Neuropathy News April 2026

FPN’s second annual Neuropathy Advocacy Day We held our second annual Neuropathy Advocacy Day on March 11. It was an important day to speak up for the 30 million Americans living with peripheral neuropathy. Together, we asked Congress to support more research and better care for people affected by this condition.   Learn more about […]

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Behind the lab coat: Q&A with Dr. Townsend  

“Science is a team sport” – Kristy Townsend, PhD  Dr. Townsend recently spoke on our webinar, Behind the lab coat: How medical research really works.   Kristy Townsend, PhD is a researcher and Professor in the Department of Neurological Surgery at The Ohio State University’s College of Medicine. Research in the Townsend Lab for Neurobiology & Energy Balance focuses on neural […]

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FPN’s second annual Neuropathy Advocacy Day 

The Foundation for Peripheral Neuropathy (FPN) held our second annual Neuropathy Advocacy Day on March 11. It was an important day to speak up for the 30 million Americans living with peripheral neuropathy (PN). Together, we asked Congress to support more research and better care for people affected by this condition.  Goals of Advocacy Day  […]

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A powerful new study to predict progression and improve care in anti-MAG neuropathy

We are proud to announce that with the help from generous donors, the Foundation for Peripheral Neuropathy is funding an important new research study. We are investing $525,000 over the next three years to support this work. This project brings hope to people living with IgM peripheral neuropathy (IgM-PNP), also including anti-MAG neuropathy. It is a rare nerve disease that can be very unpredictable.  […]

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Neuropathy News March 2026

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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 […]

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Ariel Zhang, PhD, awarded scholarship for neuropathy research 

Ariel Zhang, PhD, was awarded one of two 2026 Clinical Research Training Scholarship (CRTS) to support her important research on chemotherapy-induced peripheral neuropathy (CIPN). The CRTS is a two-year scholarship program that provides funding for emerging experts in neuropathy. The scholarship supports researchers’ efforts to advance treatments, prevention, and even cures for peripheral neuropathy (PN) and is fully funded by the Foundation for Peripheral Neuropathy.  Zhang’s research  Even though CIPN is common, it has not been studied as much as […]

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A Call to Action for Peripheral Neuropathy Research: NIH Collaboration, Funding Gaps, and the Future of PN Treatment

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Peripheral Neuropathy Affects Millions Worldwide Peripheral neuropathy (PN) affects an estimated 30 million Americans and approximately 130 million people worldwide. There are dozens of causes, but metabolic disease — including obesity, pre-diabetes, and diabetes — is by far the leading driver of PN. Metabolic Disease as the Leading Cause of Peripheral Neuropathy Metabolic dysfunction plays […]

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Dr. Erika Williams shares findings from her Clinical Research Training Scholarship 

CRTS Updates.

Meet the researcher: 2023 CRTS recipient Dr. Erika Williams  Erika Williams, MD, PhD, a neuromuscular fellow at Massachusetts General Brigham, was one of our first Clinical Research Training Scholarship recipients in 2023.  Her research focused on the autonomic nervous system (ANS), a component of the peripheral nervous system.   “The Foundation for Peripheral Neuropathy‘s Clinical Research Training Scholarship made this work possible,” Williams shared. “The transition to an independent research career is a particularly vulnerable […]

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Neuropathy News Feb. 2026

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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 […]

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Advocating for peripheral neuropathy: A conversation with FPN’s advocacy consultant, Mark Vieth   

Program Manager, Amanda Homscheid, recently sat down with Mark Vieth, our consultant who helps the Foundation for Peripheral Neuropathy advocate for neuropathy-related funding, such as the Peer Reviewed Medical Research Program (PRMRP), and connects us with important groups on Capitol Hill, like the National Institutes of Health (NIH).   Mark has been working with the Foundation for Peripheral Neuropathy for over 6 years. In this interview, he reflects on the accomplishments and progress we have made and his hopes and goals for the future.   Q. You’ve worked […]

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