GDAP1 Gene Therapy Research Fund
Supporting Hereditary Neuropathy Foundation
Created by Kohler Family
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It’s a hard disease to have,” says Alana. “Sometimes I feel embarrassed in front of my classmates. It’s not easy to keep up. The hardest part is the bullying. It makes me feel really sad that I’m not, like, normal and I feel like I shouldn’t have CMT4A. Why me? I just try and stay strong.”

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Contact Us: Hereditary Neuropathy Foundation | PO Box 1922| Midlothian, VA 23113 | 212.860.5405 [email protected] 
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