Search
Search
About
Log in
Join
Experiences with
Prion infections
Posts
Communities
28,676 public posts
Filter results
Doctors with Long Covid
Just saw the news item this morning about doctors suffering Long Covid. When COVID happened I must say I thought ‘they’ (doctors) must be prepared for anything due to their choice of job. (Perhaps a little uncharitably due to my anger about my own situation at the time). They are presumably exposed
Just saw the news item this morning about doctors suffering Long Covid. When COVID happened I must say I thought ‘they’ (doctors) must be prepared for anything due to their choice of job. (Perhaps a little uncharitably due to my anger about my own situation at the time). They are presumably exposed
arTistapple
in
Thyroid UK
1 year ago
Positive update and jopefully helpful advice/suggestions..💗
Hey guys,I haven't been on here a while, but I've been busy trying new ways to manage and get better (and also had bad anxiety for a while which is the main reason I wasn't here😕) and I wanted to share in hopes that it could help someone else. So last year a had trouble walking, looking at people when
Hey guys,I haven't been on here a while, but I've been busy trying new ways to manage and get better (and also had bad anxiety for a while which is the main reason I wasn't here😕) and I wanted to share in hopes that it could help someone else. So last year a had trouble walking, looking at people when
Turquoisesummer
in
Fibromyalgia Action UK
1 year ago
Methotrexate for the summer
Hi lovely friends, Some of you will recall back in February that I had a flare with rash that my Rheumy, Dr A, didn’t recognise as a Lupus rash. He is still adamant it wasn’t Lupus then but that the progression, which 2 weeks later was confirmed by the Dermatologist as a Lupus rash, was! 🤷🏼♀️
Hi lovely friends, Some of you will recall back in February that I had a flare with rash that my Rheumy, Dr A, didn’t recognise as a Lupus rash. He is still adamant it wasn’t Lupus then but that the progression, which 2 weeks later was confirmed by the Dermatologist as a Lupus rash, was! 🤷🏼♀️
Spotty-ewe
in
LUPUS UK
1 year ago
Want to take advantage of all our features? Just log in!
Log in
or
Join
The way to access COVID-19 treatments has changed
The way to access COVID-19 treatments has changed, and is now different in the different nations of the UK. Check our article to find out what the process is for where you live: https://www.lupusuk.org.uk/accessing-covid-19-treatments/ These changes are particularly important for people in England and
The way to access COVID-19 treatments has changed, and is now different in the different nations of the UK. Check our article to find out what the process is for where you live: https://www.lupusuk.org.uk/accessing-covid-19-treatments/ These changes are particularly important for people in England and
Debbie_kinsey
Administrator
in
LUPUS UK
1 year ago
*Sensitive* A bit of hope for those in need
After 7 years trying to conceive, 3 ICSI cycles, 7 embryo transfers ( including 2 doubles) , 1 MMC and 5 BFN, our baby girl finally arrived in the world on Sunday the 29th October. I just wanted to thank everyone in this forum for making me feel like I wasn't alone in this difficult journey. I don't
After 7 years trying to conceive, 3 ICSI cycles, 7 embryo transfers ( including 2 doubles) , 1 MMC and 5 BFN, our baby girl finally arrived in the world on Sunday the 29th October. I just wanted to thank everyone in this forum for making me feel like I wasn't alone in this difficult journey. I don't
TrendyDove
in
Fertility Network UK
10 months ago
Scared
Hi there, I'm 38 year old active, fit woman. I've been diagnosed with severe cervical stenosis at c6-7 with radiculopathy. Have had symptoms for 20+ years not realising what it was. Then last summer after having an appendectomy and 3 weeks rest, the pain behind left shoulder blade and in neck flared
Hi there, I'm 38 year old active, fit woman. I've been diagnosed with severe cervical stenosis at c6-7 with radiculopathy. Have had symptoms for 20+ years not realising what it was. Then last summer after having an appendectomy and 3 weeks rest, the pain behind left shoulder blade and in neck flared
Rewe
in
Cervical Myelopathy
1 year ago
RLS and Covid vaccine
Just for everyones awareness, my RLS was way worsened by the covid vaccine and so far it seems to have been a permanent side effect. I had RLS since I was a kid but tyically lasted 10 to 30 minutes each night whereas after the vaccine (within days) it shot up to 2 to 3 hours. I wanted to make sure I
Just for everyones awareness, my RLS was way worsened by the covid vaccine and so far it seems to have been a permanent side effect. I had RLS since I was a kid but tyically lasted 10 to 30 minutes each night whereas after the vaccine (within days) it shot up to 2 to 3 hours. I wanted to make sure I
the7thsong
in
Restless Legs Syndrome
1 year ago
Shingles vaccine
Just seen the BBC news health website. Shingles vaccines being offered to over 65’s ( was 70) and, even better, to vulnerable immune suppressed people over 55 from September 2023.
