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Medically induced zombie looking for help!
Is anyone else on Pregabalin and if so, how do you cope with 'zombiefying' side effects? I spend most of my working day on a computer and sometimes I feel like I can barely keep my eyes open. I'm also on Celecoxib and Topiramate.
Is anyone else on Pregabalin and if so, how do you cope with 'zombiefying' side effects? I spend most of my working day on a computer and sometimes I feel like I can barely keep my eyes open. I'm also on Celecoxib and Topiramate.
Fibro_warrior
in
Fibromyalgia Action UK
1 year ago
7 Covid vaccinations
Hello, I just can’t get over it that some of you had 7 COVID vaccinations! I know only about the first 2 and then 2 (maybe 3) boosters = 5 vaccines. Where are the other 2 are coming from? Or is this only in the UK? Just wondering because even my oncologist seemed to be surprised he only told me there
Hello, I just can’t get over it that some of you had 7 COVID vaccinations! I know only about the first 2 and then 2 (maybe 3) boosters = 5 vaccines. Where are the other 2 are coming from? Or is this only in the UK? Just wondering because even my oncologist seemed to be surprised he only told me there
Helma77
in
CLL Support
1 year ago
ivf/ICSI Sept/oct 2023 tww
Anyone in the TWW? 5dp5dt and all symptoms gone again. :( Any reassuring stories ?
Anyone in the TWW? 5dp5dt and all symptoms gone again. :( Any reassuring stories ?
Pkm4321
in
Fertility Network UK
9 months ago
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Eugenol
I just happened to come across some information relating to cirrhosis. It is called eugenol and it comes from cloves. The NIH as recently as 2021 has done studies and as far as I can tell it is helping the liver to heal. I am not a scientist so the big scientific words are beyond me so I am not sure
I just happened to come across some information relating to cirrhosis. It is called eugenol and it comes from cloves. The NIH as recently as 2021 has done studies and as far as I can tell it is helping the liver to heal. I am not a scientist so the big scientific words are beyond me so I am not sure
leanne5000
in
British Liver Trust
10 months ago
Problematic mucous & dry cough ..
Hello, Dad's cough is now pretty mucousy, and dry at the same time. Both are frustrating/aggravating for him, in different ways. For the mucous part - we try to do some mild chest tapping to encourage it out & I know that drinking good amounts of water is good for that too. Any
ideas
that have
Hello, Dad's cough is now pretty mucousy, and dry at the same time. Both are frustrating/aggravating for him, in different ways. For the mucous part - we try to do some mild chest tapping to encourage it out & I know that drinking good amounts of water is good for that too. Any
ideas
that have
Vip1
in
The Roy Castle Lung Cancer Foundation
11 months ago
Spring Covid 'Jab' Ten Out Of Ten.
Dear All, Today I had my Latest Covid 'Booster', I think about Seven so far, at a local 'Free' Church- of all places. Very Well 'organised' indeed😀, waiting time around an hour, and a quarter. The Jabs were supplied, via the Chemist/ Pharmacy, on a Walk In basis. I was Extremely Impressed, by the
Dear All, Today I had my Latest Covid 'Booster', I think about Seven so far, at a local 'Free' Church- of all places. Very Well 'organised' indeed😀, waiting time around an hour, and a quarter. The Jabs were supplied, via the Chemist/ Pharmacy, on a Walk In basis. I was Extremely Impressed, by the
AndrewT
in
Vasculitis UK
1 year ago
13 years on
I was put in an induced coma because of the swine flu. I was that poorly, I still have flash backs now, and the dreams I had are surreal.
I was put in an induced coma because of the swine flu. I was that poorly, I still have flash backs now, and the dreams I had are surreal.
