Author: Amanda Homscheid

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Posts by Amanda Homscheid

Dr. Erika Williams shares findings from her Clinical Research Training Scholarship 

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Meet the researcher: 2023 CRTS recipient Dr. Erika Williams  Erika Williams, MD, PhD, a neuromuscular fellow at Massachusetts General Brigham, was one of our first Clinical Research Training Scholarship recipients in 2023.  Her research focused on the autonomic nervous system (ANS), a component of the peripheral nervous system.   “The Foundation for Peripheral Neuropathy‘s Clinical Research Training Scholarship made this work possible,” Williams shared. “The transition to an independent research career is a particularly vulnerable […]

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Advocating for peripheral neuropathy: A conversation with FPN’s advocacy consultant, Mark Vieth   

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Program Manager, Amanda Homscheid, recently sat down with Mark Vieth, our consultant who helps the Foundation for Peripheral Neuropathy advocate for neuropathy-related funding, such as the Peer Reviewed Medical Research Program (PRMRP), and connects us with important groups on Capitol Hill, like the National Institutes of Health (NIH).   Mark has been working with the Foundation for Peripheral Neuropathy for over 6 years. In this interview, he reflects on the accomplishments and progress we have made and his hopes and goals for the future.   Q. You’ve worked […]

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FPN welcomes the Brigham and Women’s Hospital as a new site for the IMAGiNe Study 

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The Foundation for Peripheral Neuropathy (FPN) is excited to share that the Brigham and Women’s Hospital has joined the IMAGiNe Study as a new research site. With help from FPN, they will take part in this international study about IgM anti-MAG peripheral neuropathy, a rare autoimmune form of PN.  About the IMAGiNe Study  The IMAGiNe Study (IgM Anti-Myelin-Associated Glycoprotein Neuropathy Study) is led by Maastricht University Medical Center in the Netherlands. The study is creating a […]

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Video interview with Will Schwalbe

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Author Will Schwalbe shares an update on living with small fiber neuropathy, the power of friendship, and lessons learned along the way. In this conversation with our FPN Program Manager, he reflects on adaptation, support, and hope for those navigating life with neuropathy. Will’s original story was shared in 2020 where he shares an article […]

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Critical funding restored for medical research

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Veteran-focused Peer Reviewed Medical Research Program funding returned to 2024 funding level after 50% cut in 2025  After a huge cut in 2025, research funding for the Department of Defense’s Peer Reviewed Medical Research Program (PRMRP) is finally back to its earlier level: $370 million. This is great news for people living with peripheral neuropathy (PN), because each year we work hard […]

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IMAGiNe study progress: 2025 highlights and what’s ahead

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As we start a new year, we are excited to look back at what the IMAGiNe study achieved in 2025. We are also looking ahead to our goals for 2026 and beyond. At the Foundation for Peripheral Neuropathy (FPN), we celebrate every milestone that helps move peripheral neuropathy research forward.   About the IMAGiNe study  The IMAGiNe study (IgM Anti-Myelin-Associated Glycoprotein Neuropathy Study) is led by Maastricht University Medical […]

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Video interview with Susan W.

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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 […]

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Celebrating Caregiver’s Month!  

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November is National Family Caregivers Month, a time to honor the amazing people who give their time and energy to care for others.   Many caregivers work full-time jobs while also supporting a loved one living with peripheral neuropathy. Their kindness and dedication make a big difference every day. This month, we want to thank them and remind everyone […]

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Neuropathy patient advocacy is the answer: Widow finds hope in Foundation’s purpose  

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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 […]

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Living well with neuropathy: Reflections on 30 years of PN, 96 years of life and finding purpose through it all 

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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 […]

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