They can be life-threatening at times, and they can certainly affect the quality of the patient’s life.
There are many neurological conditions and physiotherapy can help many of them.
Alzheimer’s disease takes away the declining years of many older people.
It is surprising to note that it can occur in people 40 years old or younger.
ALS or Lou Gehrig’s disease is a disease that robs the brain and spinal cord of the ability to move.
Both of these are neurological diseases that can be helped by physiotherapy.
MS, another of the neurological conditions that affects the brain and spinal cord, can lead to a long, slow decline.
Parkinson’s disease is another of the neurological conditions of the brain.
This one can cause shaking and loss of coordination, and problems moving and walking.
Physiotherapy offers some relief to these patients.
Guillain Barre Syndrome is one of the types of neurological conditions that affect the brain and spinal cord too.
It is a case of the person’s own immune system attacking outside these areas.
It can be severe enough to require emergency hospitalization. Physiotherapy offers help with regaining strength and adapting to life with the disease.
Neurological conditions that are autoimmune diseases are difficult to treat.
Myasthenia Gravis is one such illness. It causes muscular weakness because of a lack of communication between nerves and muscles.
Like other neurological conditions, it can be very debilitating. A great amount of physiotherapy is needed to help Myasthenia Gravis patients to live with their neurological conditions.
This includes strength training, training in the use of supportive devices, and help with common tasks.
One problem physiotherapists face when working with MG patients is that too much exercise will make their condition worse and not better. Many of the patients with neurological conditions cannot carry on daily functions such as caring for themselves and their homes.
It is not uncommon for these people to be unable to work. They may even have trouble walking or getting up and down stairs at all. Difficulty swallowing or breathing; dizziness, poor balance and falls, and a total lack of endurance plague many of these patients who have neurological conditions. Medications or surgeries can help with some of their problems, but many problems are ones they will have to abide.
Physiotherapy can offer solutions that other branches of medicine cannot.
Exercises, as in most physiotherapy, include strengthening and stretching exercises.
In whatever way is possible, patients with neurological conditions need to get aerobic exercise.
Physiotherapists may be able to make a plan so that this is possible.
Part of this plan for patients with neurological conditions would include balance training and coordination training. With these two skills in place, the patient will have a more advanced ability to do aerobic and other exercises. Aquatic exercise is also used.
Patients with neurological conditions must live with many problems of lack of movement and function.
Physiotherapy can help them to overcome some of these problems.It can make their lives easier and more pleasant, besides.
30 November 2009
27 November 2009
Small Update
Hey Guys,
A late happy ThanksGiving to you all, it’s been awhile. My ThanksGiving was bitter sweet at best, the food was great. I had to huge plates of food. And then my sister was helping me walk down the stairs, and my body started to get really stiff. I tried to calm down and relax. But as I made my way down, I walked as quickly as I could to a chair and that’s when a painful back spasm gripped my back.
It was tough, and it hurt so bad. Luckily I didn’t have to go to the ER. I’m okay, just really sore today. Just wanted to give you all an update. The writing is going well, slow but very well. Please keep me in your prayers.
-Brandon
A late happy ThanksGiving to you all, it’s been awhile. My ThanksGiving was bitter sweet at best, the food was great. I had to huge plates of food. And then my sister was helping me walk down the stairs, and my body started to get really stiff. I tried to calm down and relax. But as I made my way down, I walked as quickly as I could to a chair and that’s when a painful back spasm gripped my back.
It was tough, and it hurt so bad. Luckily I didn’t have to go to the ER. I’m okay, just really sore today. Just wanted to give you all an update. The writing is going well, slow but very well. Please keep me in your prayers.
-Brandon
FELDENKRAIS:THE POWER OF MOVEMENT
by Alternative.Health
Kathy James
The Feldenkrais Method® is unusual, unusually deep, subtle, and powerful. It’s a revolutionary approach to understanding how we function both physically and mentally, as well as providing tools for our improvement. So for example, if you are someone who experiences pain and have been told to exercise it is a step but it may not be enough. Our tendency to move in the same ways, guided by the same postural habits, sensory cues and mental images are strong. What an individual needs to learn is how they are moving and how their way of moving may relate to their pain or problem. Feldenkrais Practitioners are trained movement specialists, who help people move and live with greater comfort, flexibility and ease.
Before being introduced to Feldenkrais in 1975, I had spent about twenty-five years getting ready for it. I started with dancing— tap, jazz, ballet, whatever. I danced through my entire childhood, compelled by the sheer pleasure I experienced through movement. I didn’t think much about the importance of movement for health or well-being when I was young; I just knew that it made me feel good and gave me a sense of confidence.
In college I became interested in science, but continued to dance off and on. I yearned to find a way to combine the two, somehow. Then I took this workshop consisting of simple but unusual movement sequences that seemed so trivial—yet after each class I felt great! I still remember one of the classes, just turning our heads around to look behind us and then back to the front, repeating it several times. We then turned our heads while moving our eyes in the opposite direction, still very gently, repeating each movement. After a series of these strange variations, we were asked to repeat the original movement: I was shocked to discover that my range of movement had doubled with almost no effort, just be paying attention to my movement in new ways. This was my introduction to The Feldenkrais Method®.
After completing my degree in Zoology, I continued dancing, while looking for ways to integrate my two passions—scientific inquiry, and movement. When I heard about a training program with Moshe Feldenkrais, I knew that I had to do it. The four-year program began in Amherst, Massachusetts, in the summer of 1980, and culminated in Tel Aviv, Israel, where Moshe Feldenkrais lived.
That was almost thirty years ago. Today, most people have still not heard of the Feldenkrais Method®, but many folks have tried it, and have been helped by it. The Feldenkrais Method® consists of two basic forms—one on one individual sessions, called “Functional Integration®,” and group movement classes known as “Awareness Through Movement®.”
In Awareness Through Movement® classes, the Feldenkrais practitioner verbally guides people through a sequence of gentle movements. Many of these movements focus on simple daily actions such as reaching, looking behind yourself, breathing, sitting, improving balance, bending down, walking, or more complicated patterns such as yoga postures. Regardless of the specific movement, the point is always to move gently, and work at your own level.
Functional Integration® is the one-to-one, hands-on session in which the Feldenkrais practitioner and client work together to increase the client’s movement awareness and capacity, in supportive and non-invasive ways. Usually, the practitioner works with the client (fully clothed) on a low table, using gentle touch and verbal direction to guide the movement sequences that encourage new awareness and learning. The result is improved pain-free movement and improved performance in almost any area—be it sitting, walking, running, playing tennis, playing piano, gardening—whatever involves movement.
Moshe Feldenkrais was a true innovator, developing thousands of movement lessons that produce impressive changes. Worldwide there are more than 6,000 Feldenkrais Practitioners, using movement awareness to help people with all sorts of challenges, ranging from back, neck, shoulder, knee, hand or foot pain, to neurological conditions such as cerebral palsy; head injuries from accidents or strokes; chronic conditions such as chronic fatigue or fibromyalgia; to musicians and athletes who wish to improve their performance. Some practitioners have even applied their work to animals with impressive results. My favorite quote from Moshe Feldenkrais sums up our approach nicely: “To make the impossible possible, the possible easy, and the easy elegant.”
Kathy James is a Certified Feldenkrais Practitioner, in private practice in Petaluma.
Email: kathytjames@att.net
Kathy James
The Feldenkrais Method® is unusual, unusually deep, subtle, and powerful. It’s a revolutionary approach to understanding how we function both physically and mentally, as well as providing tools for our improvement. So for example, if you are someone who experiences pain and have been told to exercise it is a step but it may not be enough. Our tendency to move in the same ways, guided by the same postural habits, sensory cues and mental images are strong. What an individual needs to learn is how they are moving and how their way of moving may relate to their pain or problem. Feldenkrais Practitioners are trained movement specialists, who help people move and live with greater comfort, flexibility and ease.
Before being introduced to Feldenkrais in 1975, I had spent about twenty-five years getting ready for it. I started with dancing— tap, jazz, ballet, whatever. I danced through my entire childhood, compelled by the sheer pleasure I experienced through movement. I didn’t think much about the importance of movement for health or well-being when I was young; I just knew that it made me feel good and gave me a sense of confidence.
In college I became interested in science, but continued to dance off and on. I yearned to find a way to combine the two, somehow. Then I took this workshop consisting of simple but unusual movement sequences that seemed so trivial—yet after each class I felt great! I still remember one of the classes, just turning our heads around to look behind us and then back to the front, repeating it several times. We then turned our heads while moving our eyes in the opposite direction, still very gently, repeating each movement. After a series of these strange variations, we were asked to repeat the original movement: I was shocked to discover that my range of movement had doubled with almost no effort, just be paying attention to my movement in new ways. This was my introduction to The Feldenkrais Method®.
After completing my degree in Zoology, I continued dancing, while looking for ways to integrate my two passions—scientific inquiry, and movement. When I heard about a training program with Moshe Feldenkrais, I knew that I had to do it. The four-year program began in Amherst, Massachusetts, in the summer of 1980, and culminated in Tel Aviv, Israel, where Moshe Feldenkrais lived.
That was almost thirty years ago. Today, most people have still not heard of the Feldenkrais Method®, but many folks have tried it, and have been helped by it. The Feldenkrais Method® consists of two basic forms—one on one individual sessions, called “Functional Integration®,” and group movement classes known as “Awareness Through Movement®.”
In Awareness Through Movement® classes, the Feldenkrais practitioner verbally guides people through a sequence of gentle movements. Many of these movements focus on simple daily actions such as reaching, looking behind yourself, breathing, sitting, improving balance, bending down, walking, or more complicated patterns such as yoga postures. Regardless of the specific movement, the point is always to move gently, and work at your own level.
Functional Integration® is the one-to-one, hands-on session in which the Feldenkrais practitioner and client work together to increase the client’s movement awareness and capacity, in supportive and non-invasive ways. Usually, the practitioner works with the client (fully clothed) on a low table, using gentle touch and verbal direction to guide the movement sequences that encourage new awareness and learning. The result is improved pain-free movement and improved performance in almost any area—be it sitting, walking, running, playing tennis, playing piano, gardening—whatever involves movement.
Moshe Feldenkrais was a true innovator, developing thousands of movement lessons that produce impressive changes. Worldwide there are more than 6,000 Feldenkrais Practitioners, using movement awareness to help people with all sorts of challenges, ranging from back, neck, shoulder, knee, hand or foot pain, to neurological conditions such as cerebral palsy; head injuries from accidents or strokes; chronic conditions such as chronic fatigue or fibromyalgia; to musicians and athletes who wish to improve their performance. Some practitioners have even applied their work to animals with impressive results. My favorite quote from Moshe Feldenkrais sums up our approach nicely: “To make the impossible possible, the possible easy, and the easy elegant.”
Kathy James is a Certified Feldenkrais Practitioner, in private practice in Petaluma.
Email: kathytjames@att.net
26 November 2009
Dance Offers Key To Mobility For Actor With Cerebral Palsy
By Michelle Diament
November 25, 2009
For three decades Gregg Mozgala struggled to walk with cerebral palsy forcing his body up on its toes and wavering from side to side. But at 31, that’s all changing thanks to a choreographer.
Mozgala, an actor, has been working with Tamar Rogoff for just eight months, but is slowly gaining use of muscles and tendons that had been off-limits all his life. In intensive sessions, the two work on one area of the body at a time focusing on tension-release. Unlike physical therapists he’d seen in the past, Mozgala says Rogoff has given him the key to access his own body.
The result is that Mozgala can now walk more smoothly and doesn’t fall like he used to. And it proves what scientists have come to believe about the brain — that it’s constantly changing and able to grow.
The pair’s success is also yielding a four-person hour-long dance premiering in December in New York City, much more than the 10-minute presentation the two envisioned at first, reports The New York Times.
November 25, 2009
For three decades Gregg Mozgala struggled to walk with cerebral palsy forcing his body up on its toes and wavering from side to side. But at 31, that’s all changing thanks to a choreographer.
Mozgala, an actor, has been working with Tamar Rogoff for just eight months, but is slowly gaining use of muscles and tendons that had been off-limits all his life. In intensive sessions, the two work on one area of the body at a time focusing on tension-release. Unlike physical therapists he’d seen in the past, Mozgala says Rogoff has given him the key to access his own body.
The result is that Mozgala can now walk more smoothly and doesn’t fall like he used to. And it proves what scientists have come to believe about the brain — that it’s constantly changing and able to grow.
The pair’s success is also yielding a four-person hour-long dance premiering in December in New York City, much more than the 10-minute presentation the two envisioned at first, reports The New York Times.
