NAF works with the most knowledgeable, accomplished Ataxia researchers in the world. We are committed to providing the resources needed to pursue a cure and better quality of life for people with Ataxia.
The National Ataxia Foundation is committed to funding the best science relevant to hereditary and sporadic types of ataxia in both basic and translational research. NAF invites research applications from U.S.A. and International non-profit and for-profit institutions. Non-U.S. citizens are eligible to apply for a research grant from NAF.
Funding for Ataxia-Telangiectasia research proposals will receive a lower priority unless they lend themselves to an overall better understanding of the ataxia disease process.
Funds provided by the National Ataxia Foundation may not be used for indirect/F&A costs.
NEW THIS YEAR
The National Ataxia Foundation has transitioned to using a Grant Application Management online program called proposalCENTRAL.
Letters of Intent and completed applications are to be submitted through the online portal. The portal is expected to “go live” at the end of Summer 2018, however, if you plan to submit an application, you are encouraged to create a user account, which you will then use when you submit the LOI and full application. Click on this link to create your user account with proposalCENTRAL.
You may contact Sue Hagen, NAF Research Services Director, at firstname.lastname@example.org with questions.
Below are descriptions of NAF’s research programs:
Letters of Intent to apply for any of the research grants must include the nameand credentials of the Principle Investigator and the name of the institution, city, state and (if out of the United States) the name of the country.
NAF Research Grants
Research Grant: One-year seed money grants of up to $15,000 but promising proposals up to a maximum of $30,000 will be considered for early or pilot phases of studies and ongoing investigations. Applicants for seed-money grants need to be faculty members.
September 14, 2018 – Date the Letter of Intent is due with a ½ to one-page abstract with specific aims of your research.
October 15, 2018 – Full application due
NAF Young Investigator Awards
Young Investigator (YI) Award: One-year grants of $35,000 to encourage young investigators to pursue a career in the field of any form of Ataxia research.
For Young Investigator award programs, candidates must have attained an MD or PhD degree, and have an appointment as a junior faculty member, senior post-doc or clinical fellow. Individuals at the Associate Professor level are not eligible. Clinicians must have finished their residency no more than five years prior to applying. PhDs must be no more than five years from end of the completion of their post-doc training.
The sponsoring institution must agree in writing to the following provision: the young investigator (MD or PhD) must be free to allocate approximately half time (50%) for Ataxia related research.
October 1, 2018 – Date the Letter of Intent is due with a ½ to one-page abstract with specific aims of your research and the name of your mentor
November 1, 2018 – Full application due
NAF Fellowship Awards
Research Post-Doc Fellowship Award: One-year grants* up to $35,000. Applicants should have completed at least one year of post-doctoral training, but not more than two at the time of application, and should have shown a commitment to research in the field of Ataxia.
October 15, 2018 – Date the Letter of Intent is due with a ½ to one-page abstract with specific aims of your researchand the name of your mentor
November 15, 2018 – Full application due
Launched in 2005, NAF’s biennial Ataxia Investigators Meeting brings together world-leading Ataxia clinicians and scientists who are working to accelerate the pace of Ataxia research, better understand the disease, and develop therapies. In 2018, more than 170 people from 13 countries participated. The 9th AIM will be in 2020. For information on AIM 2020, contact Sue Hagen at email@example.com.
Sponsorship support provided by:
The AIM 2018 Schedule is still being finalized and there may be changes, however the preliminary schedule can be viewed below.
Ataxia Patient Meeting
The National Ataxia Foundation hosts an annual patient meeting each year which is attended by those affected by Ataxia and their caregivers and family members. Attendance is often over 500 individuals. Presentations by leading Ataxia researchers and clinicians are given during the 3-day conference. Ataxia researchers are invited to participate in the exhibit area of the meeting to recruit patients for IRB approved research studies or share their research findings.
If you are interested in recruiting patients at the National Ataxia Foundation’s Annual Membership Meeting, please contact the National Ataxia Foundation at (763) 553-0020 or email firstname.lastname@example.org