Just wondering if anyone who is NOT on a disease modifying therapeutic has gotten a COVID booster? If so, did you have any increase in ms symptoms from the booster? Thanks!
MS and COVID Booster: Just wondering if... - My MSAA Community
MS and COVID Booster
Hi Donna, I am not on a DMT, and I am having my booster on Saturday. I will let you know how I am if it’s not too late for you. I am having Pfizer. 😊
Thanks jimeka! I have an appointment for December 7th, so that would be really helpful. It is for Pfizer also. Did you have any ms type reactions to the first two?
Hi Jimeka. Just wondering how your booster went? I had mine (Pfizer) on Tuesday and have had about 48 hours of feeling crummy. I think things are beginning to improve as I am getting some energy back.
Glad it’s over until the next one. Like you I felt off it for about a week. The worst with me was the pain in the hips and thighs, apparently a very common symptom with Pfizer. At least you should be up and running for Christmas 🎄
I have been off DMTs for five years and didn’t have any reaction with the Pfizer 3 shots. I had a sore arm with the first shot.
Thank you. That is great to hear. Glad you did so well with them. Right after my first and second shots I had some increase in neuropathy, some eye issues (light sensitivity) and extra systolic heart beats that went on for a couple of days. Most symptoms have resolved, but some linger. This makes me a bit cautious about the booster, but I’m sure COVID would be worse.
I had about the same effects from all three shots. Fatigue, dizziness, aches, sore arm, flu like symptoms. Lasted 3-4 days, kind of a pain but lot better than Covid 👍🏼. Good Luck 🙏👍🏼😉
Thanks Kenu! Sounds like you had the usual and expected side effects, which are a pain but which get over with. You must be really relieved to have the booster behind you!
Hello, I ended up with Optic Neuritis after my second shot. It was my introduction to all of this. Still waiting on a diagnosis. Still plan to get booster because COVID would be worse.
Thanks Jtara. So sorry to hear about your optic neuritis. Did you lose vision? When you say that it was your introduction to all this, do you mean to ms? Hope you get some resolution of your neuritis soon.
I had a cloud over my vision in the left eye. Was admitted for testing and IV steroids. Didn’t know there were any other options. I was just scared. My vision has returned for the most part but yes, it brought on all of the testing and follow-up for MS. So glad to have this community here💜
Thanks for clarifying. I had optic neuritis with my very first exacerbation of ms. I lost vision in my left eye, but after several months of fluctuating bluriness, my vision pretty much returned to normal. That was 40 years ago and my vision has been fine ever since.(Except now I have cataracts At the time of the exacerbation I also felt extreme heat and numbness down my whole left side. I assumed I was having a stroke even though I was only 32 years old. This was followed by four months of utter exhaustion. My ms has never been as bad as it was during that initial attack. I hope you will have a mild course and that your vision stays normal.
I read an article about treating optic neuritis with a sodium channel blocker. I bet kdali knows more about it. I would ask about treatment to limit lasting vision problems.
I have had a booster, and am not on dmt’s. The booster was the easiest shot for me. No increase in ms symptoms with any of them. Good luck!
To reassure you: 81 years old, never on a DMT, RRMS since 2010, mild reaction to 2 doses and 1 booster of Moderna.
BTW, booster is a smaller dose than the 1st two...and if you get a mild reaction that probably means your immune system recognizes the spike protein in the vaccine and is going to work. Unpleasant, but probably, all in all, a good thing.
Hi Donna
Not on a DMT and had booster. Had no noticeable change.
Good Luck