The Dravet Syndrome Foundation (DSF) is a volunteer run, non-profit organization based in the United States. The mission of the foundation is to aggressively raise research funds for Dravet's syndrome and related epilepsies, while providing support to affected individuals and families. The Dravet Syndrome Foundation is listed as a research and support organization on National Organization of Rare Diseases's (NORD) database.
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History
The Dravet Syndrome Foundation was founded by parents with the purpose of expediting research to find a cure and better treatments for their afflicted children. It was established in the state of Connecticut and was designated a tax-exempt public charity in the United States in September 2009 by the Internal Revenue Service under Section 501(c)3.
Programs
In accordance with their mission, the Dravet Syndrome Foundation focuses its work in four areas: Research Grants; Research Roundtable; International Ion Channel Epilepsy Patient Registry (IICEPR); and the International Patient Assistance Grant (PAG) Program.
Research Grant Program
Grants are offered for research projects directly related to Dravet syndrome and associated epilepsies. These grants fund initial research hypotheses that have not been fully explored. The results extracted from this type of research will help bring untested research to the point that it can qualify for larger governmental funding. Research applications are judged principally on novelty of the hypotheses, innovative approaches with a direct relevance and application to Dravet syndrome and related conditions, scientific quality, strength of approach, and likelihood of success.
Research Roundtable
This annual meeting allows researchers, geneticists, neurologists, and other professionals with a strong interest in Dravet syndrome and related epilepsies to establish a “research roadmap”. By allowing this consortium of specialists to establish a plan, the Dravet Syndrome Foundation can facilitate the development and implementation of better treatments by funding research projects that address the critical challenges of this syndrome and which will offer the most promising breakthroughs at the fastest pace possible. This meeting takes place each year just prior to the commencement of the American Epilepsy Society (AES) Conference.
International Ion Channel Epilepsy Patient Registry (IICEPR)
This registry (co-funded with ICE Epilepsy Alliance) is owned by University of Michigan Neurology Department and Miami Children's Hospital Brain Institute but is available to all interested researchers. It will collect basic information and genetic test results of individuals with Dravet syndrome and related epilepsies worldwide. The establishment of this registry will expedite future clinical trials and will serve to improve communication of ideas amongst interested researchers, as well as assure rapid distribution of any new information that may benefit patients and their families. The website for registration for the registry is www.iicepr.org.
International Patient Assistance Grant (PAG) Program
This program offers grants to patients with Dravet syndrome and associated epilepsies for necessary medical equipment needs associated with these conditions that are not covered through private insurance or other assistance programs.
Scientific Advisory Board
The Dravet Syndrome Foundation’s Scientific Advisory Board (SAB) oversees the organization's research activities. They review and approve all research grant applications and meet annually with other interested researchers and scientists to discuss innovative and promising research in the field of Dravet syndrome and associated epilepsies.
Board Chair
Board Members
Fundraising
In addition to private donations, private fundraising events, corporate sponsorships and grants, the Dravet Syndrome Foundation produces two major annual fundraising events: Ciara's Butterfly Bash and Steps Toward A Cure.
Ciara’s Butterfly Bash is the Dravet Syndrome Foundation's annual signature event where money is raised for research while honoring a professional who has gone above and beyond in the field of Dravet syndrome and related epilepsies. It is held each March in Greenwich, Connecticut. In 2011, over $125,000 was raised for research in one evening. Steps Toward A Cure consists of family-friendly fundraising walks, as well as the RACRE series of fundraising half-marathons. In 2010, over $165,000 was raised for research at nine walk locations across the U.S.
Delegations
In 2011, a group of parents formed a delegation of the Dravet Syndrome Foundation in Spain (DSF Spain). Both organizations share the same mission and work closely together, but have separate Boards of Directors and Scientific Advisory Boards. DSF Spain will be announcing its first research grant award in Summer 2011.
Dravet Syndrome Foundation Spain
Partner Organizations
The quickest way to a cure for a rare disease such as Dravet syndrome is by uniting families and researchers in a global collaboration. The Dravet Syndrome Foundation works with the following like-minded organizations to assure rapid distribution of information and to avoid duplication of efforts and research dollars.