25 November 2009
23 November 2009
New Isle of Wight boat for wheelchair users
Wed, 22 Apr 2009 Sally Coffey / Motor Boats Monthly
A club on the Isle of Wight has raised funds to buy a catamaran to enable people with disabilities to get on the water
The Fishbourne Sailability Club has raised funds to buy a catamaran to enable its members to get a taste of motorboating.
The Fishbourne Sailability Club was founded in 2002 to enable people with disabilities to enjoy water-based activities in both sailing and motorboats. Last year it looked into a suitable motorboat and the catamaran was chosen due to its ease of access, stability and working space.
The boat is now ready for use and to celebrate a naming ceremony will be held on Saturday 25 April at the Royal Victoria Yacht Club, Fishbourne, Isle of Wight from 12pm. The ceremony will be presided over by the High Sheriff of the Isle of Wight, Gabrielle Edwards and yachtsman, Geoff Holt.
A spokesperson from the club said, "We believe that the availability of this boat will make a real difference to many people with disabilities on the Island."
For more information call 01983 882560.
A club on the Isle of Wight has raised funds to buy a catamaran to enable people with disabilities to get on the water
The Fishbourne Sailability Club has raised funds to buy a catamaran to enable its members to get a taste of motorboating.
The Fishbourne Sailability Club was founded in 2002 to enable people with disabilities to enjoy water-based activities in both sailing and motorboats. Last year it looked into a suitable motorboat and the catamaran was chosen due to its ease of access, stability and working space.
The boat is now ready for use and to celebrate a naming ceremony will be held on Saturday 25 April at the Royal Victoria Yacht Club, Fishbourne, Isle of Wight from 12pm. The ceremony will be presided over by the High Sheriff of the Isle of Wight, Gabrielle Edwards and yachtsman, Geoff Holt.
A spokesperson from the club said, "We believe that the availability of this boat will make a real difference to many people with disabilities on the Island."
For more information call 01983 882560.
Museum wins place in guide
THE River and Rowing Museum in Henley is one of only four Oxfordshire attractions to win a place in a guide to the best visitor attractions for disabled people.
The museum, which was built 10 years ago, was designed to be fully accessible to all visitors but improvements have been made, including automatic electronic doors and programmes designed specifically for disabled people.
The Rivertime Boat Trust, which operates from the museum’s jetty, uses a specially constructed boat which can carry 12 people and is fitted with a wheelchair ramp and hydraulic lift for the disabled.
The museum also hosts Breaking Barriers, a project involving adults with sensory, physical and learning disabilities to develop new ways of learning.
It is also working with organisations including the Reading Association for the Blind and the Learning Disabilities Group in Henley to improve access, understanding and enjoyment of the galleries.
Chief executive Paul Mainds was "delighted" to be included in the Rough Guide To Accessible Britain.
He said: "It’s a great compliment, not only to our building but to our staff and the programmes we run.
The museum, which was built 10 years ago, was designed to be fully accessible to all visitors but improvements have been made, including automatic electronic doors and programmes designed specifically for disabled people.
The Rivertime Boat Trust, which operates from the museum’s jetty, uses a specially constructed boat which can carry 12 people and is fitted with a wheelchair ramp and hydraulic lift for the disabled.
The museum also hosts Breaking Barriers, a project involving adults with sensory, physical and learning disabilities to develop new ways of learning.
It is also working with organisations including the Reading Association for the Blind and the Learning Disabilities Group in Henley to improve access, understanding and enjoyment of the galleries.
Chief executive Paul Mainds was "delighted" to be included in the Rough Guide To Accessible Britain.
He said: "It’s a great compliment, not only to our building but to our staff and the programmes we run.
19 November 2009
Injection Could Help Regrow Spine, Reduce Back Pain
TheDenverChannel.com
POSTED: 6:21 pm MST November 18, 2009
About 80 percent of Americans will experience low back pain at some point in their lives.
It's the second most common reason people visit their doctors. Often, these patients have torn or ruptured discs that cause excruciating pain. But there's a new option on the horizon that could regrow healthy discs in the spine without surgery.
Rebecca Tirs spends most days curled up in bed with her pal, Jenny Bee. But this isn't how life has always been for these two.
Ten years ago, Tirs was an active 28-year-old. But then she was in a rollover car accident, where she tore two discs in her low back.
"I had a mild traumatic brain injury. I had a fractured pelvis. I had fractured scapula, fractured ribs," she said.
Tirs can barely walk. She had to quit work and give up all her favorite activities.
"It was just constant, deep down to the bone, severe pain," Tirs said. "I cried all the time."
Dr. Michael DePalma is working on a new way to heal injured backs. As part of a clinical trial, he injects growth factors, found naturally in the body, into damaged discs.
"The growth factors are that, they stimulate growth of certain tissue," said DePalma, the medical director at the VCU Spine Center in Richmond, Va.
The injection includes a growth factor called OP1, a key ingredient in the development of bone and tissue. In animals, the shot helped damaged discs grow back. Doctors say in humans, it could mean no surgery, no damage to surrounding tissue and little downtime.
"This sort of treatment may find its role in treating the disc before they get to a point beyond which only surgery is going to help," DePalma said.
Tirs doesn't know if she received a placebo or the real injection, but she noticed a slight improvement in her pain level.
"Instead of maybe an eight or a nine, I was a seven," she said.
She said every bit helps -- if it gets her one step closer to her old, vibrant self.
Researchers are still working to see if one injection is enough to ease the pain. Eligible patients have suffered lower back pain for three to six months despite physical therapy and medication.
BACKGROUND: Intervertebral discs, which form the cushions between the vertebrae of the spine and make up about a third of the spine's height, degenerate earlier than any other connective tissue in the body. When a disc degenerates, it loses height and affects the mechanics of the entire spine, possibly negatively affecting surrounding muscles and ligaments.
A major cause of back pain, research shows pain from disc degeneration affects 12 to 35 percent of the Western world, according to the journal Arthritis Research & Therapy.
"Back pain is common, and the most common source of back pain is a disc," said Michael DePalma, M.D., an interventional spine specialists at VCU Spine Center in Richmond, Va..
About 10 percent of back pain sufferers become chronically disabled. When a disc ruptures or bulges to press on a nearby nerve root, the injury is called a herniation. Experts believe some degeneration must take place before a disc herniates.
CAUSES: Aging and injury are the most common causes of disc degeneration. These factors lead to a loss of hydration in the material that makes up a disc, which ultimately leads to the loss of height. This loss of height eventually causes pressure on the nerve roots in the spine, resulting in pain.
New research suggests genes may play a larger role in back pain than once thought. A research team at the University of Alberta recently discovered eight genes linked to degeneration of discs in the lumbar region of the spine. The discovery came a year after the same team demonstrated that disc degeneration is affected in a large way by genetics.
REGENERATING DAMAGED DISCS: While medications, physical therapy and surgery can help some back patients, researchers are exploring new options for treating discs with the body's own resources. Studies examining treatments like gene therapy, stem cell therapy, cellular scaffolds and growth factor injections are underway in animals, and some in humans.
Growth factors are molecules that bind to cell membranes and activate the growth of new cells. A single injection of the growth factor OP-1 has been shown in animals to both increase the height of a disc and reduce pain, without damaging surrounding tissue. The first trial examining the treatment in humans is underway.
"This sort of treatment may find its role in treating the disc before they get to a point beyond which surgery is going to help," Dr. DePalma said.
FOR MORE INFORMATION, PLEASE CONTACT: Michael DePalma, MD
mdepalma@mcvh-vcu.edu
POSTED: 6:21 pm MST November 18, 2009
About 80 percent of Americans will experience low back pain at some point in their lives.
It's the second most common reason people visit their doctors. Often, these patients have torn or ruptured discs that cause excruciating pain. But there's a new option on the horizon that could regrow healthy discs in the spine without surgery.
Rebecca Tirs spends most days curled up in bed with her pal, Jenny Bee. But this isn't how life has always been for these two.
Ten years ago, Tirs was an active 28-year-old. But then she was in a rollover car accident, where she tore two discs in her low back.
"I had a mild traumatic brain injury. I had a fractured pelvis. I had fractured scapula, fractured ribs," she said.
Tirs can barely walk. She had to quit work and give up all her favorite activities.
"It was just constant, deep down to the bone, severe pain," Tirs said. "I cried all the time."
Dr. Michael DePalma is working on a new way to heal injured backs. As part of a clinical trial, he injects growth factors, found naturally in the body, into damaged discs.
"The growth factors are that, they stimulate growth of certain tissue," said DePalma, the medical director at the VCU Spine Center in Richmond, Va.
The injection includes a growth factor called OP1, a key ingredient in the development of bone and tissue. In animals, the shot helped damaged discs grow back. Doctors say in humans, it could mean no surgery, no damage to surrounding tissue and little downtime.
"This sort of treatment may find its role in treating the disc before they get to a point beyond which only surgery is going to help," DePalma said.
Tirs doesn't know if she received a placebo or the real injection, but she noticed a slight improvement in her pain level.
"Instead of maybe an eight or a nine, I was a seven," she said.
She said every bit helps -- if it gets her one step closer to her old, vibrant self.
Researchers are still working to see if one injection is enough to ease the pain. Eligible patients have suffered lower back pain for three to six months despite physical therapy and medication.
BACKGROUND: Intervertebral discs, which form the cushions between the vertebrae of the spine and make up about a third of the spine's height, degenerate earlier than any other connective tissue in the body. When a disc degenerates, it loses height and affects the mechanics of the entire spine, possibly negatively affecting surrounding muscles and ligaments.
A major cause of back pain, research shows pain from disc degeneration affects 12 to 35 percent of the Western world, according to the journal Arthritis Research & Therapy.
"Back pain is common, and the most common source of back pain is a disc," said Michael DePalma, M.D., an interventional spine specialists at VCU Spine Center in Richmond, Va..
About 10 percent of back pain sufferers become chronically disabled. When a disc ruptures or bulges to press on a nearby nerve root, the injury is called a herniation. Experts believe some degeneration must take place before a disc herniates.
CAUSES: Aging and injury are the most common causes of disc degeneration. These factors lead to a loss of hydration in the material that makes up a disc, which ultimately leads to the loss of height. This loss of height eventually causes pressure on the nerve roots in the spine, resulting in pain.
New research suggests genes may play a larger role in back pain than once thought. A research team at the University of Alberta recently discovered eight genes linked to degeneration of discs in the lumbar region of the spine. The discovery came a year after the same team demonstrated that disc degeneration is affected in a large way by genetics.
REGENERATING DAMAGED DISCS: While medications, physical therapy and surgery can help some back patients, researchers are exploring new options for treating discs with the body's own resources. Studies examining treatments like gene therapy, stem cell therapy, cellular scaffolds and growth factor injections are underway in animals, and some in humans.
Growth factors are molecules that bind to cell membranes and activate the growth of new cells. A single injection of the growth factor OP-1 has been shown in animals to both increase the height of a disc and reduce pain, without damaging surrounding tissue. The first trial examining the treatment in humans is underway.
"This sort of treatment may find its role in treating the disc before they get to a point beyond which surgery is going to help," Dr. DePalma said.
FOR MORE INFORMATION, PLEASE CONTACT: Michael DePalma, MD
mdepalma@mcvh-vcu.edu
18 November 2009
Independent living: A disabled man and his personal assistants
Stefano Goodman uses a wheelchair and lives independently - with the help of two personal assistants. Such uniquely intimate relationships with strangers take a bit of getting used to ...
My disability means that I need help for almost all physical activity. So, to enable me to live an independent life in my own home, I need a live-in personal assistant. Do not call them 'carers' under any circumstances. If you do, disabled people will start throwing their wheelchairs at you. Or, at least, they'll ask their PAs to do it on their behalf.
I have a couple of PAs working in three-day shifts and they usually stick around for a year. Training up and getting to know the new guys twice a year is stressful, but I have developed strategies to make these periods easier.
Living with strangers
We are in the kitchen. He asks me if I want some wine and I nod. He takes the glass, puts it between my lips and slowly starts tipping it down my throat. When I have had enough I carefully grip the glass in my teeth and gently push it down: the international sign language for 'Please don't drown me in Chilean merlot'. I can shove a computer mouse around well enough to win international design awards, but holding a wine glass is beyond my physical abilities.
I have found that the kitchen is a really good place to weigh up my new partner in this strange relationship. Strange because it resides in a grey area: too intimate to be strictly business (it's hard to think of the person helping you dry off after a bath as an employee), yet too enforced to really be friendship.
In return for bed and board and a small living allowance they have come from all over the world, for any number of reasons. I know from their passport photos what they look like, but on the first day they are strangers. Strangers who eat and sleep in my house; strangers who help me do some of the most private things possible.