Aioos
in
ICUsteps
1 year ago
PV and shingles
Hi. I am on Hydroxyurea unfortunately, since a year ago, one capsule, although I certainly need a second one with my platelets nearing 750. It lowers my immune system, years ago it did the same and I stopped it then. After a terrible cold with persistent cough this winter, that lasted one month, now
Hi. I am on Hydroxyurea unfortunately, since a year ago, one capsule, although I certainly need a second one with my platelets nearing 750. It lowers my immune system, years ago it did the same and I stopped it then. After a terrible cold with persistent cough this winter, that lasted one month, now
Kelly2
in
MPN Voice
1 year ago
Cold water!
I went swimming for the first time yesterday since my diagnosis of PAF 18 months ago. I'm on holiday in France at the moment. It was an outdoor pool and it's hot here so the water felt really cold. I went in waist deep and then ducked under. I swam for a few metres then realised I was in AF. I guess
I went swimming for the first time yesterday since my diagnosis of PAF 18 months ago. I'm on holiday in France at the moment. It was an outdoor pool and it's hot here so the water felt really cold. I went in waist deep and then ducked under. I swam for a few metres then realised I was in AF. I guess
Sandych55
in
Atrial Fibrillation Support
11 months ago
horrible taste in mouth, nothing tastes good
After looking in my mouth, my GP said, I think you have thrush. A dentist had said an X-ray showed no tooth infection was causing the bad taste. GP prescribed nystatin. After taking it the bad taste is worse than ever, especially in the morning, and the area behind my top and bottom teeth feels
After looking in my mouth, my GP said, I think you have thrush. A dentist had said an X-ray showed no tooth infection was causing the bad taste. GP prescribed nystatin. After taking it the bad taste is worse than ever, especially in the morning, and the area behind my top and bottom teeth feels
Mstiles
in
PMRGCAuk
1 year ago
Mycophenolate or Azathioprine ?
Hi friends, Some of you will remember that in February I had an intolerably itchy rash my Rheumy didn’t recognise as being a Lupus rash but was confirmed by Dermy as such. After being on Prednisolone for a total of 7 weeks tapering down by 5 mg per week, my poor innards were screaming. I couldn’t
Hi friends, Some of you will remember that in February I had an intolerably itchy rash my Rheumy didn’t recognise as being a Lupus rash but was confirmed by Dermy as such. After being on Prednisolone for a total of 7 weeks tapering down by 5 mg per week, my poor innards were screaming. I couldn’t
Spotty-ewe
in
LUPUS UK
1 year ago
Denied Covid-19 Vaccination
01/05/2023 - Received NHS email to book Spring Covid-19 Vaccination 25/05/2023 - Attended 4pm appointment at our own GP surgery with Husband who has Rituximab IV infusions + DMARDS for his RA (he is immunocompromised). I have SLE (Lupus). ~ On entering treatment room we were met with, “Neither of
01/05/2023 - Received NHS email to book Spring Covid-19 Vaccination 25/05/2023 - Attended 4pm appointment at our own GP surgery with Husband who has Rituximab IV infusions + DMARDS for his RA (he is immunocompromised). I have SLE (Lupus). ~ On entering treatment room we were met with, “Neither of
Turquoise-1
in
LUPUS UK
1 year ago
Shingles
Hi all, My friend has Shingles. With PMR is it advisable to stay away until after breakout. Reading conflicting advice. Much appreciated yet again!! Thank you.
Hi all, My friend has Shingles. With PMR is it advisable to stay away until after breakout. Reading conflicting advice. Much appreciated yet again!! Thank you.
