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Topic: new to this site- best thing out for info. (Read 197 times) |
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jckgales
New Board Newbie
I love YaBB 1G - SP1!
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new to this site- best thing out for info.
« on: Feb 8th, 2005, 6:41am » |
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Im 44 and just been diagnosed with ch. After year and a half. Doctors seem useless. No one else understands the pain but you guys. I have been searching for info but seems like a big circle. My doc says wont give me O2 but now I see I need a new doc. Just want to say to all clusterheads hang in there and thanks for all info. jckgales11@charter.net
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Langa
CH.com Alumnus New Board Hall of Famer
So many donuts, such little time...
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Re: new to this site- best thing out for inf
« Reply #1 on: Feb 8th, 2005, 8:58am » |
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Hi Jck and Welcome to the Family - I agree with you...this is definitely THE place for great info on clusters. Make sure to print as much info as you can to take to your doctor. Have you seen a Neurologist? Tell us more about yourself...are you on any meds? The oxygen works for a lot of us to abort an actual headache, but are you on a preventative? Are you episodic or chronic? Langa
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When you saw only one set of footprints, it was then that I carried you.
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nani
CH.com Alumnus New Board Hall of Famer
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Re: new to this site- best thing out for inf
« Reply #2 on: Feb 8th, 2005, 8:59am » |
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Welcome and sorry you have to be here. This is the best place for info. It wasn't until I'd looked around here and learned so much that I was able to take the upper hand in my treatment. PF wishes, nani
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Kris_in_SJ
New Board Hall of Famer
There's no place like home.
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Re: new to this site- best thing out for inf
« Reply #3 on: Feb 8th, 2005, 8:28pm » |
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Hi - Check your email. Kris
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