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Cough After Eating
This is the most recent episode of my mum’s PSP, she barely chokes, now we are dealing with after a meal cough, she coughs few mins after having her meals(different meals). I got her a cough syrup that helps after a while. Has this happened to anyone or experienced this, any solution? Her next appointment
This is the most recent episode of my mum’s PSP, she barely chokes, now we are dealing with after a meal cough, she coughs few mins after having her meals(different meals). I got her a cough syrup that helps after a while. Has this happened to anyone or experienced this, any solution? Her next appointment
Candor8
in
PSP Association
3 months ago
Covid
Two members of my family have Covid.. My mum is suffering from ET. She bever got vaccinated cos she got scared at that time due to many cases of thrombosis and sudden deaths we had in my country.. Anyone else who hasn't got the vaccine and went through Covid. We were maked and kept distance and all but
Two members of my family have Covid.. My mum is suffering from ET. She bever got vaccinated cos she got scared at that time due to many cases of thrombosis and sudden deaths we had in my country.. Anyone else who hasn't got the vaccine and went through Covid. We were maked and kept distance and all but
PHGR
in
MPN Voice
8 months ago
dental work with liver disease
I need dental work as in extractions. What procedures do I need to ask my doctor and dentist . I moved and need a new dentist.
I need dental work as in extractions. What procedures do I need to ask my doctor and dentist . I moved and need a new dentist.
Rumpleblack
in
British Liver Trust
9 months ago
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Does tibilone get better?
Hello everyone, I've just finished a 6 month course of prostap with no add back hrt. I had a pretty rough time on prostap alone, apparently I was supposed to be prescribed hrt alongside but never was, and in order to carry on my consultant has now added in tibilone. I thought the prostap was bad but
Hello everyone, I've just finished a 6 month course of prostap with no add back hrt. I had a pretty rough time on prostap alone, apparently I was supposed to be prescribed hrt alongside but never was, and in order to carry on my consultant has now added in tibilone. I thought the prostap was bad but
Womble84
in
Endometriosis UK
9 months ago
High Peak Flow but Wheezing and Phlegm x 4+ Months and Intense Fatigue
High Peak Flow but Wheezing and Phlegm x 4+ Months and Intense Fatigue I usually only get asthma as a secondary condition - with hayfever or a chest cold, etc. Since the first week of January, I've had constant fluid on the lungs - now a yellowy brown, which I cough up - but wouldn't say I have a
High Peak Flow but Wheezing and Phlegm x 4+ Months and Intense Fatigue I usually only get asthma as a secondary condition - with hayfever or a chest cold, etc. Since the first week of January, I've had constant fluid on the lungs - now a yellowy brown, which I cough up - but wouldn't say I have a
mmprospers
in
Asthma Community Forum
3 months ago
Free Covid Rapid Lateral Flow Test
Does anyone know how to obtain Covid Rapid Lateral Flow Tests free-of-charge in the U.K.? The Gov U.K. site says they are not available direct but are available via your local Pharmacy. None of my local pharmacy stores issue these tests free-of-charge under the NHS but are happy to charge £13 each, even
Does anyone know how to obtain Covid Rapid Lateral Flow Tests free-of-charge in the U.K.? The Gov U.K. site says they are not available direct but are available via your local Pharmacy. None of my local pharmacy stores issue these tests free-of-charge under the NHS but are happy to charge £13 each, even
Richardmint
in
CLL Support
8 months ago
My rheumy tele-consultation due to Covid.
