Author: Amanda Homscheid

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Posts by Amanda Homscheid

Charitable tax deductions may rise this year

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Recent tax law changes will increase deductions for charitable contributions for some donors this year. Here is a high-level summary Starting this 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 tax returns. This is an increase from the $300/$600 amounts last year. This is a […]

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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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The Foundation for Peripheral Neuropathy Received Transformational Gift

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We are honored to share that on October 20, 2025, the Foundation for Peripheral Neuropathy (FPN) received the incredible gift of a substantial sum from our longtime supporter and friend, Lynne Warner. This generous donation, given in her memory, will have a lasting impact and bring hope to the peripheral neuropathy community.  About Lynne Warner  […]

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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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