Just seen the BBC news health website. Shingles vaccines being offered to over 65’s ( was 70) and, even better, to vulnerable immune suppressed people over 55 from September 2023.
Amnesiac3637
in
NRAS
1 year ago
Hi all an update on my new rheumy
Hi everybody, yesterday evening I had an appointment with my new Rheumy. I was actually dreading it due to my last experience with the previous rheumatologist. Well I have to say he was brilliant listened to me, Then going on my symptoms and doing an ultrasound on my hands and looking at all my blood
Hi everybody, yesterday evening I had an appointment with my new Rheumy. I was actually dreading it due to my last experience with the previous rheumatologist. Well I have to say he was brilliant listened to me, Then going on my symptoms and doing an ultrasound on my hands and looking at all my blood
Wonderfullifeandmore
in
PMRGCAuk
1 year ago
Rejected for anti virals
Hi everyone I tested positive for Covid on Tuesday and reported it to my GP surgery on Wednesday. I heard from Chelsea and Westminster Hospital on Thursday. They asked about how active my Lupus had been and I told them recently it had been pretty well controlled and they asked how it affected me and
Hi everyone I tested positive for Covid on Tuesday and reported it to my GP surgery on Wednesday. I heard from Chelsea and Westminster Hospital on Thursday. They asked about how active my Lupus had been and I told them recently it had been pretty well controlled and they asked how it affected me and
BookishVibes
in
LUPUS UK
1 year ago
Paxlovid for Covid if you have PMR
hi all. Living in France for 5 months didn’t think I would get Covid here but I did. I think it came with our guests on the plane. But in any case I have Paxlovid with me but I keep seeing things that say don’t take it if you have autoimmune disorder. Is that us? My doctor gave it to me but…. I am down
hi all. Living in France for 5 months didn’t think I would get Covid here but I did. I think it came with our guests on the plane. But in any case I have Paxlovid with me but I keep seeing things that say don’t take it if you have autoimmune disorder. Is that us? My doctor gave it to me but…. I am down
bluegirl7
in
PMRGCAuk
1 year ago
Germantara
I've getting my medical summary from doctors cause as you know I'm doing pip had fantastic advice and would like to thank everyone Well I was looking at it and some I didn't understand so I googled them the copd stage I'm at I'm end stage 3 it said I've got 5 to 8 years to live I thought
I've getting my medical summary from doctors cause as you know I'm doing pip had fantastic advice and would like to thank everyone Well I was looking at it and some I didn't understand so I googled them the copd stage I'm at I'm end stage 3 it said I've got 5 to 8 years to live I thought
Germantara
in
Lung Conditions Community Forum
1 year ago
awful cough before transfer- can I take anything?
