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Compensated or Decompensated
I was diagnosed in May 2019 with Cirrhosis and my Hepatologist told me it was Compensated and I would be monitored in the liver clinic every 6 months (the pandemic put paid to that plan). I've subsequently had two endoscopies which show six varices, one of which shows some evidence of past bleeding.
I was diagnosed in May 2019 with Cirrhosis and my Hepatologist told me it was Compensated and I would be monitored in the liver clinic every 6 months (the pandemic put paid to that plan). I've subsequently had two endoscopies which show six varices, one of which shows some evidence of past bleeding.
IanM1957
in
British Liver Trust
1 year ago
Covid sent me from managed hypo to hyper…
Hi all, I had been on 60mcg T3 & 25mcg levo, 6mg LDN for two years, managed hypothyroidism. Prior to this I presented with normal tsh, low T3, and normal T4. Vit d, B12, Ferratin, Folate all normal. I caught Covid in August and a week later started having severe symptoms of — insomnia, muscle
Hi all, I had been on 60mcg T3 & 25mcg levo, 6mg LDN for two years, managed hypothyroidism. Prior to this I presented with normal tsh, low T3, and normal T4. Vit d, B12, Ferratin, Folate all normal. I caught Covid in August and a week later started having severe symptoms of — insomnia, muscle
KettlebellQueen
in
Thyroid UK
5 months ago
None of my family message me.
I deleted Facebook around a year ago, and after that I have felt very isolated. During that period of time there has been a lot of introspection and I have noticed that I never receive messages from family members. It is always me sending messages. And then they often stop responding even if I am
I deleted Facebook around a year ago, and after that I have felt very isolated. During that period of time there has been a lot of introspection and I have noticed that I never receive messages from family members. It is always me sending messages. And then they often stop responding even if I am
davidthecoder
in
Anxiety and Depression Support
5 months ago
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RA complicated by arthritis in knees
Morning, so I have increasing pain in knees, worse on left. Diagnosed with Degenerate Oesteo-Arthritis in both knees, treatment for which is steroid injection, for time being, but ultimately will need knee replacement surgery. My question is, does anyone have tips to reduce pain & swelling & preserve
Morning, so I have increasing pain in knees, worse on left. Diagnosed with Degenerate Oesteo-Arthritis in both knees, treatment for which is steroid injection, for time being, but ultimately will need knee replacement surgery. My question is, does anyone have tips to reduce pain & swelling & preserve
Mama-K
in
NRAS
5 months ago
Forstair Next
Hi, I've been on combi forstair Next inhaler and my symptoms has greatly improved! However I have 2 horrible side effects . 1 . Bouts of oral thrush and 2 . What I can only describe as a plug of mucus every morning which leads me to cough and clear my throat, does anybody have any tips? I regularly
Hi, I've been on combi forstair Next inhaler and my symptoms has greatly improved! However I have 2 horrible side effects . 1 . Bouts of oral thrush and 2 . What I can only describe as a plug of mucus every morning which leads me to cough and clear my throat, does anybody have any tips? I regularly
Mini2020
in
Asthma Community Forum
2 months ago
Covid
Just recovering from a very nasty covid bout - my first. I'm a pretty healthy, active 76 year old with no medical issues other than PV. I don't need to take any prescription medicines other than HU, and otherwise take only aspirin and vitamins. Nevertheless, I was seriously sick for 2 weeks with all
Just recovering from a very nasty covid bout - my first. I'm a pretty healthy, active 76 year old with no medical issues other than PV. I don't need to take any prescription medicines other than HU, and otherwise take only aspirin and vitamins. Nevertheless, I was seriously sick for 2 weeks with all
saltmarsh
in
MPN Voice
5 months ago
Laxido longterm use
Hi all,I've been taking 1,sometimes 2 laxido sachets daily for the past 3 months and this has helped.My gastroenteritis has suggested swapping for prucalopride 1mg but this gives me all day stomach ache.My question is,is laxido safe to use daily long term?
Hi all,I've been taking 1,sometimes 2 laxido sachets daily for the past 3 months and this has helped.My gastroenteritis has suggested swapping for prucalopride 1mg but this gives me all day stomach ache.My question is,is laxido safe to use daily long term?
