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Research Funding Opportunities

2022 Cure CMD Request for Applications (RFA)
International Research Grants in Congenital Muscular Dystrophy
 

Collagen 6, Congenital Dystroglycanopathies, LAMA2, Congenital Laminopathy, SELENON

Application Deadline: Friday, July 22, 2022, 11:59 pm Eastern Time
 

Thanks to the tremendous efforts of the CMD patient community, Cure CMD is pleased to announce the availability of $400,000 in international research grant funding for the five primary subtypes of Congenital Muscular Dystrophy

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  • Each CMD subtype constitutes a separate application for research project awards, independent of the other four CMD subtypes (funding award levels vary by subtype, see below)

  • Applications that propose research in more than one CMD subtype are also welcome (funding award capped at $100,000)

  • Applicants must be affiliated with an accredited academic institution and in good standing

  • Inclusion of junior investigators in your proposed project is also encouraged

 

Cure CMD welcomes applications for meaningful research that could translate into a treatment or care optimization, propelling our mission in support of those living with congenital muscular dystrophy.

  • Advocacy Partners
    The Cure CMD Advocacy Team works with the following rare disease organizations in the United States to support legislation that affects our community. National Organization for Rare Disorders (NORD) EveryLife Foundation for Rare Diseases Rare Disease Legislative Advocates (RDLA) Global Genes: Allies in Rare Disease Muscular Dystrophy Association (MDA)
  • International Advocacy
    Participate in the advocacy efforts of Eurodis, an organization committed to rare disease advocacy in 74 European countries. Get involved with Rare Disease International, a global alliance of persons living with a rare disease. Learn about the NGO Committee for Rare Diseases and their advocacy work. Join the international community in raising awareness about rare diseases on Rare Disease Day
  • Federal Advocacy
    Find out who represents you in the U.S. Senate and House of Representatives Learn how to build a relationship with your Senators and Representative Learn about the federal Rare Disease Congressional Caucus and ask your Senators and Representative to join if they haven't already Use RDLA's Advocacy Tools to learn more about how to advocate Familiarize yourself with RDLA's legislative scorecard Participate in RDLA's monthly legislative webinars to learn about current and proposed legislation that supports the Rare Disease community Sign up for Rare Across America Attend Rare Disease Week on Capitol Hill
  • State Advocacy
    Learn how to advocate in your state by checking out RDLA's State Advocacy Hub Join the RareAction Network for your state Check the NORD state report card to see how well your state supports the Rare Disease Community Learn about NORD's Project RDAC (Rare Disease Advisory Council) and see if one has been established in your state.
  • Other Opportunities
    Join YARR (Young Adult Representatives of RDLA) if you are 18-29 years old Celebrate Rare Disease Day in February Attend the RARE Patient Advocacy Summit sponsored by Global Genes Travel to the National Institutes of Health (NIH) to attend Rare Disease Day at NIH Participate in NORD’s Patient and Family Forum
  • Resources
    Share the Cure CMD Advocacy Fact Sheet with your legislators Create a One Pager telling your CMD story and share with your legislators. See an example.
  • Advocacy Partners
    The Cure CMD Advocacy Team works with the following rare disease organizations in the United States to support legislation that affects our community. National Organization for Rare Disorders (NORD) EveryLife Foundation for Rare Diseases Rare Disease Legislative Advocates (RDLA) Global Genes: Allies in Rare Disease Muscular Dystrophy Association (MDA)
  • International Advocacy
    Participate in the advocacy efforts of Eurodis, an organization committed to rare disease advocacy in 74 European countries. Get involved with Rare Disease International, a global alliance of persons living with a rare disease. Learn about the NGO Committee for Rare Diseases and their advocacy work. Join the international community in raising awareness about rare diseases on Rare Disease Day
  • Federal Advocacy
    Find out who represents you in the U.S. Senate and House of Representatives Learn how to build a relationship with your Senators and Representative Learn about the federal Rare Disease Congressional Caucus and ask your Senators and Representative to join if they haven't already Use RDLA's Advocacy Tools to learn more about how to advocate Familiarize yourself with RDLA's legislative scorecard Participate in RDLA's monthly legislative webinars to learn about current and proposed legislation that supports the Rare Disease community Sign up for Rare Across America Attend Rare Disease Week on Capitol Hill
  • State Advocacy
    Learn how to advocate in your state by checking out RDLA's State Advocacy Hub Join the RareAction Network for your state Check the NORD state report card to see how well your state supports the Rare Disease Community Learn about NORD's Project RDAC (Rare Disease Advisory Council) and see if one has been established in your state.
  • Other Opportunities
    Join YARR (Young Adult Representatives of RDLA) if you are 18-29 years old Celebrate Rare Disease Day in February Attend the RARE Patient Advocacy Summit sponsored by Global Genes Travel to the National Institutes of Health (NIH) to attend Rare Disease Day at NIH Participate in NORD’s Patient and Family Forum
  • Resources
    Share the Cure CMD Advocacy Fact Sheet with your legislators Create a One Pager telling your CMD story and share with your legislators. See an example.
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