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Covid Again
hi all just a quick question can Covid affected your lungs when you are on blood thinners?, I had Covid at the beginning of December which was pretty bad, i feel like I recovered well but I’m back to square one again my chest hurt and I’m a bit more breathless but I also suffer from severe anxiety and
hi all just a quick question can Covid affected your lungs when you are on blood thinners?, I had Covid at the beginning of December which was pretty bad, i feel like I recovered well but I’m back to square one again my chest hurt and I’m a bit more breathless but I also suffer from severe anxiety and
Cimmy
in
Lung Conditions Community Forum
9 months ago
Christmas Covid
Looks like our Christmas present was Covid. At my partners mothers and both tested positive one this morning and the others last Thursday but so far I’m negative but sure I’ll get it. not sure where we picked it up as been careful. I’m not sure what to do meds wise as I took my 15mg of MTX yesterday
Looks like our Christmas present was Covid. At my partners mothers and both tested positive one this morning and the others last Thursday but so far I’m negative but sure I’ll get it. not sure where we picked it up as been careful. I’m not sure what to do meds wise as I took my 15mg of MTX yesterday
Alan7690
in
NRAS
9 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
6 months ago
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My Christmas
I did not attend the family gathering unfortunately since I have anxiety inside indoor spaces with groups of people, and we have COVID and flu going around. My concern with COVID is that some people get long term symptoms like chronic fatigue, loss of smell or taste, and a few others. So it just still
I did not attend the family gathering unfortunately since I have anxiety inside indoor spaces with groups of people, and we have COVID and flu going around. My concern with COVID is that some people get long term symptoms like chronic fatigue, loss of smell or taste, and a few others. So it just still
davidthecoder
in
Anxiety and Depression Support
9 months ago
Pneumonia Vaccine
I was talking to a very friendly Doctors wife yesterday who works on his admin and we talked about the amount of people suffering and in some cases hospitalised with pneumonia. She said that the vaccine I was given about 10yrs ago is now not considered to be sufficient protection. It is thought that
I was talking to a very friendly Doctors wife yesterday who works on his admin and we talked about the amount of people suffering and in some cases hospitalised with pneumonia. She said that the vaccine I was given about 10yrs ago is now not considered to be sufficient protection. It is thought that
Ridge
in
PMRGCAuk
9 months ago
Covid update
I had a call back after 2.5 days from the covid medication delivery unit. They asked me to go to the local hospital to get an infusion of sotrovimab. The tablets form interacts with some of my medication so this one was chosen. I will let you know how I do on it.
I had a call back after 2.5 days from the covid medication delivery unit. They asked me to go to the local hospital to get an infusion of sotrovimab. The tablets form interacts with some of my medication so this one was chosen. I will let you know how I do on it.
artydutch
in
MPN Voice
9 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
6 months ago
Rash any advice?
I have noticed this rash over last 2 or 3 months. Its not itchy or raised. Any advice most welcome. Im taking 100mcg teva levo and 15mcg thybon henning. Vit d, magnesium glycinate. Any advice most welcome 🌸🌸🌸🌸🌸
I have noticed this rash over last 2 or 3 months. Its not itchy or raised. Any advice most welcome. Im taking 100mcg teva levo and 15mcg thybon henning. Vit d, magnesium glycinate. Any advice most welcome 🌸🌸🌸🌸🌸
Geegee777
in
Thyroid UK
10 months ago
sjogens?
I have post PV Myelofibrosis. When I was dx with PV I took Pegasys from April 22 @ 45mg then 60mg then 90mg fortnightly. (On Jakavi since August 23) So took Pegasys for about 16 months After a couple of months on Pegasys I started to experience close vision problems which could not be corrected with
I have post PV Myelofibrosis. When I was dx with PV I took Pegasys from April 22 @ 45mg then 60mg then 90mg fortnightly. (On Jakavi since August 23) So took Pegasys for about 16 months After a couple of months on Pegasys I started to experience close vision problems which could not be corrected with
Yanico
in
MPN Voice
10 months ago
shingles vaccine
Hi folks This is a brilliant site has keep me steady since my husband’s diagnosis of SLL now CLL. My Husband had been W&W for 6 years, now on acalabrutinib for two years with no side affect and doing well. He has been offered the shingles vaccine but he hasn’t had chickenpox’s, is it safe to get the
Hi folks This is a brilliant site has keep me steady since my husband’s diagnosis of SLL now CLL. My Husband had been W&W for 6 years, now on acalabrutinib for two years with no side affect and doing well. He has been offered the shingles vaccine but he hasn’t had chickenpox’s, is it safe to get the
Charles4
in
CLL Support
10 months ago
Covid
hi all, I have been diagnosed with tumid lupus and am currently being investigated for SLE (DR said 99.9% I have it as showing all symptoms etc). I have just tested positive for covid today. Has anyone got any advise? I’ve never had covid, let alone Covid with lupus and I’m terrified this is going
