You Can Help
There are so many ways to join the cause! The mission of the Hereditary Neuropathy Foundation is about change: changing things right here, right now, and creating change well into the future. You can be a part of this movement in so many ways.
Be an HNF Supporter
Your financial contribution to HNF fuels our mission and enables us to continue critical research, advocacy and awareness activities that will one day lead to a cure for CMT. Consider a direct donation, earmarked to match your priorities. Contributions at the Member level or above are eligible to receive a copy of our Essential Guide: What It’s Like to Live with CMT and a Mission Happy Feet bracelet!
Special Offer from Strough Real Estate
HNF Board Member Kathleen Zappola has pledged 20% of her commission for any referrals from the HNF! So if you are looking to buy or sell a home in the Hamptons, contact Kathy right away!
Advocate!
HNF continues to advocate for the needs of those living with CMT. You can help! Read more…
Shop with iGive
By shopping online through iGive, a portion of the proceeds is donated to HNF.
Use Mission Fish
Coming soon: Ebay offers buyers and sellers the option of using Mission Fish which then donates a portion of proceeds to HNF.
hello my name is kyle clark and i have CMT and i have asked CMT music to sponsor if they do i’ll contact you if you have any questions
email me @ monster_drums@hotmail.com
Hello,
I was recently diagnosed with Charcot-Marie-Tooth and I was wondering how I would be able to gain awareness in Maine about the disorder. I am a mom of 3 boys and it wasnt until I was diagnosed when my youngest was born that I even heard about the condition. I would like to have people here in Maine if there not aware of it to become aware. This condition for me is awful and has changed my way of life and if I can help someone else not have to deal with the stuggles alone like I have had to. I also would like to in time organize a walk to raise money for the disorder if someone can lead me into the direction of where I need to be would be amazing
Thank you for your comment. We certainly understand your challenges and struggles, and you’re right, awareness is such a big part of what we need to do. One of our premiere awareness efforts is our children’s book series, see http://www.hnf-cure.org/awareness/arlene-scene/. We offer free school presentations, and perhaps your sons’ schools would be interested. Contact me, carol@hnf-cure.org, to talk further about this. Also, our Team CMT, http://www.hnf-cure.org/team-cmt/, is a great way to raise awareness of Charcot-Marie-Tooth while raising money for research.
This is a very difficult disease, but we truly believe that together, we can make a difference. Looking forward to working with you!