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New to NASH and wondering if milk thistle helps ? What about vitamin E ?
Things to help my liver
Things to help my liver
Amon46
in
Living with Fatty Liver and NASH
3 years ago
Liver and bacon
Hi I was just wondering if anyone knows if you can have liver and bacon with cirrhosis because I love it but not sure if I can have it also the same with bacon and onion suet pudding thanks Mary
Hi I was just wondering if anyone knows if you can have liver and bacon with cirrhosis because I love it but not sure if I can have it also the same with bacon and onion suet pudding thanks Mary
Sexy1971
in
British Liver Trust
3 years ago
PBC and Autoimmune Hepatitis
Diagnosed with PBC 2012 last biopsy 3yrs ago stage 2. Labs not improving over the years dispite using Urso and Ocaliva combined. Now trying steroids and bone marrow suppressants incase I have autoimmune hepatitis. My Alt and Ast stabalized but still have elevated alk phos. Any body out there with
Diagnosed with PBC 2012 last biopsy 3yrs ago stage 2. Labs not improving over the years dispite using Urso and Ocaliva combined. Now trying steroids and bone marrow suppressants incase I have autoimmune hepatitis. My Alt and Ast stabalized but still have elevated alk phos. Any body out there with
Q8Cooper
in
PBC Foundation
3 years ago
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Has anyone been diagnosed with AIH wrongly?
My 20 year old son has been having blood tests for over a year (due to the pandemic all follow up appointments were cancelled) I’ve been chasing the hospital constantly to give a diagnosis but each time they’ve said do more tests. Finally last week a consultant told him he’s possibly got AIH. This has
My 20 year old son has been having blood tests for over a year (due to the pandemic all follow up appointments were cancelled) I’ve been chasing the hospital constantly to give a diagnosis but each time they’ve said do more tests. Finally last week a consultant told him he’s possibly got AIH. This has
Jess246
in
British Liver Trust
3 years ago
Advice needed! ❤️
Hi everyone! I’m brand new here & I’m looking for help/advice. So my doctor sent me for blood tests after I had intense full body itching & I got the call that I have Hep C. I’m absolutely gutted. I was an IV addict 6 years ago so I’m assuming I caught the virus through this? I’m waiting to be referred
Hi everyone! I’m brand new here & I’m looking for help/advice. So my doctor sent me for blood tests after I had intense full body itching & I got the call that I have Hep C. I’m absolutely gutted. I was an IV addict 6 years ago so I’m assuming I caught the virus through this? I’m waiting to be referred
BadDecisions
in
Hepatitis C Trust
3 years ago
MO is recommending EstroDIM
to help lower Estrogen. The ingredients are: Vitamin E 33.5mg, I3C 200mg, DIM 100mg. Should I avoid this supplement because of the Vitamin E? peace
to help lower Estrogen. The ingredients are: Vitamin E 33.5mg, I3C 200mg, DIM 100mg. Should I avoid this supplement because of the Vitamin E? peace
ocman
in
Prostate Cancer Network
3 years ago
Free ebook of 300 pages:"Parkinson's here and now. 27 years searching for a cure for Parkinson's disease (1994-2021)."
This coming Monday (if everything goes as planned) I will publish on my blog "Parkinson's here and now" the link to a free book of about 250-300 pages and in printable pdf format, which collects the most interesting of the book I published in 2015 (now translated into English) as a tribute to my father
This coming Monday (if everything goes as planned) I will publish on my blog "Parkinson's here and now" the link to a free book of about 250-300 pages and in printable pdf format, which collects the most interesting of the book I published in 2015 (now translated into English) as a tribute to my father
parkinsonshereandnow
in
Cure Parkinson's
3 years ago
Benadryl tablets for hive looking lupus rash
Hello, I hope all are safe and keeping well? I’ve only been diagnosed few months ago and still learning lots about Lupus and how to manage it. Has anyone used successfully Benadryl tablets to keep under control hive looking like lupus rash? I came off prednisolone and only on hydroxy now and these
Hello, I hope all are safe and keeping well? I’ve only been diagnosed few months ago and still learning lots about Lupus and how to manage it. Has anyone used successfully Benadryl tablets to keep under control hive looking like lupus rash? I came off prednisolone and only on hydroxy now and these
MadT
in
LUPUS UK
3 years ago
Possible Autoimmune hepatitis. Smooth Muscle Antibody detected waiting for appt with specialist. Please help.
