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Cluster Headache Help and Support >> Getting to Know Ya >> I'm new here. http://www.clusterheadaches.com/cgi-bin/yabb2/YaBB.pl?num=1240099651 Message started by Beenyweeny on Apr 18th, 2009 at 8:07pm |
Title: I'm new here. Post by Beenyweeny on Apr 18th, 2009 at 8:07pm
Hi Everyone:
I sure am glad I found this place. I didn't even know a forum for CH's existed. I knew I wasn't alone, but I didn't know where to find any of you. So a little about me... I'm 33 years old and I've been getting cluster headaches for about 2 years. Originally I was diagnosed with Trigeminal Neuralgia before I was sent to a neurologist. My neuro sent me for an MRI to rule out TIA. All clear! Other than being in excrutiating pain every night (between 11pm and 2am), I am a perfect picture of health. I have 2 small children (ages 5 and almost 4). My oldest son had a massive stroke when he was 2 yrs.old. :-( He had no prior medical history and there is still no specific reason as to why it happened. He has cognitive and physical disabilities that we are still trying to work through. The important thing is that he survived and is doing amazingly well considering the amount of damage the clot caused. My 3 year old is perfectly healthy and quite the smart a. I felt compelled to find a group like this one after last night. I woke up around 12am after feeling like someone just hit me with a giant rubber mallet. BTW I'm a righty. I sat straight up and instantly felt intense pain. I could not find the regulator to my O2 tank and almost panicked. I woke up my husband crying and begging him to get up and help me. We finally found it and I sucked that tank dry. Headache went away, fioricet kicked in....back to bed. When the pain starts I can feel a twinge in my right nostril and in my temple. I know that its coming in the next 2-3 minutes, full blown pain! My right nostril starts clogging up and dripping. My right eye swells, turns red and tears. Sometimes the pain is so intense I bang my head on the wall. Like that really helps. Besides my O2 tank, I have Fioricet on hand. Also, I take a daily regimen of Verapamil and Nortryptaline. I really don't think that either of them are doing me any good yet I continue to take them. I have officially refused to do another round of Prednisone. I gain weight and if my butt gets any bigger, I will have to buy new clothes and I hate clothes shopping. So there's my reason for that. I don't know how long my headaches last because I always take a Fioricet or breathe in the O2. Before that (in the very beginning before I had any available relief), I would walk the neighborhood just to get my mind off of the pain (even at 2am). Eventually they went away. They used to be episodic but now they seem to be chronic. I really feel like the pain is coming from my sinuses but my sinuses are clear. I just don't understand how you can feel pain that intensely and not have a reason as to why or where it's coming from. My neurologist said that when he dies and goes to heaven, the first question he is going to ask God is "What the F was up with cluster headaches?". Apparently he can't figure them out either. Brandi in FL |
Title: Re: I'm new here. Post by coach_bill on Apr 18th, 2009 at 9:02pm
welcome,
Glad you found us, CH sucks thats for sure and i thought nobody eles knew anything like what i went thourgh, but it sounds like you hit it right on the head. As you read more posts you will find different strokes for the different folks but always keep a open mind and you just might find that magic bullet. Coach Bill |
Title: Re: I'm new here. Post by Lefty on Apr 23rd, 2009 at 6:34pm Beenyweeny wrote on Apr 18th, 2009 at 8:07pm:
Hi Brandi, Glad you found us sorry you had to. Well Brandi at least you are on some abortive and preventive meds already. The 02 works a treat for me and many others on this forum. As to your statement i think most of us would like to ask the same question ( What The F**@K). Bill has already mentioned the beast affects us all in different ways and what works for one may not for another, but there's one thing we all share and that is the unbearable pain we endure during a hit. I hope you stick around because this is a great place to learn about the various treatments available and to talk to people who will totally understand and offer you support during these testing times. PS Glad to hear your son is doing better...! ;) Take care Lefty...! |
Title: Re: I'm new here. Post by Beenyweeny on Apr 23rd, 2009 at 7:14pm
Hi Coach...Hi Lefty:
Thanks for the comments. I already feel reassured by this site. I tried the water idea...didn't work for me. I'll keep trying it though. My neuro just upped my Nortryptaline to 25mg so I'll see if that makes any difference. (At least I won't be sad since it's really an antidepressant)...and I'm not depressed. Anyway, thanks again for your support. Talk to you all soon. Brandi |
Title: Re: I'm new here. Post by BarbaraD on Apr 25th, 2009 at 8:41am
What rate are you using with your O2 and are you using the RIGHT mask? Chek the O2 info on the left and BE SURE you're using it right. That's really important. ????? Why wasn't your regulator already on your tank - Boy scout motto - Always be prepared!!!!
As to the pain killers - NOT GOOD! They will cause rebounds... Vaso constrictors will kill the pain and don't cause rebounds. Imitrex or cafergot work a lot better than pain killers (even asprin will cause rebounds if taken too often). Coffee works well or RED BULL at the first sign of a HA. Melatonin at night before bedtime (9-15mg). Take for several days before you say it didn't work. It helps get thru the REM sleep and lets you get the rest you need to get thru the days. Glad you found us - we're a good bunch and do KNOW how you feel cause most of us are going thru what you are and we DO UNDERSTAND. My last episode started in 97 and I'm hoping it will end any day now :). But so far I just keep the RED Bull, coffee and O2 handy. Check the O2 info on the left and be sure your O2 is being used properly. If you need help contact Batch or Chuck - and ASK questions. They're really experts on it. (Dont' tell Chuck I said that!). Any questions you have just ask - we're here to help. Hugs BD |
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