Imagine getting a new lodger who, on their first night in your house, helps you undress and makes you comfortable in bed. Psychologically, that took a lot of getting used to, but now my concerns are more mundane.
The perils of shopping
I went to the supermarket with Raoul the other day, and we accidentally stole four tuna steaks and two fruit smoothies. After completely filling a basket, we used the compartment under my chair. We got to the checkout and unloaded - but we forgot the items stuffed away under me. Raoul was oblivious - when there is food within arm's reach you could take a hammer to him and he wouldn't notice - but I remembered just as he handed over the cash.
For a second, I thought I should mention it. Then, just as quickly, I reassessed the situation: sleepy edge-of-town branch; genuinely a complete accident so we hadn't acted suspiciously; very easy to play the disabled card (when they come for Raoul I could start drooling and gibbering - perhaps I should practise this for future use?). Anyway, no one noticed a thing until I mentioned it when we were in the car. He was wide-eyed for a minute, and then we both laughed.
Another day I asked Raoul if he could make a quick trip to the supermarket for toothpaste. On returning, his opening line was, "They didn't have your old one." I was immediately on alert. He continued, "But they had a special offer, buy two and get one free." With a showman's flourish, he showed me something made of ground chalk and minty wallfiller. In a family-sized tube. Well, what's the point of buying the wrong thing and then not buying it in the very largest size you can find? Instead of one tube of the toothpaste I have been using for half my life, I have three salamis of grout.
I wanted to turn into the drill instructor from Full Metal Jacket. I wanted to scream poetic, spittle-flecked invective inches from his pacific face. But it's only toothpaste and he's a good guy really. And I barely reach his midriff; asking someone to bend down so that I can insult him seems very laboured.
Anger management
Checking for 'work' emails. Illustration: Stefano Goodman
I remember the moment I knew I had a serious problem with my new PA, Zvonimir.
Near the end of his third shift he asked if I wanted a game of chess. I remembered him talking about chess before and, detecting that he was a fairly accomplished player, I had already mentally prepared myself for a nonchalant defeat. I convinced myself that I really should have been working anyway, and so any loss was going to be down to a lack of concentration.
We played and in no time he was beating me like a bad habit. Every now and again I made a show of checking for 'work' emails, emphasising the point that I was actually being polite in playing at all. I did mount one serious attack, but I knew I was doomed. At one point I made a desperate/stupid move and he stifled a deep sigh. Three moves later I resigned.
Breezily, I congratulated him and said that I really should get back to work. This didn't even register with him. He just stared at me. "Why did you do that?" he asked. I told him what my attack plan was. "I understand that," he said. "Yes, I understand that. But you knew you didn't have enough time to develop that attack." Disgust and anger laced his disappointment. He didn't blink during the whole exchange.
A few weeks later, Z left our working relationship. The agency that arranges for these placements does very thorough background and criminal history checking, but I am not sure where his anger management issues would show up on a normal application form. Z always treated me with respect and, despite his general intensity and occasional temper flare-ups, we got on OK, even if I had begun to be slightly wary of him.
There was no such (fragile) harmony back at the shared, off-shift volunteer house. Threatening behaviour to the housemates and staff at the local bank was a quick route out of the country.
Tea time
I await the first cup of tea from a new PA the way I await the first game of a new football season: anything could happen and the result will be a signpost for the season ahead, Gary.
More than two weeks in with Raoul, I still couldn't get through one of his afternoon cuppas. He noticed. "No better?" he asked. "Getting there …" I said, unconvincingly. It had taken a full week to successfully remind Raoul to let the kettle boil fully before using the water to make tea, and three or four days before that to convince him that water from the hot tap is not a substitute. "Really?" he had asked in genuine wonderment. "Really," I had said. "But it's so hot, almost too hot to touch!"
Sometimes I fantasise about buying every tealeaf and bag available, and ordering a scientific endeavour hitherto unknown to tea technology. Locking ourselves in the kitchen, we would try every possible combination of brewing time, temperature and method. Once we discovered the perfect process, I would get the PA to video it and post it on YouTube. From then on, it would be available to all the new PAs at the click of a mouse. One day, my friends, one day ...
The last supper
It's year-end for Gustav. He is a really easy-going guy and I will be sorry to see him go, even with his onion breath and addiction to pornography. Often it is very hard to say goodbye to someone who has been sharing my life for a year. Unless it has been a really difficult placement, I am genuinely sad as I see them leave for the last time. I have had intimate physical contact with them for a year, but I will probably never see again.
I offered Gustav his choice of our last meal together, as is my tradition. Secretly I hoped he would pick something that I usually forbid myself, thereby allowing me to gorge guilt-free. This gambit usually works very well, as almost every one of my PAs has had the appetite of a nursing sow. (I do not put Raoul in this bracket; his appetite is a mutant thing and belongs in a different league completely).
Unfortunately, Gustav was under pressure from his new girlfriend Ursula to become a vegetarian, and so he picked some macrobiotic stuff from a place run by people with hairy arms. I think I hid my disappointment very well, and I'm proud of the mental strength that prevented this incident souring my memory of a pretty good working relationship.
• Stefano Goodman is a pseudonym. All other names have been changed.
More information on independent living
Independent Living Alternatives
ilanet.co.uk/
National Centre for Independent Living
ncil.org.uk
Community Service Volunteers
csv.org.uk
My disability means that I need help for almost all physical activity. So, to enable me to live an independent life in my own home, I need a live-in personal assistant. Do not call them 'carers' under any circumstances. If you do, disabled people will start throwing their wheelchairs at you. Or, at least, they'll ask their PAs to do it on their behalf.
I have a couple of PAs working in three-day shifts and they usually stick around for a year. Training up and getting to know the new guys twice a year is stressful, but I have developed strategies to make these periods easier.
Living with strangers
We are in the kitchen. He asks me if I want some wine and I nod. He takes the glass, puts it between my lips and slowly starts tipping it down my throat. When I have had enough I carefully grip the glass in my teeth and gently push it down: the international sign language for 'Please don't drown me in Chilean merlot'. I can shove a computer mouse around well enough to win international design awards, but holding a wine glass is beyond my physical abilities.
I have found that the kitchen is a really good place to weigh up my new partner in this strange relationship. Strange because it resides in a grey area: too intimate to be strictly business (it's hard to think of the person helping you dry off after a bath as an employee), yet too enforced to really be friendship.
In return for bed and board and a small living allowance they have come from all over the world, for any number of reasons. I know from their passport photos what they look like, but on the first day they are strangers. Strangers who eat and sleep in my house; strangers who help me do some of the most private things possible.
Imagine getting a new lodger who, on their first night in your house, helps you undress and makes you comfortable in bed. Psychologically, that took a lot of getting used to, but now my concerns are more mundane.
The perils of shopping
I went to the supermarket with Raoul the other day, and we accidentally stole four tuna steaks and two fruit smoothies. After completely filling a basket, we used the compartment under my chair. We got to the checkout and unloaded - but we forgot the items stuffed away under me. Raoul was oblivious - when there is food within arm's reach you could take a hammer to him and he wouldn't notice - but I remembered just as he handed over the cash.
For a second, I thought I should mention it. Then, just as quickly, I reassessed the situation: sleepy edge-of-town branch; genuinely a complete accident so we hadn't acted suspiciously; very easy to play the disabled card (when they come for Raoul I could start drooling and gibbering - perhaps I should practise this for future use?). Anyway, no one noticed a thing until I mentioned it when we were in the car. He was wide-eyed for a minute, and then we both laughed.
Another day I asked Raoul if he could make a quick trip to the supermarket for toothpaste. On returning, his opening line was, "They didn't have your old one." I was immediately on alert. He continued, "But they had a special offer, buy two and get one free." With a showman's flourish, he showed me something made of ground chalk and minty wallfiller. In a family-sized tube. Well, what's the point of buying the wrong thing and then not buying it in the very largest size you can find? Instead of one tube of the toothpaste I have been using for half my life, I have three salamis of grout.
I wanted to turn into the drill instructor from Full Metal Jacket. I wanted to scream poetic, spittle-flecked invective inches from his pacific face. But it's only toothpaste and he's a good guy really. And I barely reach his midriff; asking someone to bend down so that I can insult him seems very laboured.
Anger management
Checking for 'work' emails. Illustration: Stefano Goodman
I remember the moment I knew I had a serious problem with my new PA, Zvonimir.
Near the end of his third shift he asked if I wanted a game of chess. I remembered him talking about chess before and, detecting that he was a fairly accomplished player, I had already mentally prepared myself for a nonchalant defeat. I convinced myself that I really should have been working anyway, and so any loss was going to be down to a lack of concentration.
We played and in no time he was beating me like a bad habit. Every now and again I made a show of checking for 'work' emails, emphasising the point that I was actually being polite in playing at all. I did mount one serious attack, but I knew I was doomed. At one point I made a desperate/stupid move and he stifled a deep sigh. Three moves later I resigned.
Breezily, I congratulated him and said that I really should get back to work. This didn't even register with him. He just stared at me. "Why did you do that?" he asked. I told him what my attack plan was. "I understand that," he said. "Yes, I understand that. But you knew you didn't have enough time to develop that attack." Disgust and anger laced his disappointment. He didn't blink during the whole exchange.
A few weeks later, Z left our working relationship. The agency that arranges for these placements does very thorough background and criminal history checking, but I am not sure where his anger management issues would show up on a normal application form. Z always treated me with respect and, despite his general intensity and occasional temper flare-ups, we got on OK, even if I had begun to be slightly wary of him.
There was no such (fragile) harmony back at the shared, off-shift volunteer house. Threatening behaviour to the housemates and staff at the local bank was a quick route out of the country.
Tea time
I await the first cup of tea from a new PA the way I await the first game of a new football season: anything could happen and the result will be a signpost for the season ahead, Gary.
More than two weeks in with Raoul, I still couldn't get through one of his afternoon cuppas. He noticed. "No better?" he asked. "Getting there …" I said, unconvincingly. It had taken a full week to successfully remind Raoul to let the kettle boil fully before using the water to make tea, and three or four days before that to convince him that water from the hot tap is not a substitute. "Really?" he had asked in genuine wonderment. "Really," I had said. "But it's so hot, almost too hot to touch!"
Sometimes I fantasise about buying every tealeaf and bag available, and ordering a scientific endeavour hitherto unknown to tea technology. Locking ourselves in the kitchen, we would try every possible combination of brewing time, temperature and method. Once we discovered the perfect process, I would get the PA to video it and post it on YouTube. From then on, it would be available to all the new PAs at the click of a mouse. One day, my friends, one day ...
The last supper
It's year-end for Gustav. He is a really easy-going guy and I will be sorry to see him go, even with his onion breath and addiction to pornography. Often it is very hard to say goodbye to someone who has been sharing my life for a year. Unless it has been a really difficult placement, I am genuinely sad as I see them leave for the last time. I have had intimate physical contact with them for a year, but I will probably never see again.
I offered Gustav his choice of our last meal together, as is my tradition. Secretly I hoped he would pick something that I usually forbid myself, thereby allowing me to gorge guilt-free. This gambit usually works very well, as almost every one of my PAs has had the appetite of a nursing sow. (I do not put Raoul in this bracket; his appetite is a mutant thing and belongs in a different league completely).
Unfortunately, Gustav was under pressure from his new girlfriend Ursula to become a vegetarian, and so he picked some macrobiotic stuff from a place run by people with hairy arms. I think I hid my disappointment very well, and I'm proud of the mental strength that prevented this incident souring my memory of a pretty good working relationship.
• Stefano Goodman is a pseudonym. All other names have been changed.
More information on independent living
Independent Living Alternatives
ilanet.co.uk/
National Centre for Independent Living
ncil.org.uk
Community Service Volunteers
csv.org.uk
Nintendo Turns Rehab Into "Wii-Hab"
Hardcore gamers may be fond of looking down on the Nintendo Wii and things like Wii Fit, but more and more physical therapists are discovering the platform's genuine medical applications.
Sometimes, surgery is necessary to save someone's life - or at least to save their health and comfort - but it can be a long and painful road to recovery. Doctors and physicians have been trying to make the rehabilitation process easier on patients for years, so when Wii Fit came along, some of them saw the opportunity to literally make rehab a game, as Lauren Admire writes in Issue 227 of The Escapist.
Since beginning the program in 2008, nearly 200 patients have taken part in this special Wii-hab therapy. Though Wii-hab doesn't replace traditional methods, it certainly helps break up the monotony of traditional physical therapy exercises. The buttons of the controller help patients with their small motor skills, while the swinging and flicking motions many games employ help with hand-eye coordination. Games that support the Wii Balance Board also assist with balance, core strengthening and even retraining muscles.