Ladydaff1
in
IBS Network
7 months ago
COVID
My husband just had a positive home covid test. My test was negative. I"ve phoned both onc and rad onc and am waiting to hear back about starting Taxol tomorrow and rads to lower spine on Thursday to see if there is any reason for me to delay either of these. I want to scream! Has anybody had
My husband just had a positive home covid test. My test was negative. I"ve phoned both onc and rad onc and am waiting to hear back about starting Taxol tomorrow and rads to lower spine on Thursday to see if there is any reason for me to delay either of these. I want to scream! Has anybody had
PJBinMI
in
SHARE Metastatic Breast Cancer
5 months ago
Bad reaction to progynova
hi, has one experienced a bad reaction to taking progynova? I’ve got a large red raw hand rash and swollen eyes because of this had to cancel my planned fet😩 seems like I have an allergy
hi, has one experienced a bad reaction to taking progynova? I’ve got a large red raw hand rash and swollen eyes because of this had to cancel my planned fet😩 seems like I have an allergy
keepfaith1982
in
Fertility Network UK
3 months ago
autoimmunity
I went to Laurie Mischley’s alumni camp in August. One of the Labs that I decided to get done called Nuro zoomer I believe, had an interesting result. Turns out I have auto immunity to my glycine receptors. There’s not a whole lot about this online, but apparently in some cases it can cause parkinsonism
I went to Laurie Mischley’s alumni camp in August. One of the Labs that I decided to get done called Nuro zoomer I believe, had an interesting result. Turns out I have auto immunity to my glycine receptors. There’s not a whole lot about this online, but apparently in some cases it can cause parkinsonism
rebtar
in
Cure Parkinson's
7 months ago
happened to see this article In a news feed regarding B and T cells, Covid and antibodies…
I have wondered why if we don’t make antibodies by getting vaccinated, then why bother. This article gives me some hope that we are protected more than I thought. Hope that this article is credible. Just wanted to post it for our information. Subject may have been touched on before in HealthUnlocked
I have wondered why if we don’t make antibodies by getting vaccinated, then why bother. This article gives me some hope that we are protected more than I thought. Hope that this article is credible. Just wanted to post it for our information. Subject may have been touched on before in HealthUnlocked
Curling123
in
CLL Support
5 months ago
Constant lower Back/Left Bum cheek pain
Hi All,I have adenomyosis and I have been having constant and chronic lower back pain and pain on my left bum cheek for 9 months. Does anyone else with adenomyosis have this problem? I've had a laparoscopy and endo wasn't found but I wouldn't be surprised if I have it too. It's tormenting me and hugely
Hi All,I have adenomyosis and I have been having constant and chronic lower back pain and pain on my left bum cheek for 9 months. Does anyone else with adenomyosis have this problem? I've had a laparoscopy and endo wasn't found but I wouldn't be surprised if I have it too. It's tormenting me and hugely
ABFr23
in
Endometriosis UK
5 months ago
Covid
l have Covid at the moment, had it about a week, l haven’t got the usual symptoms, not on any anti virals, l feel really tired, my main symptoms are very inflamed gums and very dry mouth, l have sorgens so dry mouth, but nothing like this, can l just ask has anyone else experienced this, not sure what
l have Covid at the moment, had it about a week, l haven’t got the usual symptoms, not on any anti virals, l feel really tired, my main symptoms are very inflamed gums and very dry mouth, l have sorgens so dry mouth, but nothing like this, can l just ask has anyone else experienced this, not sure what
Kate2628
in
NRAS
5 months ago
ANyone taking Prolia for osteoporosis?
Hi! I have been dealing with osteoporosis for more than 20 years and taken all the pills and Forteo shots. I have Lupus, Hyperparathyroidisn, Low Vitamin D and low body mass that all contribute to the problem. Unfortunately, it has continues to get worse. I have been hesitant to take Prolia as it will
Hi! I have been dealing with osteoporosis for more than 20 years and taken all the pills and Forteo shots. I have Lupus, Hyperparathyroidisn, Low Vitamin D and low body mass that all contribute to the problem. Unfortunately, it has continues to get worse. I have been hesitant to take Prolia as it will
Pumpkin2009
in
LUPUS UK
7 months ago
covid and pred
good morning Angels, It seems I have covid!! It’s my first time, what do I do re pred? More?
good morning Angels, It seems I have covid!! It’s my first time, what do I do re pred? More?
Alazarin
in
PMRGCAuk
5 months ago
Measles outbreak
Hi, not sure if I'm being silly so looking for abit of reassurance. I'm on rituximab, azathioprine and prednisolone. I'm up-to-date with vaccinations bit concerned about the measles outbreak in my area. Am I at risk due to being immunocompromised?
Hi, not sure if I'm being silly so looking for abit of reassurance. I'm on rituximab, azathioprine and prednisolone. I'm up-to-date with vaccinations bit concerned about the measles outbreak in my area. Am I at risk due to being immunocompromised?
Vqueen
in
Vasculitis UK
4 months ago
Tired Tavern - Discord server for people with CFS/ME and Long Covid
Hi guys, Just wanted to say that our CFS/ME and Long Covid Discord server has been up and running for two weeks now and we're close to 150 members. We're a very welcoming community that helps one another by sharing experiences, comfort and understanding. We also have server and community events coming
Hi guys, Just wanted to say that our CFS/ME and Long Covid Discord server has been up and running for two weeks now and we're close to 150 members. We're a very welcoming community that helps one another by sharing experiences, comfort and understanding. We also have server and community events coming
TiredTavern
in
Myalgic Encephalomyelitis Community
5 months ago
first time covid - symptoms expectation
Hello fellow RA warriors, I have been very careful since the start of the covid era - very limited outings/socializing, always mask up when out, no more gym exercise classes. I decided to enjoy the holiday a little bit more this year - dined out with a few family members in a crowded and popular restaurant
Hello fellow RA warriors, I have been very careful since the start of the covid era - very limited outings/socializing, always mask up when out, no more gym exercise classes. I decided to enjoy the holiday a little bit more this year - dined out with a few family members in a crowded and popular restaurant
Mymymy
in
NRAS
5 months ago
Hepatic Peliosis (What is it?)
RE: Hepatic Peliosis (What is it?) Hi all, I have been diagnosed with Hepatic Peliosis of the liver. What is it? and is there any treatments please? Does anyone else have Hepatic Peliosis ? How are your dealing with this etc? Any information would be helpful. Thank you. Regards, Kevin Walker
RE: Hepatic Peliosis (What is it?) Hi all, I have been diagnosed with Hepatic Peliosis of the liver. What is it? and is there any treatments please? Does anyone else have Hepatic Peliosis ? How are your dealing with this etc? Any information would be helpful. Thank you. Regards, Kevin Walker
kevpwalker
in
British Liver Trust
3 months ago
Covid testing
Does anybody know if home carers are still expected to do Covid tests? I have a new carer and when she came today she was coughing a lot. I asked her when she had last tested and she said she hasn’t tested since January of this year.
Does anybody know if home carers are still expected to do Covid tests? I have a new carer and when she came today she was coughing a lot. I asked her when she had last tested and she said she hasn’t tested since January of this year.
thelmar
in
NRAS
5 months ago
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