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yuneri cendradini's Fundraiser:

Juan's journey in fighting Duchenne Muscular Dystrophy

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yuneri cendradini


My sons name is Juan, which means a good looking boy well he is isn't he?. He was my wish come true I really wanted a baby boy since my youngest brother got sick of muscular disease. I Just want my parents to be happy seeing a healthy boy in the family. But one day those dreams are taken away when I am curious about how my son falls easily when learning to walk, and his ways of standing up is just uncommon. In that moment I remembered my brother, in my thoughts I was thinking does my son has the same disease like my brother?.As his falling grows frequent I brave myself to get my son to see a doctor. They did some test on him including blood test to see his CK levels or creatin kinase level, the results did show us his ck's are very high and this indicates he was also suffering a disease called the Duchenne Muscular Dystrophy. My world is crumbling around me because I know there is still no cure for this the only way I can help my son is only with therapies. But those therapies also doesn't help much in saving his life.

Now my son is 8 years old and his in a wheelchair, he use to do therapies but has stopped in some time because I have run out of money after seeing medical preferences all over the country. I wanted to start giving my son therapies again because not just his feet has beginning to loose its powers, his back also give in to this and formed a C shaped scholiosis

I needed to get this going by getting myself into fundraising and get donations for my son to continue his therapies. So any amount of money would be very appreciated by Juan and I it really means a lot to us



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