hi all, I have been diagnosed with tumid lupus and am currently being investigated for SLE (DR said 99.9% I have it as showing all symptoms etc). I have just tested positive for covid today. Has anyone got any advise? I’ve never had covid, let alone Covid with lupus and I’m terrified this is going
JLAR01
in
LUPUS UK
9 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
6 months ago
Periods delayed after steroid injections
Hi,Has anyone had the experience of their periods being delayed after having steroid injections. If so, for how long? I'm a week late. They haven't been this late in a long while. I have an IVF consultation next month so I'm worried they won't return Thanks
Hi,Has anyone had the experience of their periods being delayed after having steroid injections. If so, for how long? I'm a week late. They haven't been this late in a long while. I have an IVF consultation next month so I'm worried they won't return Thanks
ABFr23
in
NRAS
9 months ago
shingrix
Does anyone know how long you have to leave it after rutuximab before having the shingles vaccine. I had infusion in December & my GP has never offered this or the pneumonia jab so was going to chase this up. Tia
Does anyone know how long you have to leave it after rutuximab before having the shingles vaccine. I had infusion in December & my GP has never offered this or the pneumonia jab so was going to chase this up. Tia
juli-pa
in
Vasculitis UK
9 months ago
New to Texas, lok long for advice on insurance and doctor selection
Hi, I landed in San Antonio texas two weeks back and may stay here for a year for work reason. I am advanced prostate cancer patient since March 2023, aged only 45 now, but veteran of 10 chemo abd currently on generic abiraterone, triplet therapy keeps me in remission till now, see details in my bio.
Hi, I landed in San Antonio texas two weeks back and may stay here for a year for work reason. I am advanced prostate cancer patient since March 2023, aged only 45 now, but veteran of 10 chemo abd currently on generic abiraterone, triplet therapy keeps me in remission till now, see details in my bio.
Soumen79
in
Advanced Prostate Cancer
4 months ago
RA and (periodontitis)gum disease 😱
morning all! So yesterday I went to the dentist because a large filling on a back tooth that I’ve had for many years fell out!when I got there the dentist popped a temporary one in and he did some X-rays he then said I have periodontitis gum disease 😱with bone loss he said to start with I need to have
morning all! So yesterday I went to the dentist because a large filling on a back tooth that I’ve had for many years fell out!when I got there the dentist popped a temporary one in and he did some X-rays he then said I have periodontitis gum disease 😱with bone loss he said to start with I need to have
Mybirthday1975
in
NRAS
8 months ago
Covid
I should have been at a relatives tonight but they phoned to say they’d got covid but thought I’d be ok to visit if I wore a mask. I said I wouldn’t be going, they think I’m being over cautious as “it’s just a cold these days”. I’m on Rux which I’ve been told will make me susceptible to infections.
I should have been at a relatives tonight but they phoned to say they’d got covid but thought I’d be ok to visit if I wore a mask. I said I wouldn’t be going, they think I’m being over cautious as “it’s just a cold these days”. I’m on Rux which I’ve been told will make me susceptible to infections.
lizzziep
in
MPN Voice
9 months ago
Pain management Team
I have been waiting for 4 years to see someone in the pain management clinic at our local hospital. What a complete joke. When are the doctors and so called specialists going to help a patient who is in considerable pain and saying to him I want to cut my foot off. He was a complete waste of time, why
I have been waiting for 4 years to see someone in the pain management clinic at our local hospital. What a complete joke. When are the doctors and so called specialists going to help a patient who is in considerable pain and saying to him I want to cut my foot off. He was a complete waste of time, why
Imagine1
in
Pain Concern
9 months ago
Flu won’t go away.
I was diagnosed four years ago with emphysema. I have had no symptoms. Six weeks ago I got the flu. It’s been a rough six weeks. Getting my breath back and my energy back. Now every morning I can’t breathe and have to use an inhaler. Never had to before. I’ve had a CAT scan of my lungs, and it has not
I was diagnosed four years ago with emphysema. I have had no symptoms. Six weeks ago I got the flu. It’s been a rough six weeks. Getting my breath back and my energy back. Now every morning I can’t breathe and have to use an inhaler. Never had to before. I’ve had a CAT scan of my lungs, and it has not
Rkdevo
in
Lung Conditions Community Forum
6 months ago
Post COVID UC flare - Mezavant probs
Hi I'm new, feeling a bit scared as it's Christmas time and my gastro not back til 8 January. I had COVID mid November, very nauseous and some diahhrea and very soft sticky stool. Mild proctosigmoiditis (low down UC) for 30 years. Been off meds for 20 years until now. Following COVID my bowel symptoms
Hi I'm new, feeling a bit scared as it's Christmas time and my gastro not back til 8 January. I had COVID mid November, very nauseous and some diahhrea and very soft sticky stool. Mild proctosigmoiditis (low down UC) for 30 years. Been off meds for 20 years until now. Following COVID my bowel symptoms
Bunnygirl1
in
Crohn's and Colitis Support
9 months ago
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