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Cluster Headache Help and Support >> Getting to Know Ya >> First Time here http://www.clusterheadaches.com/cgi-bin/yabb2/YaBB.pl?num=1266190110 Message started by travisk on Feb 14th, 2010 at 6:28pm |
Title: First Time here Post by travisk on Feb 14th, 2010 at 6:28pm
Im a newbie here. Really happy to have found this place. My attacks started 7 months ago. Usually have at least five attacks a week usually one a day. Havent had a break yet more than four days. Dont have medical insurance so havent seen a doc yet. Would have went to the hospital with the first one because i thought i was going to die but was hiking the appalachian trail and was a 10 mile hike to a road so i just sat there. By the time i got off the trail knew i wasnt going to die so i thought i could tuff it out. Fast foward 7 months and i am now depressed and have considered suicide during the attacks. Going to the neurologist asap dont care if i have to spend all my money on docs and meds. Honestly cant think of a better way to spend it. It took 7 months but these ch's have broken me. Even when im not hurting im sad and scared. hard to type this without cryin. Just need a break. And some sleep. Looking foward to seeing the doctor and hopefully get at least a week without a CH. My record so far 4 days but when they come after a break they are longer about 2 hrs instead of 1 and much more painful. Well thats my story thanks for bein here and its good to know im not the only one who screams and pulls out my hair. I prefer to pull out my leg hair because i can hide the bald patches. p.s. it really sucks when i run out of hot water in my shower
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Title: Re: First Time here Post by BC_Battler on Feb 14th, 2010 at 6:59pm
Welcome,
I am so sorry you are having a hard time right now, but this is a good place to come for support. I am also sorry that you are unable to see a doctor; I can't imagine what that must be like. I do hope you get to see one soon, though, so you can treat your situation appropriately. Please do know that many of us have been where you are now, and many of has had similar thoughts to yours. But we have found ways to cope, ways to even thrive and survive; and so will you - this CH thing is something that you can beat, or at the least, learn to to co-exist with. When you need a group to listen / to vent to / to ask questions of, you are always welcome here. I wish you all the best, Travis. Please feel free to message me if you ever need some support. Take care - |
Title: Re: First Time here Post by travisk on Feb 14th, 2010 at 7:32pm
Thank you i will found this place last night and my moral has improved a hundred fold
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Title: Re: First Time here Post by Guiseppi on Feb 14th, 2010 at 7:58pm
Good news is there are some very effective treatments. For now, go buy some energy drinks, Rock Star, Monster, any containing caffeine and taurine. Chug one of these at the first sign of a hit, many can abort or at least really reduce a hit with these.
Read the oxygen info link on the left and really push for it with your doc. It's been a very effective treament for many, I can abort an attack in less then 10 minutes with just oxygen. I'm a 31 year episodic sufferer and haven't found anything that'll touch oxygen for effectiveness with the total lack of side effects. Good luck in getting in to see the neuro. An accurate diagnosis is critical as there are so many variants of headaches. Joe |
Title: Re: First Time here Post by travisk on Feb 14th, 2010 at 9:04pm
thanks already bought the drinks got ten for now and the doc my dad worked for for twenty years as an eeg tech will hopefully get me in and get me a script for the o2 thanks for readin my story and the tips lookin forward to less painful attacks shorter will be nice to
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Title: Re: First Time here Post by bejeeber on Feb 14th, 2010 at 9:59pm
Hey Travisk - great that you have a line on some O2 - there's a very good chance it will work well for you if you follow the oxygen info to the letter, including non-rebreather mask.
Considering the severity of your case, I imagine a hi flow regulator will likely need to be ordered too. GOOD thing you found this site - there are many potentially effective ways to beat back this beast we call CH. Please keep hanging around, researching here and chatting - lots to learn and discuss. If you haven't found out the hard way already, alcohol triggers a massive hit for most of us BTW. Also, I hate to tell you this, but doctors have a particularly lousy track record treating CH patients and they are generally ill informed, to put it politely. Your best hope is to find a headache specialist type neuorologist. |
Title: Re: First Time here Post by travisk on Feb 15th, 2010 at 8:26am
Drank a monster at the onset of a ch last night. The way it started i was petrified because it was painful almost instantly so i slammed a monster 3-5 min later nothing no pain no shadows i am amazed!!!!!!!!!!!!!
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Title: Re: First Time here Post by LasVegas on Feb 16th, 2010 at 12:05pm
do you have a neurologist you are pleased with? what city are you in?
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Title: Re: First Time here Post by bejeeber on Feb 16th, 2010 at 3:06pm travisk wrote on Feb 15th, 2010 at 8:26am:
Wow - that's fantastic to hear. I was becoming a little skeptical about the energy drinks (since they hadn't ever come close to aborting an attack for me when I tried them), but this report has me remembering that there's almost no treatment that is guaranteed to work for everyone with this dodgy CH condition. It's a voonderbar thing to see someone come on here and find out about something that'll bring them some immediate relief. :) |
Title: Re: First Time here Post by Newsh on Feb 16th, 2010 at 6:03pm
Travis, welcome, it feels good to be part of something so crappy, caffeine is the way forward for me as well but there are so many people with great ideas, views and advice on this site. We should all get together and rub our heads in unison.
Good luck to you Newsh |
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