Hi All. I recently went to my doctor for some pain I sustained during a work out in my upper right quadrant. He sent me for an ultrasound and it was found I have an enlarged liver at 17.2cm (also fatty liver). He did some autoantibodies/autoimmune bloods and I tested positive for Amooth Muscle Antibodies
Hi All. I recently went to my doctor for some pain I sustained during a work out in my upper right quadrant. He sent me for an ultrasound and it was found I have an enlarged liver at 17.2cm (also fatty liver). He did some autoantibodies/autoimmune bloods and I tested positive for Amooth Muscle Antibodies
Scared3
in
British Liver Trust
3 years ago
Muscle weakness
I have hashimoto's, triggered by a virus which has left me with the usual symptoms, including muscle weakness. Has anyone found either a remedy or medication to help this symptom? I can function on a daily basis but tire very easily with extra activity. I don't have much strength in my muscles. I take
I have hashimoto's, triggered by a virus which has left me with the usual symptoms, including muscle weakness. Has anyone found either a remedy or medication to help this symptom? I can function on a daily basis but tire very easily with extra activity. I don't have much strength in my muscles. I take
Highland49
in
Thyroid UK
3 years ago
ask recommendation for vitamin e and any one experience with toxiprofilene( i think wrong spelled this med)
hi everyone, good afternoon, today i just received call from the clinic director as my follow up investigation and he prescribe me the toxiprofelene or toxi something i forget the all details of the name of the drugs. but it will works same like the viagra or baby aspirin to make the blood thinner because
hi everyone, good afternoon, today i just received call from the clinic director as my follow up investigation and he prescribe me the toxiprofelene or toxi something i forget the all details of the name of the drugs. but it will works same like the viagra or baby aspirin to make the blood thinner because
qido
in
Fertility Network UK
3 years ago
Any one know ......
Hi due to have my pneumonia vacination next week it's been 8 years since my last vaccination back in 2013 and they only gave me the adult one pneumovax 23 ( pnn23) then I phoned up my GPs to book this and Spoke to the practice nurse explained it's been 8 years since my last one and I wanted the
Hi due to have my pneumonia vacination next week it's been 8 years since my last vaccination back in 2013 and they only gave me the adult one pneumovax 23 ( pnn23) then I phoned up my GPs to book this and Spoke to the practice nurse explained it's been 8 years since my last one and I wanted the
stewie
in
CLL Support
3 years ago
Hepatitis B carrier since last 21 years.
21 yrs ago when when I had blood test done during my first pregnancy, dr told mr I have Australian antigen positive. I didn’t kone what was that. Then had test few years after and dr told me I’m a hepatitis b carrier and I should do regular tests. I ask my dr to do my liver test yearly and he says don
21 yrs ago when when I had blood test done during my first pregnancy, dr told mr I have Australian antigen positive. I didn’t kone what was that. Then had test few years after and dr told me I’m a hepatitis b carrier and I should do regular tests. I ask my dr to do my liver test yearly and he says don
Kalujacky
in
British Liver Trust
3 years ago
New here...anyone from Ontario?
