10/14/2026
Today is FPN Day, marking 19 years since Jack Miller, who lives with peripheral neuropathy, started the Foundation for Peripheral Neuropathy.
What began with one person's determination to find cures has grown into a community of patients, caregivers, researchers, and supporters all driving towards answers for those living with PN.
That community has power.
In 2020, after FPN and our community advocated for it, Congress made peripheral neuropathy eligible for federal Department of Defense research funding, opening the door for researchers to apply.
This past March, 19 of us held 34 meetings with congressional offices in 11 states to keep it that way.
These are just a few ways the community moves research forward: we fund promising research, speak up for it, share trusted education, and raise awareness of PN.
Next year, we celebrate 20 years, still working toward a future without peripheral neuropathy and making life better for people living with it today.
Join our mailing list to see how you can get involved. Link in the first comment