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Infective conjunctivitis
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ZERO TASTE AFTER PAXLOVID COVID
I had Covid back in September 2022. I am pretty healthy at 71 and had my shots. First time to get it and it was pretty intense. I was given Paxlovid and afte 2 weeks I felt better however my taste was zero with little smell. I went through the holdups with no taste and come March I got it again out in
I had Covid back in September 2022. I am pretty healthy at 71 and had my shots. First time to get it and it was pretty intense. I was given Paxlovid and afte 2 weeks I felt better however my taste was zero with little smell. I went through the holdups with no taste and come March I got it again out in
oznaf
in
Acid Reflux Support
1 year ago
Duration of a first NHS Endocrinologist Appointment
Is a first, initial NHS Endocrinology appointment for hypothyroidism, which appears to be possible central hypo, genetic and suggestive of a pituitary tumour of 30 minutes duration, then thrown out regardless of time required to discuss the problem? G.P. appointments are 10 mins. maximum. Are hospital
Is a first, initial NHS Endocrinology appointment for hypothyroidism, which appears to be possible central hypo, genetic and suggestive of a pituitary tumour of 30 minutes duration, then thrown out regardless of time required to discuss the problem? G.P. appointments are 10 mins. maximum. Are hospital
Wua13262348
in
Thyroid UK
1 year ago
Internal tremble - frequency and cause
Since having covid in 2020 there are times when I suddenly feel trembly inside. I feel less steady, movement and sensation can be affected slightly. Nobody would notice but I don't feel right. This happens after being very busy, more stressful times (eg, being in a meeting) or having to be out in the
Since having covid in 2020 there are times when I suddenly feel trembly inside. I feel less steady, movement and sensation can be affected slightly. Nobody would notice but I don't feel right. This happens after being very busy, more stressful times (eg, being in a meeting) or having to be out in the
StriatedCaracara
in
LUPUS UK
1 year ago
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Covid jab and return of PMR symptoms
I had successfully reduced to 3mg after a year of taking pred. A week after having the covid jab as I was supposedly vulnerable my PMR symptoms are bad again. Neck ,shoulders and buttock pains as before. Have gone upto 5mg for the past four days on GPs recommendation but no relief . Had blood test
I had successfully reduced to 3mg after a year of taking pred. A week after having the covid jab as I was supposedly vulnerable my PMR symptoms are bad again. Neck ,shoulders and buttock pains as before. Have gone upto 5mg for the past four days on GPs recommendation but no relief . Had blood test
simps999
in
PMRGCAuk
1 year ago
bronchiectasis, asthma and long covid
Hi, I’m about 3 months into my bronchiectasis journey since my diagnosis earlier this year. My 3 month azithromycin trial went well and is now on my repeat prescription list (with it feels like a million other things ) I went for assessment for pulmonary rehab and the physio decided I’m too affected
Hi, I’m about 3 months into my bronchiectasis journey since my diagnosis earlier this year. My 3 month azithromycin trial went well and is now on my repeat prescription list (with it feels like a million other things ) I went for assessment for pulmonary rehab and the physio decided I’m too affected
Emily-G
in
Lung Conditions Community Forum
1 year ago
Bronchiectasis and long covid
Hi, I’m about 3 months into my bronchiectasis journey since my diagnosis earlier this year. My 3 month azithromycin trial went well and is now on my repeat prescription list (with it feels like a million other things ) I went for assessment for pulmonary rehab and the physio decided I’m too affected
Hi, I’m about 3 months into my bronchiectasis journey since my diagnosis earlier this year. My 3 month azithromycin trial went well and is now on my repeat prescription list (with it feels like a million other things ) I went for assessment for pulmonary rehab and the physio decided I’m too affected
Emily-G
in
Bronchiectasis Support
1 year ago
Official Statistics Liver disease profiles, July 2023 update - published 4 July 2023
For those of you who may be interested, the latest liver disease profiles for England were released this morning at 9:30 am, by the Office for Health Improvement & Disparities. It will come as no surprise to find that liver disease has increased exponentially. These latest set of figures incorporate
For those of you who may be interested, the latest liver disease profiles for England were released this morning at 9:30 am, by the Office for Health Improvement & Disparities. It will come as no surprise to find that liver disease has increased exponentially. These latest set of figures incorporate
