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79 is a blog that shares the the latest news on genetic research and care for Duchenne Muscular Dystrophy. Nick Catlin has a son Saul who lives with Duchenne and has many years experience of campaigning and supporting the fight for a cure and new treatments. Follow me!

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79 is neither promoting research nor involved in conducting any clinical trials. It is a blog and website that does not provide medical advice, diagnosis or treatment. This content is not intended to be a substitute for professional medical advice, diagnosis, or treatment. Always seek the advice of your physician or other qualified health provider with any questions you may have regarding a medical condition. Never disregard professional medical advice or delay in seeking it because of something you have read on this blog or website

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If you would like to contribute to 79 then please email me. It is important that we can all work together and share ideas and knowledge. This will be the only way to find a cure for Duchenne.

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Any news or views on research or current best practice in medical care or education for young people living with Duchenne? Please email 79.

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