Email Brad Pittman |
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Email Terry Terry just discovered he has SMA III Terry has agreed to join my site, so if you have any questions feel free to email him. |
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Email Adrain |
Click on images for larger view |
I would like to build a network of friends with SMA-III on this page. Not just SMA but anyone that has a form of Muscular Dystrophy. Parents with children that have MD. Everybody and anyone is welcome. just contact me.
Email Moana
Her 3 year old daughter has SMA III. I was fortunate to have her find my web site and contact me.
Melissa's Page
My site is about my personal experiences growing up with Spinal Muscular Atrophy. It also includes links to many disability related sites.
Teresa
Lost her father to SMA III, she can talk to others that had a family member with SMA, and help others that don't have this disorder to cope.
(To the best of her ability)
Please note these people are not professionals in the Medical Industry (meaning Doctors). I thought it would be cool and got everyone's ok to list them at this page. This is to help the many others out there with SMA III.
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