HAPPY NEW YEAR. Hope you all enjoy much better health in 2024. An update. A couple of weeks back I had a tele-consultation with my rheumy as I had Covid. This was my 1st encounter with Covid after 3 years and 8 months! On the tele-consult app I was able to upload a brief resumé of my last
HAPPY NEW YEAR. Hope you all enjoy much better health in 2024. An update. A couple of weeks back I had a tele-consultation with my rheumy as I had Covid. This was my 1st encounter with Covid after 3 years and 8 months! On the tele-consult app I was able to upload a brief resumé of my last
IdasMum
in
PMRGCAuk
8 months ago
Pneumonia and Pleurisy- pain
Hi. I'm new here. I haven't been well since before Christmas. Initially I had a bit of a sore throat which I thought then turned into a virus- cough and sinus symptoms, shivers etc. A fortnight ago I felt pain in my chest- centre and at left hand side along ribs and behind breastbone area. Also at
Hi. I'm new here. I haven't been well since before Christmas. Initially I had a bit of a sore throat which I thought then turned into a virus- cough and sinus symptoms, shivers etc. A fortnight ago I felt pain in my chest- centre and at left hand side along ribs and behind breastbone area. Also at
Poppy16
in
Lung Conditions Community Forum
7 months ago
FISH TESTING - ‘Admin Edit’ - please read sad update on this post before replying.
I apologize if I am incorrect with the name of the testing results below. My husbands first CLL Dr 5 years ago had him on watch and wait. When he received the following results Tumor/ Prognostic Markers: CD38+ ZAP70+ Trisomy 12. IgVH unmutated, I researched the results which were very concerning to
I apologize if I am incorrect with the name of the testing results below. My husbands first CLL Dr 5 years ago had him on watch and wait. When he received the following results Tumor/ Prognostic Markers: CD38+ ZAP70+ Trisomy 12. IgVH unmutated, I researched the results which were very concerning to
Debcap61
in
CLL Support
8 months ago
PAF well controlled till I got covid
hi, I’m new to this forum and hope you can give me some hope. I’ve had PAF for 13 years, well controlled on propranolol 80mg slow release - other beta blockers seem to affect my chest/throat and give me dreadful indigestion and can’t tolerate the newer ones. However in November whilst on holiday in
hi, I’m new to this forum and hope you can give me some hope. I’ve had PAF for 13 years, well controlled on propranolol 80mg slow release - other beta blockers seem to affect my chest/throat and give me dreadful indigestion and can’t tolerate the newer ones. However in November whilst on holiday in
Clifflove
in
Atrial Fibrillation Support
8 months ago
obrilant bronchiolitis
hello all...my son was diagnosed he have obrilant bronchiolitis...he is in early position....only hard breathing when he runs around but without any oxygen...what can i expect from this?how long he can live with his own lungs?how fast this dissease progresive?
hello all...my son was diagnosed he have obrilant bronchiolitis...he is in early position....only hard breathing when he runs around but without any oxygen...what can i expect from this?how long he can live with his own lungs?how fast this dissease progresive?
care20
in
Lung Conditions Community Forum
3 months ago
Fatigue..again...Moderna jab?
Hello everyone. Reduced to 2.75, working slowly towards 2.5. Back from lovely break in Ireland tracing my roots. Had Moderna jab, aching arm and headache, then, coincidentally, full flu, nose like a tap, cough etc. Altho some neighbours had flu and not the jab. Cold symptoms finally going after 2 weeks
Hello everyone. Reduced to 2.75, working slowly towards 2.5. Back from lovely break in Ireland tracing my roots. Had Moderna jab, aching arm and headache, then, coincidentally, full flu, nose like a tap, cough etc. Altho some neighbours had flu and not the jab. Cold symptoms finally going after 2 weeks
Temoral
in
PMRGCAuk
3 months ago
Small Airways Disease
I had an infection the end of Jan (still not sure what it was - maybe RSV). Didn’t really start like a cold but airways closed up & excessive mucus. Mucus tested & nothing so no antibiotics. Things slowly got worse, although I was continuing to exercise to clear my chest of mucus (my primary issues is
I had an infection the end of Jan (still not sure what it was - maybe RSV). Didn’t really start like a cold but airways closed up & excessive mucus. Mucus tested & nothing so no antibiotics. Things slowly got worse, although I was continuing to exercise to clear my chest of mucus (my primary issues is
PW_R
in
Lung Conditions Community Forum
3 months ago
On Venetoclax, lymph node appeared
Trying not to worry but a lymph node in my armpit swelled up. I feel fine, no colds, fevers or recent vaccinations. Even did a Covid test because I have had Covid totally asymptomatic but negative. Has anyone have this happen and it turned out to be nothing. Hoping this is just a fluke but it seems
Trying not to worry but a lymph node in my armpit swelled up. I feel fine, no colds, fevers or recent vaccinations. Even did a Covid test because I have had Covid totally asymptomatic but negative. Has anyone have this happen and it turned out to be nothing. Hoping this is just a fluke but it seems
Alex830
in
CLL Support
8 months ago
Covid 19 vaccine UK
Hi there, I’d welcome any information you have on eligibility for Covid 19 vaccination in the U.K. I’ve looked at the .gov.uk website and in one place it includes epilepsy under neurological conditions, in another place it doesn’t. I did have an in invitation from my GP for flu, but not for Covid.
