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
Launch an online fundraising page – Close to 3 million people have CMT or a related inherited neuropathy. Our mission it to fund and seek out treatments that will halt, reverse and ultimately cure CMT. Contact firstname.lastname@example.org for assistance.
Join the Global Registry for Inherited Neuropathies (GRIN) – by joining and sharing de-identified information on your CMT symptoms, age of onset, type of CMT, level of pain, etc. you are helping the research community gather data and pertinent information that can help us find the treatments needed to help you.
Share our Essential Guide What It’s Like to Live CMT – you can post on Facebook, and other CMT and health related communities to spread the word on CMT, email to friends and family and tweet. By taking a moment, more people will know about CMT.
Launch a letter writing campaign – join board member Iris Adler and raise funds for research. Fundraising coordinator Courtney Hollett and Iris will help you through the entire process and earmark funds raised for translational research. Contact email@example.com for assistance.
Join Team CMT – by joining the team and sporting our Team CMT singlet you can help spread awareness. You can wear it to the gym, physical therapy or if you are an athlete participating in events, you can have a dedicated fundraising page.
Join iGive – by joining iGive and downloading the button to your website or smartphone you can help our mission. Every time you shop through iGive a portion of your purchase pre-tax will be donated to HNF.