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Cluster Headache Help and Support >> Getting to Know Ya >> New here! http://www.clusterheadaches.com/cgi-bin/yabb2/YaBB.pl?num=1320445938 Message started by Nikirae on Nov 4th, 2011 at 6:32pm |
Title: New here! Post by Nikirae on Nov 4th, 2011 at 6:32pm
Hi, My name is Nicole and I am 44 years old and live in Green Bay, WI (Go Packers!! sorry had to say that)
I am very new to having Cluster Headaches. I have been having them for 6 weeks. It was great to finally get an answer to what this pain was today. I have been getting an avg of 8 a day for the past 6 weeks. I have been told everything from head spasms in my head and eyes to migraines. After a visit to the ER on Monday, I was referred to specialist and she gave me the diagnosis today. As I was with the neurologist, I felt an attack coming on, she had nurse take me to the ER right across the street and have them give me Oxygen, it was amazing how well it helped. I wanted to take it home with me. LOL I was given Indocin 50 mg 2 x day and was told if that does not help me by Monday, to call and she will start Oxygen and lithium and see if that works. I am already a chronic pain patient due to other issues and luckily already on disability, cause I am sure I would have been fired by now if I was able to work. So there is a little about me. I am so glad I found this site. I have learned so much already and I am sure there is so much more to learn and having the extra support will be great, as I live alone and my cats think I am insane when I am rolling around on the floor and hitting my head on the walls in the middle of the night. ~Nicole |
Title: Re: New here! Post by Linda_Howell on Nov 4th, 2011 at 6:48pm
Hi Nicole,
To be diagnosed correctly after only 6 weeks is a miracle around here !!!!!!! MANY here go decades. Go the left of where you are reading this. There is a list of links. Open the one in yellow (oxygen) and read to the end. There is almost nothing it doesn't cover and if there is, there are lots of us who will be glad to answer questions. 02 works for the majority of us if it is done right. I can abort a headache in under 10 mins. if I get on it at the very first twinge of a headache and stay on it for a while after it's gone. As you have already experienced it is a Godsend. Don't stop at the 02 link however. Start reading everything including posts here and on other forums on this page. Knowledge is power & the more you know the better. We're glad you found us here and you now know that you're not alone. We're family and you are our newest member. :) Linda |
Title: Re: New here! Post by Nikirae on Nov 4th, 2011 at 7:03pm
Thanks for the info :)
I will for sure run out and get some energy drinks tomorrow!! I am reading all I can on here. And yes, the neuro is a headache specialist. But I have noticed since I moved to Green Bay, doc's of all kinds are so conservative in their treatment. I think I got lucky with the diagnosis quickly because I refuse to take I can't help you for an answer, as a chronic pain patient already (Fibrobmyalgia and Failed Back Syndrome) I have lots of practice in getting an answer and getting bs from doctors. lol I sure have lots to learn thou!!! I am clicking away on the left side of page and making notes for myself and questions to ask my doctor as well. ~Nicole |
Title: Re: New here! Post by Guiseppi on Nov 4th, 2011 at 7:56pm
Incidentally......I have decided not to communicate with you anymore until Monday.....on account of I'm a charger fan. Nothing personal, it's business! ;)
Joe |
Title: Re: New here! Post by Nikirae on Nov 4th, 2011 at 11:07pm
LOL
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Title: Re: New here! Post by Mike NZ on Nov 4th, 2011 at 11:17pm Guiseppi wrote on Nov 4th, 2011 at 7:56pm:
It's just a game, nothing serious. I can't see why it matters so much. Obviously it's different when the ABs are playing the Wallabies, but then everyone knows who will win an epic encounter like that. (The above will probably only make sense to any Kiwis and Aussies). |
Title: Re: New here! Post by wimsey1 on Nov 7th, 2011 at 8:06am
Are the Wallabies in San Diego? Never hear of 'em.
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Title: Re: New here! Post by Linda_Howell on Nov 7th, 2011 at 5:45pm
O.k. here's a newbie needing our help and all you guys can do is talk *smack*
I'm ashamed. Ashamed I tell ya. ;D ;D ;D ;D Don't mind these guys Nicole. |
Title: Re: New here! Post by Nikirae on Nov 8th, 2011 at 5:24pm
LOL Smack talk is okay...it keeps my mind off of other things. And since the Packer's won..all is good ;D
On a side note, my meds have been changed to verapamil for maintenance and currently started a cycle of Prednisone. And waiting on insurance to approve oxygen. Crossing fingers this works! |
Title: Re: New here! Post by wimsey1 on Nov 9th, 2011 at 8:07am
I am also ashamed...maybe not. Any whoo, good for you, Nicole. It does sound as if you are on the right track. Line it all up, start using the O2, and one word of caution: while this lineup has helped many of us, it is not a universal panacaea. Please keep reading, and keep taking notes, especially of those interventions others have used, just in case the verapamil doesn't quite do the trick. What dose are you on? There may be a lot of room there for you and your doctor to make adjustments before giving up on it altogether. Then again, it might work first time out. Good luck, and God bless. lance
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Title: Re: New here! Post by Guiseppi on Nov 9th, 2011 at 9:01am
Even though we lost....I've decided to be the better man and still talk to you. >:(
As Lance said, don't assume the first round of meds you try will work. Keep researching to have a back-up plan to suggest in case it doesn't work. Verapamil has an awesome track record with CH, that's why it's still the first line prevent. Some go as high as 960 mg a day to get relief. If it doesn't help at even the higher doses, consider adding lithium. We used to call this the "chronic cocktail" as it helped many of our chronics when nothing else would. And if the insurance company won't cover the oxygen, don't panic. I was out of pocket for many years. A regulator can be bought for $20 on E-Bay. Mask costs you another $20. E-Tanks rent for $5-7 a month, refills run around $15. So it's not big money. If you're willing to go the welding oxygen route....MANY on the board do, it's even cheaper. joe |
Title: Re: New here! Post by Nikirae on Nov 11th, 2011 at 3:48pm
They started me on 180MG ER of the Verapamil, but I am thinking I will need to have them raise it. Still having problems during the day hours, but last 2 nights I have not been woke up by the beast. First time in almost 2 months!!!
Nice to know that the O2 out of pocket cost is not high if insurance decides not to approve. |
Title: Re: New here! Post by Nikirae on Nov 20th, 2011 at 7:31pm
I have gone two days without a headache!!!! I am so happy!!
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Title: Re: New here! Post by Guiseppi on Nov 21st, 2011 at 9:17am
Well that's great news. Don't let your guard down and keep educating yourself. here's hoping it's the start of a LONG pain free stretch. [smiley=sayyes.gif]
Joe |
Title: Re: New here! Post by Nikirae on Nov 25th, 2011 at 3:13am
Yeah I got one today >:( But it was a stressful day. But I have the O2 now and was able to abort it quickly. Also found out my stepmother has been having these for years and just got her first outbreak in 3 years yesterday :(
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