November 6, 2012
I met Hannah in 2011. I was moved by her spirit, the dedication and adoration of her friends, and most of all the perseverance of her mom and dad to find treatment and therapies for this rare, fatal disease. The grace and determination of her parents is unbelievable. Being involved in Hannah's Hope Fund has provided endless opportunities to help teach my kids about compassion and character. My five year-old son emptied his piggy bank and donated its entirety to Hannah’s Hope Fund, and discussed GAN with his pediatrician to ensure he (the doctor) knew what this rare disease was. I spend countless hours every week utilizing social media and researching opportunities for this organization. It is a honor to be part of the world dedicated to developing a cure for GAN.
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