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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
Year wait on 6 week follow up of heart attack.
Hiya everyone I'm on for a bit of a rant..been waiting a year now for app with cardiologist after a minoca HA had mri scan which shows no significant heart muscle damage 😃😃. I still get chest pains/arm/shoulder and stomach haven't been able to get dental treatment for a year as she keeps referring
Hiya everyone I'm on for a bit of a rant..been waiting a year now for app with cardiologist after a minoca HA had mri scan which shows no significant heart muscle damage 😃😃. I still get chest pains/arm/shoulder and stomach haven't been able to get dental treatment for a year as she keeps referring
Bran_flow
in
British Heart Foundation
1 year ago
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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
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
Loaded with a heavy COLD
Hi there guys. Can anyone help with this one. For the last two weeks I have had a heavy cold. Coughing, and bringing up heaps of mucus. I feel actually quite breathless since having the cold and it is making me feel really low and down. My peak flow is only 330 is this normal when you have an
Hi there guys. Can anyone help with this one. For the last two weeks I have had a heavy cold. Coughing, and bringing up heaps of mucus. I feel actually quite breathless since having the cold and it is making me feel really low and down. My peak flow is only 330 is this normal when you have an
Lizzy54
in
Asthma Community Forum
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
has anyone here undergone Lung Surgery for cancer?
hi there, newbie here who has just joined and who is looking to connect with some people who have experienced treatments for lung cancer, in this instance, surgery. my mum has been diagnosed with stage 3a lung cancer and is in the process of gathering information in order to make a decision over what
hi there, newbie here who has just joined and who is looking to connect with some people who have experienced treatments for lung cancer, in this instance, surgery. my mum has been diagnosed with stage 3a lung cancer and is in the process of gathering information in order to make a decision over what
Chambertin-1
in
Lung Conditions Community Forum
1 year ago
What is your experience with oral thrush and nystatin?
I’m experiencing a bad taste in my mouth that’s affecting my taste of food and sometimes feeling like there’s a lump in my throat when swallowing. . My GP looked in my mouth and said “you may have thrush”. She prescribed Nystatin. I don’t have the white plaques that bleed, etc., just
I’m experiencing a bad taste in my mouth that’s affecting my taste of food and sometimes feeling like there’s a lump in my throat when swallowing. . My GP looked in my mouth and said “you may have thrush”. She prescribed Nystatin. I don’t have the white plaques that bleed, etc., just
Mstiles
in
PMRGCAuk
1 year ago
Gamma light and Alzheimers - free app
I know this is not specific to PD, but thought I'd share this article. You all have been so kind to share new advancements, thank you. This looks very interesting!!! https://www.cogentica.com/alzheimers-research-gamma/ Direct from the article: (also talks about bacteria and gamma light and sound
I know this is not specific to PD, but thought I'd share this article. You all have been so kind to share new advancements, thank you. This looks very interesting!!! https://www.cogentica.com/alzheimers-research-gamma/ Direct from the article: (also talks about bacteria and gamma light and sound
Kat343
in
Cure Parkinson's
11 months ago
stress/upset at waiting times
Hi All, We are still waiting to start our treatment after being referred for ICSI in August this year. We had a further consult today and have decided to go down the donor route due to male factor infertility ( severely low count ). We have been told that we could be looking up to a 12 month wait and
Hi All, We are still waiting to start our treatment after being referred for ICSI in August this year. We had a further consult today and have decided to go down the donor route due to male factor infertility ( severely low count ). We have been told that we could be looking up to a 12 month wait and
Summeringreece
in
Fertility Network UK
7 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
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
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
Mould Issues
Has anyone experience with mould allergy/mycotoxins? My health is pretty good but I have a lingering oral problem (persistent leak/discharge from top left gum) and a few cognitive issues that come and go. I have turned every stone and latest MRI’s and CT scans still show nothing unremarkable but a
Has anyone experience with mould allergy/mycotoxins? My health is pretty good but I have a lingering oral problem (persistent leak/discharge from top left gum) and a few cognitive issues that come and go. I have turned every stone and latest MRI’s and CT scans still show nothing unremarkable but a
radd
in
Thyroid UK
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
Continuous Cough
11 month old has just started nursery and got a horrible cold from there. I gave him calpol last week Thursday for a few days as he had puffy eyes and didn’t look well at all. He still has a really bad cough which is making him puke at times and keeping him up at night. I heard you can only give calpol
11 month old has just started nursery and got a horrible cold from there. I gave him calpol last week Thursday for a few days as he had puffy eyes and didn’t look well at all. He still has a really bad cough which is making him puke at times and keeping him up at night. I heard you can only give calpol
RKesh
in
Pregnancy and Parenting Support
1 year ago
Hepatitis Advice please community - Got lots of question on LFT - thank you so much
So, I am having a bit of a spin out on this... viral hepatitis questions! ALT on the 10th May was 171. GGT was 120. I had an operation on 5th May (previous post had medication details). 15th May until 1st June - nausea, night sweats, lack of appetite bit of itching on back and thigh (Dr said it was
So, I am having a bit of a spin out on this... viral hepatitis questions! ALT on the 10th May was 171. GGT was 120. I had an operation on 5th May (previous post had medication details). 15th May until 1st June - nausea, night sweats, lack of appetite bit of itching on back and thigh (Dr said it was
GBB82
in
British Liver Trust
1 year ago
Husband refusing to accept his weekend drinking is an issue for our fertility.
Husband refusing to accept his weekend drinking is an issue for fertility. At the beginning of our fertility journey (Feb 2023) his results were drastic. ICSI for male factor infertility. By August when we had ICSI they had improved but not great. Three eggs were fertilised but non reached day 5 blast
Husband refusing to accept his weekend drinking is an issue for fertility. At the beginning of our fertility journey (Feb 2023) his results were drastic. ICSI for male factor infertility. By August when we had ICSI they had improved but not great. Three eggs were fertilised but non reached day 5 blast
Cuppppatea
in
Fertility Network UK
7 months 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
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