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Chest infection
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A little, very quiet, thumbs up đź‘Ť
Well, I've been keeping quiet about returning (again!) to C25K but I have just managed Week 4, Run 3 without any problems so I am HOPING I can finally get back on the trotting pony regularly now. After literally a whole year of Covid, colds, sinus and chest infections, PVF/Long Covid, post-Covid cough
Well, I've been keeping quiet about returning (again!) to C25K but I have just managed Week 4, Run 3 without any problems so I am HOPING I can finally get back on the trotting pony regularly now. After literally a whole year of Covid, colds, sinus and chest infections, PVF/Long Covid, post-Covid cough
Over60sRunner
Graduate
in
Couch to 5K
6 months ago
Long Covid
Hi All Last week I was diagnosed with post covid viral syndrome (long Covid) I am feeling so unwell and fatigued, just wonder if anyone on here is coping with that too Thanks Annie
Hi All Last week I was diagnosed with post covid viral syndrome (long Covid) I am feeling so unwell and fatigued, just wonder if anyone on here is coping with that too Thanks Annie
Annieosb
in
Lung Conditions Community Forum
6 months ago
QoL: Exhibition space offered
The first is that I have been in the throes of a
chest
infection
these past weeks that has prevented me from doing much at all. Every time I think it has passed, a new wave hits me, knocking me out for hours and inducing ages of sleep. What a bummer.
The first is that I have been in the throes of a
chest
infection
these past weeks that has prevented me from doing much at all. Every time I think it has passed, a new wave hits me, knocking me out for hours and inducing ages of sleep. What a bummer.
BrentW
in
Advanced Prostate Cancer
5 months ago
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trauma after icu stay
hi in2020 I was rushed to kings hospital London with septic shock due to ulcers on my liver. I was in an induced coma for a week and in hospital for 5 weeks. During the last 3 months I have been having really bad nightmares about being in a coma, specifically that my doctor is trying to kill me (i really
hi in2020 I was rushed to kings hospital London with septic shock due to ulcers on my liver. I was in an induced coma for a week and in hospital for 5 weeks. During the last 3 months I have been having really bad nightmares about being in a coma, specifically that my doctor is trying to kill me (i really
ZoeH1974
in
ICUsteps
3 months ago
PMR and Pfizer Covid Vaccine
Within 5 days of my husband and I receiving the first Pfizer Covid jab, he started getting pains in his legs and shoulders. He took paracetamol & used Bio Freeze, similar to deep heat. He got progressively worse, a GP diagnosed Frozen Shoulder over the phone, prescribed Co-Codamol & Naproxen. Within
Within 5 days of my husband and I receiving the first Pfizer Covid jab, he started getting pains in his legs and shoulders. He took paracetamol & used Bio Freeze, similar to deep heat. He got progressively worse, a GP diagnosed Frozen Shoulder over the phone, prescribed Co-Codamol & Naproxen. Within
heartsonfire
in
PMRGCAuk
6 months ago
Update on Rheumy visit
I explained we were following slow taper with approval of our wonderful gp (who she knows very well) and that we had stayed at 15mg for 7 weeks as my mum had
chest
infection
and we had stress of my niece wedding after which our gp suggested we reduce by 1mg per month which suited me perfectly.
I explained we were following slow taper with approval of our wonderful gp (who she knows very well) and that we had stayed at 15mg for 7 weeks as my mum had
chest
infection
and we had stress of my niece wedding after which our gp suggested we reduce by 1mg per month which suited me perfectly.
