Biohaven announced that the FDA has issued a Complete Response Letter (CRL) for the New Drug Application of VYGLXIA (troriluzole), intended for the treatment of Spinocerebellar Ataxia (SCA). We're very disappointed in this decision. (1/2)

Today is International Ataxia Awareness Day and we need your help to spread the word! Are you ready to make this the biggest #IAAD yet? Kick it off by sharing this graphic to let everyone know what day it is!

Ataxia doesn’t wait—and neither should treatment. NAF has launched a petition on Change.org calling on the FDA to prioritize treatment options for rare diseases with urgent unmet needs, including Spinocerebellar Ataxia (SCA). (1/4)

Today is Friedreich Ataxia Awareness Day to bring awareness to one of the most common forms of recessive hereditary Ataxia. On average, the disease’s onset is in people from ages 5-25.

Learn more about Friedreich Ataxia (FA) on our website: www.Ataxia.org/FA

The first Ataxia gene mutation (responsible for SCA1) was discovered in 1993 by Dr. Huda Yahya Zoghbi & Dr. Harry Orr. Since then, scientists have continued to unlock the genetic secrets of Ataxia as they work toward developing treatments & eventually a cure. (2/3)

April 25th is National DNA Day! It commemorates the 1953 discovery of DNA's Double Helix Structure & the completion of the 2003 Human Genome Project. Our knowledge of DNA has expanded in less than a century but when did researchers start discovering the genes that cause hereditary Ataxias? (1/3)

This Friday! Join us April 11th at 1pm CDT for our “Ask the Expert” webinar with Dr. Susan Perlman to answer your questions about Ataxia. You will have the opportunity to ask any questions you have related to Ataxia.

Register here: us02web.zoom.us/webinar/regi...

Did you know? The cerebellum is the part of the brain responsible for movement coordination in the body. Ataxia symptoms occur when the cerebellum is not functioning properly. Cerebellar dysfunction can be caused genetically or by physical injury. #AtaxiaAwareness

Today is #RareDiseaseDay which is meant to bring awareness to rare diseases around the world, including the various types of #Ataxia! How are you championing Rare Disease Day today?

For more information on Rare Disease Day, visit: www.rarediseaseday.org

The National Ataxia Foundation is conducting an online survey with help from Savanta. We need your insights. If you’re living with ataxia or caring for someone with ataxia, your feedback can help shape NAF’s future programs.