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Cluster Headache Ontario Canada

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Uploaded on Jan 27, 2009

http://clusterheadsurvivor.blogspot.ca/
PLEASE READ THIS DESCRIPTION BEFORE COMMENTING OR EMAILING ME
ALL COMMENTS SUBJECT TO APPROVAL FIRST. THANK YOU
This is me, an actual Cluster Headache Attack. I put this video on to educate, not get pitty. For people to realize and understand what us Cluster Headache people go through. Iam chronic. Have had these since June 25,2005 over 8 years without one day relief. I suffer 3 to 15 times per day lasting 30 min to 3 hours long. Some severe, some not. Please share this video with someone who doesnt understand what we go through. Perhaps it will educate some. I wake up smiling each day and love my son and he is the reason I go on each day. I am a cluster head survivor !!! My heart goes out to all you cluster heads, friends and families. May this beast be cured one day!
Please read all posts before commenting on medications I should try. OXYGEN does NOT work for me and I WILL NEVER USE NOR CONDONE or CONDEMN THE USE OF ANY ILLEGAL DRUGS WHATSOEVER nor will I approve posting for it. I am not a doctor and will not make recommondations for your CH. Please speak to your own Doctor/Nuerologist and Nuerosurgeon if you have one.I am happy to offer a warm hello and discuss CH with anyone needing a friend/support.
I am a proud member of ClusterBusters and full support what they do. Just not for me.
Please respect my wishes and my own choice. If curious read my blog to find out why instead of nasty comments which I wont publish anyway.
Michael J. Fox is my hero,please give generously to MJFF. The research/funding they do on DBS is part of why I am the 2nd person in Canada and the 17th on the planet to have DBS for Cluster Headaches.


-see my other videos- or read my blog
www.clusterheadsurvivor.blogspot.ca

thank you. Help me reach 1 million hits to spread awareness.
Hope it goes viral
thank you,God Bless

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