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Hemiplegic migraine
I was diagnosed with hemiplegic migraines and these present as a stroke (all the symptoms) but are not a stroke they are a migraine. They are caused by stress on the body physical, emotional, etc. I was posting to raise awareness and to see if possibly anyone else shares this diagnosis. It is rare disease and can be terrifying to not have information on a person to person level. I have read all the information the Internet had to offer 😂
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I had been diagnosed with Hemiplegic migraines years ago when I had stroke-like symptoms that landed me in the ER several times. They didn’t last long and I rarely got a headache. Until about 2 weeks after I took the COVID vaccine. I noticed the symptoms of light-headedness, forgetfulness, episodes where I couldn’t speak or compile sentences and others returned. As I was waiting for testing with my neurologist, a full blown attack happened and I was put into the hospital overnight for testing. That’s when I was actually diagnosed with hemolytic migraines. I was told I could not drive or work because the attacks made one side of my body go numb, or I’d go blind in one eye or I would be unable to focus or speak correctly in a conversation. They tried different migraine meds and I went back to work 3 months later. I got better and got off the meds. But now I’m getting some of the symptoms again. I wake up tired with a swoosh feeling in my head, mild ringing in my ears, brain fog and my friends and coworkers noticed I say some off the wall things during the day. I’m trying to control the symptoms so I don’t get a full blown attack like I had years ago. I read Magnesium and Vitamin B2 are good supplements to try. Also stay away from ingesting the “5 C’s”. Anybody with a similar problem out there? What have you tried?
Welcome to Mayo Clinic Connect, @loupy. I wanted to let you know I moved your post here to an existing discussion on hemiplegic migraine so you could talk with others such as @guderianj @azza1 @vahank @danralph and others.
Hi Loupy. My, still difficult to think,… I got Covid 1st then all the things you describe happened to me. Drag my foot. Can’t think, talk. Shake. Nothing mild about it tho. I’m glad you had a break and sorry they’re coming back. The terror in the beginning when I had no idea what was going on. 3 times 1 day I figured I was dying. The 1st 2 I figured what’s the point? I’d rather go here than at the hospital. The 3rd I went to ER. Guy just said not even looking up, you’re not having a sroke. That’s it. Ok, well, that’s good. Gave me a gabapentin. I can’t imagine what it was like to continue work. I was going thru this everyday multiple times. I couldn’t leave my room. Just thinking of that is terrifying. I had no idea what was happening. It’s worse now but at least I know and I learned, for the most part, not to panic.
Good luck. Haven’t been here long and it’s still uncomfortable sharing but not as rough as keeping everything inside.
Hey eastbaydave!
Wow it sounds like you’ve been going through it! I had a few bad headaches with my situation but mostly the neurological symptoms. If you haven’t yet, you might want to find a good neurologist and I recommend getting started soon on a preventative medication. Of course they may have to control your pain with other meds. But a good doctor will start you on something to prevent the attacks. When we were trying to see what would stop them, they put me on several different ones. I don’t remember what the side effects were that made me switch so often, but finally the Aimovig worked for me and the symptoms stopped. That was 4 years ago and here we are. I’m actually feeling much better than last week. I’ve been trying to stay away from triggers (look up the 5 “C’s”) and I think that has helped a lot. Other meds that I was on were Quilpta, Ajovy (injectable) and PO Nurtec, which did not work for me.
I really hope you start getting relief and can go back to work soon! I was out of work for three months until the meds started working well.
Gods bless!!