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I am Shrey Nilesh Ratambe, 5 year old and I am suffering from genetic rare disease called 'Duchenne Muscular Dystrophy' (DMD).
07/09/2021
Today is World Duchenne Awareness Day
23/07/2021
*Hi AlI! I May Not Know You Nor Little Shrey Knows You - BUT We Know One Thing 'Gifting Someone Life Is An Unmatched Act of Giving'*
Help Me To Raise Funds For My Son's Treatment Nilesh D Ratambe wants to raise funds for his son Shrey Nilesh Ratambe to fight Duchenne Muscular Dystrophy. Your donation can guide them to reach their fund goals. Please help.
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