Hereditary Neuropathy Foundation

Hereditary Neuropathy Foundation

In support of our MISSION and VALUES, the Neuropathy Support Network is pleased to announce that the Network for Neuropathy Support, Inc., a non-profit 501c3 dba the Neuropathy Support Network has joined as a partner with The Hereditary Neuropathy Foundation to increase support for patients with the hereditary neuropathies AND to increase resources available to patients.

The NSN is making available to their patients a copy of the DVD “Coping with Chronic Neuropathy”.

The Hereditary Neuropathy Foundation (HNF) is a non-profit 501(c)3 organization which raises awareness, funds scientific research, and educates the medical community as well as the general public about Charcot-Marie-Tooth disease (CMT). HNF is committed to providing support to people living with CMT and their families.

To learn more about their wonderful mission and work CLICK HERE:

About the Author

LtCol Eugene B Richardson, USA (Retired) BA, MDiv, EdM, MS

Col Richardson has suffered with severe neuropathy for over 45 years. A 27 year military veteran and veteran of the Vietnam War, he was diagnosed with a progressive chronic peripheral neuropathy resulting in severe disability. This diagnosis has been confirmed as due to exposure to Agent Orange. It was not until 2010, 42 years after his exposure to Agent Orange, that his diagnosis was recognized by Veterans Affairs as service connected.

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