Hi everyone, I was wondering if anyone ever feels like they have the flu but really don’t? In the past I’ve realized that I start to have flu like symptoms prior & during a relapse which is not fun at all. The last several days my head feel heavy, I have a constant headache or dull pain behind my eyes, extreme fatigue & weakness in limbs. I’m currently not taking any meds as I had a really bad reaction to Copaxone 2 months ago. I’m scheduled to see my neurologist on Thursday. I just hope I start to feel better soon, I really don’t like the solumedrol (steroid) treatment. 😔
MS giving flu like symptoms : Hi everyone... - My MSAA Community
MS giving flu like symptoms
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![Eveliz profile image](https://images.hu-production.be/avatars/9cabbb2fc1eb9afc4e4215344c9d1e3e_small@2x_100x100.jpg)
The last two attacks I got extremely achy all over, at least I thought they were attacks. I felt like I had the flu so I went to my Primary Doctor and he put me on steroids. I had no other symptoms.
Hi Eveliz! Ive often wondered that same question..same symptoms.I wonder virus on top of it all, did i eat something, is it the flu etc...If i go with the flow i usually get thru it but wish id gone to the doc.You are in good hands.Pls let us know how you are doing.best wishes!
I’m surprised your doc has allowed you to go 2 months with no meds. That’s a recipe for a relapse. I too had a horrible reaction to copaxone. It took a few weeks because of insurance to get me switch to tecfideria. That unfortunately didn’t work and I had to be switched again which took a few more weeks because of insurance. I have the worst relapse that l ever had at that time. I hope your doc sees you soon and a new med is started! Good luck!
Ive been struggling with flu symptoms off and on for the last year or so. I started Mayzent in September 2020 and still happens off and on. Where are you at with this or what have you learned? thanks