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Sinusitis (sinus infection)
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Covid antivirals - why?
NHS have told me I have a condition that entitles me to antivirals for Covid. But haven't told me what is or which are the qualifying condition(s). GP doesn't know either. I think this is off! Makes me worry, and I'm not easily fazed. Is it an existing condition, if so which, or is it a new condition
NHS have told me I have a condition that entitles me to antivirals for Covid. But haven't told me what is or which are the qualifying condition(s). GP doesn't know either. I think this is off! Makes me worry, and I'm not easily fazed. Is it an existing condition, if so which, or is it a new condition
Coppernob
in
Aspergillosis and Rare Fungal Infection Support
1 year ago
covid
hi all. I have severe asthma. Which I have had for many years. I had covid in June last year. Followed by chest infection, then I was hospitalised with RSV. I spent all of Xmas in hospital after I also got flu a few weeks after that , I have never been right since I had covid. I went to the post
hi all. I have severe asthma. Which I have had for many years. I had covid in June last year. Followed by chest infection, then I was hospitalised with RSV. I spent all of Xmas in hospital after I also got flu a few weeks after that , I have never been right since I had covid. I went to the post
Denae011
in
Lung Conditions Community Forum
1 year ago
Dr appt updates
Saw my pulmonologist on Tues. “Why haven’t you been using your Cpap?” Me: “Sometimes I feel claustrophobic and it’s hard to breathe. I also have had shortness of breath since I had Covid last June after coming home from our trip.” This led her to have me do a 6 minute walking test - my oxygen didn’t
Saw my pulmonologist on Tues. “Why haven’t you been using your Cpap?” Me: “Sometimes I feel claustrophobic and it’s hard to breathe. I also have had shortness of breath since I had Covid last June after coming home from our trip.” This led her to have me do a 6 minute walking test - my oxygen didn’t
PWilli
in
My MSAA Community
1 year ago
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Vaccination, Paxlovid decrease risk of long Covid, studies show
Vaccination, Paxlovid decrease risk of long Covid, studies show By Janelle Chavez, CNN Published 11:00 AM EDT, Thu March 23, 2023 https://www.cnn.com/2023/03/23/health/long-covid-vaccination-paxlovid/index.html https://www.cnn.com/2023/03/23/health/long-covid-vaccination-paxlovid/index.html#:~:text
Vaccination, Paxlovid decrease risk of long Covid, studies show By Janelle Chavez, CNN Published 11:00 AM EDT, Thu March 23, 2023 https://www.cnn.com/2023/03/23/health/long-covid-vaccination-paxlovid/index.html https://www.cnn.com/2023/03/23/health/long-covid-vaccination-paxlovid/index.html#:~:text
lankisterguy
Volunteer
in
CLL Support
1 year ago
Skin rash due to prednisolone?
Hi coming up to a year on Pred and on 5 mg one day 4 mg the next. Was going well but now have some kind of fungal infection around top half of my body. Not all over but enough to be uncomfortable and itchy. Been given some topical steroid treatment but not keen on using it. Has anyone else had similar
Hi coming up to a year on Pred and on 5 mg one day 4 mg the next. Was going well but now have some kind of fungal infection around top half of my body. Not all over but enough to be uncomfortable and itchy. Been given some topical steroid treatment but not keen on using it. Has anyone else had similar
Tanner145
in
PMRGCAuk
1 year ago
fibro and covid
hi, I had Covid over Christmas 2021 (15 months ago) since then I constantly feel I’m in one long flare of relentless fatigue and pain whereas before I had times of feeling ‘better’. Anyone else noticed this since having covid? Thanks
hi, I had Covid over Christmas 2021 (15 months ago) since then I constantly feel I’m in one long flare of relentless fatigue and pain whereas before I had times of feeling ‘better’. Anyone else noticed this since having covid? Thanks
Belleross
in
Fibromyalgia Action UK
1 year ago
Hi, I'm new here. It all sucks a bit doesn't it!
