Living with spinal muscular atrophy requires knowledge, strength and support. Find resources and support for your journey here.
Shellie L. knows true love when she looks into her daughter’s eyes each morning. Finding out her daughter had a severe form of spinal muscular atrophy was a devastating blow but each day with Aubriana is a blessing that makes her appreciate life. I was 23-years-old when I had my daughter Aubriana. She was my second… Continue reading Caring for a Child with Special Needs: Meet Aubriana