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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
3 months ago
Urodynamics test or not?
Hi. Just a brief background. I am on the waiting list for pelvic organ prolapse. I have incontinence issues and I was prescribed Solifenacin by the hospital consultant which worked for about a month then stopped. Because of this the doctor has delayed me signing the consent forms for my surgery and
Hi. Just a brief background. I am on the waiting list for pelvic organ prolapse. I have incontinence issues and I was prescribed Solifenacin by the hospital consultant which worked for about a month then stopped. Because of this the doctor has delayed me signing the consent forms for my surgery and
Mummybear0213
in
Pelvic Pain Support Network
5 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
3 months ago
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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
3 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
3 months ago
Feel like giving up.
For unknown reasons other than we think Rituxumab is not working for you any more my medication was changed to Kevzera (Sarilulmab) in November. The work up checks were done and good to go apart from a Chest X Ray as I hadn't had one for a while. A shadow area was found on my lung with suspected
For unknown reasons other than we think Rituxumab is not working for you any more my medication was changed to Kevzera (Sarilulmab) in November. The work up checks were done and good to go apart from a Chest X Ray as I hadn't had one for a while. A shadow area was found on my lung with suspected
3LittleBirds2
in
NRAS
3 months ago
Cardiovascular issues
Anybody out there with extra-cranial GCA / LVV, have any cardiovascular issues? I was having some shortness of breath, sleepiness & lightheadedness. I'm in the middle of testing for that, but a CAT scan showed I have a dilated aortic root and pericardial effusion. Those explained my symptoms, but neither
Anybody out there with extra-cranial GCA / LVV, have any cardiovascular issues? I was having some shortness of breath, sleepiness & lightheadedness. I'm in the middle of testing for that, but a CAT scan showed I have a dilated aortic root and pericardial effusion. Those explained my symptoms, but neither
winfong
in
PMRGCAuk
5 months ago
Shingles jab
Hi everyone, just had second shingles vaccine and suddenly thought should I stop taking methotrexate this week also on sulfasalazine as is recommended after covid jab, I didn't stop taking meds after the first shingles jab,it just didn't even enter my head, think I'm losing it đ wishing you all as much
Hi everyone, just had second shingles vaccine and suddenly thought should I stop taking methotrexate this week also on sulfasalazine as is recommended after covid jab, I didn't stop taking meds after the first shingles jab,it just didn't even enter my head, think I'm losing it đ wishing you all as much
Jeremycfc
in
NRAS
5 months ago
Vestibular Neuritis
Hi everyone, I woke up on New Year's Day with the room spinning around me. Very scary! Diagnosed as vestibular neuritis. My question is, I usually self inject weekly which I have continued to do. I don't know if I'm imagining it but the vertigo symptoms seem to greatly improve for a couple of days
Hi everyone, I woke up on New Year's Day with the room spinning around me. Very scary! Diagnosed as vestibular neuritis. My question is, I usually self inject weekly which I have continued to do. I don't know if I'm imagining it but the vertigo symptoms seem to greatly improve for a couple of days
Ipsofacto01
in
Pernicious Anaemia Society
5 months ago
Severely bitter taste when eating & drinking - ?FostairNEXThaler
Wondering if anyone else has experienced a very bitter taste in the mouth - both whilst eating & drinking (& generally too) when taking FostairNEXThaler? Iâve recently been discharged home after another hospital admission (asthma exacerbation secondary to Covid) so the dysguesia may very well be Covid-related
Wondering if anyone else has experienced a very bitter taste in the mouth - both whilst eating & drinking (& generally too) when taking FostairNEXThaler? Iâve recently been discharged home after another hospital admission (asthma exacerbation secondary to Covid) so the dysguesia may very well be Covid-related
Easybreath
in
Asthma Community Forum
5 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
3 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 canât 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 canât book through that line and hangs up. Both
grumpygirl
in
NRAS
3 months ago
Bursitis of toes & Steroid Injection
I've had pain from between the second & third toe since last May. It hurts to stand & walk especially barefoot or in shoes. I tend to wear trainers when I can as the base is soft & spongy. I had surgery Oct 22 for severe arthritis in the large toe & at first I feared it had spread. Two trips to GP (
I've had pain from between the second & third toe since last May. It hurts to stand & walk especially barefoot or in shoes. I tend to wear trainers when I can as the base is soft & spongy. I had surgery Oct 22 for severe arthritis in the large toe & at first I feared it had spread. Two trips to GP (
sarahsch
in
Scleroderma & Raynaud's UK (SRUK)
3 months ago
Bursitis of the toes & Steroid Injection.
I've had pain from between the second & third toe since last May. It hurts to stand & walk especially barefoot or in shoes. I tend to wear trainers when I can as the base is soft & spongy. I had surgery Oct 22 for severe arthritis in the large toe & at first I feared it had spread. Two trips to GP (
I've had pain from between the second & third toe since last May. It hurts to stand & walk especially barefoot or in shoes. I tend to wear trainers when I can as the base is soft & spongy. I had surgery Oct 22 for severe arthritis in the large toe & at first I feared it had spread. Two trips to GP (
sarahsch
in
LUPUS UK
3 months ago
friend has shingles - advice please
hi, Can I have some advice please. my friend who is a beautician is scheduled to do a facial & nails for me tomorrow. Iâve had chicken pox and her Dr has said she shouldnât pass it in because itâs on her bottom and she wonât be touching it so in that respect itâs in a good place. Any thoughts? Thank
hi, Can I have some advice please. my friend who is a beautician is scheduled to do a facial & nails for me tomorrow. Iâve had chicken pox and her Dr has said she shouldnât pass it in because itâs on her bottom and she wonât be touching it so in that respect itâs in a good place. Any thoughts? Thank
MalloryMoss
in
PMRGCAuk
6 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
3 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
3 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 canât 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 canât 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
3 months ago
Recovery from colds/flu whilst on Adalimumab
Hello,I was diagnosed with Crohn's 18 months ago and have been on Adalimumab for the last 12 months. In that time I have managed to avoid colds/flu until a couple of weeks ago. Have felt quite unwell and presently doesn't seem to be ending. My question is really to other people who have a reduced immune
Hello,I was diagnosed with Crohn's 18 months ago and have been on Adalimumab for the last 12 months. In that time I have managed to avoid colds/flu until a couple of weeks ago. Have felt quite unwell and presently doesn't seem to be ending. My question is really to other people who have a reduced immune
UmaDaisy
in
Crohn's and Colitis Support
6 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 âhappyâ to have it done privately at a cost of ÂŁ100 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 âhappyâ to have it done privately at a cost of ÂŁ100 approx but would need to travel some distance at the moment. Thanks for any advice
Main1234
in
Vasculitis UK
3 months ago
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