Welcome to Team Hannah's Hope Fund and Justin's Triumph over GAN. We raise funds to support the development of a treatment and cure for Giant Axonal Neuropathy (GAN), and to be the resource for doctors, scientists and families world-wide. GAN is an extremely rare and fatal genetic disease. There are only 63 known cases world-wide. The life expectancy for these children is only into their 20's. In 2015, the FDA approved an experimental trial -- so far, 2 patients have been injected. Help us raise money to continue our search for a cure for GAN.
I race to save the lives of my fraternal twin brother and little sister who have Giant Axonal Neuropathy (GAN).
We are rasing fund to find a treatment and cure of GAN.
Please support me!
|Donor||Donation Amount||Donation Date||Comment|
|HMSA Classical||$400.00*||12/15/2017||Congratulations and thank you for participating in the HMSA Classical Charity Challenge.|
|Heritage Texas||$191.00*||10/16/2017||Jeans for Genes|
|* offline donation|