In July 2020 I lost my Nan. She had a stroke and went to hospital, then a palliative nursing home. We couldn't go an visit because of stupid Covid. Only my Grandad could go, once a day, for an hour. She had 4 married sons, 4 grandchildren and 3 great grandchildren. She passed alone. Before that my Grandad
In July 2020 I lost my Nan. She had a stroke and went to hospital, then a palliative nursing home. We couldn't go an visit because of stupid Covid. Only my Grandad could go, once a day, for an hour. She had 4 married sons, 4 grandchildren and 3 great grandchildren. She passed alone. Before that my Grandad
Ronnietheblonde
in
Bereavement Care & Share
1 year ago
long covid
My fibro had a flare that got a lot worse and stayed after I had covid in Dec 2021, and I now think this is a comorbidity esp as the symptoms overlap with fibro, but for me the severity and longevity has become so much worse since I had covid in a way my fibro never was before, the GP wanted to put everything
My fibro had a flare that got a lot worse and stayed after I had covid in Dec 2021, and I now think this is a comorbidity esp as the symptoms overlap with fibro, but for me the severity and longevity has become so much worse since I had covid in a way my fibro never was before, the GP wanted to put everything
DavidCB
in
Fibromyalgia Action UK
1 year ago
Morphine
Hi i have had a cronic cough for many years and Asthma my doctor suggested trying 5 mg of morphine which i wasn't happy about but within a few days my cough has almost gone. Has anyone else tried this
Hi i have had a cronic cough for many years and Asthma my doctor suggested trying 5 mg of morphine which i wasn't happy about but within a few days my cough has almost gone. Has anyone else tried this
nottowell
in
Lung Conditions Community Forum
10 months ago
Seeking advice for London private fertility clinics
Hi everyone, I’m now 36, living in NW London. Previously diagnosed abroad with PCOS and prescribed oral clomiphene citrate with an unsatisfactory result. Only conducted basic tests and screening requested by GP for the sake of secondary care referral in NHS. While waiting for my first appointment at
Hi everyone, I’m now 36, living in NW London. Previously diagnosed abroad with PCOS and prescribed oral clomiphene citrate with an unsatisfactory result. Only conducted basic tests and screening requested by GP for the sake of secondary care referral in NHS. While waiting for my first appointment at
fupafupa
in
Fertility Network UK
11 months ago
Any advice on getting Covid
I’ve just tested Positive for Covid this morning, my first time, ahhh….. hoping I don’t fall back into AF. I’ve read others here have gone into AF on getting Covid. I’m on low dose Metoprolol and low dose aspirin. Any precautions I should be doing to prevent AF coming back?. So far my symptoms are
I’ve just tested Positive for Covid this morning, my first time, ahhh….. hoping I don’t fall back into AF. I’ve read others here have gone into AF on getting Covid. I’m on low dose Metoprolol and low dose aspirin. Any precautions I should be doing to prevent AF coming back?. So far my symptoms are
OzJames
in
AF Association
1 year ago
Graves Disease, Covid and Paxlovid
Hello. My husband was just diagnosed with Covid on Sunday. He is on Paxlovid. Has anyone in the group taken Paxlovid for Covid and if so we’re there any problems with it? I also have multiple sclerosis and another autoimmune disease called Polymyalgia Rheumatica. Thanks!
Hello. My husband was just diagnosed with Covid on Sunday. He is on Paxlovid. Has anyone in the group taken Paxlovid for Covid and if so we’re there any problems with it? I also have multiple sclerosis and another autoimmune disease called Polymyalgia Rheumatica. Thanks!
Donna5658
in
Thyroid UK
1 year ago
Paxlovid and MS
My husband was diagnosed with Covid on Sunday night and is taking Paxlovid. I’m wondering if there are people in the group who have taken Paxlovid for Covid and if so, were there any problems with their ms? Thanks!
My husband was diagnosed with Covid on Sunday night and is taking Paxlovid. I’m wondering if there are people in the group who have taken Paxlovid for Covid and if so, were there any problems with their ms? Thanks!
