Maryland Stroll for IRSF

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October is Rett Syndrome Awareness Month. 💜

Though first identified in the 1960s, Rett syndrome did not receive worldwide recognition as a distinct disorder until 1983. Through the 1980s and 1990s, diagnostic criteria were developed and research continued, culminating in the landmark discovery of the MECP2 gene mutation as the primary cause of Rett by Dr. Huda Zoghbi’s lab in 1999.

In 2006, the Natural History Study began collecting vital data on the progression of Rett syndrome—data that continues to guide care standards and inform today’s gene therapy clinical trials. And in 2023, after decades of relentless research and advocacy, the FDA approved the first-ever treatment for Rett syndrome, marking a historic milestone for the entire community.

Each discovery, study, and breakthrough over the past 40 years has brought us closer to better treatments and, one day, a cure. 💜 But we're not done yet. This October, we need your help to raise awareness and critical funds in our fight against Rett. Learn more and get started today at rettsyndrome.org/october.

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While Rett syndrome IS genetic, it is NOT an inherited disorder. This is because it is typically caused by a mutation on the X chromosome. This October, in honor of Rett Syndrome Awareness Month, learn more about from the International Rett Syndrome Foundation: https://www.rettsyndrome.org/about-rett-syndrome/