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Hi everyone! Hope you're all doing OK. So, for a second Christmas in a row, I have coronavirus. I feel absolutely dreadful, worse than when I had it last year. I've had 5 covid vaccinations in total. I sent my lateral flow test result to the NHS and have been told they are only offering treatment t...

Covid is terrible I am still dealing with the after effects from when I almost died from the Delta Variant. I had the vaccine but my MS only let it be half as effective. So when I finally went to the hospital my O2 level was at 40% I was out in a medically induced coma for 13 days they gave me some ...

Had a exacerbation of symptoms mainly do to "Covid" with Multiple Sclerosis. 10/15/2022. Saline I.V. helped, and Paxlovid. Muscle spasms and ankle curls on my right side of body.

Hey Everyone, I tested positive for Covid 4days ago and I have been having symptoms for 8 days. I feel horrible still. Apparently there was a pill I could have taken before day 5 of symptoms however, I found out about the pill and called my doctor on day 6. So they can’t prescribe it. I feel like ...

Hi this is my first post. I had covid a week ago and I still feel dizzy, I feel like my breathing is a little different and my eye site it’s more blurred. Has anyone eles had this?

All that shielding, all that worry, all that stress and I have a cold! And they told me that the vaccines didn't work on me.

In July 2021 I had my first jab, then got Covid the week after. Second jab in september. Then had my third jab in November so there would be enough time before my Ocrevus, which was beginning of January. All jabs were Pfizer. I am way more sick this time than last, I thought Omikron was supposed to ...

I’m still feeling the affects of the Covid I’m having numbness tingling but now it’s moved to my good side now . I’m not having any injections at the moment I have to leave it for two weeks before I start REBIF . Hope everyone has a wonderful Sunday

My youngest son had Covid two weeks ago now my husband has it he’s had both jabs and now he’s got it .I’m so worried that I’m going to get it I’ve had both jabs but it doesn’t look like that makes any difference. I’m having numbness in my face at the moment I’m hoping I don’t get it and relapse. I h...

Hi all I'm in South Africa and we are slowly being allowed to take the vaccine I am currently on gilenya I just want to know about people's experiences with the Johnson and Johnson vaccine

so has anyone taken the covid shot? Do tell.

Has anyone else had the coronavirus? I cant taste anything and I am freaking out slightly!! I had a spoon of chilli powder and NOTHING

Hi there! I'd like to ask those MSers, diagnosed before Covid, how did you manage fears of viral infections? My partner is even more worried than I am about going to places without a mask. How did you cope before when you had sneezing people around you? What about, post-covid? How are you handling i...

**Thanks for the replies. Looks like everyone does what they are comfortable with. I am not ready to "go back to normal", so I will continue doing what I have been. Take care, all! :) How are you all handling covid-19? Especially those on B cell depleting treatments. I've been shielding at home (...

I currently have Covid FOR THE THIRD TIME in a year! My first time having Covid is what lead to my MS diagnosis due to bizarre symptoms that came with it (my entire right side of my tongue, cheek, throat, and face went numb). I live in BC, Can, and was lucky to get onto Paxlovid by day 2 of my sympt...

I have had covid for 2 weeks now and seems there is no end to it, my symptoms are through the roof. Anxiety is oh my god I cant even discribe and my brain fog is uncontrolable. any advice on this will be great help.

After I was diagnosed with MS in october last year, I asked for a second medical opinion. The second neurologist told me that in her opinion the COVID infection I had last year in january would have triggered the MS, knowing that in 2012 I had Lyme disease, when I went blind and was initially though...

Hi everyone 😊 I was wondering if anyone had some experience with Covid treatment. I was just tested positive yesterday. (It's my second time, the first time I had in June last year. I had Paxlovid tablets, which I was not feeling great on it and it was swapped to Sotrovimab infusion - I was happy w...

I have RRMS and recently had Covid. Is there anyone out there (who may deal with MS brain fog as a regular occurrence) suffering the additional brain fog following Covid? I’m finding it very difficult to navigate and have been feeling terribly frustrated. Thanks in advance. Wishing you all well!

Hello everybody! Today I woke up with extreme difficulty in breathing and very persistent cough. I had just gotten a negative Covid result 3 days back and was relieved that this time I wasn't ill for that many days, like the first time I got Covid, cause it was forbidding me from going back on track...