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Colds
Have another really bad cough and cold (not COVID) - is this related to the immune system being reduced by pred ? I am on 6 mg after about 5 years
Have another really bad cough and cold (not COVID) - is this related to the immune system being reduced by pred ? I am on 6 mg after about 5 years
Daffodilia
in
PMRGCAuk
11 months 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
11 months 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
11 months ago
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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
11 months ago
Has anyone had more fertilised eggs 2nd time round with ICSI?
Hi everyone, I'm wondering if anyone undergoing ICSI had a more successful round of fertilised eggs 2nd time round and if there was anything you done differently? We had our first round in August and they managed to use 10 mature eggs after collecting 15 eggs, 24 hours later we were told that only
Hi everyone, I'm wondering if anyone undergoing ICSI had a more successful round of fertilised eggs 2nd time round and if there was anything you done differently? We had our first round in August and they managed to use 10 mature eggs after collecting 15 eggs, 24 hours later we were told that only
WMolly88
in
Fertility Network UK
5 months 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
Olaparib side effects - cough and breathlessness
Hi all. I've been taking Olaparib since May this year and have had a constant cough and breathlessness. It's getting me down a bit and I was wondering if anyone else has had this side effect and how long it lasted x
Hi all. I've been taking Olaparib since May this year and have had a constant cough and breathlessness. It's getting me down a bit and I was wondering if anyone else has had this side effect and how long it lasted x
Demelzatheseagull
in
My Ovacome
9 months 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
11 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
11 months 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
11 months 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
11 months ago
How often and duration of the Tass gloves?
Just completed the build. Wife used first time for 2 hrs with improved gait was able to walk in house without walker. Used walking sticks just due to fear of falling. Hand printing improved. However today after 2 hrs she said she felt very jittery, kind of like a residual feeling of vibratio So she
Just completed the build. Wife used first time for 2 hrs with improved gait was able to walk in house without walker. Used walking sticks just due to fear of falling. Hand printing improved. However today after 2 hrs she said she felt very jittery, kind of like a residual feeling of vibratio So she
Furch
in
Cure Parkinson's
7 months ago
A number of over the counter cold medicine in the USA in jeopardy
Here's the link to the artIcle https://www.wsj.com/health/healthcare/decongestant-cold-medicine-ineffective-f68df3f7?st=b0jipkx3rqa2o0a&reflink=article_copyURL_share
Here's the link to the artIcle https://www.wsj.com/health/healthcare/decongestant-cold-medicine-ineffective-f68df3f7?st=b0jipkx3rqa2o0a&reflink=article_copyURL_share
pdpatient
in
Cure Parkinson's
9 months ago
Immunocompromised people aged 50+ are now eligible for the shingles vaccine
Immunocompromised people aged 50 and over are now eligible for the shingles vaccine. The vaccine reduces your chances of getting shingles and reduces the risk of complications if you still develop it. Read more on our website, including answers to some commonly asked questions, here: https://www.lupusuk.org.uk
Immunocompromised people aged 50 and over are now eligible for the shingles vaccine. The vaccine reduces your chances of getting shingles and reduces the risk of complications if you still develop it. Read more on our website, including answers to some commonly asked questions, here: https://www.lupusuk.org.uk
Debbie_kinsey
Administrator
in
LUPUS UK
9 months 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
11 months 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
11 months ago
Methylene Blue
Has anyone used or considered Methylene Blue in very low dosages for their Parkinson's? Franciso Gonzalez-Lima of the University of Texas, Austin is an expert on its advantages for treating neurological diseases. Mercola did an interview with him on the subject. Mercola does not promote synthetic drugs
Has anyone used or considered Methylene Blue in very low dosages for their Parkinson's? Franciso Gonzalez-Lima of the University of Texas, Austin is an expert on its advantages for treating neurological diseases. Mercola did an interview with him on the subject. Mercola does not promote synthetic drugs
Trailing
in
Cure Parkinson's
1 year ago
Cold!
After doing the 20 min run on Saturday I rested Sunday. Haven't slept well for three nights now. Now I think I've got a cold. Headache, etc. Will rest with a short walk until Wednesday now. See how I feel then. Feeling very frustrated.
After doing the 20 min run on Saturday I rested Sunday. Haven't slept well for three nights now. Now I think I've got a cold. Headache, etc. Will rest with a short walk until Wednesday now. See how I feel then. Feeling very frustrated.
Basil73
in
Couch to 5K
9 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
11 months 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
10 months ago
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