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Daily Chat >> General Posts >> I have hope, I think. http://www.clusterheadaches.com/cgi-bin/yabb2/YaBB.pl?num=1257867438 Message started by BigMatt on Nov 10th, 2009 at 10:37am |
Title: Re: I have hope, I think. Post by lorac on Nov 10th, 2009 at 11:51am
Good luck big matt.....keep us posted ok.
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Title: Re: I have hope, I think. Post by BigMatt on Nov 13th, 2009 at 12:51pm
I went to see my doctor yesterday and he decided it was worth a try to go on the new medication. It is a bit of a ramp up one pill to start and increase by one every three days until I am at three twice a day so it will be a few weeks before I am at full strength. I forget the name of the med and the bottle is at home and at this point they all sound the same. Lol I am hopeful that I will be able to get to full strength without any nasty side effects I hope, I have had a hard time with most medications tried on me most make it to hard to take them, this one could cause a nasty rash and if it does I will have to stop taking it so I hope I don’t get the rash.
PF wishes to everyone for the weekend. :) |
Title: Re: I have hope, I think. Post by Linda_Howell on Nov 13th, 2009 at 1:03pm Quote:
Matt, as soon as you can, please let us know the name of this med. Every once and awhile I have people who contact me re: SUNCT, and if this works works for you, it might also help others. Keep us updated on your progress, O.K.? |
Title: Re: I have hope, I think. Post by BigMatt on Nov 13th, 2009 at 6:33pm
I will update this weekend and put what the med is, if you do meet someone with SUNCT, please give them my email and ask them to contact me. I really would like to talk to someone that has SUNCT as I do, it would make me feel less alone with this I think and who knows maybe I could help them or they could help me, as we all know knowledge is power. :)
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