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Peyronie's disease
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liver ast/alt
Good day, i recently got Bloodwork done. My billirubine was raised 71u/mol and AST 81. My ALT was 25, GGT normal and ALP also. I was a binge drinker for 15 years. Never drank daily. My fear is cirrhosis, with the ast alt ratio. Have had 2 ultrasounds that were complete normal and 1 MRI with out contrast
Good day, i recently got Bloodwork done. My billirubine was raised 71u/mol and AST 81. My ALT was 25, GGT normal and ALP also. I was a binge drinker for 15 years. Never drank daily. My fear is cirrhosis, with the ast alt ratio. Have had 2 ultrasounds that were complete normal and 1 MRI with out contrast
Che1985
in
British Liver Trust
9 months ago
Update after cardiac catheterization.
First a BIG THANK YOU for all the advice and support. I felt you with me every step of the way. The catheterization showed no narrowing of the major cardiac arteries. But head cardiologist came and said all my symptoms were classic heart attack and clearly something was blocked...so i have a bucket
First a BIG THANK YOU for all the advice and support. I felt you with me every step of the way. The catheterization showed no narrowing of the major cardiac arteries. But head cardiologist came and said all my symptoms were classic heart attack and clearly something was blocked...so i have a bucket
agingfeminist
in
PMRGCAuk
6 months ago
Paroxysmal and permanent Afib
Does anybody know when paroxysmal Afib becomes permanent? I was diagnosed with paroxysmal Afib towards the end of 2022, after I had been fitted with a Linq loop recorder. I was only ever having short episodes lasting up to 8 hours, then on 13th October just gone I started with an episode which is still
Does anybody know when paroxysmal Afib becomes permanent? I was diagnosed with paroxysmal Afib towards the end of 2022, after I had been fitted with a Linq loop recorder. I was only ever having short episodes lasting up to 8 hours, then on 13th October just gone I started with an episode which is still
Beatle45
in
AF Association
6 months ago
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What causes sudden return to sinus rhythm from permanent AF, even when it only lasts an hour or two?
I have permanent AF and of late is has been fairly normal to find walking difficult and feeling very breathless and easily tired. I am used to the routine of just carrying on and making myself stay as occupied and busy as I can. What I just found today, was that I found the daily walk (40 minutes,
I have permanent AF and of late is has been fairly normal to find walking difficult and feeling very breathless and easily tired. I am used to the routine of just carrying on and making myself stay as occupied and busy as I can. What I just found today, was that I found the daily walk (40 minutes,
oscarfox49
in
AF Association
6 months ago
Thrombocytopenia
Hi all, I have just been diagnosed with autoimmune thrombocytopenia, which is very low platelet count and can cause bruising and excessive bleeding. Diagnosed with PBC in 2018. Just wondered if anyone else has this as I know that we can be prone to more than one autoimmune condition.
Hi all, I have just been diagnosed with autoimmune thrombocytopenia, which is very low platelet count and can cause bruising and excessive bleeding. Diagnosed with PBC in 2018. Just wondered if anyone else has this as I know that we can be prone to more than one autoimmune condition.
nunbrook
in
PBC Foundation
7 months ago
First ever park run
Well, I’ve finally done it! First parkrun in the bag and it was enjoyable- as everyone had said, brilliantly well organised, friendly and absolutely no pressure. I wasn’t going to take the dog because I wanted to suss it out myself first but she did those puppy dog eyes at me when I put the gear on
Well, I’ve finally done it! First parkrun in the bag and it was enjoyable- as everyone had said, brilliantly well organised, friendly and absolutely no pressure. I wasn’t going to take the dog because I wanted to suss it out myself first but she did those puppy dog eyes at me when I put the gear on
SweatyHettie
Graduate
in
Couch to 5K
6 months ago
Permanent AF how do you manage?
