Learn about BIO, register for events and explore member services. The CMT Research Foundation was created by two patients who have over 20 years of experience advancing CMT research and drug development. 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. CMT Research Foundation funds Shift to explore novel series of drugs created to control the expression of PMP22 gene. The CMT Research Foundation is ensuring that I will have at least one treatment option within my lifetime. Christopher “Topher” Delamarter grew up the son of an army brat with a wanderlust for travel and adventure. Thank you. The approach focuses on silencing the gene that is causing the disease in each disease subtype, and replacing it with a functional gene. Inherited mutations in the MFN2 gene lead to degeneration of muscle-controlling … 355 talking about this. Yes, that means you. Federal tax exempt status as a public charity under Section 501 (c)(3) is pending by the U.S. Internal Revenue Service. The Biotechnology Innovation Organization is the world's largest biotech trade association. Today is the first day of our CMT Action Month, a time to rally toge... ther as a CMT community to transform awareness into action. CMT Research Foundation. CMT Research Foundation Personal Fundraising. Our Vision Donate  Hunter’s CMT4B3 Research Foundation Inc. (Tax ID: 85-3259676) is a Delaware corporation. Our Vision Donate  Hunter’s CMT4B3 Research Foundation Inc. (Tax ID: 85-3259676) is a Delaware corporation. The CMT Research Foundation (CMTRF) wants to turn September from Awareness Month into “CMT Action Month.”. About. 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.. About. Atlanta, Georgia, United States Founder and CEO Gary Donaldson Communications Sep 2017 - Present 3 years 4 months. Help us make a difference! Your donation WILL make a differece. Help us make a difference! The ongoing hunt for CMT genes has given insights into treatments that might be used to stop or reverse the disorder. Launched in 2018 by two CMT patients, Susan Ruediger … When you give by December 31, 2020, a generous group of donors will match your donation up to $100,000. Read More. The CMT Research Foundation is solely dedicated to funding research that will yield a cure or treatment for CMT. Charcot-Marie-Tooth type 1A, or better known as CMT1A, is a … 1 Cognipharma Team $23,717.90 raised; 2 Susan Ruediger $12,426.00 raised; 3 Chelsea Layton $1,494.30 raised; 4 Gary Donaldson $1,068.59 raised; 5 Karina Wilgeroth $1,065.00 raised; View Full Leaderboard. All donations are tax-deductible to the full extent of the law. CMT4B3 Research Foundation. September 1 at 5:54 AM. Working with a network of respected scientists and industry professionals, the foundation will accelerate treatments and a cure for CMT. Patients and families. Do you know what CMT researchers say is the most powerful and influential force to speed treatments for CMT? 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). 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. Currently, the STAR Drug Development Pipeline involves more than 30 research partners in more than 50 research studies. They won't stop until they do so. Any donation that you make will be matched dollar by dollar by Cognipharma! Attend Events; Advocate; Support; Close; for Patient Organizations. Federal tax exempt status as a public charity under Section 501 (c)(3) is pending by the U.S. Internal Revenue Service. Find a Patient Organization; Rare Disease Day® Patient Stories; Take Action. Help us bring hope to all these families all over the world. Federal tax exempt status as a public charity under Section 501 (c)(3) is pending by the U.S. Internal Revenue Service. “The CMT Research Foundation will play a unique role in the CMT community by limiting overhead and focusing on funding research that will help speed cures not only for various levels of CMT, but also other neurological degenerative diseases including amyotrophic lateral sclerosis (ALS) and Alzheimer’s,” Livney said in a press release. Chris Delamarter Topher's Personal Fundraising Page Help us reach this important goal before the end of September! Hunter’s CMT4B3 Research Foundation Inc. (Tax ID: 85-3259676) is a Delaware corporation. CMTA Annual Reports The 2019 Annual Report is now available. 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. The CMT Research Foundation has one single focus: deliver treatments and cures for CMT. Research. Find out what CMTA is doing to advance research, create awareness, and make life better for everyone affected by CMT. CMT4B3 Research Foundation. While expected to treat multiple CMT … Since 2008, STAR has invested more than $16 million in CMT research. CMT Research Foundation Jan 2020 - Present 1 year. 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. They have one single focus: find treatments for CMT with our lifetimes. Synonyms: CMT 4B1, Charcot-Marie-Tooth disease, Type 4B, CMT 4B, Charcot Marie Tooth disease type 4B1 Charcot-Marie-Tooth disease type 4B2 Synonyms: CMT 4B2, Charcot Marie Tooth disease type 4B2, CHARCOT-MARIE-TOOTH DISEASE, WITH FOCALLY FOLDED MYELIN SHEATHS, AUTOSOMAL RECESSIVE, TYPE 4B2, CHARCOT-MARIE-TOOTH NEUROPATHY, TYPE 4B2 Please help us get there by donating what you can. 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. 77 Garden Road Scarsdale, NY 10583 info@cmt4b3.org Contact us: (917) 453-2319. We would like to show you a description here but the site won’t allow us. As the CMT gene hunt continues, MDA-funded scientists are investigating how and why specific genetic mutations lead to different types of CMT. Read More. Join Membership Network. 77 Garden Road Scarsdale, NY 10583 info@cmt4b3.org Contact us: (917) 453-2319. 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 … Patient Assistance Programs; Other Financial Assistance ; Connect with Others. 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. The CMT Research Foundation is solely dedicated to funding research that will yield a cure or treatment for CMT. Information on Clinical Trials and Research Studies; COVID-19 Resources; Help to Access Medications. Edinburgh, United Kingdom Gary Donaldson Communications was founded to offer clients a reliable, forward-thinking and creative partner that will help engage their target audiences and inspire business growth. Born in Washington, D.C., they moved to Brooklyn when he was 7 years old. You can give Angelique and everyone living with CMT more than hope by making a donation to the CMT Research Foundation to fund the most promising research that’s solely focused on delivering treatments and cures during our lifetime. … 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. 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