Our Friends’ blogs
Many of our Friends also write their own blogs about ataxia. Check them out below!
Wendy’s Is This the Wheel Life?
Wendy discusses her experiences in dealing with the public perceptions and societal limitations that impact her life with ataxia: “the reality of disability in modern Britain,” including how to plan a wedding when you have ataxia. Great for: well-written prose and reflections on life as someone with ataxia.
Iain’s Kilted Walker
Follow Iain as he walks … pretty much everywhere around the world in his kilt! Iain has worked hard to get into every local newspaper he can along the way, raising awareness of his condition, and fundraising as he goes. Great for: fundraising inspiration and taking control.
Amanda’s Boy Number Two and Me
Amanda is the mother of Sebastian, aged six, who has episodic ataxia. Her blog discusses her personal experiences in caring for a child who has additional needs. Great for: parents of children with ataxia.
Arran’s Eleanor Creative Blog
Read Arran’s professional blog about running her own Creative Marketing company after receiving her SCA6 diagnosis. Great for: people with ataxia wanting to read about employment, and taking control.