Hi everyone , I had AF for about six years I was diagnosed after I was fond to have a leaky heart valve,I could manage my AF while I was only getting episodes say once a month but then once a week but for the last week I’m having them every day ,not sure how to cope ,perhaps some of you lovely people
Hi everyone , I had AF for about six years I was diagnosed after I was fond to have a leaky heart valve,I could manage my AF while I was only getting episodes say once a month but then once a week but for the last week I’m having them every day ,not sure how to cope ,perhaps some of you lovely people
Fattypatty
in
AF Association
3 months ago
Warning, ugly face
I am not diagnosed with Lupus, but I do have Ehlers Danlos Syndrome and Generalised multi joint Osteoarthritis, fibromyalgia and am hypothyroid.However, I am trying to get to the bottom of the terrible sores that come up on my face and neck. They can be terrible and then clear up a bit, but never fully
I am not diagnosed with Lupus, but I do have Ehlers Danlos Syndrome and Generalised multi joint Osteoarthritis, fibromyalgia and am hypothyroid.However, I am trying to get to the bottom of the terrible sores that come up on my face and neck. They can be terrible and then clear up a bit, but never fully
Lozza812
in
LUPUS UK
7 months ago
Has anyone taken 25mg of Metropolo twice a day! Any side effects?
I have AFIB and a lot of other medications bother me so they are going to try Metropolo twice a day for blood pressure and heart rate! I AM going to do this tomorrow! Any comments I would appreciate it!
I have AFIB and a lot of other medications bother me so they are going to try Metropolo twice a day for blood pressure and heart rate! I AM going to do this tomorrow! Any comments I would appreciate it!
BaileyC57
in
AF Association
6 months ago
Covid vaccines and Lupus Flare - up
Everytime I get a Covid shot I get a painful Lupus Flare- up for 4 to 5 months . In the 30 years of having Lupus I have never been so sick as since I have been taking Covid shots . I am thinking I will wait at least 1 year , if not longer for another one .
Everytime I get a Covid shot I get a painful Lupus Flare- up for 4 to 5 months . In the 30 years of having Lupus I have never been so sick as since I have been taking Covid shots . I am thinking I will wait at least 1 year , if not longer for another one .
seabreezegirl
in
LUpus Patients Understanding and Support
7 months ago
Emergency cardiac admission to hospital. Advice please.
I had severe left sided pain Wednesday evening. Grabbed my hospital bag and took a taxi to emergency. It wasn't a heart attack but i was admitted to cardiology ward because of irregular ecg. On Sunday morning i am having a cardiac catheterization to look for and treat any narrowing of arteries. I
I had severe left sided pain Wednesday evening. Grabbed my hospital bag and took a taxi to emergency. It wasn't a heart attack but i was admitted to cardiology ward because of irregular ecg. On Sunday morning i am having a cardiac catheterization to look for and treat any narrowing of arteries. I
agingfeminist
in
PMRGCAuk
6 months ago
A really long post, I’m sorry.
Hello, this might turn into a ramble, so apologies in advance. My husband was diagnosed with F3/F4 Bridging fibrosis about 6 weeks ago. It’s been a very emotional and scary few weeks made worse by lots of googling! I found this forum this week, and since reading, feel a lot more positive going forward
Hello, this might turn into a ramble, so apologies in advance. My husband was diagnosed with F3/F4 Bridging fibrosis about 6 weeks ago. It’s been a very emotional and scary few weeks made worse by lots of googling! I found this forum this week, and since reading, feel a lot more positive going forward
Booksand
in
British Liver Trust
9 months ago
strange feeling
wondering if anyone can help for about 4 months now I have had a stitch like feeling that comes and goes in kidney area! I see doctor who said not to worry all seems fine 🤷♀️. So I made another appointment had bloods and kidney function was ok! Since then I still have the stitch feeling, have had UTI
wondering if anyone can help for about 4 months now I have had a stitch like feeling that comes and goes in kidney area! I see doctor who said not to worry all seems fine 🤷♀️. So I made another appointment had bloods and kidney function was ok! Since then I still have the stitch feeling, have had UTI
Readbecgar
in
Early CKD Support
9 months ago
Cirrhosis child a
