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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
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
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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
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
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
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
Feeling Frustrated!
Hi everybody, never posted on here but I read every now and again. Soo where to start. We have gone through 1 Live ICSI and Two FET. Live ended in a chemical pregnancy they told me but didn't really explain exactly what it is but it failed neathertheless. Both FET with 2 5day Blastocyst didn't take either
Hi everybody, never posted on here but I read every now and again. Soo where to start. We have gone through 1 Live ICSI and Two FET. Live ended in a chemical pregnancy they told me but didn't really explain exactly what it is but it failed neathertheless. Both FET with 2 5day Blastocyst didn't take either
Janechar10
in
Fertility Network UK
11 months 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
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
Phlegmy covid cough and recovery times
Update: His doctor said that his phlegmy cough was “normal” and wasn’t too concerned. After 18 days he’s finally tested negative for covid and his cough has improved. Thanks everyone for your input! Has anyone had a covid infection with a phlegmy cough? How long did it take to clear it? My one parent
Update: His doctor said that his phlegmy cough was “normal” and wasn’t too concerned. After 18 days he’s finally tested negative for covid and his cough has improved. Thanks everyone for your input! Has anyone had a covid infection with a phlegmy cough? How long did it take to clear it? My one parent
Bebopcoober
in
CLL Support
1 year ago
I think it’s all over 😢
After having a miracle BFP from a natural conception following our first failed round of ICSI I think I’m having a miscarriage and feel so heartbroken. I couldn’t believe it when I tested positive after my period didn’t come - it just seemed too good to be true… and now I think I’m losing it at 5 and
After having a miracle BFP from a natural conception following our first failed round of ICSI I think I’m having a miscarriage and feel so heartbroken. I couldn’t believe it when I tested positive after my period didn’t come - it just seemed too good to be true… and now I think I’m losing it at 5 and
HoneyB11
in
Fertility Network UK
11 months ago
Fatigue
Hi all, I tested positive for Covid on 14th February after carefully avoiding it for almost three years. It has really knocked me out. I work 3days a week and have been unable to return since Covid diagnosis. I am so, so tired and having at least two naps a day. I feel Covid has exacerbated all the existing
Hi all, I tested positive for Covid on 14th February after carefully avoiding it for almost three years. It has really knocked me out. I work 3days a week and have been unable to return since Covid diagnosis. I am so, so tired and having at least two naps a day. I feel Covid has exacerbated all the existing
SanG55
in
PMRGCAuk
1 year ago
Belated thank yous
Thank you everyone for the birthday wishes back in August. It’s been a rough, bumpy road since I had Covid last June (fortunately it was 2 days after returning from Oberammergau to see the Passion Play.) The tour was postponed in 2020, I can’t remember the reason….oh yes, it was Covid! 😆 The illness
Thank you everyone for the birthday wishes back in August. It’s been a rough, bumpy road since I had Covid last June (fortunately it was 2 days after returning from Oberammergau to see the Passion Play.) The tour was postponed in 2020, I can’t remember the reason….oh yes, it was Covid! 😆 The illness
PWilli
in
My MSAA Community
1 year ago
Singulair - Flu Like Symptoms Side Effect
Hey All! A little bit of background on me. Early October I was infected with COVID-19, I’m 4 times vaxxed, and while it was only two days of symptoms, I ended up with SOB on day 3 which later turned into Long COVID. I was prescribed Flovent and Salbutamol by the ER Doctor, my NP then prescribed me Symbicort
Hey All! A little bit of background on me. Early October I was infected with COVID-19, I’m 4 times vaxxed, and while it was only two days of symptoms, I ended up with SOB on day 3 which later turned into Long COVID. I was prescribed Flovent and Salbutamol by the ER Doctor, my NP then prescribed me Symbicort
SandanChitoRyu
in
Asthma Community Forum
1 year ago
DuoStim ivf / icsi
Looking to see if anyone can share their experience of doing DuoStim? Where you do 2 stimulation cycles in one back to back. After egg collection you have a few days off stim then restart towards another collection. I am considering it, my clinic is happy for me to do it (on my request) just unsure
Looking to see if anyone can share their experience of doing DuoStim? Where you do 2 stimulation cycles in one back to back. After egg collection you have a few days off stim then restart towards another collection. I am considering it, my clinic is happy for me to do it (on my request) just unsure
Lotofluckneeded
in
Fertility Network UK
1 year ago
Pseudomonas and carpets?
Does anyone know if Pseudomonas is in carpets? I tore out 2 rooms a few yrs ago and put Laminate in and so glad i did it but still have carpeting in my bedroom and office in my house and wonder if maybe Pseudomonas is in it as I have had 6 courses of Iv antibiotics for colonized Pseudomonas this year
Does anyone know if Pseudomonas is in carpets? I tore out 2 rooms a few yrs ago and put Laminate in and so glad i did it but still have carpeting in my bedroom and office in my house and wonder if maybe Pseudomonas is in it as I have had 6 courses of Iv antibiotics for colonized Pseudomonas this year
Lapis5
in
Lung Conditions Community Forum
1 year ago
Covid
I tested positive for Covid on Thu. 16th March and I have had an email telling me I am "vunerable". I have asthma as well as CLL, on W&W for CLL. I am 80 years old. I did the test and phoned the result through and answered all the questions. I was told someone would contact me. Well, I am still
I tested positive for Covid on Thu. 16th March and I have had an email telling me I am "vunerable". I have asthma as well as CLL, on W&W for CLL. I am 80 years old. I did the test and phoned the result through and answered all the questions. I was told someone would contact me. Well, I am still
Motorman
in
CLL Support
1 year ago
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