Blog
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Jul 11, 2024Join the NEPTUNE-17 clinical trial for Diabetic Peripheral Neuropathic Pain (DPNP)
Does diabetic peripheral neuropathic pain (DPNP) disrupt your daily life and keep you awake at night despite your current treatment? You are not alone. The NEPTUNE-17 clinical trial, hosted by… -
Jun 25, 2024
Announcing Our New Partnership with GlaxoSmithKline (GSK)
We are thrilled to announce a new partnership between the Foundation for Peripheral Neuropathy (FPN) and GlaxoSmithKline (GSK) as a 2024 Research Impact Partner. This collaboration, with GSK’s generous support,… -
Jun 13, 2024The Foundation for Peripheral Neuropathy Receives Largest Gift to Date
We are honored to announce that on May 16, 2024, the Foundation for Peripheral Neuropathy (FPN) received an extraordinary and transformational donation of over $660,000. This unprecedented gift, given posthumously,… -
Jun 12, 20242024 CRTS in PN
The Foundation for Peripheral Neuropathy (FPN) is pleased to announce the 2024-25 cycle of our early career research grants, offered through the American Academy of Neurology (AAN) and American Brain… -
May 23, 2024Living with Peripheral Neuropathy: A 30-Year Journey of Challenges and Hope
Meet Jason B., a husband, father, supporter of FPN, and an SFN patient, as he shares his journey living with peripheral neuropathy. January 2, 1994, 24 years old, a recent… -
Apr 24, 2024Exercise for CIPN
By Sumedha ShastryHave you ever been watching TV and stumbled upon an advertisement promoting an 80s aerobics class—filled with bright workout outfits and groovy background music? For many, it brings… -
Apr 15, 2024A Proclamation for PN Awareness
By Stacey Udell, PN patient and FPN supporter The Town of Huntington’s (NY) board meeting, on April 11, 2024, was a truly unforgettable experience for me, as I had the… -
Apr 9, 2024Make Your Voice Heard: Join the Call to Action for PN Advocacy!
Help Advocate for Government Funding for Peripheral Neuropathy Research in 2025 Due to the Foundation for Peripheral Neuropathy’s (FPN) advocacy efforts on the Hill, and countless letters from PN patients…