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Update on previous post
So just to update my previous post ... I have been informed today that despite having lupus, receiving letter for flu jab and having to get 2 lots of public transport to get to work, I have to get there. NHS Occ Health person said βyou are increased risk but are you happy with having to go to workβ
So just to update my previous post ... I have been informed today that despite having lupus, receiving letter for flu jab and having to get 2 lots of public transport to get to work, I have to get there. NHS Occ Health person said βyou are increased risk but are you happy with having to go to workβ
Ronie23
in
LUPUS UK
4 years ago
Just thinking
I know I always am, but next year I'll be first in the queue for that flu jab !!!! πππππππππππππππ
I know I always am, but next year I'll be first in the queue for that flu jab !!!! πππππππππππππππ
allanah
in
NRAS
4 years ago
Advice re shielding
Hi, jus new to group. Am confused as to whether I should be shielding or not. Brief history, diagnosed approx 8 yrs with asthma at the time thought due to work, subsequently found other employment 2017, after about 8months in new job condition improved significantly and after visiting hospital asthma
Hi, jus new to group. Am confused as to whether I should be shielding or not. Brief history, diagnosed approx 8 yrs with asthma at the time thought due to work, subsequently found other employment 2017, after about 8months in new job condition improved significantly and after visiting hospital asthma
Stormywater
in
Asthma Community Forum
4 years ago
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Anyone here diagnosed with POLYCYSTIC LIVER DISEASE?
Anybody here been diagnosed with PLD, what treatments are you having and what precautions are you taking during Coronavirus?
Anybody here been diagnosed with PLD, what treatments are you having and what precautions are you taking during Coronavirus?
Nicsopami
in
British Liver Trust
4 years ago
MELATONIN FOR COVID-19 / Part 1
One possible problem for moderate to severe Covid-19 patients is the potential for significant damage to the lungs and possibly other organs like the liver based on what is being seen in patients. At this point, treatment options to try and prevent, repair or ameliorate this damage is very limited and
One possible problem for moderate to severe Covid-19 patients is the potential for significant damage to the lungs and possibly other organs like the liver based on what is being seen in patients. At this point, treatment options to try and prevent, repair or ameliorate this damage is very limited and
chartist
in
Cure Parkinson's
4 years ago
Corona virus and us !
Hi After having a heart attack 2 years ago my cardiologist suggested I get a flu jab every year and one off anti pneumonia jab,which I did . Iβve read that a lot of people who have the virus with underlying conditions and unfortunately pass away, do so as the result of pneumonia. So am I right in thinking
Hi After having a heart attack 2 years ago my cardiologist suggested I get a flu jab every year and one off anti pneumonia jab,which I did . Iβve read that a lot of people who have the virus with underlying conditions and unfortunately pass away, do so as the result of pneumonia. So am I right in thinking
Auctioneerjim
in
British Heart Foundation
4 years ago
Polycystic liver and coroavirus
Hi. I have polycystic liver disease very large cysts and bloods not the best. Does any one know if ishould I be self isolating not due to see consultant till September as they have rescheduled my appointment?
Hi. I have polycystic liver disease very large cysts and bloods not the best. Does any one know if ishould I be self isolating not due to see consultant till September as they have rescheduled my appointment?
Nicsopami
in
British Liver Trust
4 years ago
Chronic headaches after receiving the flu shot.
Iβm so glad I fount this! I got the flu shot last year and the next day I started getting a headache which was told was a migraine that lasted 5 weeks! It has been a year now and Im still getting these horrible headaches that last a few days at least every month. Prior to this I was really healthy.
Iβm so glad I fount this! I got the flu shot last year and the next day I started getting a headache which was told was a migraine that lasted 5 weeks! It has been a year now and Im still getting these horrible headaches that last a few days at least every month. Prior to this I was really healthy.
Head_ache
in
National Migraine Centre
4 years ago
Elocon Not working
Hi All Prescribed Elocon 3 weeks ago for lupus profundus on my nose. I have started losing tissue which is upsetting. The redness is slightly reduced and 2 of the bigger bumps but I was told not to use it for more than 2 weeks and then have a break. If it has not cleared what do I do now ? Wait to lose
Hi All Prescribed Elocon 3 weeks ago for lupus profundus on my nose. I have started losing tissue which is upsetting. The redness is slightly reduced and 2 of the bigger bumps but I was told not to use it for more than 2 weeks and then have a break. If it has not cleared what do I do now ? Wait to lose
Montysmum1
in
LUPUS UK
4 years ago
Second wave of NHS letters?
Dear all, I received a 'at risk of severe illness' letter from NHS on 8/04/20 saying to stay at home for at least 12 weeks from receipt of letter. I have MCTD and am on hydroxychloroquine, should note I also have coeliac disease and am offered the flu jab annually Just wondering if anyone else has got
Dear all, I received a 'at risk of severe illness' letter from NHS on 8/04/20 saying to stay at home for at least 12 weeks from receipt of letter. I have MCTD and am on hydroxychloroquine, should note I also have coeliac disease and am offered the flu jab annually Just wondering if anyone else has got
BellaC79
in
LUPUS UK
4 years ago
Anyone here taking Tenofovir Alafenamide (TAF) instead of Tenofovir Disoproxil Fumarate (TDF) for Hepatits B?