Jamie Weinman is a recent survivor of a brain tumor. After her tumor was removed, the entire left side of her body was affected. She's been using Wii-hab to help with her balance and coordination. "It's more fun because you don't feel like it's therapy," she reports to CNET, "[Wii-hab] helped my leg get stronger, it helped me with my balance and coordination. The more you use it, the better you get, and it gets you excited to do it again because I'm trying to beat my last score."
Sometimes, surgery is necessary to save someone's life - or at least to save their health and comfort - but it can be a long and painful road to recovery. Doctors and physicians have been trying to make the rehabilitation process easier on patients for years, so when Wii Fit came along, some of them saw the opportunity to literally make rehab a game, as Lauren Admire writes in Issue 227 of The Escapist.
Since beginning the program in 2008, nearly 200 patients have taken part in this special Wii-hab therapy. Though Wii-hab doesn't replace traditional methods, it certainly helps break up the monotony of traditional physical therapy exercises. The buttons of the controller help patients with their small motor skills, while the swinging and flicking motions many games employ help with hand-eye coordination. Games that support the Wii Balance Board also assist with balance, core strengthening and even retraining muscles.
Jamie Weinman is a recent survivor of a brain tumor. After her tumor was removed, the entire left side of her body was affected. She's been using Wii-hab to help with her balance and coordination. "It's more fun because you don't feel like it's therapy," she reports to CNET, "[Wii-hab] helped my leg get stronger, it helped me with my balance and coordination. The more you use it, the better you get, and it gets you excited to do it again because I'm trying to beat my last score."
17 November 2009
Wrap Up a Wish: Hopes for greater mobility
Published online on Monday, Nov. 16, 2009
By Ron Orozco / The Fresno Bee
About the series
The wish: Criselda Ruiz wishes for an EasyStand Magician chair. Cost: $2,236
How to help: For the 17th year, The Fresno Bee, in partnership with the United Ways of Fresno, Tulare and Madera counties, is publishing Wrap Up a Wish, a series of stories about families, individuals and organizations with special needs -- and inviting readers to help with cash contributions. It's The Bee's hope that you, after reading these stories, will help make your neighbors' wishes come true. Just use a coupon that will appear inside The Bee through Dec. 10 to designate the recipient of your donation. On Christmas Eve, we'll follow up with a report on your response to Wrap Up a Wish.
Criselda Ruiz is the mother of seven children, including two sets of twins. She says she loves all her children the same but devotes quite a bit of attention to Janessa, 7. Janessa has cerebral palsy. All the other children, ages 2 to 13, are healthy, including Janessa's twin, Jonathan.
At 6 months old, Janessa began hemorrhaging. Doctors diagnosed her with cerebral palsy, a disorder resulting from damage to the brain that can affect coordination and muscle movement.
She wears leg braces and can't walk. She speaks just a handful of words, including "agua."
"I still love her either way," Ruiz says, tears welling in her eyes. "She's my special kid." The doctors told Ruiz that Janessa needed to sit up on her own by age 5. Otherwise, it may be harder for her to eventually walk on her own.
Sitting up hasn't happened yet -- and that concerns Ruiz.
Doctors believe an EasyStand Magician, a system that helps support a child in sitting and standing positions and can be easily moved, could help the girl. The device costs more that $2,000.
Ruiz's income is limited to $486 she receives monthly from Fresno County to care for Janessa. She lives in government-subsidized housing and receives food stamps.
"It's hard every month," says Ruiz, who has been separated from her husband for six months. "After all the bills are paid, there's a little left."
Janessa previously attended Storey Elementary School, which offered therapy programs suited for her. For a while, she needed the help of oxygen tanks. She now is in the second grade at Lane Elementary School.
Ruiz says Janessa is constant with her smile. "She is always happy," Ruiz says, adding that she is hopeful that Janessa will be able to walk.
"I pray for her all the time."
The reporter can be reached at rorozco@fresnobee.com or (559) 441-6304.
By Ron Orozco / The Fresno Bee
About the series
The wish: Criselda Ruiz wishes for an EasyStand Magician chair. Cost: $2,236
How to help: For the 17th year, The Fresno Bee, in partnership with the United Ways of Fresno, Tulare and Madera counties, is publishing Wrap Up a Wish, a series of stories about families, individuals and organizations with special needs -- and inviting readers to help with cash contributions. It's The Bee's hope that you, after reading these stories, will help make your neighbors' wishes come true. Just use a coupon that will appear inside The Bee through Dec. 10 to designate the recipient of your donation. On Christmas Eve, we'll follow up with a report on your response to Wrap Up a Wish.
Criselda Ruiz is the mother of seven children, including two sets of twins. She says she loves all her children the same but devotes quite a bit of attention to Janessa, 7. Janessa has cerebral palsy. All the other children, ages 2 to 13, are healthy, including Janessa's twin, Jonathan.
At 6 months old, Janessa began hemorrhaging. Doctors diagnosed her with cerebral palsy, a disorder resulting from damage to the brain that can affect coordination and muscle movement.
She wears leg braces and can't walk. She speaks just a handful of words, including "agua."
"I still love her either way," Ruiz says, tears welling in her eyes. "She's my special kid." The doctors told Ruiz that Janessa needed to sit up on her own by age 5. Otherwise, it may be harder for her to eventually walk on her own.
Sitting up hasn't happened yet -- and that concerns Ruiz.
Doctors believe an EasyStand Magician, a system that helps support a child in sitting and standing positions and can be easily moved, could help the girl. The device costs more that $2,000.
Ruiz's income is limited to $486 she receives monthly from Fresno County to care for Janessa. She lives in government-subsidized housing and receives food stamps.
"It's hard every month," says Ruiz, who has been separated from her husband for six months. "After all the bills are paid, there's a little left."
Janessa previously attended Storey Elementary School, which offered therapy programs suited for her. For a while, she needed the help of oxygen tanks. She now is in the second grade at Lane Elementary School.
Ruiz says Janessa is constant with her smile. "She is always happy," Ruiz says, adding that she is hopeful that Janessa will be able to walk.
"I pray for her all the time."
The reporter can be reached at rorozco@fresnobee.com or (559) 441-6304.
Conjoined twins op 'successful'
An operation lasting over 24 hours to separate conjoined twins has been successful, say doctors in Australia.
Bangladeshi twins Trishna and Krishna, who are nearly three years old, were joined at the top of the head.
On Tuesday, Chief of Surgery Leo Donnan said both girls were "doing well" following the surgery at the Royal Children's Hospital in Melbourne.
The still photographs of the girls were taken before separation
Watch here
Bangladeshi twins Trishna and Krishna, who are nearly three years old, were joined at the top of the head.
On Tuesday, Chief of Surgery Leo Donnan said both girls were "doing well" following the surgery at the Royal Children's Hospital in Melbourne.
The still photographs of the girls were taken before separation
Watch here
16 November 2009
We found we were not alone
Your world is turned on its head and suddenly even the everyday tasks that we all take for granted become so much harder.
She and husband, Bernard, are full-time carers for their grandson, Kyle.
The 12-year-old has cerebral palsy, epilepsy, asthma, global development delay and learning difficulties.
“Caring for a disabled child you tend not to go out and about as much,” says Mary, 61.
She considers the family lucky as Kyle is mobile, but she says: “People whose children are severely disabled can find it difficult to even go on the bus - simple things that we take for granted.”
That is why the Middlesbrough couple decided to join Parents 4 Change, a network that brings together parents, carers and service users to share their experiences and work alongside the professionals to find solutions to everyday challenges.
“We have learned an awful lot about different disabilities and how people cope,” says Mary. “It makes you feel as though you are not alone and it puts your own child’s disabilities into perspective.”
She and husband, Bernard, are full-time carers for their grandson, Kyle.
The 12-year-old has cerebral palsy, epilepsy, asthma, global development delay and learning difficulties.
“Caring for a disabled child you tend not to go out and about as much,” says Mary, 61.
She considers the family lucky as Kyle is mobile, but she says: “People whose children are severely disabled can find it difficult to even go on the bus - simple things that we take for granted.”
That is why the Middlesbrough couple decided to join Parents 4 Change, a network that brings together parents, carers and service users to share their experiences and work alongside the professionals to find solutions to everyday challenges.
“We have learned an awful lot about different disabilities and how people cope,” says Mary. “It makes you feel as though you are not alone and it puts your own child’s disabilities into perspective.”
15 November 2009
Hydrocephalus can create balance issues for older adults
Published: Saturday, November 7, 2009
Submitted by Dr. Alis Vidinas
While you may not be familiar with hydrocephalus, chances are at some time you’ve heard the phrase “water on the brain.” This used to be what hydrocephalus was known as -- although the “water” was actually cerebrospinal fluid, which surrounds the brain and spinal cord. This fluid is what cushions our brains. But too much of it may result in dangerous pressure on the brain tissues and negatively affect how the brain works.
Some individuals are born with hydrocephalus, others develop it. Normal pressure hydrocephalus is the form that occurs most often among older adults. It can be brought on by any one of a number of factors, such as a head injury, an infection, surgery or a brain hemorrhage. Sometimes, there’s no apparent cause. If a cause can be determined and corrected, however, symptoms may improve.
As the condition progresses, the symptoms become more pronounced. In the early stages there may be changes in how the individual walks and in their ability to walk. Legs may feel weak, and the person may fall without warning.
The National Institute of Neurological Disorders and Stroke lists other possible symptoms of normal pressure hydrocephalus as headache followed by vomiting, nausea, problems with balance, poor coordination, urinary incontinence, lethargy, drowsiness, irritability or other changes in personality or cognition, including memory loss. These symptoms, and others, can vary with age, disease progression and each person’s tolerance for the condition.
Many of these symptoms also occur with other illnesses that affect seniors, such as Alzheimer’s and Parkinson’s diseases. Because of this, normal pressure hydrocephalus may be misdiagnosed. Among the tests that may be used to determine whether an individual has this condition are CT scan, MRI, spinal tap and neuropsychological exams. These tests can also rule other health issues in or out. The determination of which test or tests to use varies between individuals and will depend on a number of factors such as their age, symptoms and physical condition.
There are treatment options for persons with hydrocephalus. The most common one is a shunt, or tube, that’s placed in the brain during surgery. The excess fluid is moved away from the brain and absorbed into the circulatory system. It’s important for the patient to continue to see his or her physician regularly after undergoing this procedure to ensure that no infection has set in and that the shunt is working properly and that no adjustments are needed.
How well a patient recovers can depend on how far the condition has progressed and, of course, how well they respond to the treatment. Some people respond extremely well. As with other conditions and illnesses, early detection and intervention is important to eventual recovery. Left untreated, the symptoms generally worsen and lead to death.
When should an individual seek medical attention? It’s always important to be aware of changes to your overall health. Changes in balance, coordination and memory are among those that should be brought to your health care provider’s attention. They could be a symptom of normal pressure hydrocephalus or an indication there’s another issue that needs to be treated. Abrupt changes in someone’s level of awareness or overall mental state require immediate medical attention, and 911 should be called or the person should be taken to an emergency room.
Alis Vidinas, M.D., is a family practitioner at the Henry Ford Medical Center-Fairlane in Dearborn. For an appointment call (800) HENRYFORD.
Submitted by Dr. Alis Vidinas
While you may not be familiar with hydrocephalus, chances are at some time you’ve heard the phrase “water on the brain.” This used to be what hydrocephalus was known as -- although the “water” was actually cerebrospinal fluid, which surrounds the brain and spinal cord. This fluid is what cushions our brains. But too much of it may result in dangerous pressure on the brain tissues and negatively affect how the brain works.
Some individuals are born with hydrocephalus, others develop it. Normal pressure hydrocephalus is the form that occurs most often among older adults. It can be brought on by any one of a number of factors, such as a head injury, an infection, surgery or a brain hemorrhage. Sometimes, there’s no apparent cause. If a cause can be determined and corrected, however, symptoms may improve.
As the condition progresses, the symptoms become more pronounced. In the early stages there may be changes in how the individual walks and in their ability to walk. Legs may feel weak, and the person may fall without warning.
The National Institute of Neurological Disorders and Stroke lists other possible symptoms of normal pressure hydrocephalus as headache followed by vomiting, nausea, problems with balance, poor coordination, urinary incontinence, lethargy, drowsiness, irritability or other changes in personality or cognition, including memory loss. These symptoms, and others, can vary with age, disease progression and each person’s tolerance for the condition.
Many of these symptoms also occur with other illnesses that affect seniors, such as Alzheimer’s and Parkinson’s diseases. Because of this, normal pressure hydrocephalus may be misdiagnosed. Among the tests that may be used to determine whether an individual has this condition are CT scan, MRI, spinal tap and neuropsychological exams. These tests can also rule other health issues in or out. The determination of which test or tests to use varies between individuals and will depend on a number of factors such as their age, symptoms and physical condition.
