The - Epilepsy Support Group - Community Forum
September 04, 2010, 01:21:43 PM *
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Author Topic: Are You Searching For Support Groups?  (Read 727 times)
admin
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« on: September 22, 2008, 11:17:04 PM »

Currently, there are a lot of empty sections in this category of 'Epilepsy Support Groups -or- Events'. So I would like to ask for some help. No matter if you are a member, or just a Guest, of this one online epilepsy support group, please feel free to share some information about any epilepsy support group(s) and or any events that pertains to epilepsy, available in your area, state, or country. Then I can add the information to the appropriate topic threads in this category. A topic thread, by the way, are any of the individual sections that contain information, just as the very one you're looking at right here, right now. This is the 'topic thread' titled 'Are You Searching For Support Groups?'

What's shared in this community forum, may very well become helpful for someone else who is looking for answers and support, now, or in the future.

For the Guests, you can send the information to support-team@epilepsysupportgroup.com

Thank you Smiley
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*I'm not a doctor, but the information I share is what I've either learned and or experienced due to having epilepsy myself.

Never argue with idiots. They bring you down to their level and then beat you with experience.

ruthbrown
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« Reply #1 on: October 21, 2008, 10:42:23 PM »

Hi Bruce

That is a good question. I belong to WebMD Epilepsy Support Group, Epilepsy Support Yahoo groups. My favorite is the new one. The Epilepsy Support Group-Community Forum. This is my favorite one.

Why, you ask? It is more personal. We can talk directly to each other. Just to say hi in a personal message. I can talk to the Admin any time I want to. He helps all of us and gives us ideas.

Ruth
« Last Edit: November 20, 2008, 01:04:20 PM by admin » Logged

Birdbomb
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« Reply #2 on: April 01, 2010, 05:58:18 PM »

www.vnsmessageboard.com


The VNS Message Board is an independent support forum for patients or family members who have the VNS (vagal nerve stimulator) or for those seeking more information about it.  This site is NOT associated with nor does it accept any funding by Cyberonic$ (maker of VNS) or any affiliate.  Our supportive and caring staff have first hand experience with VNS, most have had it implanted and all with varying degrees of success and or failure.
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http://www.vnsmessageboard.com

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