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Hi all, this is the third week on my new batch of T3, i already posted about my energy levels which dropped to zero again and then improved but only after taking my B Vitamins again which i was hoping not to have too as they send my eyes yellow. I do not know if they go yellow because my system is sluggish
Hi all, this is the third week on my new batch of T3, i already posted about my energy levels which dropped to zero again and then improved but only after taking my B Vitamins again which i was hoping not to have too as they send my eyes yellow. I do not know if they go yellow because my system is sluggish
Angelic69
in
Thyroid UK
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 . I’ve 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 . I’ve 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
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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
Chronic headaches after receiving the flu shot.
I’m 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.
I’m 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
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
TSH Finally Out of Range - Advice Please
I've got Hashimoto's (thyroglobulin antibodies 230 in a range of 0-130), and have been medicated for coming up around 11 months following my diagnosis last year. Started on 25mg of thyroxine, now on 150mg. I have blood tests every 8 weeks, and these are my most recent ones from this week. Things are
I've got Hashimoto's (thyroglobulin antibodies 230 in a range of 0-130), and have been medicated for coming up around 11 months following my diagnosis last year. Started on 25mg of thyroxine, now on 150mg. I have blood tests every 8 weeks, and these are my most recent ones from this week. Things are
Fluffysheep
in
Thyroid UK
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
B vitamins query
Somebody mentioned Marmite for B vitamins; is the B9 in it the best form? I e , folate, as opposed to folic acid?
Somebody mentioned Marmite for B vitamins; is the B9 in it the best form? I e , folate, as opposed to folic acid?
Noelnoel
in
Thyroid 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
Help please I'm PREGNANT
Good afternoon. I have had this text message this afternoon from my GP. 'Thank you for your enquiry about B12 injection. Your records show that immunological blood tests for Pernicious Anaemia have been normal, therefore it is safe to have B12 injections 6 monthly. To help reduce Coronavirus transmission
Good afternoon. I have had this text message this afternoon from my GP. 'Thank you for your enquiry about B12 injection. Your records show that immunological blood tests for Pernicious Anaemia have been normal, therefore it is safe to have B12 injections 6 monthly. To help reduce Coronavirus transmission
Yoshi12
in
Pernicious Anaemia Society
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 I’m 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 I’m 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 😔. 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 😔. 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
Should I be shielding if I am offered the flu jab via my doctors?
I am 48 year old asthmatic and have been offered the flu jab from my doctors for years. Although I have never been admitted to hospital with my asthma, I was almost admitted 3 years due to a respiratory virus (which I had 3 courses of oral steroids for). Last may I had a chest infection and was given
I am 48 year old asthmatic and have been offered the flu jab from my doctors for years. Although I have never been admitted to hospital with my asthma, I was almost admitted 3 years due to a respiratory virus (which I had 3 courses of oral steroids for). Last may I had a chest infection and was given
Gentlechelle11
in
Asthma Community Forum
4 years ago
7 years with this bladder cancer
After having bladder cancer for 7years numerous turbt operations each time having chemo this last bout consultants going to put me on bcg treatment
After having bladder cancer for 7years numerous turbt operations each time having chemo this last bout consultants going to put me on bcg treatment
64Andy
in
Fight Bladder Cancer
4 years ago
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