hannah's hope fund

I think it's so wonderful to have a presence on the web, albeit a small one. But to get the word out on something so important means so much to me. I recently got an email from my friend, Pam, back in New York. Two of her dearest friends, Matt and Lori Sames, learned just a few months back that their little girl, Hannah, is suffering from a disease called Giant Axonal Neuropathy, or GAN. This family is now dedicated to not only treating their daughter, but bringing awareness of this terrible disease with the hopes of saving a few very precious lives. Please visit www.hannahshopefund.org to learn more about Hannah and this disease, and spread the word in any way you can.