SPECIAL ANNOUNCEMENTS


Help for those with Autonomic Neuropathy

For patients needing help with Autonomic Neuropathy, The American Autonomic Society is an important resource. In the left column of their site is a patient resource link to a listing of information about Autonomic Neuropathy and doctors around the U.S. which understand and specialize in the diagnosis and treatment of this illness.

To visit their site click here: American Autonomic Society


May 22nd - Drs. Noah Kolb and A. Gordon Smith to Host
“Autoimmune Neuropathies” Facebook Chat

Facebook Chat: “Autoimmune Neuropathies”
Where: www.facebook.com/NeuropathyAssociation
Guest Hosts: Noah Kolb, MD and A. Gordon Smith, MD (University of Utah School of Medicine—1 of 15 Neuropathy Association-designated Centers of Excellence)
When: May 22nd, 7:00 - 8:30 pm ET

Click here to learn about “Autoimmune Neuropathies” Facebook Chat


Register Today for The Neuropathy Action Foundation’s 7th Annual “Neuropathy Action Awareness Day”

The 7th Annual “Neuropathy Action Awareness Day” provides an exciting opportunity for patients to interact with other patients, physicians and exhibitors. After six years of hosting this event in San Francisco or Sacramento we are holding our first event in Los Angeles. Past events drew over 300 neuropathy patients, family members, health care providers and others to learn about neuropathy, policy issues and patient advocacy. This year the morning consists of an Exhibit Area and educational sessions. There will be a sit down luncheon. The afternoon consists of additional educational sessions and Exhibit Area with refreshments. The event features a celebrity speaker, elected officials and others.

      Date: Thursday, June 20, 2013       Location: Mr. C Hotel Beverly Hills, 1224 Beverwil Drive, Los Angeles, CA 90035

Click here for more information and to register


Welcome to The Neuropathy Support Network. We are here to Help!

The purpose of the Neuropathy Support Network is to provide volunteer support, guidance, counseling and information to neuropathy patients. Our mission includes creating a coalition of neuropathy patient advocates and neuropathy organizations that neuropathy patients can turn to for help; and to raise awareness among physicians and medical organizations of the seriousness of neuropathy, the suffering that neuropathy patients endure, and awareness of the possible treatments and medicines that exist.

If you suffer from Neuropathy, or have a friend or loved one who does, we are here to help. Go to the Contact Us page and fill out the contact form with your neuropathy question(s) and we will get back to you. Questions are answered in the order in which they are received.


ABOUT OUR BANNER

A human figure stands alone in a large field, buried waist deep in grass, arms reaching out in lonely isolation, seeking answers. Millions of neuropathy patients reach out blindly toward some sense of help, from “somewhere.”

The human figure symbolizes many patients, experiencing neuropathy in an isolated world of strange symptoms. Feeling buried under negative opinions, loss of purpose and friends, often alone in their struggle, with courage they reach out. In this simple act they find hope in a network of patients and a few professionals.

ABOUT THE DVD

The purpose of the Coping with Chronic Neuropathy DVD is to help others reach out, find answers, spread hope and raise funds for neuropathy research.

Discussed is the power of faith, increasing your neuropathy knowledge, getting and giving patient support, and learning to adapt to the changes neuropathy brings to lives - while remaining focused on getting help for your neuropathy.

Answers to your neuropathy questions.

“A story of hope and courage as told from the perspective of the real world of the Neuropathy patient”

Thomas H. Brannagan III, MD, Neurologist, Medical Advisor to The Neuropathy Association, Director of the Neuropathy Center of Excellence, Columbia University, NYC



. JOIN the NSN TODAY
and get updates on

Special Reports,
and Upcoming Events!

.


Online Neuropathy Support Groups

To view Facebook sites of online support groups available for those who cannot attend in person click below:

“Support for Neuropathy” , Ms. Jessica Benjamin - Administrator, Janet Cate - Co-Administrator

“Our Neuropathy Friends” , Ms. Kathy Moore and Mr. Paul Maziarz - Administrators

“Peripheral Neuropathy Support Group” , Mary Siniard - Administrator

“Neuropathy Pain Support UK” , Lizzy Harvey - Administrator - UK Internet support group

HAVING A CONFERENCE? – Are you having a SPECIAL neuropathy meeting, conference, or seminar? Advertise it here by sending the information on WHO, WHAT, WHERE, HOW to gene@neuropathysupportnetwork.org and we will post the information. We are approaching over 2000 visits a month to this site for information every month from all parts of the U.S. and worldwide.


DISCLAIMER: The information on this web site or the links or in the guidance provided is intended to be educational and informative and not medically prescriptive or diagnostic. All patients are encouraged to consult with their own medical doctor when considering any information contained in this web site or other web sites noted.

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