Nominations Open: PRMRP Consumer Reviewer (Due March 17) The Congressionally Directed Medical Research Programs (CDMRP) is looking for new consumer reviewers to join upcoming scientific review panels. If you are a PN patient and want to review research grants, this opportunity is for you! This year, $370 million has been approved for the program. Peripheral […]
For nearly two decades, the Foundation for Peripheral Neuropathy (FPN) has been a trusted place for people living with peripheral neuropathy (PN). We provide information, support, and a sense of community. As our work has expanded, our audience has grown too. Because of this, it’s important that our visual identity shows who we are now […]
Critical funding restored for medical research After a huge cut in 2025, research funding for the Department of Defense’s Peer Reviewed Medical Research Program is finally back to its earlier level: $370 million. This is great news for people living with peripheral neuropathy. Each year, we work hard to make sure PN is one of the topics that can receive this funding. The more […]
November was Diabetes Awareness Month Diabetes affects millions of people. It is a major cause of peripheral neuropathy. Last month, we shared information to help you understand how diabetes develops. We explained why it can damage nerves, and what you can do to stay healthy. Learning the signs early and managing blood sugar can lower […]
Diabetes is the main cause of peripheral neuropathy. We’re supporting diabetes awareness month by promoting diabetes education. By learning about what can increase your risk of getting diabetes and the signs that show you might have it, you can take steps to prevent it or manage it better. And keeping your diabetes under control reduces […]
We are honored to share that on October 20, 2025, the Foundation for Peripheral Neuropathy (FPN) received the incredible gift of a substantial sum from our longtime supporter and friend, Lynne Warner. This generous donation, given in her memory, will have a lasting impact and bring hope to the peripheral neuropathy community. About Lynne Warner […]
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Research update with Dr. Michelassi Francesco Michelassi, MD, PhD, Physician and Lead Scientist at the University of Virginia Health and the 2024 Clinical Research Training Scholarship (CRTS) recipient, shares his work studying Chemotherapy-Induced Peripheral Neuropathy (CIPN). He explains how his research could help protect nerves and lead to new treatments. Learn how FPN helped Dr. […]
Celebrating Jack Miller, FPN’s founder on FPN Day Tomorrow, FPN celebrates its 18th anniversary. In honor of our founding, we are proud to celebrate Jack Miller, the man who founded the Foundation for Peripheral Neuropathy. In his previous patient story from 2011, Jack shared the complete history of why he started FPN and his own long journey with peripheral neuropathy. […]
Chemotherapy induced peripheral neuropathy (CIPN) can impact up to 70% of chemo patients. The effects can linger long after chemotherapy has ended. Patients can be left with issues in their hands or feet ranging from pain and tingling to muscle weakness. Treating CIPN is really hard Scientists don’t fully understand what causes CIPN. Studies have shown that […]
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We’re pleased to announce our newest board member, Jennie Starr. Starr started her career as a lawyer, then worked for both tech and biotech companies. She also ran a nonprofit while raising her children. Now she’s bringing all of that experience to help support our mission. About Jennie Starr Starr has always liked building new […]
Read More… from New Board Member Jennie Starr: A Builder with a Big Heart