
Navigating Life With Friedreich’s Ataxia
The Who and the Why?
Freddie’s Ataxia Fund (FAF) is a charity established in 2025 for people diagnosed with the rare genetic condition Friedreich’s Ataxia (FA). We provide financial grants to contribute to the costs of adapting to life with FA. Based in Dundee, Scotland, we were founded by the family and friends of Eilidh Kiddie, who was diagnosed with FA in 2019.
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The Wheeling Wanderer
As an aspiring journalist, Eilidh has started a travel blog. Please read her blog and follow her on Instagram