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Mental health?
I developed EPI after having Covid. In August of 2021. My fist attempt at eating after my fever broke sent my to the emergency room with sever pain. At the time they suspected pancreatitis, but because I was still recovering from covid they ran other tests, told me I had covid pneumonia and sent me home
I developed EPI after having Covid. In August of 2021. My fist attempt at eating after my fever broke sent my to the emergency room with sever pain. At the time they suspected pancreatitis, but because I was still recovering from covid they ran other tests, told me I had covid pneumonia and sent me home
Ethelknows
in
Chronic Pancreatitis Support
28 days ago
Covid and lung cancer
My husband has Covid and so far I'm not showing any symptoms, but I'm concerned about how it might affect someone with lung cancer. Any advice welcome. I'm being very careful, wearing a mask My husband is banished to the upstairs TV or the other end of the garden to avoid contact ! I've never
My husband has Covid and so far I'm not showing any symptoms, but I'm concerned about how it might affect someone with lung cancer. Any advice welcome. I'm being very careful, wearing a mask My husband is banished to the upstairs TV or the other end of the garden to avoid contact ! I've never
Gingergus
in
The Roy Castle Lung Cancer Foundation
29 days ago
New here looking for some help!
Hi all. I’ve just found this forum as I’ve been lokkkng for help for quite some time. I’ve had the weirdest thing happen…… Bit of a back story first…..I never had asthma my entire life. Until I got COVID for the first time in August 2021. I was considered high risk as it was as I also have rheumatoid
Hi all. I’ve just found this forum as I’ve been lokkkng for help for quite some time. I’ve had the weirdest thing happen…… Bit of a back story first…..I never had asthma my entire life. Until I got COVID for the first time in August 2021. I was considered high risk as it was as I also have rheumatoid
Gonewiththewindddddd
in
Asthma Community Forum
29 days ago
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Good news/bad news
hi all. The nurse rang last week to say that my liver results had improved somewhat but were still outside normal range. Because I have such active disease she didn’t want to leave me with no meds at all, so we decided to restart the leflunomide and see how the blood results go in two week, then make
hi all. The nurse rang last week to say that my liver results had improved somewhat but were still outside normal range. Because I have such active disease she didn’t want to leave me with no meds at all, so we decided to restart the leflunomide and see how the blood results go in two week, then make
HeadInASpin
in
NRAS
1 month ago
Post covid oxygen levels.
Hi, I have recently had covid which left me with a dreadful COPD exacerbation. I was given anti virals and taken rescue pack followed by another course of Doxycycline. Although I feel a lot better my oxygen levels have dropped dreadfully. I am prescribed ambulatory oxygen but am finding I am using it
Hi, I have recently had covid which left me with a dreadful COPD exacerbation. I was given anti virals and taken rescue pack followed by another course of Doxycycline. Although I feel a lot better my oxygen levels have dropped dreadfully. I am prescribed ambulatory oxygen but am finding I am using it
Maggity
in
Lung Conditions Community Forum
1 month ago
Dreaded Covid
Having started with a bad cold last week after having a gastroscope, at my local hospital, I didn’t think too much about it at first, eventually went to doctors said it was a virus and chest was clear just drink plenty fluids, then my daughter thought best check covid and it was positive, can’t hear
Having started with a bad cold last week after having a gastroscope, at my local hospital, I didn’t think too much about it at first, eventually went to doctors said it was a virus and chest was clear just drink plenty fluids, then my daughter thought best check covid and it was positive, can’t hear
Alibongo60
in
Headway
1 month ago
clonazepam lethargy
has anyone experienced extreme fatigue since taking Clonazepam. My husband has been taking this now for around 10 days. He seems to be sleeping better at night but extremely tired during the day and i think this might be impacting his ability to walk as he can barely stand up without falling backwards
has anyone experienced extreme fatigue since taking Clonazepam. My husband has been taking this now for around 10 days. He seems to be sleeping better at night but extremely tired during the day and i think this might be impacting his ability to walk as he can barely stand up without falling backwards
Licquoricelover
in
PSP Association
1 month ago
MSK Community Care
Hello All Just had my latest check up at the Hospital. After a terrible flare about a year and a half ago, which took ages to get under control, Sulfa was finally added to my Mthx and has really been a game changer. I have also been lucky enough to have an absolutely amazing Rheumatologist and I have
Hello All Just had my latest check up at the Hospital. After a terrible flare about a year and a half ago, which took ages to get under control, Sulfa was finally added to my Mthx and has really been a game changer. I have also been lucky enough to have an absolutely amazing Rheumatologist and I have
Chockyuk
in
NRAS
2 months ago
covid related?
