Advocacy Day & the critical need for research dollars Thanks to all our Peripheral Neuropathy Awareness Week contributors From our live webinar participants who submitted great questions, to our social followers who shared content to educate on PN, and all those who talked to their community about their personal experience last week, thank you! Increased […]
Advocacy Day & the critical need for research dollars On March 18, FPN staff and board members traveled to Washington, D.C. to speak up for the 30 million Americans who have peripheral neuropathy (PN). Our visit was urgent because earlier in March, the U.S. Congress passed a bill that cut funding for medical research by 57%. Read […]
Protect PN research from proposed funding cuts Proposed cuts to federal research funding threaten critical studies across many conditions, including neuropathy. Research funding, which totals billions annually, supports essential work on nerve regeneration, pain management, and new treatments for PN. As soon as today, the House will be voting on a continuing resolution to fund […]
In December 2020, Amy, a 74-year-old New Yorker with a career in construction, was working remotely to avoid COVID-19. After a rare on-site meeting, she tested positive for the virus. Along with the typical symptoms, there was an added surprise; Amy developed peripheral neuropathy (PN). Though she’d experienced mild numbness in her toes the previous […]
The Foundation for Peripheral Neuropathy (FPN) welcomes Amanda Peltier, MD, MS, to our board of directors, effective Jan. 1, 2025. Her distinguished career in neurology, extensive research experience, and dedication to advancing care for peripheral neuropathy patients make her an exceptional addition to our leadership team. About Amanda Peltier, MD, MS Peltier is an Associate Professor at Vanderbilt University Medical […]
The Foundation for Peripheral Neuropathy (FPN) welcomes Shanna K. Patterson, MD, MS, who joined our Board of Directors effective January 1, 2025. She brings an exceptional blend of clinical expertise, academic leadership, and a long-standing commitment to improving the lives of individuals living with peripheral neuropathy. Patterson has deep roots in the neurology profession and community Patterson currently serves as the […]
Read More… from Shanna Patterson, MD, MS, joins our Board of Directors
The Foundation for Peripheral Neuropathy (FPN) is proud to announce Ronald Lissak named President of the Board of Directors, effective January 1, 2025. With a distinguished career in the medical device industry and a personal connection to peripheral neuropathy (PN), Ron brings a wealth of experience, dedication, and a clear vision to his new role. A Leader in Medical […]
The Foundation for Peripheral Neuropathy (FPN) is a 100% donor supported 501(c)3 charitable organization. Through research funding, awareness, and patient education, our work advances our mission to improve the lives of patients living with peripheral neuropathy and accelerates the development of treatments, and one day, cures. A Donor Advised Fund (DAF) We view our supporters as valued partners, and thus FPN […]