I need to appreciate what muscular dystrophy is. I read about it on smudge but I need someone to break it down within words an idiot can understand. Thanks contained by advance for anyone trying to abet me.
Answers: The Muscular Dystrophy Association treats 40 different diseases. Muscular Dystrophy as a disease comes in two variation Becker, which is the milder form, and Duchene, which is more aggressive. In people near Muscular Dystrophy the body makes to little or none of a protein (dystrophin), which help muscles to keep their strength and shape. In Becker the body does not produce ample, in Duchene the body produces none. My son have Duchene when I got his diagnosis I run home and looked up all I could find and be devastated. What you read is usually the worse case and I found it vary greatly some people plateau for years at guaranteed stages and some do not. I will tell you how my son progressed but everyone is different. At 8 he be diagnosed he could not run, took stairs one step at a time and when he got up from the floor he did what the doctor call a crab motion spreading his arms and legs out and inching his way up. The first muscle the disease attacks is the leg muscles, it moves from the larger muscles that do most of the work to the subsequent smaller set of muscles. He was surrounded by a wheelchair at age 10 and he also needed surgery to release his heel cords (In kids with MD the treat cords start to shorten and there foot start to point down). Then it started affecting his arms at age 13 which made him have to jump into an electric wheelchair. He developed scoliosis and had to hold a spinal fusion and to Herrington rods put along his spine, which meant he could not longer turn contained by bed by himself. He then plateau and be losing just rather arm strength so he needed a little more minister to. He is know 23 and the next stage hit this ultimate summer it moved to the diaphragm muscle with effects his skilfulness to exhale air and push CO2 out of the lungs he have a build up of CO2 and his Oxygen went down and he go into a seizure and we almost loss him he is very soon on oxygen during the day and a ventilator at hours of darkness to let his heart rest and to find a good night rest. The diaphragm will slowly get weaker and he will requirement to be on the ventilator all the time and lastly the subsequent muscles the disease attacks is the heart muscle. The only entity I can add is my son have showed me the definition of what courage is.
Muscular Dystrophy is a series of diseases which damage the muscular system of the body. There are going on for 100 or more different kinds of it. Many are highly serious even deadly some are not as risky.
Great strides have be made against this disease and the life expectancy of nation with it have been growing for the end century. This is a result of the Jerry Lewis Telethon on labor day. He have raised millions upon millions for research.
If you know a child next to muscular dystrophy contact the muscular dystrophy association.
www. mdausa.org
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Are ridges contained by my year dated sons person in charge usual the vanished side is different than the right side?
Answers: The Muscular Dystrophy Association treats 40 different diseases. Muscular Dystrophy as a disease comes in two variation Becker, which is the milder form, and Duchene, which is more aggressive. In people near Muscular Dystrophy the body makes to little or none of a protein (dystrophin), which help muscles to keep their strength and shape. In Becker the body does not produce ample, in Duchene the body produces none. My son have Duchene when I got his diagnosis I run home and looked up all I could find and be devastated. What you read is usually the worse case and I found it vary greatly some people plateau for years at guaranteed stages and some do not. I will tell you how my son progressed but everyone is different. At 8 he be diagnosed he could not run, took stairs one step at a time and when he got up from the floor he did what the doctor call a crab motion spreading his arms and legs out and inching his way up. The first muscle the disease attacks is the leg muscles, it moves from the larger muscles that do most of the work to the subsequent smaller set of muscles. He was surrounded by a wheelchair at age 10 and he also needed surgery to release his heel cords (In kids with MD the treat cords start to shorten and there foot start to point down). Then it started affecting his arms at age 13 which made him have to jump into an electric wheelchair. He developed scoliosis and had to hold a spinal fusion and to Herrington rods put along his spine, which meant he could not longer turn contained by bed by himself. He then plateau and be losing just rather arm strength so he needed a little more minister to. He is know 23 and the next stage hit this ultimate summer it moved to the diaphragm muscle with effects his skilfulness to exhale air and push CO2 out of the lungs he have a build up of CO2 and his Oxygen went down and he go into a seizure and we almost loss him he is very soon on oxygen during the day and a ventilator at hours of darkness to let his heart rest and to find a good night rest. The diaphragm will slowly get weaker and he will requirement to be on the ventilator all the time and lastly the subsequent muscles the disease attacks is the heart muscle. The only entity I can add is my son have showed me the definition of what courage is.
Muscular Dystrophy is a series of diseases which damage the muscular system of the body. There are going on for 100 or more different kinds of it. Many are highly serious even deadly some are not as risky.
Great strides have be made against this disease and the life expectancy of nation with it have been growing for the end century. This is a result of the Jerry Lewis Telethon on labor day. He have raised millions upon millions for research.
If you know a child next to muscular dystrophy contact the muscular dystrophy association.
www. mdausa.org