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Spring COVID vaccination
Hi all, I was told when I was diagnosed with PMR last year that the condition would mean I was immuno-suppressed. Consequently I thought I would be entitled to a free spring COVID jab which is being widely advertised now for over-75s (not me yet) and people with weakened immune systems (like me, I
Hi all, I was told when I was diagnosed with PMR last year that the condition would mean I was immuno-suppressed. Consequently I thought I would be entitled to a free spring COVID jab which is being widely advertised now for over-75s (not me yet) and people with weakened immune systems (like me, I
Hedgehogfriend
in
PMRGCAuk
2 months ago
COVID jab
Is anyone wary of having another COVID jab this spring after having A F after the jab.
Is anyone wary of having another COVID jab this spring after having A F after the jab.
Myflowers2
in
Atrial Fibrillation Support
2 months ago
Latest COVID jab.
Am in the early days of PMR and have just been notified I can get a free COVID.jab. I am a bit worried as the only other person I know who has PMR got it the day after a her jab along with diabetes. There is no rush but I wonder if you have any advice as it is a while until I see a doctor.
Am in the early days of PMR and have just been notified I can get a free COVID.jab. I am a bit worried as the only other person I know who has PMR got it the day after a her jab along with diabetes. There is no rush but I wonder if you have any advice as it is a while until I see a doctor.
tinlid
in
PMRGCAuk
2 months ago
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Covid jab
I have been invited for a booster Covid jab. However I have seen that there is a connection between afib symptoms commencing after having a jab on a ,gov website. Has any one any experience of this?
I have been invited for a booster Covid jab. However I have seen that there is a connection between afib symptoms commencing after having a jab on a ,gov website. Has any one any experience of this?
Prawnsalad
in
Atrial Fibrillation Support
2 months ago
B-12 Def in Mexico (no health insurance)
Here is my (ongoing) thread to detail my B12 journey. Here goes! 2-3 years before diagnosis I began having the following symptoms. Numbness in toes which slowly spread to feet then ankles, then calves. A slow deterioration of muscle tone all over. Periods of intermittent dizziness/vertigo and fatigue
Here is my (ongoing) thread to detail my B12 journey. Here goes! 2-3 years before diagnosis I began having the following symptoms. Numbness in toes which slowly spread to feet then ankles, then calves. A slow deterioration of muscle tone all over. Periods of intermittent dizziness/vertigo and fatigue
GracePV
in
Pernicious Anaemia Society
2 months ago
People with hypothyroidism and ME
Those who suffer with both hypothyroidism and ME, do you find that your exhaustion is somewhat abated if your vitamins and minerals are optimal? I have posted previously about a friend who has had hypothyroidism for many years. But after contracting Covid she started to feel exhausted and eventually
Those who suffer with both hypothyroidism and ME, do you find that your exhaustion is somewhat abated if your vitamins and minerals are optimal? I have posted previously about a friend who has had hypothyroidism for many years. But after contracting Covid she started to feel exhausted and eventually
AnneEvo
in
Thyroid UK
2 months ago
Spring Covid booster
Have had text from my surgery offering me a Spring Booster for Covid. Have been on 4.5mg Prednisolone for a couple of months now. Would my immune system still be classed as compromised on such a low dose?
Have had text from my surgery offering me a Spring Booster for Covid. Have been on 4.5mg Prednisolone for a couple of months now. Would my immune system still be classed as compromised on such a low dose?
jaycee444
in
PMRGCAuk
2 months ago
Cold water!
I went swimming for the first time yesterday since my diagnosis of PAF 18 months ago. I'm on holiday in France at the moment. It was an outdoor pool and it's hot here so the water felt really cold. I went in waist deep and then ducked under. I swam for a few metres then realised I was in AF. I guess
I went swimming for the first time yesterday since my diagnosis of PAF 18 months ago. I'm on holiday in France at the moment. It was an outdoor pool and it's hot here so the water felt really cold. I went in waist deep and then ducked under. I swam for a few metres then realised I was in AF. I guess
Sandych55
in
Atrial Fibrillation Support
10 months ago
Spring COVID Vaccine 2024 booster eligibility
Spring COVID Vaccine 2024 booster eligibility The government has announced a Spring 2024 dose of COVID-19 vaccine for: people aged 75 years and over those in care homes those with a weakened immune system (aged 6 months and over) https://www.vasculitis.org.uk/news/covid-boosters
Spring COVID Vaccine 2024 booster eligibility The government has announced a Spring 2024 dose of COVID-19 vaccine for: people aged 75 years and over those in care homes those with a weakened immune system (aged 6 months and over) https://www.vasculitis.org.uk/news/covid-boosters
Suzi70
Administrator
in
Vasculitis UK
2 months ago
Covid booster
Hi. I am travelling abroad to Asia at the end of April and have been trying to find out if I can get my Covid booster before I go. Gp not doing them. NHS website says booking service no longer available and no Clinics open. 119 recorded message says you can’t book through that line and hangs up. Both
Hi. I am travelling abroad to Asia at the end of April and have been trying to find out if I can get my Covid booster before I go. Gp not doing them. NHS website says booking service no longer available and no Clinics open. 119 recorded message says you can’t book through that line and hangs up. Both
grumpygirl
in
NRAS
2 months ago
Breastfeeding, skin on skin and contractions (c-section)
Hey everyone, I gave birth about 10 days ago (emergency c section at 29+3 due to HELLP/Pre eclampsia/slowinf fetus heart) and I now have 2 kids in NICU. They encourage us to do skin on skin and after I started doing that, I have been having severe contractions even when I am very far from them; i am
