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Title: im new Post by genericmo on Mar 11th, 2005, 7:39pm this is a great site :)just got diagnosed cluster headache with horners syndrome had a lode of tests at hospital a couple of weks ago . im still suffering with the headaches. thought id taken a stroke got a bit scared. the horners showed up when i had my worsed headache of all time. still waiting for more test to be done in hospital , i would like someone too talk too me . thanks |
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Title: Re: im new Post by Jonny on Mar 11th, 2005, 7:49pm on 03/11/05 at 19:39:20, genericmo wrote:
What would you like me to say? If you will be needing talk about women having sex with horses....press 1 For homo sex press 2 (That will get you Dons direct line) For another menu press 3 LMAO ;;D |
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Title: Re: im new Post by nani on Mar 11th, 2005, 7:52pm Hi mo (can I call you mo?). Welcome and I'm sorry you're here. What kind of meds are you using as preventatives and abortives. Oxygen is a very effective abortive for many of us. Look over at the links on the left for oxygen info. Look around the site here and at the OUCH site (there is also an OUCH UK site) and learn all you can about this. Information is our best weapon. Have a look at this promising new treatment as well. Read through it and pay attention to potential meds interactions. Good luck and pain free wishes, nani :) http://www.clusterheadaches.com/cgi-bin/yabb/YaBB.cgi?board=meds;action=display;num=1107368408 |
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Title: Re: im new Post by genericmo on Mar 11th, 2005, 8:21pm hi thanks for talking to me i only got a morphine drug for the pain and a a drug called migraleve dont seem to be doing any good the pain starts in my face around the sinussus then goes up into my head its the worst pain ever when its in my head like some one is hitting in the eye with a knife its seems to be around the eye mostly. and i can feel sick too i just wish sometimes it would go away. but i soppose most people feel like that thanks for listening to me . my name is mary :) |
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Title: Re: im new Post by pubgirl on Mar 11th, 2005, 8:29pm Mary You can talk to a Ch sufferer in person on the OUCH UK Helpline. It has an answerphone where you leave a message and a knowledgeable sufferer will ring you back and help. I have messaged you the telephone number. Wendy |
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Title: Re: im new Post by pubgirl on Mar 11th, 2005, 8:33pm Mary Just seen where you live! There is an OUCh UK meeting of Clusterheadache sufferers in your home city this weekend, everyone welcome, sufferers and supporters alike. see your messages for details Wendy |
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Title: Re: im new Post by genericmo on Mar 11th, 2005, 8:42pm thanks wendy , sent you a message, i hope u can get me a place at the meeting [smiley=laugh.gif]in glasgow . mary |
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