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W8r3 developed a dry cough?
been enjoying my runs and really proud to reach 28 minutes running ! never been able to run ( well jog) before due to knee problems but yep am there! this week though I seem to have a very dry throat and tickly cough? I’ve been running on the treadmill- gym is air conditioned- and the dry tickly throat
been enjoying my runs and really proud to reach 28 minutes running ! never been able to run ( well jog) before due to knee problems but yep am there! this week though I seem to have a very dry throat and tickly cough? I’ve been running on the treadmill- gym is air conditioned- and the dry tickly throat
JoggingAnnie4
in
Couch to 5K
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
Rash .
Hi I'm just looking for a bit of advice . I'm having a flare right now due to not being on my Biological drug since having an operation on my foot again . However this time seems longer and the flare is much more intense . Been up to see Rheumatology the Dr didn't know me didn't examine me even though
Hi I'm just looking for a bit of advice . I'm having a flare right now due to not being on my Biological drug since having an operation on my foot again . However this time seems longer and the flare is much more intense . Been up to see Rheumatology the Dr didn't know me didn't examine me even though
Weemillie
in
NRAS
1 year ago
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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
Not sure what to expect?
Hi all I’ve managed to get an appointment with the Rheumy nurse today f2f. I started on Sulfasalazine just over 2 years ago, I was slow to improve and had steroid injections to help along the way. I changed trusts after one year due to lack of appointments and just general mayhem prompted by my GP.
Hi all I’ve managed to get an appointment with the Rheumy nurse today f2f. I started on Sulfasalazine just over 2 years ago, I was slow to improve and had steroid injections to help along the way. I changed trusts after one year due to lack of appointments and just general mayhem prompted by my GP.
Akaka
in
NRAS
1 year 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
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
Neck and calf mussles pain
I am suffering from neck and calf muscles pain from past Couple of years. Taking neuro medicine like Pregabanyl M but still suffering from pain. I cannot turn head left side fully due to pain. Can not walk due muscles sprain in one leg. Any advice. I got treatment from psychiatrist . Any good advise
I am suffering from neck and calf muscles pain from past Couple of years. Taking neuro medicine like Pregabanyl M but still suffering from pain. I cannot turn head left side fully due to pain. Can not walk due muscles sprain in one leg. Any advice. I got treatment from psychiatrist . Any good advise
Mohannandigana1952
in
Diabetes India
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
constant pain following hypoxia BI after cardiac arrest
hello all , looking for advice - my husband has a brain injury following cardiac arrest last spring. He has moderate impairment. He is home and slowly improving. But - He is suffering from constant pain in shoulders, arms and his armpits. We have tried everything- pain killers don’t touch it, heat/
hello all , looking for advice - my husband has a brain injury following cardiac arrest last spring. He has moderate impairment. He is home and slowly improving. But - He is suffering from constant pain in shoulders, arms and his armpits. We have tried everything- pain killers don’t touch it, heat/
Weloveajigsaw
in
Headway
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
chilblain damage to finger nails?
Hi folks, I wonder if anyone else has had the same problem. I had chilblains on 3 fingers, next to the finger nail base. 3 or 4 weeks later the skin has healed but the half moons are red and tender and the skin has retracted from the nail base so it looks as if the nail might come away. I can't
Hi folks, I wonder if anyone else has had the same problem. I had chilblains on 3 fingers, next to the finger nail base. 3 or 4 weeks later the skin has healed but the half moons are red and tender and the skin has retracted from the nail base so it looks as if the nail might come away. I can't
redmaggie
in
Scleroderma & Raynaud's UK (SRUK)
1 year ago
Interferon-Alpha 2-a and Its Dual Effect in Treating Two Diseases (Hepatitis C and Polycythemia Vera)
»Here, we report a 56-years-old male patient with hepatitis C virus infection and PV, who was treated with IFN for his chronic hepatitis C, which resulted in significant improvement of HB as well as normalization of his bone marrow and eradication of the clone (Jak2V617F). …The patient received pegylated
»Here, we report a 56-years-old male patient with hepatitis C virus infection and PV, who was treated with IFN for his chronic hepatitis C, which resulted in significant improvement of HB as well as normalization of his bone marrow and eradication of the clone (Jak2V617F). …The patient received pegylated
Manouche
in
MPN Voice
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
Going down down down
I won’t bore anyone with the full length story, as so many suffering from Lyme disease and related secondary conditions have been through similar experiences however I’ll just give you a quick overview so perhaps you can give me some advice and I’d particularly love to hear from anyone in the UK (or
I won’t bore anyone with the full length story, as so many suffering from Lyme disease and related secondary conditions have been through similar experiences however I’ll just give you a quick overview so perhaps you can give me some advice and I’d particularly love to hear from anyone in the UK (or
Elenaleeuk
in
Living with Lyme Disease UK
1 year ago
Syphilis recovery / retesting question
hello! I have recently received a reactive result for syphilis, and was given the one shot of penicillin treatment. I work on a cruise ship, and so regular testing is not available sadly, and the doctor said I won’t be retested for another 3 months… this is driving me mad as my symptoms have calmed
hello! I have recently received a reactive result for syphilis, and was given the one shot of penicillin treatment. I work on a cruise ship, and so regular testing is not available sadly, and the doctor said I won’t be retested for another 3 months… this is driving me mad as my symptoms have calmed
Lostatsea04
in
BASHH
1 year ago
Covid 19 has it worsen your ME/CFS symptoms?
Good morning all! I was wondering if any of you caught Covid 19 that made their ME symptoms worse. The reason I ask is that I am pretty much still "terrified" not to wear a mask and to travel just in case I get covid. I discussed with my GP they advice the as my mom lives in a sunny place I should go
Good morning all! I was wondering if any of you caught Covid 19 that made their ME symptoms worse. The reason I ask is that I am pretty much still "terrified" not to wear a mask and to travel just in case I get covid. I discussed with my GP they advice the as my mom lives in a sunny place I should go
theia
in
Myalgic Encephalomyelitis Community
1 year ago
Covid/PMR Questions
My husband just tested positive for Covid. My doctor had warned me that because of the prednisone, I needed to contact her if I had exposure to or showed symptoms of Covid or any other bug. My recollection is that she said if I got sick, she would increase my dose of prednisone since my own immune system
My husband just tested positive for Covid. My doctor had warned me that because of the prednisone, I needed to contact her if I had exposure to or showed symptoms of Covid or any other bug. My recollection is that she said if I got sick, she would increase my dose of prednisone since my own immune system
Donna5658
in
PMRGCAuk
1 year ago
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