does anyone feel ike the tinnitus started after covid? Just interested in any links, I’ve recently had a bad virus not tested for covid but it was quite nasty and I’m wondering if that’s why my tinnitus is worse
does anyone feel ike the tinnitus started after covid? Just interested in any links, I’ve recently had a bad virus not tested for covid but it was quite nasty and I’m wondering if that’s why my tinnitus is worse
Retailgirl
in
Tinnitus UK
1 month ago
I’m Back
it has been quite a while since I have been on this message board, life just happens as we all know with Lupus. Many changes have occurred from multifocal, pneumonia, aspergillus in my lung and tumor in my lung upper right lobe… however, it is benign right now and they’re just going to watch it. I
it has been quite a while since I have been on this message board, life just happens as we all know with Lupus. Many changes have occurred from multifocal, pneumonia, aspergillus in my lung and tumor in my lung upper right lobe… however, it is benign right now and they’re just going to watch it. I
SunflowerYiayia
in
LUPUS UK
5 months ago
How do you get diagnosed on the NHS
Hello all. I've just joined this forum and have a bit of a perplexing question. For years I've suffered from food intolerances and mild allergies. I have had (and still have) various autoimmune issues. Post Covid in 2020, I developed hay fever along with an increasing number of food intolerances qand
Hello all. I've just joined this forum and have a bit of a perplexing question. For years I've suffered from food intolerances and mild allergies. I have had (and still have) various autoimmune issues. Post Covid in 2020, I developed hay fever along with an increasing number of food intolerances qand
Treetop33
in
The UK Mastocytosis Support Group
1 month ago
Covid, covid test and tapering
Very slow tapering (DL style and working well) currently at 5mg prednisolone. Just into my 3rd year PMR diagnosis, when I contracted covid. Staying put at 5 mg now. PMR bouts of fatigue and sleepiness much worse this time though just starting to improve a little. not the case on my previous covid infection
Very slow tapering (DL style and working well) currently at 5mg prednisolone. Just into my 3rd year PMR diagnosis, when I contracted covid. Staying put at 5 mg now. PMR bouts of fatigue and sleepiness much worse this time though just starting to improve a little. not the case on my previous covid infection
waltztherapy
in
PMRGCAuk
1 month ago
psoriasis flair and adalimumab
hi all, I am looking for some advice. I had severe psoriasis which was almost gone thanks to adalimumab. I saw my dermatology team back in April for my 6 monthly check where my psoriasis was flairing up. so I had an adalimumab blood test to see if it was meant to work. I got the results back a
hi all, I am looking for some advice. I had severe psoriasis which was almost gone thanks to adalimumab. I saw my dermatology team back in April for my 6 monthly check where my psoriasis was flairing up. so I had an adalimumab blood test to see if it was meant to work. I got the results back a
katienewland
in
Beyond Psoriasis
1 month ago
Experience of Covid Vaccines and Adrenals
I know the covid vaccines are a hot topic here. I don’t know if mum’s experience is helpful to share. Last years jabs were both a nightmare - led to weakness, temperature, light headedness loss of mobility and a significant down step in her dementia. Despite being a real advocate for the jabs I was
I know the covid vaccines are a hot topic here. I don’t know if mum’s experience is helpful to share. Last years jabs were both a nightmare - led to weakness, temperature, light headedness loss of mobility and a significant down step in her dementia. Despite being a real advocate for the jabs I was
RT18
in
PMRGCAuk
1 month ago
Fibro fog or long Covid?
