Melissa's Page on Spinal Muscular Atrophy

<body> <B> Melissa's Page on Spinal Muscular Atrophy </B> <P> Hi, my name is Melissa, welcome to my page about Spinal Muscular Atrophy. <P> I know that we are all different, and that a neuromuscular disease doesn't affect us all in the same way, so I decided to do this page from a totally personal point of view, on how SMA affected me as I grew up. My hope is that it might be of help to kids and/or their parents, who might just be finding out they have a neuromuscular disease, who don't know much about it, how it might affect them or what they might expect on down the line. It is my hope that kids and/or their parents not only find my page informative, but also that when they leave here, they might leave with a little less fear of, and a little more hope for, the future. <P> If you are viewing this text, your browser lacks the ability to read frames. Don't worry, you can still visit my site. Please come inside! <P> <a href="right.html">Melissa's Page</a> </body>