Depending on the the type of MD suffered, and therefore the level of physical impairment, the possibilities are extensive. Choosing a career that fits your level of mobility is wise. Some sufferers may be unable to work or can only manage part time or casual work.
I suffer from Charcot - Marie - Tooth (CMT) and when I was younger I wanted a career in hospitality. However, I was unable to manage the physical demands of being on my feet. So I went to University and completed a B. Sc Psychology. I have worked as a Counsellor and Trainer for almost 15 yrs on & off apccording to my health fluctuations. I have modified my practices to meet my CMT needs, such as rest breaks, ergonomic aids & sitting whilst I train. My career is successful & has even led me to do workshops & counselling for other MD sufferers. I have met nurses, banker, admin staff & childcare workers with forms of MD.
So, work out realistic goals, work to your strengths and best of luck in your career!
I have SMA type III (spinal muscular atrophy), a form of muscular dystrophy, and I have always seen and/or been treated by neurologists recommended by MDA. You can contact the national Muscular Dystrophy Association (MDA) either locally or online at http://www.mda.org for additional information or if you have questions you've been unable to find answers for. They are invaluable to families and individuals alike. Further personal research can be done using a search engine such as Google and entering the terms "neurology" and "muscular dystrophy."
First, there are nine types of muscular dystrophy listed in the attached links. If you read the link, you will see the difference between them; some of them are mild, not too seriously affect the sufferers quality or length of life, others do. Without knowing which type is your son suffering of, it is impossible to write anything specific. The only common between these types is the cause. With the exception of a few cases, where the genetic mutation, some kind of abnormality, happens after births, the vast majority is inherited. In either case, the mutated (abnormal) gene is unable to supply any or enough of the necessary protein what the muscle needs for proper function. While there are a great amount of research going on for muscular dystrophy, cure is not found yet. Until a method is found to correct or replace the faulty gene or supply the needed protein, the treatments can only focus on decreasing the symptoms and increasing the comfort, thus the quality of life, as much as possible, for the sufferers'.
As noted, aldolase is elevated in skeletal muscle diseases, such as muscular dystrophies. Duchenne's muscular dystrophy, the most common type of muscular dystrophy, will increase the aldolase level more than any other disease.
When contractures become more pronounced, tenotomy surgery may be performed. In this operation, the tendon of the contractured muscle is cut, and the limb is braced in its normal resting position while the tendon regrows
Swimming.
Swimming.
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The kind of muscular control needed for gymnastics is called?
Martial arts
anyway if your asking the biological kind (i hope you are) then some x-liked traits i know are hemophilia A and B, color blindness, muscular dystrophy, alport syndrome, dent's disease and lots more try this site.... http://en.wikipedia.org/wiki/Sex-linked
People who develop weakness of the diaphragm or other ventilatory muscles may require a mechanical ventilator to continue breathing deeply enough. Air may be administered through a nasal mask or mouthpiece, or through a tracheostomy tube
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