Wow. What a roller coaster ride this week. I had gone amost two weeks without a major incapacitating migraine and thought (silly me) that there was some light at the end of my tunnel. Thinking that the preventatives were finally working and that the daily little spits and sputters of pain on the left side were all that would be coming my way. I was looking forward to more days of being pain-free versus pain-full.
Wednesday dawned like a regular day -- Little twinges on the left side and some throbbing at the base of my head. By mid-morning the electrical jolts on the left were coming more strongly and frequently, and my throat was starting to get tight. By late afternoon, I was rocking and rolling with a full-on headache. My brain/mouth connection couldn't find the words and I had a rasping voice when they did manage to come out. Headed home from work and took a Maxalt. Nothing. The pressure built, so for the first time, I took a 2nd Maxalt. Again, nothing. All I could do was rock in my chair and cry -- it hurt so bad. I just wanted to be unconscious. I kept telling myself that if this keeps up, I'll ask my husband to take me to the ER... but of course I kept moving the time. Just give it another hour, it will break. I know it will break, maybe just another hour.
Sleep didn't come and the pain lasted all night. By morning, I was still in tears and called my doc. I'd never had a migraine go this long or hurt this bad before. Into his office first thing, and a shot of demerol --the headache finally broke just before noon. Good heavens.
Today, the usual residual pain/melon-head is still hanging in there, but at least I am functioning again. Don't know if there are any answers here, but I needed to vent some of how this episode scared me. I hate the idea that the usual meds no longer work to knock down the headaches. Having to get an injection seems so extreme. I feel like such a whiner -- was the pain really that bad or am I just getting timid and weak? I don't know. I just don't know.
Thanks for giving me a place to vent.


Hey friend, sorry to hear about the setback when things were going so well. Hope the recovery wasn't too bad.
Had the same thing 3 years ago w/Imitrex. Ended up in the ER at 2 in the morning. Changed to Relpax. Now also on Topamax. I am sure I will change again within a year or two. Nothing lasts and our stupid heads keep changing on us. Keep your chin up and don't let the monster win!
Thanks for the kind thoughts. I really appreciate this forum and the folks who participate.