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atrial fibrillation and Covid vaccination
since lockdown and having the regular booster Covid vaccinations my atrial fibrillation has increased dramatically over the last 6 months since the two boosters one in April this year and further one in October this year since then I’ve been getting them at least 2 to 3 times a week prior to that, it
since lockdown and having the regular booster Covid vaccinations my atrial fibrillation has increased dramatically over the last 6 months since the two boosters one in April this year and further one in October this year since then I’ve been getting them at least 2 to 3 times a week prior to that, it
colingee
in
Atrial Fibrillation Support
8 months ago
Human Rights Day - 75th Anniversary
Today marks the 75th Anniversary of Human Rights Day. This year’s theme is
Freedom, Equality and Justice for All
. Please remember this. In 2010, Dr Matt Jameson Evans (Chief Medical Officer) and an entrepreneur, Jorge Armanet founded HealthUnlocked. They wished to reshape how data and information
Today marks the 75th Anniversary of Human Rights Day. This year’s theme is
Freedom, Equality and Justice for All
. Please remember this. In 2010, Dr Matt Jameson Evans (Chief Medical Officer) and an entrepreneur, Jorge Armanet founded HealthUnlocked. They wished to reshape how data and information
Narwhal10
in
Pernicious Anaemia Society
8 months ago
Sorted -,covid anti viral treatment
I managed to get covid a month after Rituxumab infusions, got free lateral flow test from independent pharmacy (boots and Tesco were hopeless and not signed up to the scheme) all the pharmacist needed was sight of a clinical letter confirming diagnosis. After testing positive I called 111 and an anti
I managed to get covid a month after Rituxumab infusions, got free lateral flow test from independent pharmacy (boots and Tesco were hopeless and not signed up to the scheme) all the pharmacist needed was sight of a clinical letter confirming diagnosis. After testing positive I called 111 and an anti
Pompey3
in
Vasculitis UK
8 months ago
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Is this lupus?
Hi, I'm just into my sixties and have developed symptoms that are tempting to pigeonhole "getting older" or menopause, but I don't think that they are. I do know though that the flare ups became much worse following a viral infection Feb 2020 (maybe covid?). I also reacted dramatically to the astra
Hi, I'm just into my sixties and have developed symptoms that are tempting to pigeonhole "getting older" or menopause, but I don't think that they are. I do know though that the flare ups became much worse following a viral infection Feb 2020 (maybe covid?). I also reacted dramatically to the astra
Foodwithfriends83
in
LUPUS UK
8 months ago
Cold & sore throat PAF
hi, I’ve had a cold and cough for 7 days now and having been having AF episodes lasting from 30mins - 5hours almost daily. Normally I would get an episode once a month at worst. Can colds and coughs bring on more regular occurances of AF?
hi, I’ve had a cold and cough for 7 days now and having been having AF episodes lasting from 30mins - 5hours almost daily. Normally I would get an episode once a month at worst. Can colds and coughs bring on more regular occurances of AF?
tom0985
in
Atrial Fibrillation Support
5 months ago
internal shingles
hi, I’ve been diagnosed with internal shingles and it’s the most painful thing I have ever experienced. I’m on my last day of Aciclovir, I’m taking paracetamol and codeine during the day and 3 amitriptyline at night, this has been going on for over a week. Is this normal? Any advice gladly accepted
hi, I’ve been diagnosed with internal shingles and it’s the most painful thing I have ever experienced. I’m on my last day of Aciclovir, I’m taking paracetamol and codeine during the day and 3 amitriptyline at night, this has been going on for over a week. Is this normal? Any advice gladly accepted
Mongoose123
in
PMRGCAuk
8 months ago
Wearing NHS Phonak hearing aids for one week
hello I suffer from mild/moderate high frequency hearing loss which was picked up by the Audiologist when I had two severe bouts of vertigo last year. I can hear ok most of the time but find it hard to hear/understand voices clearly on the television and sounds in the distance like church bells.
hello I suffer from mild/moderate high frequency hearing loss which was picked up by the Audiologist when I had two severe bouts of vertigo last year. I can hear ok most of the time but find it hard to hear/understand voices clearly on the television and sounds in the distance like church bells.
