SMS Research Foundation

About the Smith-Magenis Syndrome Research Foundation

Founded in 2010 by dedicated parent advocates, the Smith-Magenis Syndrome Research Foundation is committed to enhancing the understanding of Smith-Magenis Syndrome (SMS) to develop viable therapeutic options.

Impact on Lives

Through funding comprehensive research projects, the SMS Research Foundation aims to improve the quality of life for children and individuals affected by SMS worldwide.

Why Donate?

Increased funding for research is essential to create innovative treatment options for those living with Smith-Magenis Syndrome. Your tax-deductible donation supports life-changing research and brings hope to families impacted by this complex disorder.

Join the Cause

Make a difference today! Your contribution, whether in cryptocurrency or cash, can help unlock new possibilities for individuals with Smith-Magenis Syndrome. Together, we can pave the way for groundbreaking research and improved lives.