My name is Vicki, and I have bilateral progressive peripheral neuropathy. I have had this condition for over 15 years, and I am ok with it! In the Beginning My... read more →
MICHAEL WRIGHT has had neuropathy for about six years. Living in Charlotte, NC, with a supportive family, Michael has not let his neuropathy get the best of him. He has... read more →
Our friends at LivOn Labs, producer of vitamins and supplements, share information on supplements for nerve health with us. LivOn Labs is a supporter and partner of FPN. FPN recommends... read more →
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 →