Hey everyone, I gave birth about 10 days ago (emergency c section at 29+3 due to HELLP/Pre eclampsia/slowinf fetus heart) and I now have 2 kids in NICU. They encourage us to do skin on skin and after I started doing that, I have been having severe contractions even when I am very far from them; i am
Tryinglate
in
Pregnancy and Parenting Support
2 months ago
Treatment for fibro, MCAS, hypermobility syndrom (after catching covid) and long term covid sufferers
Good afternoon to all. I wanted to go straight to the findings I have done, diagnostic tests with top consultants in London. I was diagnosed with hypermobility syndrome and I had a horrible reaction to a covid infection last xmas which caused me long covid: fatigue, pain in bones, muscles and joints,
Good afternoon to all. I wanted to go straight to the findings I have done, diagnostic tests with top consultants in London. I was diagnosed with hypermobility syndrome and I had a horrible reaction to a covid infection last xmas which caused me long covid: fatigue, pain in bones, muscles and joints,
Divinesoul
in
Fibromyalgia Action UK
2 months ago
Covid
hi all forum people hope your all as well as you can be. I have lupus and got covid and now as result been off work since mid December now advised I have fibromyalgia and long covid and can’t walk as far even with walking aids. I only have min daily living and wondered if I should update pip but will
hi all forum people hope your all as well as you can be. I have lupus and got covid and now as result been off work since mid December now advised I have fibromyalgia and long covid and can’t walk as far even with walking aids. I only have min daily living and wondered if I should update pip but will
Geeforce99
in
LUPUS UK
2 months ago
Covid booster vaccines
hi Does anyone know if partners / carers of clinically extremely vulnerable people are eligible for the Covid boosters in April. I am under 75 years of age. I am “happy” to have it done privately at a cost of £100 approx but would need to travel some distance at the moment. Thanks for any advice
hi Does anyone know if partners / carers of clinically extremely vulnerable people are eligible for the Covid boosters in April. I am under 75 years of age. I am “happy” to have it done privately at a cost of £100 approx but would need to travel some distance at the moment. Thanks for any advice
Main1234
in
Vasculitis UK
2 months ago
Spring 2024 Covid Vaccine invitation.
Good evening everyone. I’m enquiring if anyone has been contacted with an invitation to have a Spring Covid vaccination booster and if so, how many are or have taken this up? My G.P’s Surgery messaged me recently and I have an appointment for this on 1st May. I have since heard of three people who have
Good evening everyone. I’m enquiring if anyone has been contacted with an invitation to have a Spring Covid vaccination booster and if so, how many are or have taken this up? My G.P’s Surgery messaged me recently and I have an appointment for this on 1st May. I have since heard of three people who have
azaelea
in
MPN Voice
2 months ago
Should I ask to go up on my levothyroxine dosage?
Hi everyone! As suggested, I followed everyone's advice regarding the blood test, and also I've been taking the levothyroxine earlier (leaving more of a gap before eating or taking other medications) for a month, and my latest results are: Serum free T4 level 12.0 pmol/L [7.9 - 14.4] Normal 05 Apr
Hi everyone! As suggested, I followed everyone's advice regarding the blood test, and also I've been taking the levothyroxine earlier (leaving more of a gap before eating or taking other medications) for a month, and my latest results are: Serum free T4 level 12.0 pmol/L [7.9 - 14.4] Normal 05 Apr
melissa-b
in
Thyroid UK
2 months ago
IBS, possibly menopause, any advice
Hello, I’m looking for any advice if possible, I was diagnosed with IBS over 20 years ago now. I think I had it as a child, it seemed to come about right around the same time I got my periods at 11. Every month I would have horrendously heavy menstrual cycles that were so painful I’d almost pass out
Hello, I’m looking for any advice if possible, I was diagnosed with IBS over 20 years ago now. I think I had it as a child, it seemed to come about right around the same time I got my periods at 11. Every month I would have horrendously heavy menstrual cycles that were so painful I’d almost pass out
Droidus
in
IBS Network
2 months ago
Do I have hypothyroidism?
Hello Thabk you so much for allowing me to join 💗My husband came across this website and thought it would be an amazing place to get help advice. So sorry for long post. I have had vestibular dysfunction since August 2022. I've suffered with muscle joint pain in my neck(I have had an injury to this
Hello Thabk you so much for allowing me to join 💗My husband came across this website and thought it would be an amazing place to get help advice. So sorry for long post. I have had vestibular dysfunction since August 2022. I've suffered with muscle joint pain in my neck(I have had an injury to this
Tinkerbell_84
in
Thyroid UK
2 months ago
slightly anxious and just looking for moral support
Hoping you all had a good Christmas. Mine has been a bit rough as the whole family has been unwell including me with this cold/throat bug that is going around. It didn’t go to my chest this year, thankfully and I was recovering okay when I noticed my throat and ears started hurting again and my mouth
Hoping you all had a good Christmas. Mine has been a bit rough as the whole family has been unwell including me with this cold/throat bug that is going around. It didn’t go to my chest this year, thankfully and I was recovering okay when I noticed my throat and ears started hurting again and my mouth
Abcd123455
in
PMRGCAuk
5 months ago
Starting Pegasys soon
Hi all and merry belated Christmas So… chemo…. I was diagnosed with ET about a year ago and finally found an MPN specialist in Montreal after a few months with a hemo who, unfortunately, knew very little about ET. I should be starting Pegasys sometime in January and I have a few questions :
Hi all and merry belated Christmas So… chemo…. I was diagnosed with ET about a year ago and finally found an MPN specialist in Montreal after a few months with a hemo who, unfortunately, knew very little about ET. I should be starting Pegasys sometime in January and I have a few questions :
IsabelleHo
in
MPN Voice
5 months ago
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