Putting Patients at the Center: Two Days in Washington with Sanofi and the Milken Institute

By Amanda Homscheid, Programs Manager, Foundation for Peripheral Neuropathy How do we keep the voice of the patient at the forefront? This question was the guiding light during my two days in Washington DC. Here are the ideas I’m bringing home to the Foundation for Peripheral Neuropathy (FPN) and our community from my discussions at the […]

Read More… from Putting Patients at the Center: Two Days in Washington with Sanofi and the Milken Institute

Finding Another Way to Write

By Ayoposi Ojelabi Ayoposi Ojelabi lost the use of his hands to CIDP. Here is how assistive technology let him write again. I write with my head now. A few years ago, that sentence would have sounded strange to me. I was a network engineer and had spent much of my working life solving technical […]

Read More… from Finding Another Way to Write

90 Years Old and Still Fighting Peripheral Neuropathy

My problems started 22 years ago when I had my left knee replaced. I started to feel numbness in my left leg and some pain in the top of my toes. Then two years later I had my right knee replaced and the same problems that I had in my left leg began to appear […]

Read More… from 90 Years Old and Still Fighting Peripheral Neuropathy

Shedding Light on Idiopathic PN: Interview with Dr. Patterson 

Idiopathic peripheral neuropathy is a common diagnosis, but many people still have questions about what it means, whether an underlying cause may eventually be found, and how symptoms may change over time.  Following her popular webinar on idiopathic PN during Neuropathy Awareness Week in May, FPN sat down with Dr. Shanna Patterson for a follow-up […]

Read More… from Shedding Light on Idiopathic PN: Interview with Dr. Patterson 

Highlights from the 2026 Peripheral Nerve Society Annual Meeting 

The Foundation for Peripheral Neuropathy (FPN) is proud to have participated in the 2026 Peripheral Nerve Society (PNS) Annual Meeting in Maastricht, The Netherlands, alongside leading peripheral neuropathy (PN) researchers and clinicians from around the world. By engaging with the latest scientific discoveries and collaborating with experts across the field, FPN remains committed to bringing the most promising research developments in PN research and therapeutics to the neuropathy community.   […]

Read More… from Highlights from the 2026 Peripheral Nerve Society Annual Meeting 

From patient to advocate: Jayne’s journey of raising awareness for PN

Living with peripheral neuropathy can be challenging, but for Jayne S., it has also become a source of purpose. After developing chemotherapy-induced peripheral neuropathy (CIPN), Jayne turned her experience into action by volunteering with the Foundation for Peripheral Neuropathy and raising awareness in her community. From speaking at local events to organizing outreach efforts during […]

Read More… from From patient to advocate: Jayne’s journey of raising awareness for PN

IMAG±iNe 2.0 study welcomes new PhD researcher 

We are excited to share an important update from the IMAG±iNe 2.0 Biomarkers in IgM Peripheral Neuropathy study.  With support from the Foundation for Peripheral Neuropathy research grant, UMC Utrecht has hired Lisa Bos, MD as a new PhD student to help lead this important research.   About Lisa Bos, MD  Dr. Bos recently completed a neurology internship, where she cared for […]

Read More… from IMAG±iNe 2.0 study welcomes new PhD researcher 

2027 Next generation training grant in PN 

The Foundation for Peripheral Neuropathy (FPN) is pleased to announce the 2027-2029 cycle of our early career Clinical Research Training Scholarship in Peripheral Neuropathy (CRTS in PN), offered through the American Brain Foundation (ABF). Since 2023, we have funded $900,000 in these next generation training grants.  The goal of this funding mechanism is to support promising early career investigators (MD or PhD) who are likely to continue their careers in peripheral neuropathy […]

Read More… from 2027 Next generation training grant in PN 

I’m Still Here! 

By: Jane A.  Why am I still here?  I’ve often wondered why I’m still here. Why I say this begins with my being “run over” by a car in 1993. As my husband and I were crossing a street on a crosswalk, a car stopped for us. Unfortunately, another car didn’t see the stopped car and ran into it. The stopped car then ran into me and […]

Read More… from I’m Still Here! 

FY26 Peer Reviewed Medical Research Program funding opportunities are now available! 

For the sixth consecutive year, peripheral neuropathy (PN) has been renewed as an eligible condition for research funding by the Department of Defense (DOD) Peer Reviewed Medical Research Program (PRMRP)’s $127 million fund for FY26. Below are the FY26 funding mechanisms, pre-application and application deadlines, award amounts, maximum direct costs and how to apply.   FY26 Peer Reviewed Medical Research Program award mechanisms and pre-application deadlines:  Get […]

Read More… from FY26 Peer Reviewed Medical Research Program funding opportunities are now available!