November 8, 2012
I had been following Hannah's Hope since it's foundation but I didn't truly see the depth of its impact until I met Hannah this past summer. Hannah is such a bright and positive young lady. It is amazing how much this family has done for her and for all the children with GAN. Just because a disease is rare doesn't mean that no one should try to find a treatment for it. Who knows maybe the treatment for this illness could lead to the discovery of treatments for other illnesses.
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