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Title: For those who need help getting people to understa Post by guesst on Mar 10th, 2005, 9:59am nd http://www.clusterheadaches.org.uk/home/index.cfm?address=../clusters/note_colleagues.cfm&added=04/01/04&code=CB |
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Title: Re: For those who need help getting people to unde Post by Frank_W on Mar 10th, 2005, 10:28am This is pretty good, Thomas. I printed this out, last cycle and have given copies to a few friends. |
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Title: Re: For those who need help getting people to unde Post by guesst on Mar 10th, 2005, 10:32am Just wanted to make sure the new peeps got a look at it. ;;D |
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Title: Re: For those who need help getting people to unde Post by Yikes on Mar 10th, 2005, 12:07pm Excellent! No one really believes me when I try to talk about it, I think. Maybe this will help. |
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Title: Re: For those who need help getting people to unde Post by Chasityb on Mar 10th, 2005, 3:38pm I printed out info from this and gave to my co-workers. After that I had no problems. |
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Title: Re: For those who need help getting people to unde Post by TonyG1 on Mar 15th, 2005, 7:59pm on 03/10/05 at 12:07:15, Yikes wrote:
I've never had issue with my co-workers, usually the only thing CH does is make me run a little late until I can get my proverbial "stuff" together -- When I do talk about it, I get the same feeling -- they don't really believe it, etc. Today one of them was suprised when I told her I was having brain scans this Thursday. Kind of an interesting response .... like Oh, there is something going on there... It is much worse to have your GP refer to CH as migranes.... mine did and I promptly asked for a referral to a Neurologist... |
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