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GPA flare, is it likely even if I only have 1 symptom
I was diagnosed with GPA in 2017, I have had 3 flares since initial diagnosis and although the symptoms have got milder each time, I always have the same symptoms - pain and loss of hearing in my ear, discomfort and blood in my nose, pain and stiffness in my finger joints and extreme fatigue. I regularly
I was diagnosed with GPA in 2017, I have had 3 flares since initial diagnosis and although the symptoms have got milder each time, I always have the same symptoms - pain and loss of hearing in my ear, discomfort and blood in my nose, pain and stiffness in my finger joints and extreme fatigue. I regularly
stuc
in
Vasculitis UK
6 months ago
enlarged sore breasts
hi - rather embarrassing but here goes! Approximately 2 weeks ago I had to increase levothyroxine to 100 mcgs- breasts are now enlarged and sore. I can’t be pregnant- I happen to of had routine breast scan just prior to meds increase and no abnormalities detected. Has anyone else experienced this
hi - rather embarrassing but here goes! Approximately 2 weeks ago I had to increase levothyroxine to 100 mcgs- breasts are now enlarged and sore. I can’t be pregnant- I happen to of had routine breast scan just prior to meds increase and no abnormalities detected. Has anyone else experienced this
Purplepuffin
in
Thyroid UK
6 months ago
Nicotine Patch helps immensely.
For the last week, I’ve been wearing a 7mg nicotine patch with amazing results. Almost every night since I’ve slept through the night. My symptoms have improved, I have a much better sense of wellbeing. Nicotine has been known for years for its medicinal properties. Eggplant has the second most nicotine
For the last week, I’ve been wearing a 7mg nicotine patch with amazing results. Almost every night since I’ve slept through the night. My symptoms have improved, I have a much better sense of wellbeing. Nicotine has been known for years for its medicinal properties. Eggplant has the second most nicotine
38yroldmale
in
Cure Parkinson's
4 months ago
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first orthotics
disappointed. The podiatrist hardly looked at the foot and spent most of the appointment typing then without any measurements or gait test said he’s ordered me a pair that would arrive by post in the fullness of time. I suspect these will be no better than the well known brand I ordered online and
disappointed. The podiatrist hardly looked at the foot and spent most of the appointment typing then without any measurements or gait test said he’s ordered me a pair that would arrive by post in the fullness of time. I suspect these will be no better than the well known brand I ordered online and
Stills
in
NRAS
4 months ago
cellulitis
Hello, Has anyone had cellulitis? I have had it for just over a week. I have just completed a 2 day course of Ciprobay 500 and it didn’t work then I had a 2 day of Meronam 1gm tds by injection and I can tell it works good. Now, I need your advice if I can travel for a week with my oral antibiotic Augmentin
Hello, Has anyone had cellulitis? I have had it for just over a week. I have just completed a 2 day course of Ciprobay 500 and it didn’t work then I had a 2 day of Meronam 1gm tds by injection and I can tell it works good. Now, I need your advice if I can travel for a week with my oral antibiotic Augmentin
ANA4
in
CLL Support
6 months ago
Asthma and work .
Hi all , Just wondering if anyone else has been in the same position and if so what they did . I have been in job now for five years, they knew I had asthma when I started and it can have very badly behaved periods , like recently when i had to take two rescue packs of prednisolone 5mg for 5 days
Hi all , Just wondering if anyone else has been in the same position and if so what they did . I have been in job now for five years, they knew I had asthma when I started and it can have very badly behaved periods , like recently when i had to take two rescue packs of prednisolone 5mg for 5 days
Jazz70
in
Asthma Community Forum
4 months ago
How effective is fenofibrate for itch?
My doctor suggested a few different drugs, like rifampricin, naltrexone, and fenofibrate for my itch. He prescribed fenofibrate as he thinks it works best. Does anyone here take it and if so, has it helped? I'm worried about the warnings it comes with about severe liver damage.
