- NNPDF Mission & Goals
- Foundation History
- Organizational History
- About Our Logo
National Niemann-Pick Disease Foundation
Mission & Goals
We are a non-profit group dedicated to supporting and empowering patients and families affected by Niemann-Pick disease through education, collaboration and research.
Vision for the Future
We envision an enduring patient support community that embodies strength, hope and empathy for those affected by all Niemann-Pick Disease types. We believe deeply in the future of research that promotes clinical treatments with potential to improve patient quality of life and with intent to ultimately cure all Niemann-Pick Disease types.
We are committed to:
- Supporting and empowering patients and families affected by NPD by meeting them where they are in their NPD journey.
- Upholding a balanced, unbiased approach with families, researchers, clinicians and industry to move treatment forward to provide a variety of therapies and to work together toward a cure. We encourage full transparency among all stakeholders in the Niemann-Pick Disease community.
- Supporting basic science and clinical research through awareness and collaborative funding initiatives.
- Adhering to a written code of conduct that fosters respect for all, regardless of treatment choices or research perspectives, which maintains patient privacy and follows the national HIPPA regulations.
- Encouraging and promoting advocacy and collaborative community partnerships across the NPD community, both in the U.S. and internationally.
- Respecting the diversity of Board members, employees, families, researchers, clinicians and industry, and governing the NNPDF ethically and transparently according to NNPDF Bylaws.
The National Niemann-Pick Disease Foundation is a national non-profit 501(c)(3), rare disease network of families dedicated to providing empowerment resources, support and education for families, caregivers and patients affected by all Niemann-Pick Disease types.
We are families, patients and compassionate friends across the U.S. that share hope, promote research and raise awareness for NPD. We are dedicated to supporting and empowering one another, through education of potential therapies for all Niemann-Pick Disease types. We work tirelessly as volunteers, caregivers, counselors, and fundraisers for patient support, research and clinical treatment.
On February 10, 1992, six families with children suffering from Niemann-Pick disease met at the National Institutes of Health at Bethesda, Maryland. Concerned with cutbacks in funds for medical research and knowing without research there was little hope for their children, they decided to form a foundation – The Niemann-Pick Type C Foundation, Inc. Bylaws were drafted and a board of directors was selected. Service activities began immediately and the first year saw many accomplishments.
- A Newsletter offering information and support was sent out.
- A Directory of families affected by NPC was compiled and distributed to the families.
- An informational pamphlet was written and mailed to hundreds of professionals and organizations in the medical field to create awareness of this rare disease.
- Fundraising began to channel money into medical research.
- A Scientific Advisory Board of doctors and researchers was established.
- A paragraph was added to the Appropriations Bill for NIH to ensure continued funding for Niemann-Pick Disease research at the federal level.
1993 was another busy year. The Foundation name was changed to the National Niemann-Pick Disease Foundation, Inc., nonprofit status was awarded by the IRS, the first family conference was held, and the first research grant was awarded to Dr. Eugene Carstea to identify the genetic cause of NPC. Dr. Carstea announced the discovery of the NPC1 gene four years later.
All of these services have continued and expanded over the years.
- The enewsletter goes out to over 1000 households.
- The NNPDF is a co-founder of the International Niemann-Pick Disease Alliance (INPDA)
- The Family Conference has grown 15-fold with separate sessions for ASMD and NPC. Top researchers attend to interact with families and share their expertise.
- NNPDF was a founding member of the Lysosomal Disease Research Consortium, which awards over $1,000,000 in related research grants annually.
The National Niemann-Pick Disease Foundation currently has over 450 Niemann-Pick families as members. Thousands of medical, corporate, professional, friend and family sponsors assist in supporting our goals through contributions and donations of services. NNPDF is the largest Niemann-Pick Disease family support organization in the world and one of the largest private funders of Niemann-Pick Disease research.
The NNPDF’s board continues to be comprised mainly of parents with children affected by NPD. All board members donate their time to the NNPDF on a volunteer basis.
Of the six original families, all have lost a child to Niemann-Pick Disease. All six are still NNPDF members.
The Foundation has a record of getting things done. The NNPDF was founded in 1992. Since then, the Foundation has:
- Raised over $5.5 million for research on NPA, NPB, and NPC, family support, education, and other activities
- Funded research that led to the discovery of the NPC1 gene
- Funded research that has led to the identification of numerous gene mutations for use by researchers, clinicians, and in genetic testing
- Funded research to study the neurological effects of NPD
- Co-sponsored the first International Symposium on NPC
- Promoted awareness of NPD by publishing educational materials
- Held an annual conference every year since 1993 for families affected by all types of NPD, scientists, and others
- Published regular newsletters to keep families informed about the Foundation and the latest advancements in understanding NPD
- Provided opportunities for NPD families to communicate with each other and share their thoughts, ideas, and experiences
The National Niemann-Pick Disease Foundation’s logo represents our commitment to support families affected by Niemann-Pick Disease and research toward finding treatments and a cure. With the passing of time there has been a need to change and update our logo, but the NNPDF board has worked to keep the spirit and inspiration of the below drawing as our underlying promise of “HOPE”. The rainbow colors are from our original rainbow logo, which was designed by Tommy Kenny.
Tommy passed away in 1995 from Niemann-Pick C. Although he knew he was seriously ill, he took strength from the rainbow as a symbol of hope and faith. We continue to share his hope and faith with the rainbow colors, our support of NP families, and our support for research.
Special thanks to Tommy’s Mother, Barbara Kenny, for sharing these pictures of Tommy with us and to Hunt Ozmer for contributing Tommy’s original drawing from his files.
Original Logo ~ 1992-2006
2008 – 2018
This new logo was designed to reflect the positive spirit of the Niemann-Pick community, to continue the hopeful nature of the rainbow’s arc, and to capture the essence of those who have passed with the butterfly image, maintaining the spirit and inspiration of the original drawing as an underlying promise of hope.
The National Niemann-Pick Disease Foundation does not collect any identifying information about individuals visiting this web site (name, email address, etc). We do collect demographic information on the number of hits, number of unique visitors, etc to help us improve the site.
Information voluntarily provided by visitors to the site through email or forms is not sold to other organizations. Information may be shared with officers or members of NNPDF, affiliated researchers and physicians, or other organizations to provide a proper response to questions or concerns.
Information provided to companies listed on the NNPDF Stores is subject to the privacy policies of those companies.
At times, data may be collected for research studies, surveys, etc. When this is done, the recipient of the information will be clearly identified and visitors will have the option of not participating.