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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
Bloodshot eyes
I've accidentally got shampoo in my dry eyes and made them bloodshot I'm really fatigued today and yesterday
I've accidentally got shampoo in my dry eyes and made them bloodshot I'm really fatigued today and yesterday
Oldbloke1
in
PBC Foundation
8 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
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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
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
News on functional cure for chronic Hep B?
May be of interest to those on anti-virals for chronic Hep B https://liverdiseasenews.com/news/gsks-hepatitis-b-candidate-bepirovirsen-wins-fda-fast-track-designation/
May be of interest to those on anti-virals for chronic Hep B https://liverdiseasenews.com/news/gsks-hepatitis-b-candidate-bepirovirsen-wins-fda-fast-track-designation/
Tiger800xrt
in
British Liver Trust
5 months 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
Itraconazole.
is anybody having problems with Itraconazole. I first found I had Aspergillosis after a bout of pneumonia. I went into hospital for a couple of days. I kept telling the Drs I couldn’t breathe first thing in the morning after I returned home. They didn’t really acknowledge it until one morning I passed
is anybody having problems with Itraconazole. I first found I had Aspergillosis after a bout of pneumonia. I went into hospital for a couple of days. I kept telling the Drs I couldn’t breathe first thing in the morning after I returned home. They didn’t really acknowledge it until one morning I passed
Mavary
in
Lung Conditions Community Forum
5 months 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
PID abcess laposcopy adhesiolysis
In November I had severe pelvic pain and back pain and I went to my GP where they said they suspected I had kidney stones. That evening the pain was so severe my Husband called 999 who told him to take me to A&E. There again I was sent home shortly after saying I was fine, and they booked me in for a
In November I had severe pelvic pain and back pain and I went to my GP where they said they suspected I had kidney stones. That evening the pain was so severe my Husband called 999 who told him to take me to A&E. There again I was sent home shortly after saying I was fine, and they booked me in for a
Busy23
in
Pelvic Pain Support Network
5 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
2 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
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
Pain Relief
I have posted before regarding Scleroderma and Raynauds and the problems which relate to this. I have osteoarthritis in my knees and they are so very painful. I was coping with the help of steroid injections, paracetamol and Ibuprofen however steroid injections are now limited with less relief and
I have posted before regarding Scleroderma and Raynauds and the problems which relate to this. I have osteoarthritis in my knees and they are so very painful. I was coping with the help of steroid injections, paracetamol and Ibuprofen however steroid injections are now limited with less relief and
creditcrunchie
in
Scleroderma & Raynaud's UK (SRUK)
2 months 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
Is it back? 🙈
Hi Everyone, Tapered off Pred in Jan24 after being diagnosed with PMR May 18. . I had my routine Rheumie appointment 2 weeks ago which was with a Registrar for the first time. I told him I had increasing neck, shoulders and wrist, hand pain for the past few weeks especially bad upon waking. He told
Hi Everyone, Tapered off Pred in Jan24 after being diagnosed with PMR May 18. . I had my routine Rheumie appointment 2 weeks ago which was with a Registrar for the first time. I told him I had increasing neck, shoulders and wrist, hand pain for the past few weeks especially bad upon waking. He told
Croft9232
in
PMRGCAuk
2 months ago
Covid Vaccination
Good Morning. In 2021 I had Covid my CA125 went down.A fortnight ago I had my Covid Vaccination ,I had a blood test on Wednesday and got the result yesterday My CA125 have gone down 70 .Has any one else experienced this ? Thank you
Good Morning. In 2021 I had Covid my CA125 went down.A fortnight ago I had my Covid Vaccination ,I had a blood test on Wednesday and got the result yesterday My CA125 have gone down 70 .Has any one else experienced this ? Thank you
Inchellon
in
My Ovacome
2 months ago
Covid vaccine or not
A retired cardiologist’s advice is very simple - Covid can kill steroids cannot.
A retired cardiologist’s advice is very simple - Covid can kill steroids cannot.
Porridgeandgrapes
in
PMRGCAuk
2 months ago
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