Story about Spinal Muscular Atrophy .

Sophies story

Feb 25, 2017

By: Jennie


Sophie (6) was diagnosed at 20 months with SMA type 2. After 4 long months of doctors visits, x-rays, MRIs, and ECE/ECG, and a final blood test to confirm. Sophie has never been able to stand or crawl, but she does sit rather well without support. We're open to play dates as well!! 

Know someone who should read this story? Share it

0 comments

Login or register to leave a comment


Spinal Muscular Atrophy treatments

What are the best treatments for Spinal Muscular Atrophy?

Spinal Muscular Atrophy symptoms

Which are the symptoms of Spinal Muscular Atrophy?

Do I have Spinal Muscular Atrophy?

How do I know if I have Spinal Muscular Atrophy?

Spinal Muscular Atrophy prognosis

Spinal Muscular Atrophy prognosis

Spinal Muscular Atrophy life expectancy

What is the life expectancy of someone with Spinal Muscular Atrophy?

Spinal Muscular Atrophy and depression

Spinal Muscular Atrophy and depression

Natural treatment of Spinal Muscular Atrophy

Is there any natural treatment for Spinal Muscular Atrophy?

Living with Spinal Muscular Atrophy

Living with Spinal Muscular Atrophy. How to live with Spinal Muscular ...