Choralmusic
in
Tinnitus UK
12 days ago
my day took a dive.
My brother was diagnosed with pancreatic cancer. His surgery early this morning revealed the cancer had spread undetected. They ended the procedure and sent him home giving him 6 months to live. Life seems random and impersonal. My son’s dog Roxie understands.
My brother was diagnosed with pancreatic cancer. His surgery early this morning revealed the cancer had spread undetected. They ended the procedure and sent him home giving him 6 months to live. Life seems random and impersonal. My son’s dog Roxie understands.
Gobbsofjoy
in
Cure Parkinson's
15 days ago
Pain in lower left abdomen for 5 years and now a very little bright red blood in stool once in a while
Hi All,When I was 24 (10 years ago)years old I consulted a gastroenterologist with stomach discomfort and bloating. He did an colonoscopy and an endoscopy..One polyp was found and was benign on biopsy.I was diagnosed with IBS..Time passed stomach problems were a daily concern for me.5 years ago suddenly
Hi All,When I was 24 (10 years ago)years old I consulted a gastroenterologist with stomach discomfort and bloating. He did an colonoscopy and an endoscopy..One polyp was found and was benign on biopsy.I was diagnosed with IBS..Time passed stomach problems were a daily concern for me.5 years ago suddenly
S_searching
in
Colon Cancer Connected
8 months ago
Advice after possible Covid
Hi all, I've been horribly ill with what is probably Covid (no positive LFT test but typical weird breathlessness, fluid lungs, fatigue, dizziness and all the rest). However, three weeks later and a course of antibiotics, and I'm still feeling rotten - massive fatigue, pains everywhere, dizziness
Hi all, I've been horribly ill with what is probably Covid (no positive LFT test but typical weird breathlessness, fluid lungs, fatigue, dizziness and all the rest). However, three weeks later and a course of antibiotics, and I'm still feeling rotten - massive fatigue, pains everywhere, dizziness
Treetop33
in
LUPUS UK
8 months ago
Questions about experience with rinvoq
Have had to stop rinvoq a few times lately due to infections, this last time I stopped rinvoq for ear infection for 5 days. The infection has not cleared up so they're giving me another antibiotic for 10 days. I was just wondering if most people have a flare when stopping rinvoq for that length of
Have had to stop rinvoq a few times lately due to infections, this last time I stopped rinvoq for ear infection for 5 days. The infection has not cleared up so they're giving me another antibiotic for 10 days. I was just wondering if most people have a flare when stopping rinvoq for that length of
gnstric66
in
NRAS
10 months ago
advice
Hello! I havnt posted before but was looking on the lupus Uk website and wanted some advice if possible. I have been struggling with weird symptoms for a while since my son was born 4 years ago- ( then cot covid and was really unwell so was all put down to long covid) I have positive APS antibodies
Hello! I havnt posted before but was looking on the lupus Uk website and wanted some advice if possible. I have been struggling with weird symptoms for a while since my son was born 4 years ago- ( then cot covid and was really unwell so was all put down to long covid) I have positive APS antibodies
Ell5
in
LUPUS UK
8 months ago
Advice needed please
I've had GPA for 25 years with 2 relapses. I last had Rituximab in June 21, I then in November had Covid with 2 hospital admissions. I now have long Covid. I cannot have RTmab because my Immune system is so low, Igg 3.4IgA 0.48 IgM 0.42p Yesterday I was walking around and felt extreme fatigue,
I've had GPA for 25 years with 2 relapses. I last had Rituximab in June 21, I then in November had Covid with 2 hospital admissions. I now have long Covid. I cannot have RTmab because my Immune system is so low, Igg 3.4IgA 0.48 IgM 0.42p Yesterday I was walking around and felt extreme fatigue,
Fleen
in
Vasculitis UK
8 months ago
immune system
I am on immune suppressants, Is it advisable to take vitamins to help immune system fight against Cold and flu therefore also general Feeling crappy. Thank you for advice in advanc
