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Duchenne Muscular Dystrophy

Fighting Duchenne Muscular Dystrophy Together

Jakub and Martin write their blog for pleasure and to cheer up others. Not only does that unite them, but they both share a rare disease called Duchenne Muscular Dystrophy too. Living with Duchenne comes with thousands of downs and ups. We do not fight by a brute force, but rather by a power within. One just needs to find it within him or herself.

Do not say: "It’s not possible!" It's always possible to find a way how to continue. Believe in yourselves and fight for every single day. You may not like every day, but you can find something unique and beautiful in every single day.

Thanks to all who have signed up for a subscription of the intergalactic content of http://nevzdavejto.cz. Those, who have not yet decided, you have another chance to do so.

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Jakub and Martin write their blog for own pleasure and to cheer up others. Not only that unites them. They both share a rare disease called Duchenne muscular dystrophy, too.

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Jakub Šudák

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Duchenne Muscular Dystrophy

Jakub and Martin write their blog for pleasure and to cheer up others. Not only does that unite them, but they both share a rare disease cal
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