Donna5658
in
My MSAA Community
1 year ago
Myelin Sheath Repair
This isn't technically a B12 question but since a lot of us have peripheral neuropathy I thought I'd post it here. Has anyone read about a newly discovered use for an old antihistamine, clemastine? They say it can repair the myelin sheath for MS patients. Here is a blurb I read: "[i]Now, researchers
This isn't technically a B12 question but since a lot of us have peripheral neuropathy I thought I'd post it here. Has anyone read about a newly discovered use for an old antihistamine, clemastine? They say it can repair the myelin sheath for MS patients. Here is a blurb I read: "[i]Now, researchers
MoKayD
in
Pernicious Anaemia Society
11 months ago
Live Yoghurt
Hi there - just to run this past everyone - I have just recovered from Covid which has left me with either Covid tongue or oral thrush - not sure which yet - but the gel I have been given to cure the thrush doesn't seem to be doing any good so assume it is Covid tongue which can happen with Lupus patients
Hi there - just to run this past everyone - I have just recovered from Covid which has left me with either Covid tongue or oral thrush - not sure which yet - but the gel I have been given to cure the thrush doesn't seem to be doing any good so assume it is Covid tongue which can happen with Lupus patients
posthinking01
in
LUPUS UK
1 year ago
Covid anti viral meds
Has anyone taken the Covid anti-viral meds? I reported my positive test online this morning and have just been called by the nurse at the local hospital to triage me. They are sending the tablets by courier later this afternoon.
Has anyone taken the Covid anti-viral meds? I reported my positive test online this morning and have just been called by the nurse at the local hospital to triage me. They are sending the tablets by courier later this afternoon.
Blueskysunshine
in
NRAS
1 year ago
IMPORTANT INFORMATION ABOUT TREATMENTS FOR CORONAVIRUS
I received a letter March 20th with this heading from the NHS.At first I was totally disoriented by it because I thought we were over the worst of Covid, I mean everyone is walking carefree, not wearing masks, there are no reports on the News about it so why did I get this letter? This letter informs
I received a letter March 20th with this heading from the NHS.At first I was totally disoriented by it because I thought we were over the worst of Covid, I mean everyone is walking carefree, not wearing masks, there are no reports on the News about it so why did I get this letter? This letter informs
MjRock
in
NRAS
1 year ago
round two!
remember how I was short of breath a few weeks ago, went to the ER, sent home on oxygen and told it was a cold. I spent four days on oxygen, then coughed like crazy for two weeks, staring the muscle under my ribs and throwing out a few ribs as well. then silly me, thinking it’s just a cold and I
remember how I was short of breath a few weeks ago, went to the ER, sent home on oxygen and told it was a cold. I spent four days on oxygen, then coughed like crazy for two weeks, staring the muscle under my ribs and throwing out a few ribs as well. then silly me, thinking it’s just a cold and I
StacyHayward
in
My MSAA Community
1 year ago
Wk7 run2
Ive had sinusitis the last few days but managed to make a speedy recovery. A few rest days and i am back on it today. I did stop a few times but glad i feel well enough to run again 😌. Not going to push myself too much this week , just concentrating on getting myself back to were i was 😊
Ive had sinusitis the last few days but managed to make a speedy recovery. A few rest days and i am back on it today. I did stop a few times but glad i feel well enough to run again 😌. Not going to push myself too much this week , just concentrating on getting myself back to were i was 😊
Natashasoraya
in
Couch to 5K
1 year ago
Hello...struggling today
Hi everyone, I am really struggling today. My issue is terrible health anxiety triggered by the pandemic. I work as a massage therapist and was doing fine before the pandemic having one flare up in 2014 where I believed I had a contagious skin disease and was contaminating everyone. Getting a good
Hi everyone, I am really struggling today. My issue is terrible health anxiety triggered by the pandemic. I work as a massage therapist and was doing fine before the pandemic having one flare up in 2014 where I believed I had a contagious skin disease and was contaminating everyone. Getting a good
redcedar91
in
My OCD Community
1 year ago
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