08/27/2026
August is Spinal Muscular Atrophy (SMA) Awareness Month! 🧬💙
Founded in 1996 by Cure SMA, this month is dedicated to spreading knowledge, supporting individuals and families affected by SMA, and advocate for continued research toward a cure.
💡 Key Facts to Know About SMA:
What it is: Spinal Muscular Atrophy is a rare, genetic neuromuscular condition that affects nerve cells in the spinal cord, leading to muscle weakness that impacts mobility, swallowing, and breathing.
Carrier Rate: Approximately 1 in 50 people in the U.S. carry the gene for SMA.
Preserved Cognition: While SMA affects physical motor skills, it does not impact a person's intelligence, learning ability, or cognitive development.
Types: There are four main types of SMA that can present at different stages—ranging from infancy to adulthood.
For special education advocates, educators, and families, understanding SMA is vital for ensuring students receive the necessary physical, architectural, and classroom accommodations—such as assistive technology, mobility support, and tailored 504 Plans or IEPs—to thrive academically and socially alongside their peers.
Let's use this month to uplift voices, promote accessibility, and support the remarkable individuals and families living with SMA! 🌟
👉 Learn more about advocacy and accommodations for students with physical disabilities:
https://www.dayanlawfirm.com/special-education-services/