Richard-Allen
in
British Liver Trust
1 year ago
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
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
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
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
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
Flare and due COVID jab Friday
Hi all. I hope you are all well or as well as can be. 🙂 I'm booked for my spring COVID booster tomorrow but I'm starting to flare, sore hands and shoulders etc and they are starting me on hydroxychloroquine next week as well as the 3g if sulfasalazine I'm already on. Have any of you had the jab whilst
Hi all. I hope you are all well or as well as can be. 🙂 I'm booked for my spring COVID booster tomorrow but I'm starting to flare, sore hands and shoulders etc and they are starting me on hydroxychloroquine next week as well as the 3g if sulfasalazine I'm already on. Have any of you had the jab whilst
Haz58
in
NRAS
1 year ago
Long awaited/ Neglected review
Hello,, My name is Cat, I had a heart attack in 2018. I was put on the Gold standard medications, after having two stents fitted to my LAD. I had my cardiac rehabilitation and later reviewed . I was given the all clear. I started working full time again and then covid hit. Everything was okay until
Hello,, My name is Cat, I had a heart attack in 2018. I was put on the Gold standard medications, after having two stents fitted to my LAD. I had my cardiac rehabilitation and later reviewed . I was given the all clear. I started working full time again and then covid hit. Everything was okay until
Katydl
in
British Heart Foundation
1 year ago
New job
Good morning fellow Lupies! I was hoping for some opinions please. I recently accepted a new 12 week temp job (with the possibility to go perm later) and was due to start tomorrow. However, I started feeling unwell yesterday and woke up feeling worse and with a temperature and tested positive for Covid
Good morning fellow Lupies! I was hoping for some opinions please. I recently accepted a new 12 week temp job (with the possibility to go perm later) and was due to start tomorrow. However, I started feeling unwell yesterday and woke up feeling worse and with a temperature and tested positive for Covid
BookishVibes
in
LUPUS UK
1 year ago
Feeling safe in public after transplant
Hi all, I’m 3 1/2 months out from transplant. My husband and I have been isolating since COVID-19 with a few instances of freedom with a few road trips when cases were down And we did attend a wedding that was mostly outside and everyone had to test for Covid. My husband did have to attend a business
Hi all, I’m 3 1/2 months out from transplant. My husband and I have been isolating since COVID-19 with a few instances of freedom with a few road trips when cases were down And we did attend a wedding that was mostly outside and everyone had to test for Covid. My husband did have to attend a business
Jamok
in
Kidney Transplant
1 year ago
COVID anxiety
As you know from previous posts, three days ago I saw a comedy show at a small arena. I was going to wear a mask and it fell out of my boyfriends pocket. I’m not scared I’ll get covid. I tested negative this morning. Today we are going to the beach, the same beach I went to a few days before I tested
As you know from previous posts, three days ago I saw a comedy show at a small arena. I was going to wear a mask and it fell out of my boyfriends pocket. I’m not scared I’ll get covid. I tested negative this morning. Today we are going to the beach, the same beach I went to a few days before I tested
Daisy425
in
Anxiety and Depression Support
1 year ago
Recurring UTI’s
Had appointment with Rheumatology nurse this week and she wanted to check my recent urine infection had cleared. I didn’t have any symptoms and was feeling quite well so surprised when she rang on Thursday to say test showed an infection and I needed antibiotics and to get these from my GP, which I
Had appointment with Rheumatology nurse this week and she wanted to check my recent urine infection had cleared. I didn’t have any symptoms and was feeling quite well so surprised when she rang on Thursday to say test showed an infection and I needed antibiotics and to get these from my GP, which I
Baner
in
PMRGCAuk
1 year ago
Covid
I have Covid. At bedtime when I take ibuprofen and paracetamol without Gaviscon my acid reflux is worse. When I take Ibruprofen and paracetamol with Gaviscon my Covid symptoms are worse. Any thoughts please?
I have Covid. At bedtime when I take ibuprofen and paracetamol without Gaviscon my acid reflux is worse. When I take Ibruprofen and paracetamol with Gaviscon my Covid symptoms are worse. Any thoughts please?
AHG123
in
Acid Reflux Support
1 year ago
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