Hi everyone , A fellow sufferer of PMR (who has been on steroids for 3 years and still on 10mgs due to ongoing symptoms ) recently heard that people with auto immune disease on steroids may not be suitable to have the vaccine.
I will explore this myself but wondered if any of you had further information.
Also can someone answer at what point ,if ever , are you classified as immunocompromised if you have been on long term steroids
No-one knows the answer to that yet - not even the developers. It will require clinical trials in such patients to see what happens. In theory it is no different from having the flu vaccine - and we all have that if we are sensible. So at present that will be speculation.
NONE of the vaccines are what is called "live" so the risk for the immunocompromised there doesn't apply. The question might be whether you will develop a good immune response having been vaccinated. Or whether the stimulation of the immune respose might be excessive in some autoimmune disorders.
Thankyou for your response, it is going to be interesting investigating this !Of course I have an annual flu vaccine which i have been fine with and i am desperate
not sure what happened then but my post was interrupted. I was going to say I am desperate to return to seeing my family and want to have a vaccine but want to make a relatively informed decision.Currently feeling positive as diagnosed in June and down to 11mgs (taken any time between 2am and 4am )using a slow wean .
Have walked every day but have help in the garden and rest most afternoons.
Pain still there a bit ,but under control and not planning to wean any more just at the moment. There is no rush with this illness or any race or goal to win.
As an ex ITU nurse I know only too well how important it is to have vaccinations and will be doing my own research into the pros and cons. Will look out for any info on this helpful site.
I haven't seen my lot since before Covid - and not sure I want to see the nurse anyway - she works on Covid ICU now! The other is an ACP and briefly was working on a unit with ?Covid patients but was shielded first time round and when her new letter arrived asked to carry on working - until occy health said sorry, but we must send you home as you have the highest level of vulnerable! Have to admit I'm not sorry ...
But there would be all the quarantine stuff too - they live in the UK, I'm in Italy!
Your comment... "Or whether the stimulation of the immune respose might be excessive in some autoimmune disorders"... is the main concern I have regarding having the vaccine.
My reaction to this years flu vaccine fuels that concern. First two days after the vaccine I felt pretty rough but thought that was a good thing as meant my immune system was doing its job and (hopefully), producing antibodies.
Three of four days later I had an acute ME/CFS relapse that lasted around ten days before settling down. But by the end of that period a PMR flare decided to rear its head and aside from the accompanying overwhelming fatigue the bi-lateral hip and thigh pain was severe enough at times to reduce me to whimpering.
Finallly, decided to increase pred by 5mg for ten days to try to bring everything under control. Day ten - better than I was but not better.
I would say my immune system reaction to the flu vaccine was excessive but whether clinical trials would be able to identyfy those autoimmune illnesses that may react in that way will remain to be seen.
Although it's been a pretty unpleasant seven weeks my view is the flu would have been worse!
hi Pipalina, so sorry to hear of your suffering following the flu vaccine . I had my vaccine in November with no side effects apart from prolonged pain in the muscle at the site of injection. Individual responses are so variable.You are right to say Flu could have been worse and of course there is the slim possibility it had nothing to do with the vaccine . I hope you are recovering from your flare and that you have managed to reduce your pred back.
These are challenging times made all the more difficult by underlying health problems and we must continue to support each other and keep informed as possible by sharing information
I had the flu jab this year, as I always do, and no reaction to it!
Yes - I think it is likely to remain a great unknown because I suspect it is a very idiosyncratic response with no way of predicting who will and who won't react. I had real flu once - and I have no desire to ever have it again! My husband missed his flu jab a few years ago and ended up with flu, in bed for 3 weeks and developing pneumonia and fluid on the lung which took 6 months to resolve completely. I had absolutely no adverse effects this year - not even a sore arm. No idea which vaccine we get here in northern Italy - GP didn't know there were various versions!!!
They all seem pretty ill informed on this. I'm still waiting for my latex free vaccination - it's been a month now since I passed on the info you gave me about the Sequirus vaccine and I have phoned weekly only to get the response that they are investigating it. In the meantime I got a call from someone else in the practice asking why I hadn't had my flu jab which I patiently explained and was told that they hadn't read the notes on my file. Yesterday I got the standard NHS letter reminding me about the jab so called surgery again got a promise that they will give me a ring back - guess what? I'll try again in a few days but I'm close to giving up.
Left hands, right hands - looks like no hands!
I've now sent them an e-mail - wait to see what that brings.
Hi Pipalina, I had my Flu vaccine on 13 October and 3 hours later my PMR symptoms also returned from my left hip down my thigh, arms, shoulders and neck. It was the pain from this radiating into my head that was unbearable.
Checking online I read an article that said this would be a temporary flare so put up with it for 3 weeks as I was had reduced my prednisolone dose to 8.5mg for the first time in nearly 3 years and was reluctant to increase the dose.
I couldn't bear it any longer so increased my dose up to 13mg. Continued with this dose for 2 weeks but was still in pain so increased to 15mg 8 days ago. This has made it so much more bearable and I am coping much better at the moment, hoping it will improve further.
Having got down to 8.5mg and now back up to 15mg I feel I am almost back to square one with this reaction from the flu vaccine.
Who knows if it will happen again with the Covid vaccine, my GP said he doesn't know.
Hello Norski1 - I'm very sorry to hear about your reaction to the flu vaccine. especially as you had managed to taper down to 8,5mg.
I too had just managed to taper down to 8.5mg when I had the flu jab and also had to increase to 13.5mg in an attempt to bring the flare-up under control.
I hope being at 15mg for a few weeks will keep your symptoms at bay, if not, maybe you need some imput from your GP or rheumatogist.
Very best wishes to you - Kathy