CMTA Annual Reports The 2019 Annual Report is now available. Patient-led research organisations are changing the landscape for rare disease research and drug development one disease at a time and the CMT Research Foundation are no exception. Information on Clinical Trials and Research Studies; COVID-19 Resources; Help to Access Medications. All donations are tax-deductible to the full extent of the law. The approach focuses on silencing the gene that is causing the disease in each disease subtype, and replacing it with a functional gene. CMT Research Foundation funds Shift to explore novel series of drugs created to control the expression of PMP22 gene. CMT Research Foundation. Help us bring hope to all these families all over the world. AcuraStem has identified 37 compounds that improve nerve cell survival and might help treat Charcot-Marie-Tooth disease type 2A (CMT2A), according to a press release from the CMT Research Foundation.. CMT2 accounts for roughly one-third of CMT cases and CMT2A is its most common subtype. Founded by Susan Ruediger and Patrick Livney, who have over 20 years of collective experience working with the CMT research community, the CMT Research Foundation is solely devoted to funding research projects that will deliver a cure or treatment for CMT. This year, the foundation is seeking to turn awareness of Charcot-Marie-Tooth (CMT) disease into action through useful and informative videos, personal fundraising pages, and a “double-your-donation” fundraising campaign.. Overland Park: In late January, the CMT Research Foundation announced a partnership with Shift Pharmaceuticals to further research in treatments for CMT1A, a familiar form of Charcot-Marie-Tooth (CMT). Any donation that you make will be matched dollar by dollar by Cognipharma! Please help us get there by donating what you can. The CMT Research Foundation is ensuring that I will have at least one treatment option within my lifetime. When you give by December 31, 2020, a generous group of donors will match your donation up to $100,000. Chris Delamarter Topher's Personal Fundraising Page Help us reach this important goal before the end of September! Find out what CMTA is doing to advance research, create awareness, and make life better for everyone affected by CMT. Our Vision Donate  Hunter’s CMT4B3 Research Foundation Inc. (Tax ID: 85-3259676) is a Delaware corporation. Christopher “Topher” Delamarter grew up the son of an army brat with a wanderlust for travel and adventure. Launched in 2018 by two CMT patients, Susan Ruediger … Hereditary Neuropathy Foundation (HNF) is a non-profit 501(c)3 organization which mission is to increase awareness and accurate diagnosis of Charcot-Marie-Tooth (CMT) and related inherited neuropathies, support patients and families with critical information to improve quality of life, and fund research that will lead to treatments and cures. CMT4B3 Research Foundation. The ongoing hunt for CMT genes has given insights into treatments that might be used to stop or reverse the disorder. Hunter’s CMT4B3 Research Foundation Inc. (Tax ID: 85-3259676) is a Delaware corporation. Born in Washington, D.C., they moved to Brooklyn when he was 7 years old. 355 talking about this. CMT Research Foundation Personal Fundraising Leaderboard. Inherited mutations in the MFN2 gene lead to degeneration of muscle-controlling … September is Charcot-Marie-Tooth (CMT) Awareness month and we are delighted to welcome George Simpson, volunteer media relations advisor, as our guest blogger to educate our community on this little … About. The CMT Research Foundation has launched a new research program that will seek to develop a precision medicine approach to treat people with Charcot-Marie-Tooth (CMT) disease, the foundation announced in a press release. The Biotechnology Innovation Organization is the world's largest biotech trade association. The CMT Research Foundation is solely dedicated to funding research that will yield a cure or treatment for CMT. CMT Research Foundation Jan 2020 - Present 1 year. While expected to treat multiple CMT … September 1 at 5:54 AM. About. Hereditary Neuropathy Foundation (HNF) is a non-profit 501(c)3 organization which mission is to increase awareness and accurate diagnosis of Charcot-Marie-Tooth (CMT) and related inherited neuropathies, support patients and families with critical information to improve quality of life, and fund research that will lead to treatments and cures. Help us make a difference! Cognipharma have partnered with the CMT Research Foundation to find treatments and cure for CMT, and are fundraising as a team to deliver on that goal. They have one single focus: find treatments for CMT with our lifetimes. Help us get there by donating what you can 85-3259676 ) is a Delaware corporation for Events and member. Drug development Pipeline involves more than 30 Research partners in more than $ 16 million in Research. Hunter ’ s CMT4B3 Research Foundation was created by two CMT patients, Susan Ruediger … the Innovation. 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