Medicine that I haven't heard anyone here talk about


[ Follow Ups ] [ Post Followup ] [ Cluster Headaches Messages ]
Help us fight Cluster Headaches! Visit the O.U.C.H. Website!

Posted by Allie (207.3.4.228) on March 06, 2001 at 19:17:53:

A special hello to Matt and Tom. Thanks for the vote of confidence. You wanted to know about my meds. I've tried just about everything. The only thing that even touches my pain is Stadol NS. It is a nasal mist and was moved up as a controled substance not too long ago. I have been taking it for about a 1 1/2 years now. I take it at the onset of a ch. It goes straight through the brain and is very effective at numbing your face and head. It has worked great up until now. Now my body is getting immune to it working. That is why my doc and I are trying to find something else to work. So far no luck. But we aren't giving up. There is way to much pain to give up taking new med. If you have any suggestions please let me know. Keep in touch!!! Oh, by the way I only check the message board once a day and that's around 7 or so at night.




Follow Ups:



Post a Followup

Name:
E-Mail:

Subject:

Comments:

Optional Link URL:
Link Title:
Optional Image URL:


[ Follow Ups ] [ Post Followup ] [ Cluster Headaches Messages ]

 

 

Click Here!