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Cluster Headache Help and Support >> Medications, Treatments, Therapies >> just have to say http://www.clusterheadaches.com/cgi-bin/yabb2/YaBB.pl?num=1238634550 Message started by Lissa on Apr 1st, 2009 at 9:09pm |
Title: just have to say Post by Lissa on Apr 1st, 2009 at 9:09pm
It's just incredible how much had been done in just a decade as to the treatment of CH. When I first came to this board, all there was was Imitrex tablets, Verapamil and a few other meds. There was hardly anything available to us, medication wise AND information wise. I never even heard of a hypothagamus 10 years ago! I remember when Imitrex injections just came out and everybody was like HELL YEAH. lol I'm so glad that research is actually being done on clusters because they are just awful (to say the very least). It seems like every time I come to this forum, there is a new treatment available. That's so great. :)
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Title: Re: just have to say Post by Lissa on Apr 1st, 2009 at 9:27pm
It is awesome! Things have really changed for the better!
My story? It's probably in the archives. :p I wish I could find my older posts but I can't for some reason. :-/ |
Title: Re: just have to say Post by Mrs Deej on Apr 1st, 2009 at 9:31pm Lissa wrote on Apr 1st, 2009 at 9:27pm:
Yeah, they are probably on the old message board. Good to have you back though, sorry for the circumstance!! Stick around, it's good to hear from old faces!!! :) |
Title: Re: just have to say Post by Lissa on Apr 1st, 2009 at 9:36pm Mrs Deej wrote on Apr 1st, 2009 at 9:31pm:
I haven't been hit yet, just a few shadows here and there. *crosses fingers* Thanks for the friendly welcome! |
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