There are treatment options for persons with hydrocephalus. The most common one is a shunt, or tube, that’s placed in the brain during surgery. The excess fluid is moved away from the brain and absorbed into the circulatory system. It’s important for the patient to continue to see his or her physician regularly after undergoing this procedure to ensure that no infection has set in and that the shunt is working properly and that no adjustments are needed.
How well a patient recovers can depend on how far the condition has progressed and, of course, how well they respond to the treatment. Some people respond extremely well. As with other conditions and illnesses, early detection and intervention is important to eventual recovery. Left untreated, the symptoms generally worsen and lead to death.
When should an individual seek medical attention? It’s always important to be aware of changes to your overall health. Changes in balance, coordination and memory are among those that should be brought to your health care provider’s attention. They could be a symptom of normal pressure hydrocephalus or an indication there’s another issue that needs to be treated. Abrupt changes in someone’s level of awareness or overall mental state require immediate medical attention, and 911 should be called or the person should be taken to an emergency room.
Alis Vidinas, M.D., is a family practitioner at the Henry Ford Medical Center-Fairlane in Dearborn. For an appointment call (800) HENRYFORD.
Study looks at whether back braces offer benefit for scoliosis
ST. LOUIS POST-DISPATCH
11/12/2009
Scoliosis screenings in middle schools find thousands of teenagers with curved spines each year.
What happens next isn't as well planned.
Treatment for scoliosis hasn't changed in five decades — if the spine is curved to a certain degree, the teenager gets a back brace. But research has not conclusively proved the benefits of the braces.
Some young people who don't wear a brace never have any problems and their curves never worsen. Others wear the braces for years and still end up needing back surgery.
A long-term study at Washington University and more than 20 other research centers hopes to figure out why.
"If we can say that bracing doesn't change (the progression of a spinal curve) then it's a treatment regimen that we shouldn't offer," said Dr. Matthew Dobbs, a pediatric orthopedic surgeon and lead investigator at Washington University. "Why do school screenings? Why identify a child with a small curve and put them through years of bracing if it's not going to alter natural curve?"
Half of the participants in the study will receive back braces to wear at least 18 hours a day, and the other half won't wear braces. Both groups will receive regular X-rays to check their spinal curves.
Braces aren't thought to correct the curves but to prevent progression.
"But again we have no data to support that, despite all of us doing this for years and years and years," Dobbs said. "We don't know what the best treatment is; we don't know who's going to progress."
Curves that progress to 50 degrees — about 10 percent of cases — are generally thought to require spinal fusion surgery.
Dobbs predicts the research will show that certain patients benefit from bracing and others don't, depending on the type of spinal curve.
Adolescent idiopathic scoliosis occurs in about one in 1,000 teenagers, and is 10 times more common in girls. It can cause back pain, and in severe cases can affect heart and lung function.
The cause is unknown, although Dobbs and other researchers are studying the disorder's genetic factors.
Most states conduct scoliosis screenings by checking students' backs, typically in sixth and eighth grades. The Missouri health department estimates that 84 percent of schools voluntarily perform the checks. A bill working through the Illinois legislature would require the checks.
Smaller spinal curves are typically monitored by a doctor, but patients whose curves reach between 20 and 40 degrees are usually recommended for back braces.
If it's found that fewer teens need braces, the research could save money on treatments plus spare some teenagers the psychological stress of wearing a brace.
Braces are "mostly put on young teenage girls who are very concerned about appearance in general and don't want anything that makes them look different," Dobbs said.
That's why patients in the study are also monitored psychologically to see how they're handling the brace.
"If we see a child in the study who dips on their mood and mental health during the study, we need to figure out what's going on," Dobbs said.
Kelli Sargent of Belleview, Mo., has worn a brace for 20 hours every day since January, after doctors measured a 27-degree curve in her spine.
The seventh-grader hasn't let scoliosis keep her from activities including volleyball and basketball, which she plays without the brace.
But starting middle school this fall was sometimes tough when new kids asked Kelli about the brace. She also had to start changing for gym class, making it obvious that she wears it.
But "if you just act like it's no big deal," then other kids will too, she said.
Kelli does have a difficult time picking up books from the bottom of her locker and tying her shoes, because the brace can dig into her upper thighs when she bends. And now she has to buy jeans and tops a little bit bigger to fit over the brace.
Otherwise, she's gotten used to it and even nicknamed the brace "Shelly" since it feels like she's wearing a shell.
11/12/2009
Scoliosis screenings in middle schools find thousands of teenagers with curved spines each year.
What happens next isn't as well planned.
Treatment for scoliosis hasn't changed in five decades — if the spine is curved to a certain degree, the teenager gets a back brace. But research has not conclusively proved the benefits of the braces.
Some young people who don't wear a brace never have any problems and their curves never worsen. Others wear the braces for years and still end up needing back surgery.
A long-term study at Washington University and more than 20 other research centers hopes to figure out why.
"If we can say that bracing doesn't change (the progression of a spinal curve) then it's a treatment regimen that we shouldn't offer," said Dr. Matthew Dobbs, a pediatric orthopedic surgeon and lead investigator at Washington University. "Why do school screenings? Why identify a child with a small curve and put them through years of bracing if it's not going to alter natural curve?"
Half of the participants in the study will receive back braces to wear at least 18 hours a day, and the other half won't wear braces. Both groups will receive regular X-rays to check their spinal curves.
Braces aren't thought to correct the curves but to prevent progression.
"But again we have no data to support that, despite all of us doing this for years and years and years," Dobbs said. "We don't know what the best treatment is; we don't know who's going to progress."
Curves that progress to 50 degrees — about 10 percent of cases — are generally thought to require spinal fusion surgery.
Dobbs predicts the research will show that certain patients benefit from bracing and others don't, depending on the type of spinal curve.
Adolescent idiopathic scoliosis occurs in about one in 1,000 teenagers, and is 10 times more common in girls. It can cause back pain, and in severe cases can affect heart and lung function.
The cause is unknown, although Dobbs and other researchers are studying the disorder's genetic factors.
Most states conduct scoliosis screenings by checking students' backs, typically in sixth and eighth grades. The Missouri health department estimates that 84 percent of schools voluntarily perform the checks. A bill working through the Illinois legislature would require the checks.
Smaller spinal curves are typically monitored by a doctor, but patients whose curves reach between 20 and 40 degrees are usually recommended for back braces.
If it's found that fewer teens need braces, the research could save money on treatments plus spare some teenagers the psychological stress of wearing a brace.
Braces are "mostly put on young teenage girls who are very concerned about appearance in general and don't want anything that makes them look different," Dobbs said.
That's why patients in the study are also monitored psychologically to see how they're handling the brace.
"If we see a child in the study who dips on their mood and mental health during the study, we need to figure out what's going on," Dobbs said.
Kelli Sargent of Belleview, Mo., has worn a brace for 20 hours every day since January, after doctors measured a 27-degree curve in her spine.
The seventh-grader hasn't let scoliosis keep her from activities including volleyball and basketball, which she plays without the brace.
But starting middle school this fall was sometimes tough when new kids asked Kelli about the brace. She also had to start changing for gym class, making it obvious that she wears it.
But "if you just act like it's no big deal," then other kids will too, she said.
Kelli does have a difficult time picking up books from the bottom of her locker and tying her shoes, because the brace can dig into her upper thighs when she bends. And now she has to buy jeans and tops a little bit bigger to fit over the brace.
Otherwise, she's gotten used to it and even nicknamed the brace "Shelly" since it feels like she's wearing a shell.
14 November 2009
Gene Therapy Technique Slows Brain Disease - Health News - redOrbit
These findings appear in the November 6, 2009 issue of the journal Science, which is published by AAAS, the nonprofit science society.
In a pilot study of two patients monitored for two years, an international team of researchers slowed the onset of the debilitating brain disease X-linked adrenoleukodystrophy (ALD) using a lentiviral vector to introduce a therapeutic gene into patient's blood cells. Although studies with larger cohorts of patients are needed, these results suggest that gene therapy with lentiviral vectors, which are derived from disabled versions of human immunodeficiency virus (HIV), could potentially become instrumental in treating a broad range of human disorders.
Gene Therapy Technique Slows Brain Disease - Health News - redOrbit
In a pilot study of two patients monitored for two years, an international team of researchers slowed the onset of the debilitating brain disease X-linked adrenoleukodystrophy (ALD) using a lentiviral vector to introduce a therapeutic gene into patient's blood cells. Although studies with larger cohorts of patients are needed, these results suggest that gene therapy with lentiviral vectors, which are derived from disabled versions of human immunodeficiency virus (HIV), could potentially become instrumental in treating a broad range of human disorders.
Gene Therapy Technique Slows Brain Disease - Health News - redOrbit
Wheelchair-user makes council move meetings (From Darlington and Stockton Times)
HURWORTH Parish Council came down in the world this week – in order to comply with the law and out of courtesy to a wheelchair-user.
The decision to meet in a ground-floor room in the Grange Community Centre was readily agreed to after a request by villager Anthony Coates.
Wheelchair-user makes council move meetings (From Darlington and Stockton Times)
The decision to meet in a ground-floor room in the Grange Community Centre was readily agreed to after a request by villager Anthony Coates.
Wheelchair-user makes council move meetings (From Darlington and Stockton Times)
12 November 2009
Accepting Your Disability - Disabilities
Living your life with a disability isn't easy, but not everything in life is easy, is it? Some of us with disabilities were born with challenges. Others acquired their disabilities through injuries, particular veterans coming back from combat. Still others are finding the disability experience through the symptoms of an illness, such as multiple sclerosis, arthritis, chronic fatigue syndrome and others.
Accepting Your Disability - Disabilities
Accepting Your Disability - Disabilities
New brain findings on dyslexic children
Good readers learn from repeating auditory signals, poor readers do not
The vast majority of school-aged children can focus on the voice of a teacher amid the cacophony of the typical classroom thanks to a brain that automatically focuses on relevant, predictable and repeating auditory information, according to new research from Northwestern University.
But for children with developmental dyslexia, the teacher’s voice may get lost in the background noise of banging lockers, whispering children, playground screams and scraping chairs, the researchers say. Their study appears in the Nov. 12 issue of Neuron.
Recent scientific studies suggest that children with developmental dyslexia — a neurological disorder affecting reading and spelling skills in 5 to 10 percent of school aged children — have difficulties separating relevant auditory information from competing noise.
The research from Northwestern University’s Auditory Neuroscience Laboratory not only confirms those findings but presents biological evidence that children who report problems hearing speech in noise also suffer from a measurable neural impairment that adversely affects their ability to make use of regularities in the sound environment.
“The ability to sharpen or fine-tune repeating elements is crucial to hearing speech in noise because it allows for superior ‘tagging’ of voice pitch, an important cue in picking out a particular voice within background noise,” said Nina Kraus, Hugh Knowles Professor of Communication Sciences and Neurobiology and director of the Auditory Neuroscience Laboratory.
In the article “Context-dependent encoding in the human auditory brainstem relates to hearing speech-in-noise: Implications for developmental dyslexia,” Kraus and co-investigators Bharath Chandrasekaran, Jane Hornickel, Erika Skoe and Trent Nicol demonstrate that the remarkable ability of the brain to tune into relevant aspects in the soundscape is carried out by an adaptive auditory system that continuously changes its activity based on the demands of context.
Good and poor readers were asked to watch a video while the speech sound “da” was presented to them through an earphone in two different sessions during which the brain’s response to these sounds was continuously measured.
In the first session, “da” was repeated over and over and over again (in what the researchers call a repetitive context). In the second, “da” was presented randomly amid other speech sounds (in what the researchers call a variable context). In an additional session, the researchers performed behavioral tests in which the children were asked to repeat sentences that were presented to them amid increasing degrees of noise.
“Even though the children’s attention was focused on a movie, the auditory system of the good readers ‘tuned in’ to the repeatedly presented speech sound context and sharpened the sound’s encoding. In contrast, poor readers did not show an improvement in encoding with repetition,” said Chandrasekaran, lead author of the study. “We also found that children who had an adaptive auditory system performed better on the behavioral tests that required them to perceive speech in noisy backgrounds.”
The study suggests that in addition to conventional reading and spelling based interventions, poor readers who have difficulties processing information in noisy backgrounds could benefit from the employment of relatively simple strategies, such as placing the child in front of the teacher or using wireless technologies to enhance the sound of a teacher’s voice for an individual student.
Interestingly, the researchers found that dyslexic children showed enhanced brain activity in the variable condition. This may enable dyslexic children to represent their sensory environment in a broader and arguably more creative manner, although at the cost of the ability to exclude irrelevant signals (e.g. noise).
