SMArt Moves start with you! Join us to save lives.
Cure SMA is dedicated to the treatment and cure of spinal muscular atrophy (SMA), a rare genetic neuromuscular disease. It remains the leading congenital cause of death amongst children under the age of two. Today there is new hope.
Since 1984, we’ve directed and invested in comprehensive research that has shaped the scientific community’s understanding of SMA and drives breakthroughs in treatment and care, including the Newborn Screening Registry. We also provide families the support they need for today. We are currently on the verge of breakthroughs that will strengthen bodies, extend life, and lead to a cure. With new, effective treatments now available and other promising treatments on the horizon, Cure SMA’s SMArt Moves wants all healthcare professionals and parents to:
• Know the critical SMA signs, and how it may affect a child’s motor development
• Access the necessary tools and resources to take swift action and follow their instincts
Learn more at https://smartmoves.curesma.org/ or www.curesma.org
Register now for the Cure SMA Product Theater:
The Importance of Newborn Screening and Early Detection to Maximize Clinical Outcomes in Spinal Muscular Atrophy
with Mary Schroth, MD, FAAP, FCCP, Chief Medical Officer, Cure SMA
Sunday, October 10 at 12 pm CDT