The Foundation for Peripheral Neuropathy works to educate the public and healthcare professionals, provide state-of-the-art treatment for patients with peripheral neuropathy,
and will be the catalyst for advancing innovative therapeutic developments and accelerating a cure for painful neuropathies.
WE NEED YOUR HELP!
Do you or someone you know suffer from painful peripheral neuropathy?
Click here to learn more about the opportunity to participate in a important research study.
To find a
support group near you
Thank you to those of you who have become members of FPN. Your support is crucial if we are to continue to provide the resources you need! Membership renewal starts soon...you will receive an email with all the details!
Make sure to check out events in your area! Local support groups are constantly having meeting with guest speakers click hereto find one near you today!
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inbox bi- monthly. Full of information, news, tips and event updates!
PN RESEARCH REGISTRY
The PNRR will allow for various types of research, education and outcome improvement initatives.
Find out more about how YOU can get involved!
Please continue to play an active part in spreading our
invitation of hope by joining with the Foundation in
a pivotal way. Any donation - $100, $500, $1000 - may mean someday you will hear, 'Our winter is over and a cure is finally on the way.'
Orthostatic hypotension (OH), a common feature of autonomic neuropathy can be a part of PN.
OH is a form of low blood pressure that can make you feel dizzy, lightheaded and maybe make you feel faint. Click here for more information.