Neuropathy patient education matters. Everyone neuropathy touches needs resources to understand PN. Patients, caregivers, practitioners, friends, family all play a role in PN care

Today is FPN Day | Celebrating 18 years of FPN
#neuropathy #FPNday #neuropathyeducation

Its FPN Day. There's still time for us to reach our $18K goal today. Help us celebrate our 18th anniversary by donating now https://www.foundationforpn.org/donate/

Today is FPN Day | Celebrating 18 years of FPN
#neuropathy #FPNday

Research funding advances understanding and future treatments for neuropathy. We want more researchers to study neuropathy and more funding for promising projects.

Today is FPN Day | Celebrating 18 years of FPN
#neuropathy #neuropathyresearch #FPNday

Our board members share why they're dedicated to our work:
youtube.com/playlist

They're supporting FPN Day to continue our work for the neuropathy community

Today is FPN Day | Celebrating 18 years of FPN
#neuropathy #FPNday

Advocacy work pays off:
Nearly $20 million in DoD funds for PN research in recent years.

We make sure PN is an eligible research topic by getting it renewed every year

Today is FPN Day | Celebrating 18 years of FPN
#peripheralneuropathy #peripheralneuropathyresearch #FPNday

Today is FPN Day! We're raising $18K in honor of our 18th anniversary.
Help us celebrate 18 years of increased neuropathy support and research, donate now for FPN Day: https://www.foundationforpn.org/donate/

#neuropathy #FPNday

It's one week until FPN day! In honor of our 18th anniversary, we talked to our founder, Jack Miller, about living with PN for 30 years.

Read Jack's update: www.foundationforpn.org/jack-miller-96-years-liv...

#FPNday #givingday #neuropathy