I am on immune suppressants, Is it advisable to take vitamins to help immune system fight against Cold and flu therefore also general Feeling crappy. Thank you for advice in advanc
Toiletseat
in
NRAS
5 months ago
overlapping symptoms
hi all I’ve finally seen a rheumatologist and he wasn’t able to give me a diagnosis as he says I don’t present the classic symptoms for any one particular autoimmune disease but I have overlapping symptoms of more than one condition. The hair loss and rash seem to be puzzling them too. I’ve been prescribed
hi all I’ve finally seen a rheumatologist and he wasn’t able to give me a diagnosis as he says I don’t present the classic symptoms for any one particular autoimmune disease but I have overlapping symptoms of more than one condition. The hair loss and rash seem to be puzzling them too. I’ve been prescribed
TheRedOnes
in
LUPUS UK
9 months ago
Shocking story about women dying of CRF/ME
Did anyone read about the women who died from CFS/ME? https://news.sky.com/story/woman-with-me-died-after-begging-gp-for-help-inquest-told-13183530 Why didn't anyone try B12 and see if it could help her? If you look online there is masses of information about how B12 can help CFS/ME. For example
Did anyone read about the women who died from CFS/ME? https://news.sky.com/story/woman-with-me-died-after-begging-gp-for-help-inquest-told-13183530 Why didn't anyone try B12 and see if it could help her? If you look online there is masses of information about how B12 can help CFS/ME. For example
charks
in
Pernicious Anaemia Society
25 days ago
Long covid
Im struggling to get over covid and im on day 13. I have symptoms of long covidfever, diarrhea, loss of smell and taste. I have hashimotos and taking levothyroxine 100mcg alongside t3 15mcg. Any advice on how to deal with this will be very welcome
Im struggling to get over covid and im on day 13. I have symptoms of long covidfever, diarrhea, loss of smell and taste. I have hashimotos and taking levothyroxine 100mcg alongside t3 15mcg. Any advice on how to deal with this will be very welcome
Geegee777
in
Thyroid UK
8 months ago
Covid question
I’ve avoided Covid up until now. My partner and I picked it up in Cuba. Started with what we thought was food poisoning, the dreaded diarrhea. It’s now been 14 days. We’ve had chills, fevers, fatigue and daily diarrhea. I’m at the final three months of V treatment so was advised to start the antiviral
I’ve avoided Covid up until now. My partner and I picked it up in Cuba. Started with what we thought was food poisoning, the dreaded diarrhea. It’s now been 14 days. We’ve had chills, fevers, fatigue and daily diarrhea. I’m at the final three months of V treatment so was advised to start the antiviral
Cottager1989
in
CLL Support
8 months ago
EMED A200 Piston Nebuliser.
Just back home from Hospital with pneumonia Good morning all COPD Warriors, thankfully I am back home from now after a stay in hospital with pneumonia. whilst I was in hospital my Respiratory Nurses noticed that it was time for my nebuliser to be serviced as it had been 12 months since last done.
Just back home from Hospital with pneumonia Good morning all COPD Warriors, thankfully I am back home from now after a stay in hospital with pneumonia. whilst I was in hospital my Respiratory Nurses noticed that it was time for my nebuliser to be serviced as it had been 12 months since last done.
Joseph260268
in
Lung Conditions Community Forum
5 months ago
Hi all I'm newbie. Anyone here have lung damage due to Amiodarone treatment?
Rather than going into too much detail I will keep it brief. Was prescribed Amiodarone for AFib and took it for a total of four months six days. After being on it for 3 months I started coughing mostly while asleep. Also started to get really bad pain in left lung lobe that was much worse if I lay on
Rather than going into too much detail I will keep it brief. Was prescribed Amiodarone for AFib and took it for a total of four months six days. After being on it for 3 months I started coughing mostly while asleep. Also started to get really bad pain in left lung lobe that was much worse if I lay on
DizzyD
in
Lung Conditions Community Forum
8 months ago
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