On Friday the 13th of March 2020, when the world stopped for COVID-19, I finally got an answer from my neurologist about the burning pain in my feet and, sometimes,... read more →
In our blogpost. How to Get Support Without Leaving Home published in July 2020, we provided a summary of virtual support groups and social media sites for patients with PN. ... read more →
Following over a year's delay due to the COVID-19 pandemic, the IMAGiNe Study is finally back on track! The IMAGiNe Study (Immunoglobulin M(IgM)-Anti-myelin-associated-glycoprotein (MAG) Peripheral Neuropathy Study) is a research program that... read more →
The Foundation for Peripheral Neuropathy is pleased to welcome our newest Member of the Board of Directors, Kristy Townsend, Ph.D, effective June 1, 2021. Kristy Townsend holds a Ph.D. in... read more →
When Jen set out to raise awareness for PN,, she did more than she expected. Her outreach helped others and brought people together. Jen shares her story here. Jen's Story... read more →
Raise Awareness for Peripheral Neuropathy With 30 million people in the US alone with peripheral neuropathy, it is a wonder that more people are not aware of the condition. We... read more →
My PN Story My journey with PN began in 2019 with the onset of burning pain in my toes and fingers that quickly spread up my legs and arms. Within... read more →
Mental health can become a concern for patients with chronic conditions such as peripheral neuropathy. During recent months when the pandemic has disrupted many of our usual routines, mental health... read more →
Helping Others, Help Yourself! My issues started probably 5-6 years ago. We we know, PN is very hard to diagnose. With that being said, I was treated for carpal tunnel,... read more →
The U.S. Department of Defense's Peer Reviewed Medical Research Program (PRMRP) included peripheral neuropathy as a condition eligible for research funding for the first time in 2021. The Foundation for... read more →
