Blog
-
Sep 8, 2021Vicki’s Story: The Road to Fulfillment
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… -
Aug 16, 2021Michael’s Story: Let Your Birthday Help Us All!
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 become a… -
Aug 4, 2021Vitamins and Supplements for Nerve Health
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… -
Jul 15, 2021Terry’s Story: Local Support Group Offers Help
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, hands…. -
Jul 14, 2021Support Group Primer: Update July 2021
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. Here, we update… -
Jul 8, 2021Research Study Back on Track!
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 aims to… -
Jun 4, 2021FPN Welcomes New Board Member, Kristy Townsend
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… -
May 25, 2021Jen’s Story: Raising Awareness for PN Brings People Together
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…