Hi everyone ?? my name is Chelsea and I have CMT1A. I have been an ambassador with the CMT Research Foundation for a couple years now and I'm excited to participate in this year's September CMT Action Month! CMT was first described in 1886; almost 135 years ago. At this point, we need more than awareness to find a cure, we need ACTION. So I'm asking my friends and family to help me take action this year by donating to the CMT Research Foundation, an organization that is laser focused on researching treatments and cures for CMT. For the month of September, every donation will be matched by a generous donor of up to $25,000! Thanks for following my journey and help making a difference in not only my future, but the future of so many wonderful people who are also afflicted with this disease.