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Cluster Headache Help and Support >> Getting to Know Ya >> New to site NOT TO CH!!!!
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Message started by FrankWyo on May 8th, 2009 at 3:42pm

Title: New to site NOT TO CH!!!!
Post by FrankWyo on May 8th, 2009 at 3:42pm
Hello, My name is Frank and I have been and am now suffering with clusters, started in 1979, and have had some really hard times. After all these years I still have major problems dealing with this. Doctors not much help anymore. Sorry, can't concentrate to good right now. Just want to say I am glad to know I am not alone with this. :'(

Title: Re: New to site NOT TO CH!!!!
Post by Jimi on May 8th, 2009 at 3:45pm
Welcome Frank.

We have been here for many years and there are thousands of us.

Tell us what you are taking and maybe we can help.

Title: Re: New to site NOT TO CH!!!!
Post by BarbaraD on May 8th, 2009 at 5:03pm
Welcome to Clusterville Frank.

Let us know how we can help you.

Hugs BD :-*

Title: Re: New to site NOT TO CH!!!!
Post by Callico on May 8th, 2009 at 5:48pm
Welcome aboard.  You have come to the right place.  Take a deep breath and relax, as you are now home with the family.  You will go a long way before you find a more caring group than these people I call friends, and more importantly, family.  

Give us a bit of history, how ong you've suffered w/ch, how long you have been diagnosed, what meds/treatments you have tried, what has/ has not/did but doesn't work for you, etc.  Most important, check out the Oxygen info button highlighted on the left in yellow.  O2 has been a Godsend for many here.

Jerry

Title: Re: New to site NOT TO CH!!!!
Post by Guiseppi on May 9th, 2009 at 12:58am
Answer all of us nosey people, now! ;)

Welcome to the board. The strength of this board is its combined "real world" experience. Let us know what you've tried and how you've tried it, what has and hasn't worked. Could be you'll drop a new idea on us, maybe we can tweak your regimen and help you get some relief. So glad you found us.

Joe

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