We are delighted that the first ever Kennedy's Disease Patient day was held in the UK in March 2017. This was a landmark occasion where we met many families who...
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We have seen at first hand how passionate and driven the research team at UCL is. What we didn’t know is that alongside being a hugely talented and dedicated researcher,…
What a fantastic way to raise awareness and great fundraising for KD-UK by holding a 'Chinwag, Cake and a Cuppa' morning. This fundraising event could be held at your home, a...
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Ian Renouf-Watkins shares his thoughts, strategies and outlook on living with KD. My family’s journey with Kennedy’s, I now realise, began many years ago when, as a 14 year old,...
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My name is Tom Stroud and in September I will be running the New Forest Marathon to raise funds for Kennedy’s Disease UK. I was five years old when my...
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We all love to do something fun, something that puts a smile on people’s faces. Here at KDUK, we’re putting together a calendar featuring some of Dorchester’s amazing businesses. It’s...
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Colin shares his thoughts, strategies and outlook on living with KD. My name is Colin. I was born in 1953 and, along with my two brothers, I have Kennedy’s Disease...
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Even driving winds and rain can’t dampen Lou and Kate’s joy at raising new funds for KD-UK. One month before Yeovil half marathon I casually asked Kate, my sister and chairman of...
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The KD team at UCL have some fantastic news. A clinic specifically dedicated to KD will start next month (May) and will run on Friday mornings at the National Hospital...
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The Neverest Girls aim high to help fund KD-UK. The Neverest Girls, a group of passionate female runners from Chamonix in France, are busy preparing for their biggest challenge yet...
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