“The study brings us closer to understanding sensory processing in children who experience difficulty excluding irrelevant noise. It provides an objective index that can help in the assessment of children with reading problems,” Kraus says.
For nearly two decades, Kraus has been trying to determine why some children with good hearing have difficulties learning to read and spell while others do not. Early in her work, because the deficits she was exploring related to the complex processes of reading and writing, Kraus studied how the cortex — the part of the brain responsible for thinking –encoded sounds. She and her colleagues now understand that problems associated with the encoding of sound also can occur in lower perceptual structures.
Northwestern University
The vast majority of school-aged children can focus on the voice of a teacher amid the cacophony of the typical classroom thanks to a brain that automatically focuses on relevant, predictable and repeating auditory information, according to new research from Northwestern University.
But for children with developmental dyslexia, the teacher’s voice may get lost in the background noise of banging lockers, whispering children, playground screams and scraping chairs, the researchers say. Their study appears in the Nov. 12 issue of Neuron.
Recent scientific studies suggest that children with developmental dyslexia — a neurological disorder affecting reading and spelling skills in 5 to 10 percent of school aged children — have difficulties separating relevant auditory information from competing noise.
The research from Northwestern University’s Auditory Neuroscience Laboratory not only confirms those findings but presents biological evidence that children who report problems hearing speech in noise also suffer from a measurable neural impairment that adversely affects their ability to make use of regularities in the sound environment.
“The ability to sharpen or fine-tune repeating elements is crucial to hearing speech in noise because it allows for superior ‘tagging’ of voice pitch, an important cue in picking out a particular voice within background noise,” said Nina Kraus, Hugh Knowles Professor of Communication Sciences and Neurobiology and director of the Auditory Neuroscience Laboratory.
In the article “Context-dependent encoding in the human auditory brainstem relates to hearing speech-in-noise: Implications for developmental dyslexia,” Kraus and co-investigators Bharath Chandrasekaran, Jane Hornickel, Erika Skoe and Trent Nicol demonstrate that the remarkable ability of the brain to tune into relevant aspects in the soundscape is carried out by an adaptive auditory system that continuously changes its activity based on the demands of context.
Good and poor readers were asked to watch a video while the speech sound “da” was presented to them through an earphone in two different sessions during which the brain’s response to these sounds was continuously measured.
In the first session, “da” was repeated over and over and over again (in what the researchers call a repetitive context). In the second, “da” was presented randomly amid other speech sounds (in what the researchers call a variable context). In an additional session, the researchers performed behavioral tests in which the children were asked to repeat sentences that were presented to them amid increasing degrees of noise.
“Even though the children’s attention was focused on a movie, the auditory system of the good readers ‘tuned in’ to the repeatedly presented speech sound context and sharpened the sound’s encoding. In contrast, poor readers did not show an improvement in encoding with repetition,” said Chandrasekaran, lead author of the study. “We also found that children who had an adaptive auditory system performed better on the behavioral tests that required them to perceive speech in noisy backgrounds.”
The study suggests that in addition to conventional reading and spelling based interventions, poor readers who have difficulties processing information in noisy backgrounds could benefit from the employment of relatively simple strategies, such as placing the child in front of the teacher or using wireless technologies to enhance the sound of a teacher’s voice for an individual student.
Interestingly, the researchers found that dyslexic children showed enhanced brain activity in the variable condition. This may enable dyslexic children to represent their sensory environment in a broader and arguably more creative manner, although at the cost of the ability to exclude irrelevant signals (e.g. noise).
“The study brings us closer to understanding sensory processing in children who experience difficulty excluding irrelevant noise. It provides an objective index that can help in the assessment of children with reading problems,” Kraus says.
For nearly two decades, Kraus has been trying to determine why some children with good hearing have difficulties learning to read and spell while others do not. Early in her work, because the deficits she was exploring related to the complex processes of reading and writing, Kraus studied how the cortex — the part of the brain responsible for thinking –encoded sounds. She and her colleagues now understand that problems associated with the encoding of sound also can occur in lower perceptual structures.
Northwestern University
11 November 2009
Cord Blood Reverses Cerebral Palsy in Colorado Girl - Incredible Health - FOXNews.com
Chloe Levine was born seemingly perfect — she was the happy and healthy baby her parents had dreamed of.
But by the time she was 9 months old, Chloe was not reaching the milestones her older sister Shayla had met at that age.
Cord Blood Reverses Cerebral Palsy in Colorado Girl - Incredible Health - FOXNews.com
But by the time she was 9 months old, Chloe was not reaching the milestones her older sister Shayla had met at that age.
Cord Blood Reverses Cerebral Palsy in Colorado Girl - Incredible Health - FOXNews.com
The Bi-College News Online » Blog Archive » What Does It Mean to “Be” Autism?
The world of autism often seems like a theater filled with people and deprived of oxygen—nearly any noise is treated like shouts of “fire.”
So the media covered the latest controversy—a video produced for Autism Speaks, the nation’s largest autism advocacy group – like any other episode in the decades-long saga to understand the mysterious disorder. But this debate differs fundamentally from those surrounding the role of vaccines or genetics in contributing to autism—those contest science, while this contests the core identity of what it means to live with autism
The Bi-College News Online » Blog Archive » What Does It Mean to “Be” Autism?
So the media covered the latest controversy—a video produced for Autism Speaks, the nation’s largest autism advocacy group – like any other episode in the decades-long saga to understand the mysterious disorder. But this debate differs fundamentally from those surrounding the role of vaccines or genetics in contributing to autism—those contest science, while this contests the core identity of what it means to live with autism
The Bi-College News Online » Blog Archive » What Does It Mean to “Be” Autism?
10 November 2009
Disabled daughter, live on web: News24: SciTech: News
Paris - Diagnosed with severe cerebral palsy, 32-year-old Anne Lamic spends her days in south-eastern France mostly in bed, surrounded by stuffed animals and dolls. She cannot speak or walk, and she sometimes has seizures.
Disabled daughter, live on web: News24: SciTech: News
Disabled daughter, live on web: News24: SciTech: News
Sci-Tech Today | A Glimpse of the Future: Robots Aiding the Elderly
Among the products in development in Japan: A robotic bed from Panasonic that transforms into a joystick-controlled wheelchair on the user's spoken command. There's also Riba, a robot nurse disguised as a giant teddy bear, which can lift patients weighing up to 134 pounds. Those seeking companionship can turn to the robotic, seal-like Paro.
Sci-Tech Today | A Glimpse of the Future: Robots Aiding the Elderly
Sci-Tech Today | A Glimpse of the Future: Robots Aiding the Elderly
05 November 2009
Danielle’s Foundation Empowers Special Needs Families with Free Book
Growing non-profit devoted to helping families of children with cerebral palsy and brain injury commits to mission of informing and supporting parents
PHILADELPHIA—Danielle’s Foundation, a growing non-profit organization dedicated to helping parents of children with cerebral palsy and brain injury, announces the publication of its new book, Getting the Therapy, Benefits, and Resources Your Child Needs: A Guide for Parents of Children with Cerebral Palsy and Brain Injury.
Authored by Richard P. Console Jr., one of the volunteers at Danielle’s Foundation, the book was written to help parents navigate the complexities and challenges associated with successfully raising children with brain injury and cerebral palsy.
The comprehensive, 176-page guide includes the following topics:
• Understanding your child’s diagnosis, and what it means for the future
• Funding your child’s care
• Securing effective and cutting-edge therapies
• Negotiating successfully with your insurance company
• Demystifying the often confusing world of government benefits
• Ensuring your child receives the education he or she deserves
• Estate planning for families of special needs children
“My reasons for writing this book are personal,” said Console, who helped found Danielle’s Foundation in memory of Danielle Vick, the daughter of a friend who passed away in 2008 from complications associated with anoxic brain damage at just 4 years old. “While Danielle’s life was short, it was incredibly inspirational, and though she is no longer with us, we take comfort in knowing that we can make her legacy live on forever”.
Console said the purpose of the book is to educate and empower families of children with brain injury and cerebral palsy, so they can effectively advocate for their children. While he admits that families of special needs children face difficult challenges, he feels that with knowledge and education comes hope. “Every parent wants the best for their child, but getting the benefits their child needs is not always easy, and a lot of parents don’t know where to turn for help and support. We want Danielle’s Foundation to be that guiding light to which families can turn.”
“Getting the Therapy, Benefits, and Resources Your Child Needs: A Guide for Parents of Children with Cerebral Palsy and Brain Injury” is FREE to parents who call Danielle’s Foundation today toll free at 1-800-208-3494.
Parents interested in learning more about Danielle’s Foundation, and the support and services it offers, may visit www.DaniellesFoundation.org for more information.
About Danielle’s Foundation
Danielle’s Foundation is a non-profit resource that is committed to helping families of children with cerebral palsy and brain injury gain the knowledge to secure the therapy, benefits, and resources their children need. It was created by a team of grassroots volunteers whose mission is to help parents navigate through the challenges and complexities that arise while caring for their children. Their website, www.daniellesfoundation.org, also offers hundreds of articles related to treatments and therapies, education, estate planning, and legal and financial issues. Join Danielle’s Foundation today to become a part of their support network, where parents can unite to share and exchange their knowledge to educate and empower each other via their online forum.
Contacts
Danielle’s Foundation
Kristin Testa
1-800-208-3494
press@daniellesfoundation.org
PHILADELPHIA—Danielle’s Foundation, a growing non-profit organization dedicated to helping parents of children with cerebral palsy and brain injury, announces the publication of its new book, Getting the Therapy, Benefits, and Resources Your Child Needs: A Guide for Parents of Children with Cerebral Palsy and Brain Injury.
Authored by Richard P. Console Jr., one of the volunteers at Danielle’s Foundation, the book was written to help parents navigate the complexities and challenges associated with successfully raising children with brain injury and cerebral palsy.
The comprehensive, 176-page guide includes the following topics:
• Understanding your child’s diagnosis, and what it means for the future
• Funding your child’s care
• Securing effective and cutting-edge therapies
• Negotiating successfully with your insurance company
• Demystifying the often confusing world of government benefits
• Ensuring your child receives the education he or she deserves
• Estate planning for families of special needs children
“My reasons for writing this book are personal,” said Console, who helped found Danielle’s Foundation in memory of Danielle Vick, the daughter of a friend who passed away in 2008 from complications associated with anoxic brain damage at just 4 years old. “While Danielle’s life was short, it was incredibly inspirational, and though she is no longer with us, we take comfort in knowing that we can make her legacy live on forever”.
Console said the purpose of the book is to educate and empower families of children with brain injury and cerebral palsy, so they can effectively advocate for their children. While he admits that families of special needs children face difficult challenges, he feels that with knowledge and education comes hope. “Every parent wants the best for their child, but getting the benefits their child needs is not always easy, and a lot of parents don’t know where to turn for help and support. We want Danielle’s Foundation to be that guiding light to which families can turn.”
“Getting the Therapy, Benefits, and Resources Your Child Needs: A Guide for Parents of Children with Cerebral Palsy and Brain Injury” is FREE to parents who call Danielle’s Foundation today toll free at 1-800-208-3494.
Parents interested in learning more about Danielle’s Foundation, and the support and services it offers, may visit www.DaniellesFoundation.org for more information.
About Danielle’s Foundation
Danielle’s Foundation is a non-profit resource that is committed to helping families of children with cerebral palsy and brain injury gain the knowledge to secure the therapy, benefits, and resources their children need. It was created by a team of grassroots volunteers whose mission is to help parents navigate through the challenges and complexities that arise while caring for their children. Their website, www.daniellesfoundation.org, also offers hundreds of articles related to treatments and therapies, education, estate planning, and legal and financial issues. Join Danielle’s Foundation today to become a part of their support network, where parents can unite to share and exchange their knowledge to educate and empower each other via their online forum.
Contacts
Danielle’s Foundation
Kristin Testa
1-800-208-3494
press@daniellesfoundation.org
The heartbreaking case of Baby RB
I understand the mother’s desire to protect Baby RB - but doctors, after all, can be wrong, writes Liz Hunt.
By Liz HuntPublished: 6:53AM GMT 04 Nov 2009
It’s a tug-of-love case like no other. In one corner is a mother who wants her baby son to die. She believes it will save him from a life of suffering caused by a rare neuromuscular condition that means he may never move independently, and requires assistance to breathe. In the other is a father who wants the child to be given a chance, at least, of life.
In the middle sits a judge who, once lawyers, ethicists, and medics have had their say, must pronounce on Baby RB’s future. Surely Solomon had an easier decision than that faced by Mr Justice McFarlane.
