Get involved in Peripheral Neuropathy Awareness Week

May 4-10, 2025 There are lots of ways to get involved in Sign up for our awareness week webinar: Myths vs Facts on May 8 PN Myths vs. Facts: Deepening Understanding & Raising Awareness Want to break down misconceptions of PN and address some common gaps in knowledge on the topic? Shanna Patterson, MD, MS, […]

Read More… from Get involved in Peripheral Neuropathy Awareness Week

FPN Neuropathy Advocacy Day Recap 

For the first time, we organized Neuropathy Advocacy Day and took our message directly to Congress. On March 18, 2025, staff and board members from the Foundation traveled to Washington, D.C. to speak up for the 30 million Americans who have peripheral neuropathy (PN). Our visit was urgent because earlier this month, Congress passed a […]

Read More… from FPN Neuropathy Advocacy Day Recap 

Advocating for PN research: the critical need for research dollars 

Peripheral neuropathy (PN) is vastly under-researched, despite its prevalence. While over 30 million Americans live with PN, the National Institutes of Health (NIH) funded less than $200 million in PN research from its $47 billion annual budget in 2024. That is less than $7 per PN patient.   Neurological conditions are now the leading cause of […]

Read More… from Advocating for PN research: the critical need for research dollars 

Clinical Research Training Scholarship Recipient Announced

The Foundation for Peripheral Neuropathy (FPN) is pleased to announce the 2024 Clinical Research Training Scholarship (CRTS) recipient for peripheral neuropathy (PN), Francesco E. Michelassi, MD, PhD, Neuromuscular Research Fellow, Columbia University Irving Medical Center. Michelassi’s research is fully funded by FPN and will focus on chemotherapy-induced peripheral neuropathy (CIPN), by studying how a chemotherapy […]

Read More… from Clinical Research Training Scholarship Recipient Announced

Book Fundraiser to Benefit FPN: Order by Feb. 21

Best-selling author of “The End of Your Life Book Club” and FPN friend, Will Schwalbe, has written a new book, “We Should Not Be Friends.” Chronicling a forty-year improbable, life-changing friendship, this warm, funny, irresistible book also explores Schwalbe’s experience with small fiber neuropathy. “We Should Not Be Friends is as funny, warm, brutally honest […]

Read More… from Book Fundraiser to Benefit FPN: Order by Feb. 21