My doctor suggested a few different drugs, like rifampricin, naltrexone, and fenofibrate for my itch. He prescribed fenofibrate as he thinks it works best. Does anyone here take it and if so, has it helped? I'm worried about the warnings it comes with about severe liver damage.
Carly92
in
PBC Foundation
6 months ago
I had a medical crisis, I didn't die, I wonder why
Last summer I had a medical emergency. The odds were it would kill me but I survived with few life threatening consequences. The problems I had are commonly fatal for 80 year old men. There is a message in my experience which I hope to share with you in this article. It is a bit longer than most
Last summer I had a medical emergency. The odds were it would kill me but I survived with few life threatening consequences. The problems I had are commonly fatal for 80 year old men. There is a message in my experience which I hope to share with you in this article. It is a bit longer than most
nash2
Partner
in
Living with Fatty Liver and NASH
4 months ago
COPD and Pneumonia
Hello. My mom has severe COPD and got out of the hospital last week after a 3 week stay for pneumonia. She’s had COPD for 16 years and just went on O2 about a year ago. She’s always done well with the COPD and never had an exacerbation until the pneumonia. I know it can take a very long time for the
Hello. My mom has severe COPD and got out of the hospital last week after a 3 week stay for pneumonia. She’s had COPD for 16 years and just went on O2 about a year ago. She’s always done well with the COPD and never had an exacerbation until the pneumonia. I know it can take a very long time for the
nyla668
in
Lung Conditions Community Forum
2 months ago
Potential new treatment for osteoarthritis
https://www.news-medical.net/news/20240221/Nose-cartilage-based-knee-joint-treatment-project-receives-e282ac23-million-funding.aspx?utm_source=news_medical_newsletter&utm_medium=email&utm_campaign=rheumatology_newsletter_23_february_2024 I thought people might be interested in this - not directly PMR
https://www.news-medical.net/news/20240221/Nose-cartilage-based-knee-joint-treatment-project-receives-e282ac23-million-funding.aspx?utm_source=news_medical_newsletter&utm_medium=email&utm_campaign=rheumatology_newsletter_23_february_2024 I thought people might be interested in this - not directly PMR
PMRpro
Ambassador
in
PMRGCAuk
4 months ago
Heavy cold
Apologies if this seems quite trivial but I have had a heavy cold for the past 2/3 days which at present is getting worse. Have tested negative for Covid so no concerns about that so I’m just wondering whether to miss my medication tomorrow or whether it won’t make any difference. I take 20mg MTX but
Apologies if this seems quite trivial but I have had a heavy cold for the past 2/3 days which at present is getting worse. Have tested negative for Covid so no concerns about that so I’m just wondering whether to miss my medication tomorrow or whether it won’t make any difference. I take 20mg MTX but
Hightower62
in
NRAS
4 months ago
coughing and mucus for 3 months after Covid
chest cracked and lots of mucus since October I did have Covid but still bad
chest cracked and lots of mucus since October I did have Covid but still bad
Redrum46
in
Lung Conditions Community Forum
4 months ago
dengue fever vaccinate or not?
I started off on 15mg Pred in October and am now down to 10mg. I am off to India (Rajasthan) in February and dengue fever vaccine has been suggested. As it is a live vaccine I am not sure whether having the vaccine is worth the risk of contracting dengue. Any advice? Also big thanks to the community
I started off on 15mg Pred in October and am now down to 10mg. I am off to India (Rajasthan) in February and dengue fever vaccine has been suggested. As it is a live vaccine I am not sure whether having the vaccine is worth the risk of contracting dengue. Any advice? Also big thanks to the community
Hb22
in
PMRGCAuk
6 months ago
Philip
I got covid and went to hospital. They said I have severe heart failure. Since leaving hospital my pro bnp level has dropped significantly. I think the covid caused the heart failure. Anyone hear of that happening?