Hello all, I was wondering, are there any Hep B sufferers in the UK that have been prescribed the newer formulation of Tenofovir (Tenofovir alafenamide; TAF)? I know it is associated with a significantly lower risk of reduced kidney function. From what I have read in the available medical literature
Hello all, I was wondering, are there any Hep B sufferers in the UK that have been prescribed the newer formulation of Tenofovir (Tenofovir alafenamide; TAF)? I know it is associated with a significantly lower risk of reduced kidney function. From what I have read in the available medical literature
anma
in
British Liver Trust
4 years ago
How to build up your immunity with vitamin A ,vitamin D ,iodine ,vitamin C. Preventive and maintenance protocols.
https://www.thenewamerican.com/usnews/health-care/item/35241-how-to-fight-coronavirus-without-causing-a-global-depression?fbclid=IwAR3BztLtpst2p6eUAX2osbby5Agpgzsp2d8aiFcBWWSjSQe9yxUL1wNNkxs Interesting, long time ago I read about the Miracles of vitamin D.
https://www.thenewamerican.com/usnews/health-care/item/35241-how-to-fight-coronavirus-without-causing-a-global-depression?fbclid=IwAR3BztLtpst2p6eUAX2osbby5Agpgzsp2d8aiFcBWWSjSQe9yxUL1wNNkxs Interesting, long time ago I read about the Miracles of vitamin D.
parkie13
in
Cure Parkinson's
4 years ago
From our sibling site NAH: updated 20/3 Are Thyroid Patients More Prone to Getting Sick?
[u]
Are Thyroid Patients More Prone to Getting Sick?
[/u]updated 20/3 [u]
[/u] Those with thyroid disease are familiar with its symptoms including inhibited cognitive function, fluctuations in weight, fatigue, and many others. One symptom that can easily be overlooked is reduced immune function
[u]
Are Thyroid Patients More Prone to Getting Sick?
[/u]updated 20/3 [u]
[/u] Those with thyroid disease are familiar with its symptoms including inhibited cognitive function, fluctuations in weight, fatigue, and many others. One symptom that can easily be overlooked is reduced immune function
BadHare
in
Thyroid UK
4 years ago
Liver Transplants at the QE Birmingham.
This is really for those who are on the liver transplant waiting list, and who are awaiting that elusive phone call. I have heard that for the time being, all liver transplants are on hold, until this present epidemic has calmed down. Those patients are advised to stay on contact with the transplant
This is really for those who are on the liver transplant waiting list, and who are awaiting that elusive phone call. I have heard that for the time being, all liver transplants are on hold, until this present epidemic has calmed down. Those patients are advised to stay on contact with the transplant
Hidden
in
British Liver Trust
4 years ago
Vaccines
What do you all think about vaccines? I have shunned all vaccines for years even before I was made aware I had MS. Then I thought I heard if you had ms you should not get vaccines. I was reading the mssociety web page yesterday and it says regular flu shots are not only ok but encouraged. Who knew
What do you all think about vaccines? I have shunned all vaccines for years even before I was made aware I had MS. Then I thought I heard if you had ms you should not get vaccines. I was reading the mssociety web page yesterday and it says regular flu shots are not only ok but encouraged. Who knew
MSnWV
in
My MSAA Community
4 years ago
Leukaemia Care Webinar 8th April - a bit more information
Professor Dr Chris Fegan talked about CLL and COVID19 and answered previously submitted questions. Following on from AdrianUK's post ( https://healthunlocked.com/cllsupport/posts/private/143143147/uk-cll-web-conference ) this is a second report. His main message was that ALL CLL and SLL patients should
Professor Dr Chris Fegan talked about CLL and COVID19 and answered previously submitted questions. Following on from AdrianUK's post ( https://healthunlocked.com/cllsupport/posts/private/143143147/uk-cll-web-conference ) this is a second report. His main message was that ALL CLL and SLL patients should
Jm954
Administrator
in
CLL Support
4 years ago
New Diagnosis
Hello, 51 female from Florida PBC diagnosis confirmed yesterday and already Autoimmune Hepatitis patient 2016. I was told stage 3, 2nd biopsy in 3 years. I came for information, support and feedback. I would like to know what to expect.
Hello, 51 female from Florida PBC diagnosis confirmed yesterday and already Autoimmune Hepatitis patient 2016. I was told stage 3, 2nd biopsy in 3 years. I came for information, support and feedback. I would like to know what to expect.
NativeJax
in
PBC Foundation
4 years ago
12 weeks isolation or not?
Hi Iβm confused as to who should be isolating for 12weeks. I understood anyone with asthma or receiving a free flu jab should practice social distancing strictly. But I read an article which also showed an interview with the deputy chief medical officer Prof. Van-Tam and it implied anyone offered a
Hi Iβm confused as to who should be isolating for 12weeks. I understood anyone with asthma or receiving a free flu jab should practice social distancing strictly. But I read an article which also showed an interview with the deputy chief medical officer Prof. Van-Tam and it implied anyone offered a
ML10
in
Asthma Community Forum
4 years ago
Flu Shot & Long Term Unwellness
Greetings everyone, I know this is a touchy subject to some - but I was just wondering if anyone else out there has perhaps experienced what I have. I was diagnosed with Fibro about 5 years ago, after making literally dozens of trips over the years to all GP's in my surgery complaining about major fatigue
Greetings everyone, I know this is a touchy subject to some - but I was just wondering if anyone else out there has perhaps experienced what I have. I was diagnosed with Fibro about 5 years ago, after making literally dozens of trips over the years to all GP's in my surgery complaining about major fatigue
AsheleyGreen
in
Fibromyalgia Action UK
4 years ago
Liver inflammation
Hello everyone I hope you are well in this hectic world π. I jus an appointment by phone with my gastroenterology doctor. I have had Fibroscan in January and I was told that my liver came back to almost normal and is fibrosis instead of cirrosis. I was soo happy. I've developed cirrhosis because of
Hello everyone I hope you are well in this hectic world π. I jus an appointment by phone with my gastroenterology doctor. I have had Fibroscan in January and I was told that my liver came back to almost normal and is fibrosis instead of cirrosis. I was soo happy. I've developed cirrhosis because of
monikoki
in
British Liver Trust
4 years ago
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