Hello everyone, I hope everyone is doing ok on their journey. I have my transfer on Monday morning and have the worst cough I’ve ever had, it’s so chesty and painful. I just wondered if I could take some cough medicine or anything in advance of transfer or if it will affect my lining or chances? I
Hello everyone, I hope everyone is doing ok on their journey. I have my transfer on Monday morning and have the worst cough I’ve ever had, it’s so chesty and painful. I just wondered if I could take some cough medicine or anything in advance of transfer or if it will affect my lining or chances? I
Daisy-Delilah
in
Fertility Network UK
1 year ago
**LAST CALL** Involvement Opportunity - Hepatitis B (UK)
Share your experiences to help researchers improve care for hepatitis B in the UK
Do you live with hepatitis B and want to make the way it is diagnosed, monitored, and treated in the UK better for patients? The British Liver Trust are working with researchers and clinicians to design a research
Share your experiences to help researchers improve care for hepatitis B in the UK
Do you live with hepatitis B and want to make the way it is diagnosed, monitored, and treated in the UK better for patients? The British Liver Trust are working with researchers and clinicians to design a research
BritishLiverTrust1
Partner
in
British Liver Trust
1 year ago
Runny
My nose keeps running and I have to cough to clear throat what can it be?
My nose keeps running and I have to cough to clear throat what can it be?
amberrose2
in
PSP Association
1 year ago
Last do embryo
hey all, I’ve posted here a few times. But we’re on the final leg and I have my last ever frozen transfer next Friday with our last embryo using donor eggs. This is cycle 8, with a twin MMC and endless tests. I showed I had high NKC and had the Alice, era which has shown I need an extra day of drugs
hey all, I’ve posted here a few times. But we’re on the final leg and I have my last ever frozen transfer next Friday with our last embryo using donor eggs. This is cycle 8, with a twin MMC and endless tests. I showed I had high NKC and had the Alice, era which has shown I need an extra day of drugs
Link1234
in
Fertility Network UK
11 months ago
Follow up from my post about cellulitis
Sorry should have said that I am on 10 mg of Pred.
Sorry should have said that I am on 10 mg of Pred.
Dobermanlover
in
PMRGCAuk
1 year ago
CELLULITIS
Has anyone had cellulitis? I have had it for just over a week and have just completed a 7 day course of Flucloxacillin. I did not see a doctor - just had to post a photo of my leg, so haven't had the opportunity of discussing it with him. From the web it sounds quite serious, but don't like taking
Has anyone had cellulitis? I have had it for just over a week and have just completed a 7 day course of Flucloxacillin. I did not see a doctor - just had to post a photo of my leg, so haven't had the opportunity of discussing it with him. From the web it sounds quite serious, but don't like taking
Dobermanlover
in
PMRGCAuk
1 year ago
no. of straws of sperm?
hello, I’m about to try icsi and I’m using donated sperm from EsB or cryos. I appreciate it might be like asking how long is a piece of string but how many straws should I purchase ? Happy to hear your thoughts. Best wishes
hello, I’m about to try icsi and I’m using donated sperm from EsB or cryos. I appreciate it might be like asking how long is a piece of string but how many straws should I purchase ? Happy to hear your thoughts. Best wishes
Babybaby321
in
Fertility Network UK
10 months ago
Change from Nucala to Dupixent
Hello all! I don’t post much but read daily. I have eosinophilic asthma and chronic sinusitis. I’ve been on Nucala for the last 5 years and have been relatively well controlled. After a mild case of covid I developed bronchitis and was treated, but after that, I can’t seem to stop coughing. I have constant
Hello all! I don’t post much but read daily. I have eosinophilic asthma and chronic sinusitis. I’ve been on Nucala for the last 5 years and have been relatively well controlled. After a mild case of covid I developed bronchitis and was treated, but after that, I can’t seem to stop coughing. I have constant
kdr112
in
Asthma Community Forum
1 year ago
1
...
98
99
100
Next page
50
60
70
80
90
100
Filter results
Clear filters
Posted in
All communities
Lung Conditions Community Forum
2951 results
Fertility Network UK
2841 results
NRAS
2363 results
View top 10 communities
Sort by
Most Relevant
Newest