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New Message Board Archives >> 2004 Cluster Headache Specific Posts >> Where is the letter to the employers?
(Message started by: nancyc on Sep 1st, 2004, 1:46pm)

Title: Where is the letter to the employers?
Post by nancyc on Sep 1st, 2004, 1:46pm
The one that Simon wrote? I cant find it and need it desperately to give to one pain in the butt nurse that i work for....Time to educate her on chs....smiles,nancyc

Title: Re: Where is the letter to the employers?
Post by Lizzie2 on Sep 1st, 2004, 1:56pm
http://www.clusterheadaches.org/Cluster%20Headache%20Syndrome.doc


Title: Re: Where is the letter to the employers?
Post by ExplodingEyeBall on Sep 1st, 2004, 3:24pm
I just saved a copy of this letter myself.

It explains it well. It will be a lot easier to just hand someone a print out then try to explain it and then try to control myself when they give me the 'I get migraines too' line.

A girl I work with has a daughter who gets HAs and from her explanation, I've tried to get her to visit this web site because it sounds like CH to me.

She won't tell her and just says that it's migraines. Funny that the doc gives her imitrex for it.

Oh well... I know I'm not the one who asked for the letter but thanks for posting it. It will come in handy.

Pat

Title: Re: Where is the letter to the employers?
Post by nancyc on Sep 2nd, 2004, 12:29am
Thanks, darling...smiles,nancyc



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