I have just found out that 28th Feb, is Rare Genes Day, although I believe that the whole of February is dedicated to this. I feel that I should have known, as a distant family member has a child with this diagnosis. On reading her blog, I wonder at her strength, and also that of her family. She makes me cry at times, but is always upbeat. There is no cure, but ongoing research that will hopefully help others in the future.
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