Experiences with

Coronavirus infection

Also there’s this; https://ms-uk.org/news/could-coronavirus-cause-ms/ All my issues started less than 4 weeks after Covid infection…… could I have actually got ms activated from having Covid? Should I ask my gp when I see them to get me scanned in mri machine?

experienced more frequently grade ≥3 adverse events, such as neutropenia and thrombocytopenia.¹⁸ Another important issue concerning the addition of Obinutuzumab to Acalabrutinib concerns the increased vulnerability of patients with CLL receiving anti-CD20 antibodies to severe coronavirus

https://www.nytimes.com/2024/08/12/well/coronavirus-vaccine-booster.html?smid=nytcore-ios-share&referringSource=articleShare&sgrp=c-cb

“When the COVID-19 pandemic began, we set a new goal: training our cancer platform to identify and target the coronavirus. Unlike Moderna and Pfizer, we did not rely on full protein expression via mRNA.

That’s why it’s imperative to advance a pan-coronavirus vaccine forward, for which we have recently seen an encouraging report from Walter Reed Army for induction of broad antibody and cellular immunity, and, of course, nasal vaccines, two of which are still incubating in clinical trials supported by

I have booked for a booster Covid jab on the basis that as Preds increases vulnerability it is a sensible thing to do. And then I thought, er…but is it? Mrs GnT has decided to participate partly based on her unpleasant experience with statins Although this must have been discussed before I just wondered

please has anyone any useful tips as have just been diagnosed with long covid. All the PA symptoms plus utter exhaustion I have increased my IM injections but doesn’t help very much.In my late 80s which doesn’t help either.Thank you for reading.

Hello everyone! I've been getting increasingly worried about brain fog. I am constantly forgetting words and I don't seem to be able to remember multiple things at the same time (like long lists of things to do, either at home or work). I can think to myself "I need to go to town to get x item" and

Has anyone experienced a positive covid test lasting 5 weeks so far with absolutely no symptoms while on long term steroids ? Im fed up wearing a mask ....again but the wee red line is nof going away . Thanks

Emerging from the Darkness: My Encephalitis Story By Eldon Lake A Sudden Collapse In April 2023, life as I knew it changed in an instant. It began with an ache in my lower back—something I brushed off as a minor strain. I even visited an osteopath, convinced I had just overdone it somehow. But the

Hi all, So basically three years ago I had Covid, and started to get palpitations and chest pain. Luckily, I work with a cardiology consultant who sent me for an MRI and the findings were mildly reduced EF at 54% with hypokinesia in inferior wall and septum and mildly dilated left ventricle and mass

I’m new here and write because I feel no one really understands the grief I feel. My partner and I got married in our early 30’s and a few years later we got pregnant quickly after trying. I recall we made videos in the waiting room before the first scan having no idea our dreams were about to crumble

Im so sorry for the length of this post but I don’t know what to do so feel somewhat helpless so felt I needed to explain. . It’s taken me around 5 years to pluck up the courage to reach out with regard to this, but I feel like I’ve now reached rock bottom & am hoping someone may be able to help.

There are many people in our community who are still struggling with a range of symptoms including breathlessness, since having Covid. On 12th March at 6.30pm, we will be hosting a free online webinar- Latest research into Post Covid Syndrome and treatment We will be joined by Professor Rachael

There are many people in our community who are still struggling with a range of symptoms including breathlessness, since having Covid. On 12th March at 6.30pm, we will be hosting a free online webinar- Latest research into Post Covid Syndrome and treatment We will be joined by Professor Rachael Evans

Please note this covers NHS England - and is information only at this time - https://www.gov.uk/government/publications/departmental-minute-on-the-covid-19-spring-2025-vaccination-programme/departmental-minute-from-the-department-of-health-and-social-care-notification-of-contingent-liability-covid-

Hi. I have a long-awaited consultant appointment next Friday to discuss my next rituximab infusion. The first 2 were done in June and July last year and since this January I have had an increase in pain and stiffness. I have given my consultant the heads up that this is the case. My question is about

I’ve just been diagnosed with sensory neuropathy and had bloods taken to be sure nothing is causing it, I am not diabetic. I thought it was due to my Covid infection as pins n needles in my feet were one of my early symptoms that have got worse over the last 4 years but the neurologist said no, it’s

I was recently at a new transplant center to inquire about possibly listing there in addition to my current center. While meeting with the transplant team, I also met with the transplant surgeon. He mentioned that in preparation for the surgery I should get the vaccines for Shingles, RSV and any new

Hello - has anyone being diagnosed as having grandular annulare? It started after getting Covid - a few spots at first. Now 3 Covid illnesses later and I have over two hundred spots. I have tried 4 medications thus far and none have worked. Apparently its a condition that fewer than1% get so not a lot