Thank you very much Nancy for your response. I have tried most everything (I refuse to say everything because I keep hope) my Medical team and I have exhausted most options, even going international for ideas...a few weeks ago though we thought maybe a new set of eyes would be good. That was the worst appointment I think I had ever had, because that was the first and only time I’ve been told “you’ve tried everything I can think of, I have no treatment plan.” To me that was the worst thing that could’ve been said to me. Anyway I reached out the ketamine infusion center and had a wonderful discussion with them, very professional and I felt like they had my best interest at heart, the main part is they want and are willing to work with my medical team. So I don’t know what my medical teams response is to this yet as I just had sent them the request. I’ve tried the spray in the past and had good response (it was just hard medication to keep because it has a short shelf life). I’ve had my migraines since the age of 2 my parents say that I would grab my head and cry head hurt, so this has been a 28 year thing for me. Sadly I’m sure many of other migraine sufferers agree that once a medication that works it seems to be discontinued...I’ve read many posts on here and can relate to most of them, I didn’t realize that there were so many others that go through this too. Mine get me for multiple days and I’m averaging 3 days a week. I will definitely keep my experience going forward so that others can maybe find some relief through my process.
I read a thread about imitrex and fierocet I was going to say something on that really quick. Imitrex used to be a ok medication for me until it caused a seizure, and fierocet really upsets my stomach. What I currently do is use a benzo (for the nerve property), a muscle relaxer, and a blood pressure medication, also testosterone. For my break through I use fierocet still or if I’m considering the hospital I’ve got keterolac, DHE, or last resort a pain medication.