Fredddie
in
PMRGCAuk
1 year ago
Neupro Patch
I saw a consultant in the UK a month or so ago and explained that my transition from Mirapexin to Pregabalin was not going well. At that time, I was taking 150mg Pregabalin and 4 x 0.088 Mirapexin and that at that level i was getting some relief but that any reduction from that in the Mirapexin left
I saw a consultant in the UK a month or so ago and explained that my transition from Mirapexin to Pregabalin was not going well. At that time, I was taking 150mg Pregabalin and 4 x 0.088 Mirapexin and that at that level i was getting some relief but that any reduction from that in the Mirapexin left
Ced60
in
Restless Legs Syndrome
1 year ago
Holiday Vaccinations
Morning all Looking for some advice on holiday vaccinations for Caribbean. I've seen the recommended list is yellow fever and rabies etc. Just wondering if these vaccines will be "ok" for P M R sufferers. I'm currently on a very low dose 1.5 and hope to be pred free by the time I go (next march) just
Morning all Looking for some advice on holiday vaccinations for Caribbean. I've seen the recommended list is yellow fever and rabies etc. Just wondering if these vaccines will be "ok" for P M R sufferers. I'm currently on a very low dose 1.5 and hope to be pred free by the time I go (next march) just
Millipede01
in
PMRGCAuk
1 year ago
Been a bit quiet, been a bit low. Repeating a week...
Hello all,So I've been fighting a cold/cough bug since the tail end of my hols last week. The last run I managed was on Monday of this week, so I'm feeling a bit disappointed in myself, but every intention of getting back to it today after work 🤞🏾 I've now decided it was "ok" to let my body rest,
Hello all,So I've been fighting a cold/cough bug since the tail end of my hols last week. The last run I managed was on Monday of this week, so I'm feeling a bit disappointed in myself, but every intention of getting back to it today after work 🤞🏾 I've now decided it was "ok" to let my body rest,
PuffingPanda
in
Couch to 5K
1 year ago
Flu season here!
Hello folks, I'm interested to know if long term ME sufferers end up with a totally weird immunity. I'm in my early 70's, developed ME following viral pneumonia in my 30's, then over a decade later discovered I also had Hashimoto's thyroiditis (am on thyroxine).I've managed to dodge Covid even though
Hello folks, I'm interested to know if long term ME sufferers end up with a totally weird immunity. I'm in my early 70's, developed ME following viral pneumonia in my 30's, then over a decade later discovered I also had Hashimoto's thyroiditis (am on thyroxine).I've managed to dodge Covid even though
Kimmie4
in
Myalgic Encephalomyelitis Community
1 year ago
Illness, PSP & CBD
Does anyone have any advice on PSP & CBD sufferers and the effect of another illness? Mums currently got shingles and she seems to have got worse in her mobility in the last few days since being poorly. I’m hoping this is because she’s got less energy due to her shingles. This week has been tough
Does anyone have any advice on PSP & CBD sufferers and the effect of another illness? Mums currently got shingles and she seems to have got worse in her mobility in the last few days since being poorly. I’m hoping this is because she’s got less energy due to her shingles. This week has been tough
Kelmisty
in
PSP Association
1 year ago
no GP kidney infection
I’ve just signed up for new GP and receptionist told me it would be a 2 week turn around. I had bad uti symptoms and went to pharmacist they suspects it’s a kidney infection as I have fever, vomiting, bloating, frequent peeing and painful peeing. Unable to hold my bladder, incontinece and gnawing back
I’ve just signed up for new GP and receptionist told me it would be a 2 week turn around. I had bad uti symptoms and went to pharmacist they suspects it’s a kidney infection as I have fever, vomiting, bloating, frequent peeing and painful peeing. Unable to hold my bladder, incontinece and gnawing back
Littlebug77
in
Endometriosis UK
1 year ago
Post covid secretions
My husband spent two months in icu during the first wave of covid from December 2020. He was in a coma for 3 weeks of that. We are forever grateful that he managed to come back to us and has made a huge recovery at home. He still struggles with very large and sticky secretions on a daily basis. We initially
My husband spent two months in icu during the first wave of covid from December 2020. He was in a coma for 3 weeks of that. We are forever grateful that he managed to come back to us and has made a huge recovery at home. He still struggles with very large and sticky secretions on a daily basis. We initially
Lauralou412
in
ICUsteps
1 year ago
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