FPN Program Manager Amanda Homscheid catches up with longtime FPN supporter and donor Susan W., who has been living with peripheral neuropathy for over 15 years. Susan shares how her journey has evolved since first telling her story, what helps her manage symptoms and what gives her hope for the future of PN research. Thank […]
When Matt first began showing signs of neuropathy, he and his wife, Cassie, didn’t realize how difficult the journey ahead would be. They faced confusing advice, failed treatments, and constant worries about the future. Through it all, they learned how important it is to have honest information and real support. Cassie shares their story in […]
Read More… from Neuropathy patient advocacy is the answer: Widow finds hope in Foundation’s purpose
An update 14 years later by Jack Miller, FPN founder “18 years ago, I founded the Foundation for Peripheral Neuropathy because I was looking for a cure for my (and others’) neuropathy. We haven’t found it yet, but the search is continuing, and The Foundation for Peripheral Neuropathy is helping in many ways. Your support […]
My name is Gabi, and I’m 21 with peripheral neuropathy caused by a surgical injury. But honestly, that’s just a footnote—let me tell you how I got here. Eyes on the sky Back in 2022, I was fresh out of high school, ready to take on the world. I had a supportive family, a suitcase […]