Our Friends explore more about ataxia online through the digital written word. Read their stories, thoughts, ideas and about their extra-curricular activities here.
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.
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.
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.
Arran’s Eleanor Creative Blog
Read Arran’s professional blog about running her own Creative Marketing company after receiving her SCA6 diagnosis.