hi 👋 Hope you’re all doing as well as u can has anyone had both Fibro fog and long covid? I don’t know which is affecting me I have more issues with word finding and when speaking and writing how long does it last goes then affects me random I had issues trying to read consultants pain score thing
hi 👋 Hope you’re all doing as well as u can has anyone had both Fibro fog and long covid? I don’t know which is affecting me I have more issues with word finding and when speaking and writing how long does it last goes then affects me random I had issues trying to read consultants pain score thing
Geeforce99
in
LUPUS UK
1 month ago
Struggling with antibiotics on chemo
Hi all, following chemo last week I then started with cellulitis infection in my leg. I began taking co-amoxiclav antibiotics but found i couldn’t take them orally due to sickness. On Saturday ended up in a &e having injectable antibiotics. They sent me home with the same pills and told me to take
Hi all, following chemo last week I then started with cellulitis infection in my leg. I began taking co-amoxiclav antibiotics but found i couldn’t take them orally due to sickness. On Saturday ended up in a &e having injectable antibiotics. They sent me home with the same pills and told me to take
Lyndy
in
My Ovacome
5 months ago
Maybe not PMR update 5 years on
Good morning after 5 years next month on steroids with a PMR diagnosis I am headed down a different treatment path. I spoke to a musculoskeletal specialist in UK who questioned if I had ever had PMR due to my original diagnosis blood test showing a CRP result of 6 and an ESR of 1, whilst acknowledging
Good morning after 5 years next month on steroids with a PMR diagnosis I am headed down a different treatment path. I spoke to a musculoskeletal specialist in UK who questioned if I had ever had PMR due to my original diagnosis blood test showing a CRP result of 6 and an ESR of 1, whilst acknowledging
Pawscat11
in
PMRGCAuk
2 months ago
Running with angina
prior to contracting Covid in April 23 I was very fit and regularly ran up mountains and 2/3 hour runs was my usual at least once a week plus some kind of activity every day.With COVID I developed chest tightness and breathlessness, particularly worse on exertion. I repeatedly said that it felt like
prior to contracting Covid in April 23 I was very fit and regularly ran up mountains and 2/3 hour runs was my usual at least once a week plus some kind of activity every day.With COVID I developed chest tightness and breathlessness, particularly worse on exertion. I repeatedly said that it felt like
Ayecan
in
British Heart Foundation
1 month ago
When on a weekly dose of Pegasys is it ok to occasionally alter the day you inject?
Hi everyone, I’m about to try Pegasys in a few weeks time on a weekly dose of 45. If I get any unpleasant side effects I wondered if occasionally it’s ok to put back the usual day of injecting by 24 hours if I had something special on the day of the injection. I forgot to ask my haematologist at my appointment
Hi everyone, I’m about to try Pegasys in a few weeks time on a weekly dose of 45. If I get any unpleasant side effects I wondered if occasionally it’s ok to put back the usual day of injecting by 24 hours if I had something special on the day of the injection. I forgot to ask my haematologist at my appointment
Na56
in
MPN Voice
5 months ago
Follow up to initial appt
Hi all, I had my initial appt with rheumatologist 19th April, who diagnosed seronegative inflammatory arthritis. He gave me a steroid injection, which does seem to have lessened the swelling a bit, but still stiff and in pain. But I have yet to receive a follow up letter summarising the appt and findings
Hi all, I had my initial appt with rheumatologist 19th April, who diagnosed seronegative inflammatory arthritis. He gave me a steroid injection, which does seem to have lessened the swelling a bit, but still stiff and in pain. But I have yet to receive a follow up letter summarising the appt and findings
hazelcats
in
NRAS
2 months ago
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