Hi there, I have APS and moved to Ontario (near London) from Alberta 3 years ago. I have yet to find a doctor who has any specific knowledge of APS, and would like to. I was diagnosed in 2013, after being hospitalized with multiple clots (the main one was all throughout the IVC, extending into renal
Hi there, I have APS and moved to Ontario (near London) from Alberta 3 years ago. I have yet to find a doctor who has any specific knowledge of APS, and would like to. I was diagnosed in 2013, after being hospitalized with multiple clots (the main one was all throughout the IVC, extending into renal
Dandelocat22
in
Hughes Syndrome APS Forum
3 years ago
Supplements and Radiation Therapy
I am 69 and was diagnosed approximately 4 months ago with locally advanced Ductal Adenocarcinoma of the Prostate, Gleason 8, with seminal vessel involvement. I've been on Eligard for 3 months and had blood tests yesterday but I don't have any results to share yet. I also had a CT SIM yesterday in preparation
I am 69 and was diagnosed approximately 4 months ago with locally advanced Ductal Adenocarcinoma of the Prostate, Gleason 8, with seminal vessel involvement. I've been on Eligard for 3 months and had blood tests yesterday but I don't have any results to share yet. I also had a CT SIM yesterday in preparation
TottenhamMan
in
Advanced Prostate Cancer
3 years ago
Cardiovascular Disease (CVD), Parkinson's Disease (PD) and Melatonin
Previously we discussed how melatonin can be beneficial for people with Parkinson's disease (PwP) at a dose as low as 10 mg / day. Recent studies are confirming that Parkinson's disease (PD) is a risk factor for cardiovascular disease (CVD). The relationship is not yet fully understood, but it is now
Previously we discussed how melatonin can be beneficial for people with Parkinson's disease (PwP) at a dose as low as 10 mg / day. Recent studies are confirming that Parkinson's disease (PD) is a risk factor for cardiovascular disease (CVD). The relationship is not yet fully understood, but it is now
chartist
in
Cure Parkinson's
3 years ago
Vitamin E recommendations please (HypoT4/coeliac)
Hi, I have seen a few people mentioning Vitamin E supplementation recently for anxiety, and as I also have coeliac disease to go with my autoimmune hypothyroid, and may therefore have a deficient level of Vit E due to malabsorption....I would love some recommendations as to brand and dose! Obviously
Hi, I have seen a few people mentioning Vitamin E supplementation recently for anxiety, and as I also have coeliac disease to go with my autoimmune hypothyroid, and may therefore have a deficient level of Vit E due to malabsorption....I would love some recommendations as to brand and dose! Obviously
fred1e
in
Thyroid UK
3 years ago
3. Antiparkinsonian lifestyle.
(Excerpt from the book I am writing now. I hope you find it useful). Is Parkinson's disease a lifestyle disease? 3. Antiparkinsonian lifestyle. What took my father and I the longest to understand was that not only were there lifestyles that increased or decreased risk, but that it was possible to
(Excerpt from the book I am writing now. I hope you find it useful). Is Parkinson's disease a lifestyle disease? 3. Antiparkinsonian lifestyle. What took my father and I the longest to understand was that not only were there lifestyles that increased or decreased risk, but that it was possible to
parkinsonshereandnow
in
Cure Parkinson's
3 years ago
2. Non-Parkinsonian lifestyle (lower risk of developing the disease).
(Excerpt from the book I am writing now. I hope you find it useful). Is Parkinson's disease a lifestyle disease? 2. Non-Parkinsonian style. (lower risk of developing the disease, even delaying the onset of symptoms by years). Just as we came to realise the existence of a "Parkinsonian" lifestyle (
(Excerpt from the book I am writing now. I hope you find it useful). Is Parkinson's disease a lifestyle disease? 2. Non-Parkinsonian style. (lower risk of developing the disease, even delaying the onset of symptoms by years). Just as we came to realise the existence of a "Parkinsonian" lifestyle (
parkinsonshereandnow
in
Cure Parkinson's
3 years ago
Is Parkinson's disease a lifestyle disease? 1. Parkinsonian lifestyle (higher risk).
(Excerpt from the book I am writing now. I hope you find it useful). Is Parkinson's disease a lifestyle disease? 1. Parkinsonian style (increased risk of developing the disease) I have less and less doubts about the existence of a "Parkinsonian" way of life, which predisposes and increases the risk
(Excerpt from the book I am writing now. I hope you find it useful). Is Parkinson's disease a lifestyle disease? 1. Parkinsonian style (increased risk of developing the disease) I have less and less doubts about the existence of a "Parkinsonian" way of life, which predisposes and increases the risk
parkinsonshereandnow
in
Cure Parkinson's
3 years ago
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