Buchanan16
in
PMRGCAuk
6 months ago
Off on all meds
ITS GOING TI BE 2 YEARS I AM OFF ALL TYPE OF MEDS FOR MY RA.DUE TO ALL KIND OF INFECTIONS.I MUST SAY I HAVE BEING COPING VERY WELL ONCE IN A WILE MY LEFT KNEE GETS SWOLLEN BUT U PUT ICE PADS AND OFF AGAIN.I AM 69 YEARS OLD AND HAVE RA AND SJOGRENS SINCE 40.I HAVE HAD BREAST CANCER LUNG FIBROSIS I SUFFER
ITS GOING TI BE 2 YEARS I AM OFF ALL TYPE OF MEDS FOR MY RA.DUE TO ALL KIND OF INFECTIONS.I MUST SAY I HAVE BEING COPING VERY WELL ONCE IN A WILE MY LEFT KNEE GETS SWOLLEN BUT U PUT ICE PADS AND OFF AGAIN.I AM 69 YEARS OLD AND HAVE RA AND SJOGRENS SINCE 40.I HAVE HAD BREAST CANCER LUNG FIBROSIS I SUFFER
Al1954
in
NRAS
6 months ago
Has anyone had good success with Low Dose Naltrexone (LDN) for chronically reactivated EBV?
Has anyone had good success with Low Dose Naltrexone (LDN) for chronically reactivated EBV? Answered by Sebastian Denison, RPh https://youtu.be/ifWvF7Yz52Y
Has anyone had good success with Low Dose Naltrexone (LDN) for chronically reactivated EBV? Answered by Sebastian Denison, RPh https://youtu.be/ifWvF7Yz52Y
Shewulf
Administrator
in
LDN Research Trust
3 months ago
Orphenadrine
My hwp had been using ophenadrine some time ago and stopped because of fears around using anticholinergics. However, his unrelenting battle with sciatica has me wondering if it might not be worth taking the risk. He is a well person in every other way, but the pain has him battling to do exercise. He
My hwp had been using ophenadrine some time ago and stopped because of fears around using anticholinergics. However, his unrelenting battle with sciatica has me wondering if it might not be worth taking the risk. He is a well person in every other way, but the pain has him battling to do exercise. He
ghoegap
in
Cure Parkinson's
6 months ago
Did I get this wrong
So I’ve worked my frequency’s out on the basis of when I feel breathless and achy I’ve overdone it and prob need to increase my shots or I’ve left too long a gap, but usually it’s a max of one week between them so I had a rethink as my pains increased I’ve not felt well for weeks and despite increasing
So I’ve worked my frequency’s out on the basis of when I feel breathless and achy I’ve overdone it and prob need to increase my shots or I’ve left too long a gap, but usually it’s a max of one week between them so I had a rethink as my pains increased I’ve not felt well for weeks and despite increasing
Thrones12
in
Pernicious Anaemia Society
8 months ago
pneumonia vaccination
I have been told to get my pneumonia jab , i’m not worried about sore arm, but i’m just a bit concerned i might feel poorly after. I didn’t feel poorly after my flu jab or covid booster. Any reassurance would be appreciated. Thank you.
I have been told to get my pneumonia jab , i’m not worried about sore arm, but i’m just a bit concerned i might feel poorly after. I didn’t feel poorly after my flu jab or covid booster. Any reassurance would be appreciated. Thank you.
Collie4
in
Lung Conditions Community Forum
3 months ago
Reducing pred while on antibiotics
My mum has been on 60mg pred for 4 weeks and her CRP levels are now down to 3 so our GP has said its ok to reduce to 50mg which we were happy to do.My mum has
chest
infection
and terrible cough and just been given course of antibiotics for it.
My mum has been on 60mg pred for 4 weeks and her CRP levels are now down to 3 so our GP has said its ok to reduce to 50mg which we were happy to do.My mum has
chest
infection
and terrible cough and just been given course of antibiotics for it.
Buchanan16
in
PMRGCAuk
1 year ago
tapering too rapidly after synovitis?
I have now had PMR for about 3 1/2 years; several months ago my hands became very painful, and I was diagnosed eventually with acute synovitis. I was told that if I did not go onto high doses of Pred. I might lose the use of my hands, so I agreed. This is the regime I am on: 20 mg pred for 2 weeks,
I have now had PMR for about 3 1/2 years; several months ago my hands became very painful, and I was diagnosed eventually with acute synovitis. I was told that if I did not go onto high doses of Pred. I might lose the use of my hands, so I agreed. This is the regime I am on: 20 mg pred for 2 weeks,
humlies
in
PMRGCAuk
8 months ago
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
6 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
6 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
6 months ago
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
6 months 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
6 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
6 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
6 months ago
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