Hi there, I’d welcome any information you have on eligibility for Covid 19 vaccination in the U.K. I’ve looked at the .gov.uk website and in one place it includes epilepsy under neurological conditions, in another place it doesn’t. I did have an in invitation from my GP for flu, but not for Covid.
GillyA
in
Epilepsy Action
8 months ago
Rash any advice?
I have noticed this rash over last 2 or 3 months. Its not itchy or raised. Any advice most welcome. Im taking 100mcg teva levo and 15mcg thybon henning. Vit d, magnesium glycinate. Any advice most welcome 🌸🌸🌸🌸🌸
I have noticed this rash over last 2 or 3 months. Its not itchy or raised. Any advice most welcome. Im taking 100mcg teva levo and 15mcg thybon henning. Vit d, magnesium glycinate. Any advice most welcome 🌸🌸🌸🌸🌸
Geegee777
in
Thyroid UK
9 months ago
sjogens?
I have post PV Myelofibrosis. When I was dx with PV I took Pegasys from April 22 @ 45mg then 60mg then 90mg fortnightly. (On Jakavi since August 23) So took Pegasys for about 16 months After a couple of months on Pegasys I started to experience close vision problems which could not be corrected with
I have post PV Myelofibrosis. When I was dx with PV I took Pegasys from April 22 @ 45mg then 60mg then 90mg fortnightly. (On Jakavi since August 23) So took Pegasys for about 16 months After a couple of months on Pegasys I started to experience close vision problems which could not be corrected with
Yanico
in
MPN Voice
9 months ago
shingles vaccine
Hi folks This is a brilliant site has keep me steady since my husband’s diagnosis of SLL now CLL. My Husband had been W&W for 6 years, now on acalabrutinib for two years with no side affect and doing well. He has been offered the shingles vaccine but he hasn’t had chickenpox’s, is it safe to get the
Hi folks This is a brilliant site has keep me steady since my husband’s diagnosis of SLL now CLL. My Husband had been W&W for 6 years, now on acalabrutinib for two years with no side affect and doing well. He has been offered the shingles vaccine but he hasn’t had chickenpox’s, is it safe to get the
Charles4
in
CLL Support
9 months ago
Update after3years
I was in a covid coma 3years ago and posted in here to soon after I got home my brain was so hyper for a bout a month I felt so.guilty that I survived when ppl were loosing husband's wives children mum's dad's etc when I still do but I did survive I went to therapist who helped a lot and helped me
I was in a covid coma 3years ago and posted in here to soon after I got home my brain was so hyper for a bout a month I felt so.guilty that I survived when ppl were loosing husband's wives children mum's dad's etc when I still do but I did survive I went to therapist who helped a lot and helped me
Drewc
in
ICUsteps
8 months ago
Always cold.
Hi suffer from OB since 14 have stayed stable for couple years but just wondered if its normal to be so cold all the time and my skin is so transparent and pale always has a blueish tint to it .
Hi suffer from OB since 14 have stayed stable for couple years but just wondered if its normal to be so cold all the time and my skin is so transparent and pale always has a blueish tint to it .
Cornflake123
in
Lung Conditions Community Forum
3 months ago
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