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Cluster Headache Help and Support >> Getting to Know Ya >> new kid in town http://www.clusterheadaches.com/cgi-bin/yabb2/YaBB.pl?num=1292947495 Message started by willwill on Dec 21st, 2010 at 11:04am |
Title: new kid in town Post by willwill on Dec 21st, 2010 at 11:04am
[smiley=headbanger.gif] Hi. I'M 38 and been a CH member for a long time. I don't know anyone who has CH and i don't like feeling like i never will so i decided to come aboard so to speak. Just glad to have a place to listen to others.
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Title: Re: new kid in town Post by mikstudie on Dec 21st, 2010 at 12:36pm
Welcome,share your prevents and aborts with us. Do you have your CH under some what of control?
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Title: Re: new kid in town Post by wimsey1 on Dec 21st, 2010 at 1:42pm
Yes, welcome. Do share. And as far as not meeting anyone else with CHs, they are sadly more prevalent than you might think or want. It is true most will not understand what you're going through, but we do! Look forward to hearing more and God bless! lance
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Title: Re: new kid in town Post by willwill on Dec 21st, 2010 at 3:07pm
HI, I am currently on 450mg of lithium BUT i was taking 950mgs a day untill my stomach could take no more. I also take ergotamine to help abort. This has worked really good for me for the last two years as long as i don't do alot of physical work. i have to take lithium as a preventive med and to help abort CH'S. I was on prednisone, depakote, amitriptyline, thorazine, imitrex nasal and other stuff over the past twelve years. I was diagnosed while in the Navy in 1997 and i have episodic attacks.
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Title: Re: new kid in town Post by Ginger S. on Dec 21st, 2010 at 4:55pm
Welcome Willwill Glad you found us.
Look into the O2 link to the left it Read all you can here and enjoy your new CH'er friends. PF Wishes! |
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