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  1. M

    Covid 19 Vaccination with FM/CFS

    Hi, I started this post and thnaks to all for your input. I feel it worth mentioning that I did have Covid in March 2020 (no symptons other than felt extra crap for 10 days or thereabouts and slightly out of breath when talking for a while). My first Pfizer jab left me feeling rough for a day...
  2. M

    Has anyone had a Myocardial Perfusion Scan?

    Hi all from the UK, Not firectly FM related but you no how it is, when we get referred for various other health issues they (doctros, admin, nurses) haven't got a clue of what or how anything can affect us. I'm being booked in for a 'Myocardial Perfusion Scan'. This is to deterine how much...
  3. M

    Covid 19 Vaccination with FM/CFS

    I'm only a boy at 65 although did have covid in March 2019. I didn't know I had it although felt extra rough for some 10 days and then breathless for 2/3 weeks whilst talking. When I had a CT angiogram in December, they told me my lungs were in advanced post-covid recovery. So body dealt with it...
  4. M

    Covid 19 Vaccination with FM/CFS

    Back on topic, an update having just had my 2nd Pfizer jab. had the vaccine at 14:00 was ok until around 21:00 when started to feel flaky. Went to bed and woke up during the night hot and soaked in sweat. I was very ill (temp of 38.8c with the shivers) and whole body pain until Sunday mid...
  5. M

    Covid 19 Vaccination with FM/CFS

    Well I had Covid last March although didn't find out until December from the CT Angiogram. I just felt very rough for a week and didn't die. Luck of the genes I guess but who knows what a different strain may or may not do?
  6. M

    MCS (Multiple Chemical Sensitivity) and/or fragrance intolerance

    This is something that rears it's head once in a while. For some reason, I've never considered a link with the fact that in recent years, perfumes make me reel, eyes itch like mad, rhinitis, skin heats up, nasty head/eye ache etc. Have found much info online but this is an easy read. Would be...
  7. M

    Covid 19 Vaccination with FM/CFS

    Thanks to everyone for sharing your experiences. I had my first (and only so far) Pfizer jab on 21st Feb. I've gone downhill ever since. FYI, I'm 65, was diagnosed with ME/CFS in 1994 and would say for the past 23/24 yrs had made a 98% recovery. Within the last few weeks, I'm getting weaker and...
  8. M

    Covid 19 Vaccination with FM/CFS

    I just thought it would be an interesting study amongst us. I had mine since I started this thread, had the Pfizer, sore arm during the night (couldn't raise it but wasn't about that), felt fluey and spent 24+ hrs in bed. Then all ok the next day. Now suffering with the worst case of fatigue and...
  9. M

    Covid 19 Vaccination with FM/CFS

    SUnkacola, I live in North Oxfordshire, UK
  10. M

    Cholesterol medicine

    I did post maybe 2 months ago? I was diagnosed with a blocked artery and was prescribed Rosuvastatin 40mg. My whole body was in spasm for some 5 days and I stopped taking at 12 days. I was the illest I have ever been in my life so had to stop them. Unfortunately, my consultant said alternatives...
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