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supershrimper
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Not Alone
« on: Sep 4th, 2006, 4:42pm »
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I've just found this great message board and feel for once that I am not alone.
 
I have been a CH sufferer for 2 years now, with the pain a contanst dull annoying ache always there, with extreme attacks that feels like I am being stabbed in the side of the head every 2 minutes, these attacks normally last for 3-4 weeks.  I get a week or two free from the stabbing then it rears it's head again.
 
It was nice to see that there are other people suffering the same, pacing up and down, banging their heads against brick walls (literally), rocking, crying and feeling like their head is going to explode or their eyes pop out of their sockets.
 
My Nuerologist put me on antidepressents, the pain went, but they made me depressed, morphine makes me spaced out and has side effects of making my eczema and stomach hell to the point I can not cope, although the pain goes!
 
I was beginning to think that I will be like this for the rest of my life, with no one understanding.
 
I am going to be a regular visitor and hopefully some of other peoples words of wisdom will get me through the day.
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chewy
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Re: Not Alone
« Reply #1 on: Sep 4th, 2006, 6:48pm »
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Welcome home!
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thebbz
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Re: Not Alone
« Reply #2 on: Sep 4th, 2006, 7:53pm »
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Lots of other treatments out there to try. Sorry your getting hit.
Read the site when you can and try to get some rest.
Keep in touch
all the best
jb
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Re: Not Alone
« Reply #3 on: Sep 4th, 2006, 10:39pm »
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Ever try oxygen?  Ask your doctor about verapamil, helps with the shadows too.  Good luck and welcome.
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George_J
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Re: Not Alone
« Reply #4 on: Sep 5th, 2006, 12:28am »
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Welcome.
 
Lots of great people here, and much good advice.  Look around, get to know everyone, and read, read read.  
 
Ask all the questions you'd like.  We'll help in any way we can.
 
Many UK people here--I think you'll feel at home.
 
Best wishes,
 
George
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Ah! The foreigners put on such airs
Wearing the tangerine suits
And their harlequin eyes.
The pain they inspire
Draws in harmonica melodies
And the feathers of birds
Which flame up at their touch.
It all comes to light in the sheer
Debonair.
(Ellen)
chopmyheadoff
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Re: Not Alone
« Reply #5 on: Sep 5th, 2006, 3:22am »
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welcome to the mad house matey  Grin
 
it all gets better from here - trust me !!
 
What meds has the doctor got you on ??
Has he mentioned imigran ??
 
its been a life saver for me.
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supershrimper
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Re: Not Alone
« Reply #6 on: Sep 5th, 2006, 7:43pm »
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Another visit to the GP today, suggested Beta Blockers, but I have been down that road before, and that didn't help.  He gave me Remedine which is Paracetamol, dihydrocodeine tartrate. the dihydrocodeine for blocking the pain receptors, which is dulling the pain enough to be able to function, but awaiting another nuerologist appointment.  
 
Does anyone know of what causes these damn CH and how do others cope with the pain, if indeed they can.
 
 Undecided bash
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Charlotte
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Re: Not Alone
« Reply #7 on: Sep 5th, 2006, 9:38pm »
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Only a partial answer, here...no, we don't know what causes these damn headaches.
 
Charlotte
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Jobette
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Re: Not Alone
« Reply #8 on: Sep 5th, 2006, 9:50pm »
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Welcome to "My place of refuge". Cheesy
 I am sorry that you are in hell but there are some good people there with you. Grin Most of us have been doing this dance for a long time and some of you are in training.  Wink And even though it doesn't feel like it right now, things will get better and you are not alone. Kiss  
As others have said read, read, read. With the information from this board you will have the ammunition when you visit your neuro, so that you can get your ammo to fight this thing. Cool
Keep us posted! Praying for pain free days! Melissa
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Who gave cupid those flaming arrows, and why is he shooting them into my right eye?
Where is his love?
BB
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Re: Not Alone
« Reply #9 on: Sep 6th, 2006, 1:32am »
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on Sep 4th, 2006, 4:42pm, supershrimper wrote:

 
I have been a CH sufferer for 2 years now, with the pain a contanst dull annoying ache always there, with extreme attacks that feels like I am being stabbed in the side of the head every 2 minutes, these attacks normally last for 3-4 weeks.  I get a week or two free from the stabbing then it rears it's head again.
 
 
.

 
 
Hello
 
Sorry that you have this terrible headache. Hope you will find relief soon.
 
But reading your post I am a little bit concerned if you have CH or maybe something else. As far as I know, CH does not have a constant dull ache thats there always, and shouldnt have severe attacks every 2 minutes, plus the pain doesnt really feel like someone stabs you on the side of the head and unless you are chronic you should get more than 1 or 2 weeks pain free in between. Chronic CH is rarer than episodic, the ratio is something like 9-1.
 
There are other similar but different conditions such as Paroxysmal Hemicrania, Hemicrania Continua and SUNCT which have symptoms similar to CH but are different to CH and the medications for them are quite different too.
 
You may want to read and check the criteria for CH on the left side of the Board and on the www.ouch.org website and double check with your neurologist.
 
Its not uncommon for people to be misdiagnosed especially in the early stages so it pays to be extra careful.
 
Anyway, good luck with it all. Hang in there. Things will get better.
 
Annette
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supershrimper
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Re: Not Alone
« Reply #10 on: Sep 6th, 2006, 4:00am »
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Annette
I have looked up the symptoms to Paroxysmal Hemicranial and it does seem more like my pain.
Constant dull pain, with intense attacks every few minutes.
Thank you, you should be a Dr. Wink
It is nice to have support from everyone here, I would not wish this pain on my worst enemy.
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Re: Not Alone
« Reply #11 on: Sep 6th, 2006, 7:57am »
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You are most welcome Super.  Smiley
 
My DH was misdiagnosed for several years with just about everything under the sun so I know what its like.
 
Keep reading everything you can and keep a diary of what your headache does on a daily basis, it will help greatly to understand what your body does and what triggers or helps with the condition.
 
Hope you will get the diagnosis confirmed soon and then the right treatment to make all that pain go away.
 
Painfree wishes to you, and prayers.
 
Annette
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Jonny
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Re: Not Alone
« Reply #12 on: Sep 10th, 2006, 3:57pm »
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No, your not alone!!
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It is up to YOU to educate yourself and then help your doctor plan your treatment. If you just sit down in front of your doctor and say "make me better" you are setting yourself up for a great deal of pain.

- Guiseppi


chewy
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Re: Not Alone
« Reply #13 on: Sep 10th, 2006, 10:25pm »
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Quote:
Does anyone know of what causes these damn CH and how do others cope with the pain, if indeed they can.  

 
Popular belief amongst the medical community is that CH is causedby a deformity of the hpothalamus gland.
 
How do people cope? In a million differant ways. Read. Read. Read. You will find a management technique or combinations of that will help you cope and manage both the pain and the lifestyle we are stuck with.
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