I got covid and went to hospital. They said I have severe heart failure. Since leaving hospital my pro bnp level has dropped significantly. I think the covid caused the heart failure. Anyone hear of that happening?
Kiwiphil
in
British Heart Foundation
4 months ago
Help please!
Goodmorning, I was first diagnosed with PMR back in 2014, usual treatment with pred, taper etc. Then diagnosed in 2021 with Fibromyalgia aand on 2mg maintenance dose of pred & 60mg Duloxetine plus Co codamol as needed. Then last month caught Covid for first time. Have had all vaccines. It really hit
Goodmorning, I was first diagnosed with PMR back in 2014, usual treatment with pred, taper etc. Then diagnosed in 2021 with Fibromyalgia aand on 2mg maintenance dose of pred & 60mg Duloxetine plus Co codamol as needed. Then last month caught Covid for first time. Have had all vaccines. It really hit
September17
in
PMRGCAuk
4 months ago
9 months away from running due to injury, but now able to start the programme again!
I completed the programme a few years ago, but have not run for 9 months due to injury. I have had a suspected stress fracture ( wasn’t in the end!), bilateral plantar fasciitis and peroneal tendonitis . I have had shock wave therapy, steroid injections and lots and lots of physio! However, today my
I completed the programme a few years ago, but have not run for 9 months due to injury. I have had a suspected stress fracture ( wasn’t in the end!), bilateral plantar fasciitis and peroneal tendonitis . I have had shock wave therapy, steroid injections and lots and lots of physio! However, today my
Dansac29
Graduate
in
Couch to 5K
4 months ago
New to here
I have had tinnitus for a couple of years now. It started, I believe, with a bout of COVID. I had COVID for the 3rd time in October 2023 and the tinnitus has and is continuing to get worse. It's constant buzzing sound with clicking noises and now earache.
I have had tinnitus for a couple of years now. It started, I believe, with a bout of COVID. I had COVID for the 3rd time in October 2023 and the tinnitus has and is continuing to get worse. It's constant buzzing sound with clicking noises and now earache.
Butbuts
in
Tinnitus UK
4 months ago
Steroid injection in the Bum
Hi , I had a steroid shot as I have rheumatoid Arthrits which I've had for 14 years But 2 days ago I had the steroid shot in my bottom I've had them before but that was maybe 8 years ago .2 days later I'm in pain again ..I can't remember if this is normal .
Hi , I had a steroid shot as I have rheumatoid Arthrits which I've had for 14 years But 2 days ago I had the steroid shot in my bottom I've had them before but that was maybe 8 years ago .2 days later I'm in pain again ..I can't remember if this is normal .
Trishfrog1
in
NRAS
4 months ago
Covid rebound
Hello I’ve just tested positive for Covid again, just finished a curse of Plaxoid Sunday gone. I took a test on the Tuesday it was clear. Still felt fatigued so today I felt shivery took another test and it’s positive 😭 I’m eating for a call back from my Doctor . I have heard it can come back after
Hello I’ve just tested positive for Covid again, just finished a curse of Plaxoid Sunday gone. I took a test on the Tuesday it was clear. Still felt fatigued so today I felt shivery took another test and it’s positive 😭 I’m eating for a call back from my Doctor . I have heard it can come back after
Pekingese
in
CLL Support
4 months ago
Tired Tavern - Discord community for people with CFS/ME and/or Long Covid (PACS)
Hi guys, Tired Tavern is community server for people with CFS/ME and/or Long Covid (PACS). We currently have over 350+ members since starting last December. It's a community where empathy, understanding and shared experiences thrive. We have discussions, support groups as well as community events like
Hi guys, Tired Tavern is community server for people with CFS/ME and/or Long Covid (PACS). We currently have over 350+ members since starting last December. It's a community where empathy, understanding and shared experiences thrive. We have discussions, support groups as well as community events like
TiredTavern
in
Myalgic Encephalomyelitis Community
4 months ago
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