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Pegasys side effects
Hi all Started on Pegasys 11 weeks ago, at lowest dose of 45mg, suffered terribly with side effects for the first few weeks, fatigue, nausea, painful joints, itchy rash arms legs & palms of my hands. Week 6 on Pegasys I caught a mild case of Covid & all my Pegasys side effects stopped immediately!
Hi all Started on Pegasys 11 weeks ago, at lowest dose of 45mg, suffered terribly with side effects for the first few weeks, fatigue, nausea, painful joints, itchy rash arms legs & palms of my hands. Week 6 on Pegasys I caught a mild case of Covid & all my Pegasys side effects stopped immediately!
Lilliegarden
in
MPN Voice
1 year ago
Flu vaccine
Hi My flu vaccine is all booked. I’ve only ever had one before two years ago but occurred to me that maybe I should research if it’s ok to have it as I have Hashimotos/underactive thyroid. Appreciate any advice. 🌸
Hi My flu vaccine is all booked. I’ve only ever had one before two years ago but occurred to me that maybe I should research if it’s ok to have it as I have Hashimotos/underactive thyroid. Appreciate any advice. 🌸
292426
in
Thyroid UK
10 months ago
bronciectis
had bad bouts of weasin and verry sticky mucus in large amounts it woud carm dawn for a couple of hours then start again doctor as den me for X-ray she listend to my chest and said she coud hear fluid in bottom of. Lugs sent me for X-ray 2days later phone call saying for me to go back tomorrow I’m
had bad bouts of weasin and verry sticky mucus in large amounts it woud carm dawn for a couple of hours then start again doctor as den me for X-ray she listend to my chest and said she coud hear fluid in bottom of. Lugs sent me for X-ray 2days later phone call saying for me to go back tomorrow I’m
Redrum46
in
Lung Conditions Community Forum
10 months ago
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PGT-A testing
Hi everyone, just planning my 3rd cycle and have the option of PGT-A testing...I had 2 cycles, 3 transfers and 1 pregnancy which ended with MMC 2 years ago... 😪 I just turned to 40 the dreadded number... I am new to PGT-A testing... Anybody could give me some pros and cons with it and if you recommend
Hi everyone, just planning my 3rd cycle and have the option of PGT-A testing...I had 2 cycles, 3 transfers and 1 pregnancy which ended with MMC 2 years ago... 😪 I just turned to 40 the dreadded number... I am new to PGT-A testing... Anybody could give me some pros and cons with it and if you recommend
MagicTourmaline
in
Fertility Network UK
9 months ago
Dry Cough
I was in hospital in June we’ll I was there I got a dry cough with sneezing it has stayed with me my GP thought it was hay fever which I never had before she has upended my puffer too 2 times twice a day but I’m not sure if it’s too do with my heart failure which I have had for over 5 years.
I was in hospital in June we’ll I was there I got a dry cough with sneezing it has stayed with me my GP thought it was hay fever which I never had before she has upended my puffer too 2 times twice a day but I’m not sure if it’s too do with my heart failure which I have had for over 5 years.
Shaz45
in
AF Association
10 months 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
Sensitive : BFP rainbow baby
I was in two minds if to write this post as I know how difficult it is to read these updates if you are still struggling. and the fact that I am still in shock at a positive result. But I would also like to share a story of hope. So some of you will know my history, we had success on our second ICSI
I was in two minds if to write this post as I know how difficult it is to read these updates if you are still struggling. and the fact that I am still in shock at a positive result. But I would also like to share a story of hope. So some of you will know my history, we had success on our second ICSI
butterfliez
in
Fertility Network UK
7 months ago
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
1 year ago
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
update on Steroid Injection.
Just an update on my last post. As I mentioned I had the X-ray and scan done privately as there is a long wait for scans on NHS. They were both done and the results were sent straight through to the GP. I had Hoped to get the steroid injection within a couple of days again privately. I telephoned the
Just an update on my last post. As I mentioned I had the X-ray and scan done privately as there is a long wait for scans on NHS. They were both done and the results were sent straight through to the GP. I had Hoped to get the steroid injection within a couple of days again privately. I telephoned the
Macas
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
**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
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
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
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
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
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
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