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Daily Chat >> General Posts >> Clusterbuster Conference http://www.clusterheadaches.com/cgi-bin/yabb2/YaBB.pl?num=1250378141 Message started by Melissa on Aug 15th, 2009 at 7:15pm |
Title: Clusterbuster Conference Post by Melissa on Aug 15th, 2009 at 7:15pm
Just paid my registration and am really looking forward to it!
:) mel edited to add: Who else is going? |
Title: Re: Clusterbuster Conference Post by Linda_Howell on Aug 16th, 2009 at 11:24am I am.... [smiley=wave.gif] I believe Bill Mingus, Nani and oh yeah...BobW will be there. ;) |
Title: Re: Clusterbuster Conference Post by Brew on Aug 16th, 2009 at 12:21pm
I am - Saturday only. In and out, same day.
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Title: Re: Clusterbuster Conference Post by Melissa on Aug 16th, 2009 at 1:29pm
Wonderful! Can't wait!!!
:) |
Title: Re: Clusterbuster Conference Post by gAnDo on Aug 16th, 2009 at 4:13pm
So these guys are for real with their LSD fixes etc? I was sceptical...
Instead of going through what I emailed to them (found them through Wikipedia - then found this place) I will just copy the email here. If you cant be assed reading it, it basically says I had a bit of a crazy drug addled childhood and think maybe psycadelic drugs caused my headaches and may not be the answer. Of course I have no proof of that. Quote:
BUT I would be VERY interested to hear stories from people who had LSD to fix cluster headaches. Not just the hallucination stories :P Who knows, it may work. *please excuse the profanities, I had a few beers but what I said was tue [smiley=embarassed.gif] |
Title: Re: Clusterbuster Conference Post by ClusterChuck on Aug 16th, 2009 at 4:20pm gAnDo wrote on Aug 16th, 2009 at 4:13pm:
Have you read up on the link to the left side of the screen: oxygen info ? It is a life saver for many of us. Chuck |
Title: Re: Clusterbuster Conference Post by gAnDo on Aug 16th, 2009 at 4:27pm
I did mate thanks :) Read it earlier when the forums were down.
Sounds like a breath of fresh air (ha) but seriously its something I want to try, although I want to wait until I have been to see the hospital specialist docs as am not a fan of self medication. Funnily enough I have found in the past that when I run out of pain killers and need them when in work, I need to make a brisk 10 minute walk to the chemist to get them and even though my heads really painful in there, when I get back to work its better.... Increased oxygen in my brain due to walking excercise maybe? |
Title: Re: Clusterbuster Conference Post by Karla on Aug 16th, 2009 at 4:37pm
gAnDo, I suffered from 8 cluster headaches every day. Each a level 10+ lasting 1 1/2 hrs long. That is 16 hours of 10+ pain for the day. I am chronic and repeated this ritual everyday. I had tried everything out there as a preventative and abortive and nothing was working for me. I was desperate. I took a small dose of shrooms and ate them. I had a slight buzz but no high by any means. It gave me several weeks of pain free living. That means 0 ha. Drs. could not even offer me that. I used to take coke, acid, meth, pot, alcahol etc in the years of 80-93. I quit doing all drugs in 93 and in 98 I developed ch. I dont think my earlier drug use caused ch. But I do know that I had a very successful time using shrooms. I know of others lsd, shrooms, lsa seeds, kidzu, etc and had amazing success stories with stopping ch dead in its tracks. You use such low doses you don't trip. There are drs and researchers in Harvard studing the effects of shrooms and ch. Dont knock it until you have tried it the recomended way with a ch diagnosis and you have tried everything under the sun the drs have given you and nothing is left and all hope is lost and your looking at a revolver. It can be a life saving alternative.
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Title: Re: Clusterbuster Conference Post by gAnDo on Aug 16th, 2009 at 5:20pm
Thanks for your reply.
As as I said, Im sceptical, but my mind is open to the options and its realy good to hear you got some respite, especially after the intensity of your headaches! It sounds horrible (which Im really not trying to be) but Im glad Im not as bad as some people.... I dont think Id be here typing to you if it had been anywhere near as bad a you had it. I dont have the capacity/contacts(lol) to get shrooms here in Scotland, but LSD I could find I suppose... I will certianly give it a shot if the docs cant help. Still got 6 months to wait and see. Oh, and while Im here I might as well say... Alchohol helps. Never a good thing to say, but I never have migranes hungover :-[ (although I do when starting drinking) *disclaimer - dont do it kids |
Title: Re: Clusterbuster Conference Post by Linda_Howell on Aug 16th, 2009 at 5:53pm Quote:
Alcohol is an almost universal "TRIGGER" for a clusterheadache. |
Title: Re: Clusterbuster Conference Post by gAnDo on Aug 16th, 2009 at 6:00pm
Stange eh. I pretty much drink every weekend but never thro the week and all week is when its the worst, although still happens at the weekends.
I guess my next step is to stop for a month and see what happens then? |
Title: Re: Clusterbuster Conference Post by Brew on Aug 16th, 2009 at 6:10pm
Have you been diagnosed by a physician with cluster headaches? I read where you diagnosed yourself, but I must have missed the part where you got a diagnosis from a doctor.
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Title: Re: Clusterbuster Conference Post by Redd on Aug 16th, 2009 at 8:16pm
He stated Bill...
Quote:
Not an official Dx, but that was my first stumble upon CH.com, was when it was first mentioned to me by the GP, then awaiting my appt. with the Neuro. Better he's proactive in his research than reactive..hey? |
Title: Re: Clusterbuster Conference Post by Brew on Aug 16th, 2009 at 8:20pm
I've nothing against research, but
Quote:
Just making sure everything is copasetic. |
Title: Re: Clusterbuster Conference Post by Pinkfloyd on Aug 17th, 2009 at 12:55am Melissa wrote on Aug 15th, 2009 at 7:15pm:
I'll try to get up a list soon. ;-) GaNDo....not sure where you emailed your letter to Clusterbusters but they normally come to me and I haven't seen it, if it was sent recently. I would suggest you do lots of research. Both on cluster headaches as well as the treatment information found here, on Clusterbusters.com and at the OUCH button on the left hand side. Bob |
Title: Re: Clusterbuster Conference Post by Shawn on Aug 17th, 2009 at 2:57pm
It's pretty clear that everybody has a unique experience with this wonderful condition, so I'm not going to say you're wrong or right about your drug use being a contributing factor, but I do know of several people (including myself) who have been able to see some relief using the clusterbuster methods. I had one outstanding success where I went completely pain free for 6 months, but have not been able to duplicate that since then. However, I remain convinced that BobW is on to something important and I look forward to the day when mainstream medicine starts figuring out how/why this works, and how to get reliable results. Until then, for those of us who are chronic and have been literally at the end of our rope, any hope at all is better than nothing.
Thank you again Bob, your efforts have made more difference in my life than all of my doctors combined, and I'm not just saying that. I wish I was able to go to the conference, but the budget gods have been pretty brutal this year. I'm still digging out from under my million dollar babies (technically, they were just under a million, but we got two so maybe I should call them my half-million-dollar babies) -Shawn |
Title: Re: Clusterbuster Conference Post by Pinkfloyd on Aug 17th, 2009 at 7:52pm Shawn wrote on Aug 17th, 2009 at 2:57pm:
Thanks very much Shawn. We'll be a little closer to you next year so maybe you'll be able to make it in 2010. Hope so. be well, Bob |
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