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| There are many reasons for
this page. While
there is
much information on Muscular Dystrophy on the Internet and various
other
places. I wanted to provide a place where much of that information
could
be located easily.
Let me make it perfectly clear that I am neither a doctor or any other type of health care professional. My only knowledge comes from the fact that I have a form of MD called Friedrich's Ataxia. I have spent some time looking for information and possible treatments which I will share with anyone here. I invite anyone to share any knowledge they may have with visitors to this site. Simply email me If you read as much as I
have from the
conventional medical
field you tend to lose hope of a treatment or cure. My feelings are do as much as you can. I never accept
what the doctors tell me and I do things they say I can't do. My
younger brother never let his condition stop him as long as he could
keep going he did and attempted things even I didn't consider. Do you have a poem or
story? Send
it here |
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Upcoming
Events: Events I intend to attend
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| Here I will try to cover
some of the things I
deal with
(symptoms as well as improvements) This part is purely personal for me. Archives for previous years are here |
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| Symptoms
This is what my case was based on as of May 2004. Current case This is my current case Apr 2007. |
| I hope to get feedback from people visiting this page with more options. E-Mail |
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for comments on this page email webmaster@tnt-computer.com |