Bill Moore & his daughter Jessica Oberlin, two members of NAF, recently shared their stories of living with SCA3 as part of a feature for the Critical Path to Therapeutics for the Ataxias (CPTA). The CPTA aims to optimize clinical trials for inherited Ataxias. Impact stories like theirs can help researchers & drug developers understand the realities of living with Ataxia. You can read it here: c-path.org/impact_story/cpt...
A shared story of SCA3: Bill Moore & his daughter... - Ataxia UK
A shared story of SCA3
Written by
wobblybee
To view profiles and participate in discussions please or .
Read more about...
Not what you're looking for?
You may also like...
Join a remote Study for SCA1. SCA2. SCA3. or SCA6
A new remote study from the Harding Lab at Monash University aims to better understand how...
CoQ10 and Spinocerebellar Ataxias
In my never ending search for answers I came across this study today:...
Improving diagnosis, and management of Gluten Ataxia.
🙂People in the UK
Improving diagnosis and management of Gluten ataxia
Ataxia UK, Coeliac UK,...
A new light shines on SCA3. Far infrared light therapy?
Someone pointed me to this awhile back, and I remember being intrigued, but I never followed...
Peripheral neuropathy?
Hi everyone I have gluten ataxia and am curious if peripheral neuropathy is limited to just...
Why am I a part of the Ataxia UK community?
My attempts at managing SCA3
Cerebellar Ataxia SCA3 (Machado-joseph)
Happy new year 🍾🎉🥰