For those observing this High Court drama who are swayed neither by religious belief, nor by a faith in the absolutism of medical opinion that holds Baby RB as a lost cause for whom a humane exit is the only option, it’s a tortuous intellectual and emotional debate.
I find myself ricocheting between the two positions, both of them informed by awareness of the long hours the devoted parents have spent at the child’s bedside in the 13 months since his birth. His mental development is believed to be unimpaired; the court heard yesterday claims that he responds to those around him, will wriggle his body in pleasure, and can interact with toys or when stories are read to him.
By Liz HuntPublished: 6:53AM GMT 04 Nov 2009
It’s a tug-of-love case like no other. In one corner is a mother who wants her baby son to die. She believes it will save him from a life of suffering caused by a rare neuromuscular condition that means he may never move independently, and requires assistance to breathe. In the other is a father who wants the child to be given a chance, at least, of life.
In the middle sits a judge who, once lawyers, ethicists, and medics have had their say, must pronounce on Baby RB’s future. Surely Solomon had an easier decision than that faced by Mr Justice McFarlane.
For those observing this High Court drama who are swayed neither by religious belief, nor by a faith in the absolutism of medical opinion that holds Baby RB as a lost cause for whom a humane exit is the only option, it’s a tortuous intellectual and emotional debate.
I find myself ricocheting between the two positions, both of them informed by awareness of the long hours the devoted parents have spent at the child’s bedside in the 13 months since his birth. His mental development is believed to be unimpaired; the court heard yesterday claims that he responds to those around him, will wriggle his body in pleasure, and can interact with toys or when stories are read to him.
So, yes, I understand the mother’s desire to protect him. A peaceful, drug-soothed death is surely preferable to the “pitiful existence” experts say lies ahead. But how hard it is not to sympathise with the father’s refusal to deny his child an existence at all by withdrawing ventilation, as the doctors want. Doctors can, after all, be wrong.
This is not the first time that a court has been asked to decided whether a very disabled child should live or die. In 2004, in the first case of its kind, 10-month-old Charlotte Wyatt’s life was the focus of a high-profile legal battle. Born at 26 weeks, her brain was under-developed and her hearts and lungs damaged so that she had to be supplied with oxygen. Doctors wanted to let her die, rather than resuscitate her, as they had done five times previously when her breathing failed. Blind and deaf, her suffering had reached “an unbearable level”. Her chance of surviving another year was “approximately zero”.
Charlotte’s parents disputed this assessment. They said their daughter enjoyed cuddles, reacted to her musical toys, and loved to be bathed. In short, they felt she had a worthwhile quality of life, and every intervention should be made to prolong it. A judge ruled in favour of the doctors and a do-not-resuscitate order was put in place. In the event, it was not needed, Charlotte survived, confounding the experts. It was a triumph over tragedy – of sorts. Her parents split up, and she is now believed to be in the care of foster parents.
There are similarities between the cases: the damning medical prognosis, the insistence that the baby’s life is not without comfort. But there is also a fundamental difference: should the judge find in favour of his mother, and of the NHS trust that cares for Baby RB, it will be the first time that a British court has ruled against the wishes of a parent (the baby’s father) whose child does not have brain damage.
This is the fulcrum on which the debate pivots. Michael McClonas, for the NHS trust, has argued that Baby RB’s “awareness” will make his plight unbearable, “not so much now, but as he gets older and catches glimpses of what others can do”. What dangerous presumption that statement contains; that a child should be helped to die because of what might lie ahead, that his very sentience might seal his fate.
To how many others might that argument have been applied: The late writer and cerebral palsy sufferer Christy Nolan? Perhaps even Professor Stephen Hawking, who developed a debilitating illness in early adulthood? I am not an advocate of life at any price, but Baby RB’s is worth more than this.
04 November 2009
Hyperbaric oxygen treatments effective for treating many disabilities
Hyperbaric Oxygen Treatments are effective for treating many disabilities such as Cerebral Palsy, according to an article on www.ehow.com.
Hyperbaric Oxygen Treatments also known HBO therapy was not intended to treat Cerebral Palsy or other brain injuries but when coupled with intensive physical and occupational therapy can be effective, according to the article.
The Hyperbaric Oxygen Treatment Center website, which can be found at http://www.hypertc.com states that the treatment has also been effective for treating Cerebral Palsy, ,Autism, Strokes, Multiple Sclerosis and sports related injuries.
HBO therapy usually involves the patient being put into an inflatable “room” which is just big enough for a person to lie down or sit up in. The air pressure of the room is usually two to three times normal air pressure and it filled with 100% oxygen. The increase in air allows oxygen to flow to the patients organs and body tissue, according to a second article about HBO therapy on www.ehow.com.
The Hyperbaric Oxygen Treatment Center states the one treatment session lasts an hour. Patients should have multiple treatments and the number will determined during an initial evaluation with their choose treatment center.
The cost varies depending on the number of treatments needed and type of chamber used. The website states that patients can read a book, listen to music, talk on their cell phone, play a handheld videogame and/or work on a laptop to occupy themselves while in the chamber.
People who are prone to ear infections, have ear canal or ear wax related problems should not have HBO treatments because the increased air pressures in the chamber can cause patients to feel pressure on their ears. It is recommended that patients try yawning and massaging their ears in order to relieve the pressure. People who are intoxicated or experiencing cold or flu symptoms should not have the treatments because it could be dangerous to them and others who use the chamber after them, according to the website.
People of all ages can have HBO therapy but it is more effective on young children because they are still developing. The Hyperbaric Oxygen Treatment center is located in Cumming Georgia. Many other medical facilities have been known to offer the treatment. People and or family looking into this type of treatment should keep in mind that because it was not intended to treat brain injuries many insurance companies will not pay for it. As noted above the cost varies. According to the first article about HBO therapy on www.ehow.com the cost can range anywhere from $100-$250 per treatment depending on the type of chamber used.
Patients and their families also have the option of purchasing or renting a hyperbaric oxygen chamber, according to the treatment center’s website. Those who are interested in buying or renting a chamber should visit http://www.vitao2.com/index.cfm for details. Please note that a prescription is needed to complete either transaction.
Patients and families looking for further guidance or who are skeptical may want to take the time to read the testimonials of patients and families find on the Hyperbaric Oxygen Center’s website.
For more info visit: http://www.ehow.com/how_4465058_use-hyperbaric-chamber-therapy-cerebral.html
http://www.ehow.com/way_5273455_hyperbaric-chamber-therapy.html
http:// http://www.vitao2.com/index.cfm
http://www.hypertc.com
Hyperbaric Oxygen Treatments also known HBO therapy was not intended to treat Cerebral Palsy or other brain injuries but when coupled with intensive physical and occupational therapy can be effective, according to the article.
The Hyperbaric Oxygen Treatment Center website, which can be found at http://www.hypertc.com states that the treatment has also been effective for treating Cerebral Palsy, ,Autism, Strokes, Multiple Sclerosis and sports related injuries.
HBO therapy usually involves the patient being put into an inflatable “room” which is just big enough for a person to lie down or sit up in. The air pressure of the room is usually two to three times normal air pressure and it filled with 100% oxygen. The increase in air allows oxygen to flow to the patients organs and body tissue, according to a second article about HBO therapy on www.ehow.com.
The Hyperbaric Oxygen Treatment Center states the one treatment session lasts an hour. Patients should have multiple treatments and the number will determined during an initial evaluation with their choose treatment center.
The cost varies depending on the number of treatments needed and type of chamber used. The website states that patients can read a book, listen to music, talk on their cell phone, play a handheld videogame and/or work on a laptop to occupy themselves while in the chamber.
People who are prone to ear infections, have ear canal or ear wax related problems should not have HBO treatments because the increased air pressures in the chamber can cause patients to feel pressure on their ears. It is recommended that patients try yawning and massaging their ears in order to relieve the pressure. People who are intoxicated or experiencing cold or flu symptoms should not have the treatments because it could be dangerous to them and others who use the chamber after them, according to the website.
People of all ages can have HBO therapy but it is more effective on young children because they are still developing. The Hyperbaric Oxygen Treatment center is located in Cumming Georgia. Many other medical facilities have been known to offer the treatment. People and or family looking into this type of treatment should keep in mind that because it was not intended to treat brain injuries many insurance companies will not pay for it. As noted above the cost varies. According to the first article about HBO therapy on www.ehow.com the cost can range anywhere from $100-$250 per treatment depending on the type of chamber used.
Patients and their families also have the option of purchasing or renting a hyperbaric oxygen chamber, according to the treatment center’s website. Those who are interested in buying or renting a chamber should visit http://www.vitao2.com/index.cfm for details. Please note that a prescription is needed to complete either transaction.
Patients and families looking for further guidance or who are skeptical may want to take the time to read the testimonials of patients and families find on the Hyperbaric Oxygen Center’s website.
For more info visit: http://www.ehow.com/how_4465058_use-hyperbaric-chamber-therapy-cerebral.html
http://www.ehow.com/way_5273455_hyperbaric-chamber-therapy.html
http:// http://www.vitao2.com/index.cfm
http://www.hypertc.com
03 November 2009
Learning to walk again: Neurological rehabilitation overcomes paralysis
BY BRIAN PASSEY
bpassey@thespectrum.com
James Loris is walking again. The father of five who owned his own construction business was in a wheelchair, paralyzed from the chest down following an off-highway vehicle accident that fractured his C6 vertebrae.
"When I broke my neck, it pinched my spinal cord," Loris says, adding that the injury disrupted the brain's communication with his body, causing the paralysis. "He just turned the system back on."
Loris is referring to Steven Bennett, a physical therapist at Mountain Land's Southwest Neurological Rehabilitation Center in St. George. Bennett utilizes a neuromuscular training program to restore function to paralyzed or dysfunctional muscles resulting from a variety of medical conditions, including strokes, spinal cord injuries, brain injuries cerebral palsy and other neurological and orthopedic conditions.
The program utilizes electrodes placed on a patient's muscle group to read electrical signals transmitted from the brain to the muscle. An attached computer reads electrical impulses, displaying the signals on a monitor for the therapist and patient to see during treatments.
The therapist then uses a conditioning protocol to teach the brain to use alternate paths to communicate with the muscles. This conditioning is tracked by watching the signals on the monitor.
Once the brain learns to communicate with muscles through new paths it remembers the alternate paths for future use and, in effect, overcomes the paralysis.
That is how Loris came to walk again.
"You have to have determination," Loris says.
He's not quite back to his pre-accident mobility. Loris walks with a limp and has to concentrate on lifting his leg so he doesn't trip over his foot. Bennett says they have not yet been able to restore movement to the muscles in one of Loris' feet.
It's a long way from using a wheelchair because he didn't have any movement from the neck down.
"He'll come back in and we'll tune him up and smooth out that walk," Bennett says.
It's not an easy process. It's hard work. It requires strength. Yet Loris says he was driven because he had to provide for his family. He can even drive a vehicle with a standard transmission, clutch and all.
Bob Mower
The treatment is not just effective for accidents like what happened to Loris. Bob Mower, a retired Dixie State College chemistry professor, suffered a severe stroke in May and was unable to walk because he lost mobility on his entire left side.
"It was a long time before I could even move," Mower says.
Bennett says Mower was not supposed to be able to walk again. That was before he went through the neuromuscular training program.
"We had to turn on his whole left side," Bennett says.
Because Mower had the determination to move again, he checked out of both inpatient rehabilitation and home health before he was supposed to so he could begin working with Bennett.
Mower's wife, Susan, calls Bennett a "miracle worker" and says he's "perpetually optimistic and encouraging."
"Bob's in far better shape than anyone ever thought he would be," she says.
When he first visited the Southwest Neurological Rehabilitation Center, Mower couldn't walk or move his left hand. His goals were to overcome both of those obstacles and he has.
"Now I can walk from the parking lot into the therapy office, from the parking lot into the grocery store, and from the parking lot into church," he says. "I can move my hand and fingers well enough to hold onto things. I can hold the television remote so tightly my wife can't get it away from me."
Mower also likes how Bennett appreciates a good joke, because Mower is full of them.
Richard Cox
He still uses a wheelchair to get around but Richard Cox is much farther along in his recovery than he thought he would be after his injury more than three years ago.
"I had absolutely no movement," Cox says. "I couldn't type. I couldn't write my name. It's been a long 3 1/2 years."
Now he is slowly regaining movement. Although he still needs the wheelchair for everyday movement, he can walk short distances with the aid of a walker and knee brace.
Cox was riding in the back of a Jeep when he hit the roll bar and blood began to flood his spinal cord. Blood clots suffocated the spinal cord and peripheral nerves, leaving him paralyzed.