Hi i had a fibroscan scan last week cap 162 and 14.2 last year cap 260 and 63 originally diagnosed with alchol hepatitis and cirrhosis bloods are normal now ultrasound sound recent one show ever so slightly iregular outline and mild mild cirrhosis thats the way she expressed it as its so mild she said
Hi i had a fibroscan scan last week cap 162 and 14.2 last year cap 260 and 63 originally diagnosed with alchol hepatitis and cirrhosis bloods are normal now ultrasound sound recent one show ever so slightly iregular outline and mild mild cirrhosis thats the way she expressed it as its so mild she said
D6C2L30E-48
in
British Liver Trust
9 months ago
Severe coronary atherosclerosis and ADT
My recent PET / CT scan mentions severe coronary atherosclerosis. Previous one only said The heart is normal in size with scattered coronary artery calcifications. Also the new PET ? CT said something about heart enlargement but the last one said size normal. Previous scans also said there was an enlarged
My recent PET / CT scan mentions severe coronary atherosclerosis. Previous one only said The heart is normal in size with scattered coronary artery calcifications. Also the new PET ? CT said something about heart enlargement but the last one said size normal. Previous scans also said there was an enlarged
spencoid2
in
Advanced Prostate Cancer
6 months ago
Simvastatin v Atorvastatin
Just had a conversation with my Surgery employed Pharmacist. she asked me if I would object to switching from Simvastatin to Atorvastatin as the Simvastatin was rather an old drug. I was put on it around 2007. I told her to go ahead ... no problems. The following quote is what I found during an ultra
Just had a conversation with my Surgery employed Pharmacist. she asked me if I would object to switching from Simvastatin to Atorvastatin as the Simvastatin was rather an old drug. I was put on it around 2007. I told her to go ahead ... no problems. The following quote is what I found during an ultra
BenHall1
in
Atrial Fibrillation Support
7 months ago
Thyroid antibody result
Hi there, I was just wondering if a thyroid antibody level of 822 is quite high? My T4 is 9.6 and TSH is 12.04 Have been on Levothroxine 50mg for nearly 6 weeks so awaiting another blood test to see if it’s helped bring the levels down. I haven’t had a chance to discuss the antibody result with
Hi there, I was just wondering if a thyroid antibody level of 822 is quite high? My T4 is 9.6 and TSH is 12.04 Have been on Levothroxine 50mg for nearly 6 weeks so awaiting another blood test to see if it’s helped bring the levels down. I haven’t had a chance to discuss the antibody result with
Cloud77
in
Thyroid UK
7 months ago
Parkinson's/ MSA Consultants in West Midlands
Hello, My brother was diagnosed with Parkinson's three years ago. Another Consultant thinks he might have MSA or Parkinson Plus. Has anyone had MIBG Test for the MSA in West Midlands? Any recommendations for good consultants in West Midlands or nearby? Thanks
Hello, My brother was diagnosed with Parkinson's three years ago. Another Consultant thinks he might have MSA or Parkinson Plus. Has anyone had MIBG Test for the MSA in West Midlands? Any recommendations for good consultants in West Midlands or nearby? Thanks
Sarah106
in
Cure Parkinson's
9 months ago
PSA 5.4
Slight
Peyronies
disease
. Active, run , exercise, yard work etc. Just turned 65. Retired. Dad was diagnosed with PC 20 years ago and just turned 89 himself. Dad was diagnosed at 75 yo I have a follow up test in 30 days. Thank you
Slight
Peyronies
disease
. Active, run , exercise, yard work etc. Just turned 65. Retired. Dad was diagnosed with PC 20 years ago and just turned 89 himself. Dad was diagnosed at 75 yo I have a follow up test in 30 days. Thank you
Pitch10
in
Prostate Cancer Network
2 years ago
Can LFT tests me normal with fibrosis of the liver?
Hi,I had my gallbladder removed a few weeks ago as I had gallstones which were seen on ultrasound after I'd had pain/pressure/a full feeling under my right ribs. During the op, the surgeon has seen what he has described as "excessive fibrotic changes in the liver". My GP has referred me to Hepatology
Hi,I had my gallbladder removed a few weeks ago as I had gallstones which were seen on ultrasound after I'd had pain/pressure/a full feeling under my right ribs. During the op, the surgeon has seen what he has described as "excessive fibrotic changes in the liver". My GP has referred me to Hepatology
Givemecoffee
in
British Liver Trust
5 months ago
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