
Finding Clinical Trial Information Using ClinicalTrials.Gov
Many people with Ataxia are interested in participating in clinical research, but are not sure where to start. It can be tricky to know where Read More…
The Ataxia Community Comes Together in Orlando April 9–11, 2026 for the Annual Ataxia Conference! LEARN MORE
Check out our latest articles to stay-up-to-date on the happenings at NAF and in the Ataxia community. Select a category to see all the blogs available in that category.

Many people with Ataxia are interested in participating in clinical research, but are not sure where to start. It can be tricky to know where Read More…

Walk N’ Roll events bring together individuals, families, and communities to spread awareness and support NAF’s mission of accelerating treatments and improving the lives of Read More…

Our vision is clear: a world without Ataxia. Our mission guides the way that we pursue that vision: by accelerating the development of treatments and Read More…

The new year can be a time for reflection and anticipation. At NAF, it is especially true for a change to our Board of Directors Read More…

It takes a long time to develop a new drug. Not to mention it can be very expensive. But why does it take so long Read More…

Guest Author: Day Undefined Welcome to Day Undefined’s Holiday Gift Guide for the National Ataxia Foundation – taking a fun twist on some of our Read More…

NAF is hiring a full time Clinical Research Coordinator. This person will be responsible for supporting the Clinical Operations Branch of the Research Department. This Read More…

While some begin their careers with a specific specialization – ready to focus on making a difference in a certain field – Dr. Tetsuo Ashizawa’s Read More…

The following is a high-level overview of the Katie Campbell CRC-SCA Face-to-Face Meeting held from September 11-13, 2023, in Bloomington, Minnesota. This meeting focused on Read More…
Our members are a community of individuals and families who are united in the fight against Ataxia. Read about their unique Ataxia journeys from their perspectives.
We invite you to join as a member to receive a new member story each month. It’s free, and you’ll be kept up-to-date on the latest developments in the Ataxia community.

My Ataxia journey began in 1978, following a three-month coma Read More…

I’ve been living with a genetically acquired Ataxia since birth Read More…
Thank you for your interest in contributing content to our website!
We do accept guest submissions for our blog; however, we have a few important guidelines. All content must be original (not published elsewhere online) and relevant to the Ataxia community. Submissions should aim to inform, support, or empower those affected by Ataxia, including patients, caregivers, researchers, and advocates.
Here is an example of a guest authored blog: https://www.ataxia.org/6-tips-to-improve-mental-health-while-living-with-ataxia/
If you have an idea you’d like to propose, please feel free to share a brief summary or outline for our team to review. We appreciate your interest in supporting our mission and community! Email us at naf@ataxia.org.
We appreciate your interest in supporting our mission and community!
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