Then his aunt, who lives in St. George, mailed an article about Southwest Neurological Rehabilitation to Cox in Phoenix, where he lived at the time. About six months ago Cox moved to St. George to pursue treatment.
Like others who have sought Bennett's help, Cox has damage to the pathways normally used by the brain to communicate with his muscles. Because these pathways don't regenerate, Bennett has to work with Cox to teach his brain to follow different pathways.
To do this, Cox positions his wheelchair between two horizontal bars in Bennett's office. He uses his upper-body strength to pull himself up to a standing position. From there he slowly puts weight on one leg at a time to send signals to his brain. Through trial and error of placing the weight in different spots he can train his brain to find different communication pathways to the muscles.
"Once the brain sees it a couple of times it will repeat it and repeat it until it's locked into motor memory," Bennett says.
It's not easy.
As Cox puts weight on his leg he groans loudly, almost like he's bench-pressing weights in a gym. Because of his injury, his nerves are more sensitive than normal. Cox says everything is magnified by about 10 times. The process is both painful and exhausting.
Still he's determined to push through and regain mobility.
Cox meets his goal of sending a powerful signal to his brain as tracked on the computer monitor. Yet he wheezes, "One more."
He puts his weight on his left leg again, groaning under the effort once more. He meets another goal and Bennett asks Cox if he has enough energy to go again.
Without hesitation Cox replies: "Yeah."
Then he decides to show off. With Bennett blocking Cox's weaker left leg so it doesn't give out on him, he walks a few steps, using the horizontal bars for some support.
He pulls his hands from the bars, putting his entire weight on his stronger right leg for a few seconds. He is standing without assistance.
"I can, with my right leg, support my weight," Cox says with an optimistic smile.
For about three months after his injury, Cox was one of about 20 patients in the hospital with similar injuries. He got to know the other patients quite well during that time. Now he says they have all given up except one other and him.
That is why he wants to spread the word about this treatment.
"I figure this accident had to happen for a reason," he says.
He didn't know services like this were available until his aunt sent him the newspaper article. Only about a dozen locations around the country offer the neurological rehabilitation services.
Cox has been working with Bennett for less than six months and has seen many successes during that short time. Bennett says he's walked up and down the length of the center's gym with the walker.
Ever the determined optimist, Cox pats his sleek, black wheelchair and says: "I look forward to donating this to someone else."
For more information on Mountain Land's Southwest Neurological Rehabilitation Center, call 628-5194
bpassey@thespectrum.com
James Loris is walking again. The father of five who owned his own construction business was in a wheelchair, paralyzed from the chest down following an off-highway vehicle accident that fractured his C6 vertebrae.
"When I broke my neck, it pinched my spinal cord," Loris says, adding that the injury disrupted the brain's communication with his body, causing the paralysis. "He just turned the system back on."
Loris is referring to Steven Bennett, a physical therapist at Mountain Land's Southwest Neurological Rehabilitation Center in St. George. Bennett utilizes a neuromuscular training program to restore function to paralyzed or dysfunctional muscles resulting from a variety of medical conditions, including strokes, spinal cord injuries, brain injuries cerebral palsy and other neurological and orthopedic conditions.
The program utilizes electrodes placed on a patient's muscle group to read electrical signals transmitted from the brain to the muscle. An attached computer reads electrical impulses, displaying the signals on a monitor for the therapist and patient to see during treatments.
The therapist then uses a conditioning protocol to teach the brain to use alternate paths to communicate with the muscles. This conditioning is tracked by watching the signals on the monitor.
Once the brain learns to communicate with muscles through new paths it remembers the alternate paths for future use and, in effect, overcomes the paralysis.
That is how Loris came to walk again.
"You have to have determination," Loris says.
He's not quite back to his pre-accident mobility. Loris walks with a limp and has to concentrate on lifting his leg so he doesn't trip over his foot. Bennett says they have not yet been able to restore movement to the muscles in one of Loris' feet.
It's a long way from using a wheelchair because he didn't have any movement from the neck down.
"He'll come back in and we'll tune him up and smooth out that walk," Bennett says.
It's not an easy process. It's hard work. It requires strength. Yet Loris says he was driven because he had to provide for his family. He can even drive a vehicle with a standard transmission, clutch and all.
Bob Mower
The treatment is not just effective for accidents like what happened to Loris. Bob Mower, a retired Dixie State College chemistry professor, suffered a severe stroke in May and was unable to walk because he lost mobility on his entire left side.
"It was a long time before I could even move," Mower says.
Bennett says Mower was not supposed to be able to walk again. That was before he went through the neuromuscular training program.
"We had to turn on his whole left side," Bennett says.
Because Mower had the determination to move again, he checked out of both inpatient rehabilitation and home health before he was supposed to so he could begin working with Bennett.
Mower's wife, Susan, calls Bennett a "miracle worker" and says he's "perpetually optimistic and encouraging."
"Bob's in far better shape than anyone ever thought he would be," she says.
When he first visited the Southwest Neurological Rehabilitation Center, Mower couldn't walk or move his left hand. His goals were to overcome both of those obstacles and he has.
"Now I can walk from the parking lot into the therapy office, from the parking lot into the grocery store, and from the parking lot into church," he says. "I can move my hand and fingers well enough to hold onto things. I can hold the television remote so tightly my wife can't get it away from me."
Mower also likes how Bennett appreciates a good joke, because Mower is full of them.
Richard Cox
He still uses a wheelchair to get around but Richard Cox is much farther along in his recovery than he thought he would be after his injury more than three years ago.
"I had absolutely no movement," Cox says. "I couldn't type. I couldn't write my name. It's been a long 3 1/2 years."
Now he is slowly regaining movement. Although he still needs the wheelchair for everyday movement, he can walk short distances with the aid of a walker and knee brace.
Cox was riding in the back of a Jeep when he hit the roll bar and blood began to flood his spinal cord. Blood clots suffocated the spinal cord and peripheral nerves, leaving him paralyzed.
Then his aunt, who lives in St. George, mailed an article about Southwest Neurological Rehabilitation to Cox in Phoenix, where he lived at the time. About six months ago Cox moved to St. George to pursue treatment.
Like others who have sought Bennett's help, Cox has damage to the pathways normally used by the brain to communicate with his muscles. Because these pathways don't regenerate, Bennett has to work with Cox to teach his brain to follow different pathways.
To do this, Cox positions his wheelchair between two horizontal bars in Bennett's office. He uses his upper-body strength to pull himself up to a standing position. From there he slowly puts weight on one leg at a time to send signals to his brain. Through trial and error of placing the weight in different spots he can train his brain to find different communication pathways to the muscles.
"Once the brain sees it a couple of times it will repeat it and repeat it until it's locked into motor memory," Bennett says.
It's not easy.
As Cox puts weight on his leg he groans loudly, almost like he's bench-pressing weights in a gym. Because of his injury, his nerves are more sensitive than normal. Cox says everything is magnified by about 10 times. The process is both painful and exhausting.
Still he's determined to push through and regain mobility.
Cox meets his goal of sending a powerful signal to his brain as tracked on the computer monitor. Yet he wheezes, "One more."
He puts his weight on his left leg again, groaning under the effort once more. He meets another goal and Bennett asks Cox if he has enough energy to go again.
Without hesitation Cox replies: "Yeah."
Then he decides to show off. With Bennett blocking Cox's weaker left leg so it doesn't give out on him, he walks a few steps, using the horizontal bars for some support.
He pulls his hands from the bars, putting his entire weight on his stronger right leg for a few seconds. He is standing without assistance.
"I can, with my right leg, support my weight," Cox says with an optimistic smile.
For about three months after his injury, Cox was one of about 20 patients in the hospital with similar injuries. He got to know the other patients quite well during that time. Now he says they have all given up except one other and him.
That is why he wants to spread the word about this treatment.
"I figure this accident had to happen for a reason," he says.
He didn't know services like this were available until his aunt sent him the newspaper article. Only about a dozen locations around the country offer the neurological rehabilitation services.
Cox has been working with Bennett for less than six months and has seen many successes during that short time. Bennett says he's walked up and down the length of the center's gym with the walker.
Ever the determined optimist, Cox pats his sleek, black wheelchair and says: "I look forward to donating this to someone else."
For more information on Mountain Land's Southwest Neurological Rehabilitation Center, call 628-5194
02 November 2009
About Me
hi my name is DAWN i am 44 yrs old and have a disabillity called cerebral palsey hemipligia which effects my rt side i try not 2 let it get the better of me altho some times it does get me down i live my life as full as it allows i have 4 ablebodied children aged 21 19 18 17 and 3 beautiful grandsons also able bodied im also divorced my choice lol and live very happily without x lol my disabillity doesnt stop me being a nice person and being funny and careing and very strong minded helps deal with the down falls of what i was born with so i hope by telling who ever reads this a little about me helps them if they have a disabillity 2 deal with that its not that bad and u can live your lives 2 the best of your personal abillities take care enjoy your day if you would like 2 msg me then feel free hope 2 hear from u soon bye 4 now
01 November 2009
I never know what to put here!
Hello all,
It’s time for an update. Things are going well in the world of Brandon Ryan, recently The Emotional Struggle has been flying off the shelves of a few independant bookstores. The responses from friends and people from amongst the globe have been very inspiring to me.
I’ll share with you, a review that I read a few days ago. It’s from an Athiest friend of mine:
I really enjoyed this book. I read it in one sitting. You can really feel the emotion and hard work was put into this book. After reading this book I knew that you can accomplish anything you set your mind to.I give this book 10 starts out of 10 just for being raw and being truthful. Brandon is an amazing writer I hope to read many more of his books. It was an honor to be able to read this book and see his world through his eyes.
This probably means more to me, than any other review that was written by a Christian. I’ve said this a lot, but I’m not out to convert anyone. It’s not my job, my hope from the very start is to build a bridge between hope and despair. I don’t want to make people heavenly statistics. Of course, I’d love for everyone to know the same love that has changed my life.
But if it’s going to happen, it’s going to be real and true. And I know that Jesus is at work, using his sword to poke around in our hearts. He says that he has not come to bring peace, but a sword. A lot of people use this as a comfort tool, because God’s gonna bring-eth the smack-eth-down-eth. Okay, if that works for you, cool. However I’ve to come to realize from a close friend, that this statement might just carry a deeper truth.
Are lives aren’t comfortable, at least my life isn’t. God doesn’t spoon feed me, but instead he wants for you and me, to have the best life possible. And if that means him poking at areas in my life that I’d rather not deal with, it’s not because he’s angry or that he has steam coming out of his nose. But because he cares. In other words, God wants us to live better stories with our lives.
It’s only going to be a matter of time before I sit down to pound out my next memoir. Everything is falling into place for it. I’m hoping to make it much more personal and honest than my first. I wanna make mae people laugh more and cry harder. It wasn’t my intention with my first book, but it will be with this one!
Please keep helping me plug The Emotional Struggle.
-Brandon
It’s time for an update. Things are going well in the world of Brandon Ryan, recently The Emotional Struggle has been flying off the shelves of a few independant bookstores. The responses from friends and people from amongst the globe have been very inspiring to me.
I’ll share with you, a review that I read a few days ago. It’s from an Athiest friend of mine:
I really enjoyed this book. I read it in one sitting. You can really feel the emotion and hard work was put into this book. After reading this book I knew that you can accomplish anything you set your mind to.I give this book 10 starts out of 10 just for being raw and being truthful. Brandon is an amazing writer I hope to read many more of his books. It was an honor to be able to read this book and see his world through his eyes.
This probably means more to me, than any other review that was written by a Christian. I’ve said this a lot, but I’m not out to convert anyone. It’s not my job, my hope from the very start is to build a bridge between hope and despair. I don’t want to make people heavenly statistics. Of course, I’d love for everyone to know the same love that has changed my life.
But if it’s going to happen, it’s going to be real and true. And I know that Jesus is at work, using his sword to poke around in our hearts. He says that he has not come to bring peace, but a sword. A lot of people use this as a comfort tool, because God’s gonna bring-eth the smack-eth-down-eth. Okay, if that works for you, cool. However I’ve to come to realize from a close friend, that this statement might just carry a deeper truth.
Are lives aren’t comfortable, at least my life isn’t. God doesn’t spoon feed me, but instead he wants for you and me, to have the best life possible. And if that means him poking at areas in my life that I’d rather not deal with, it’s not because he’s angry or that he has steam coming out of his nose. But because he cares. In other words, God wants us to live better stories with our lives.
It’s only going to be a matter of time before I sit down to pound out my next memoir. Everything is falling into place for it. I’m hoping to make it much more personal and honest than my first. I wanna make mae people laugh more and cry harder. It wasn’t my intention with my first book, but it will be with this one!
Please keep helping me plug The Emotional Struggle.
-Brandon
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