We’re thrilled to share a follow-up from Dieter R., an avid marathoner, passionate FPN advocate, and someone living with idiopathic polyneuropathy. After first sharing his story in our October 2024 patient feature, Dieter returns with an inspiring update as he takes on his next big challenge. A decade of determination By Dieter Reuther, PN patient […]
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Last call to apply! Early-career neuropathy research grant applications due Sept. 8 We’re pleased to announce the 2026-28 cycle of our early career research grants, offered through the American Academy of Neurology and American Brain Foundation . This grant is called the Clinical Research Training Scholarship in Peripheral Neuropathy. We are still accepting applications. Learn more and apply by September 9. […]
Recent tax law changes will increase deductions for charitable contributions for some donors after 2025. Here is a high-level summary: Starting next year, single filers who don’t itemize their contributions (about 90% of taxpayers) can claim a deduction for up to $1,000 in charitable contributions and joint filers can claim up to $2,000 on their […]
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August is National Make-A-Will Month. We’re thrilled to be celebrating by announcing the Mazawey Legacy Circle. This giving circle honors those committed to investing in a future without peripheral neuropathy (PN) by including us, the Foundation for Peripheral Neuropathy, (FPN) in their estate plans. Lou Mazawey leaves his mark on FPN, the future of neuropathy […]
Peripheral neuropathy affects thousands of veterans, causing pain, numbness, and mobility challenges. It is significantly more common among veterans than in the general population, often due to factors specific to military service, such as exposure to Agent Orange or physical injuries sustained during combat. Prevalence among Veterans A study published in the Journal of Military and […]
Our donor, Mary Ann Elliott, is supporting neuropathy research in a huge way: she’s matching donations up to $50,000 to support research scholarships in peripheral neuropathy. We did it! Thank you to those who helped us reach our goal in July. Still want to support our mission? Donate today. Read more in Mary Ann’s personal […]
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The Peripheral Nerve Society (PNS) is a global non-profit group made up of doctors, scientists, and healthcare workers. They study and treat diseases of the peripheral nervous system. Each year, the PNS hosts the PNS Annual Meeting. This event brings experts from around the world to share the newest research about peripheral nerve diseases. It’s […]
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Cystic fibrosis (CF) is a genetic condition that affects around 40,000 people in the U.S. and approximately 100,000 worldwide. It causes the body to produce thick, sticky mucus that can clog the lungs and digestive tract, leading to chronic respiratory infections, digestive problems, and other complications. CF and peripheral neuropathy: a hidden risk Many people […]
For the fourth consecutive year, peripheral neuropathy (PN) has been renewed for research funding by the Department of Defense (DoD) Peer Reviewed Medical Research Program (PRMRP)’s $150 million fund for FY25. In advance of pre-application deadlines, we are sharing the FY25 funding mechanisms, award amounts, maximum direct costs and how to apply. Want to learn more about […]
May 4-10, 2025 There are lots of ways to get involved in Sign up for our awareness week webinar: Myths vs Facts on May 8 PN Myths vs. Facts: Deepening Understanding & Raising Awareness Want to break down misconceptions of PN and address some common gaps in knowledge on the topic? Shanna Patterson, MD, MS, […]
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