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Amylase test
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bilirubin tested again
hey so I'm 30 female; I had some lft done and my bilirubin came back at 23 u/mol, i had it retested and it showed 32 u/mol and direct 10u/mol, I have had it redone this week and it's gone down to 21u/mol and direct 8u/mol. the thing I'm concerned about is the dr has said it's Gilbert's but my direct
hey so I'm 30 female; I had some lft done and my bilirubin came back at 23 u/mol, i had it retested and it showed 32 u/mol and direct 10u/mol, I have had it redone this week and it's gone down to 21u/mol and direct 8u/mol. the thing I'm concerned about is the dr has said it's Gilbert's but my direct
Megaaalee
in
British Liver Trust
1 month ago
Newly diagnosed
Hey y'all. I was recently diagnosed with pancreatitis, I had an acute attack and was hospitalized for 11 days. I've never had issues before now that I knew of, but upon doing a CAT scan they discovered a 9cm cyst on my pancreas. I don't drink, but I did eat quite poorly unfortunately. I had to wait for
Hey y'all. I was recently diagnosed with pancreatitis, I had an acute attack and was hospitalized for 11 days. I've never had issues before now that I knew of, but upon doing a CAT scan they discovered a 9cm cyst on my pancreas. I don't drink, but I did eat quite poorly unfortunately. I had to wait for
BlackCoffee2112
in
Chronic Pancreatitis Support
4 months ago
Reseach project there is hope !!
I am attending this study in March may get some answers. Thank you for your interest in our research project on Tinnitus. My name is Flavia Cardini, and I am the principal investigator of this project. Thank you for completing the online questionnaires, this was the first part of the research. I am
I am attending this study in March may get some answers. Thank you for your interest in our research project on Tinnitus. My name is Flavia Cardini, and I am the principal investigator of this project. Thank you for completing the online questionnaires, this was the first part of the research. I am
Parrcj
in
Tinnitus UK
5 months ago
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Wheat Diet may Exacerbate Multiple Sclerosis Severity
Wheat diet may exacerbate multiple sclerosis severity, research finds - Jan 2024
by Natkritta Hüppe, Universitätsmedizin der Johannes Gutenberg-Universität Mainz https://medicalxpress.com/news/2024-01-wheat-diet-exacerbate-multiple-sclerosis.html
Highlights:
A research team at the University
Wheat diet may exacerbate multiple sclerosis severity, research finds - Jan 2024
by Natkritta Hüppe, Universitätsmedizin der Johannes Gutenberg-Universität Mainz https://medicalxpress.com/news/2024-01-wheat-diet-exacerbate-multiple-sclerosis.html
Highlights:
A research team at the University
Bolt_Upright
in
Cure Parkinson's
6 months ago
Struggling
I asked for a blood
test
which showed serum
amylase
was 16 lipase was 24 both of which are low.... my doctor however says maybe they have always been low.
I asked for a blood
test
which showed serum
amylase
was 16 lipase was 24 both of which are low.... my doctor however says maybe they have always been low.
Sungirl0
in
Chronic Pancreatitis Support
5 months ago
PBC - high Amylase level
Just had my latest blood results. Amylase tested for 1st time so I don’t have anything to compare it with 201 (normal range 0 - 100) Anyone have any comments? Don’t like the idea of pancreatitis!
Just had my latest blood results. Amylase tested for 1st time so I don’t have anything to compare it with 201 (normal range 0 - 100) Anyone have any comments? Don’t like the idea of pancreatitis!
DebatDG9
in
PBC Foundation
11 months ago
Very yellow but GP says I'm not jaundiced
Hello everyone, I had my gallbladder removed in 2007. Over the past 3+ years I have noticed my skin gradually becoming more yellow. I had what I think was a biliary attack last November, extreme pain vomitting etc. I have been very unwell since, losing about 2 stones in weight since (not i tended
Hello everyone, I had my gallbladder removed in 2007. Over the past 3+ years I have noticed my skin gradually becoming more yellow. I had what I think was a biliary attack last November, extreme pain vomitting etc. I have been very unwell since, losing about 2 stones in weight since (not i tended
MePo
in
British Liver Trust
11 months ago
Anyone else with elevated blood amylase results with acid reflux?
My blood
amylase
test
came back high (133) but it looks like raised
amylase
is associated with pancreatitis and I don't appear to have symptoms of that. Getting a call from my GP to discuss results in a few days but wondered if this is common with acid reflux? Thanks
My blood
amylase
test
came back high (133) but it looks like raised
amylase
is associated with pancreatitis and I don't appear to have symptoms of that. Getting a call from my GP to discuss results in a few days but wondered if this is common with acid reflux? Thanks
Jaby86
in
Acid Reflux Support
2 years ago
First symptoms
hello, Firstly I have a chronic autoimmune disorder diagnosed aged 17 of rheumatoid specialty. I’m now 61 med free for this condition but have become unwell recently. There is only a locum at the surgery offering telephone only appointments. Symptoms; Weight loss, bloating, change in toilet habits
hello, Firstly I have a chronic autoimmune disorder diagnosed aged 17 of rheumatoid specialty. I’m now 61 med free for this condition but have become unwell recently. There is only a locum at the surgery offering telephone only appointments. Symptoms; Weight loss, bloating, change in toilet habits
Hidden
in
My Ovacome
1 year ago
LOCKDOWN500!
I am keen to know how to lower my cholesterol level, whilst still enjoying a normal healthy but enjoyable life.
I am keen to know how to lower my cholesterol level, whilst still enjoying a normal healthy but enjoyable life.
LOCKDOWN500
in
British Heart Foundation
16 hours ago
Stopping Liothyronine
hi all Sadly I can no longer afford to self fund my Liothyronine T3. I have been taking it for over 4 months at 10mg daily. please can you advise how to stop as I am concerned about stopping it suddenly. I have capsules not tablet so am unable to break in half. many thanks for your advice.
hi all Sadly I can no longer afford to self fund my Liothyronine T3. I have been taking it for over 4 months at 10mg daily. please can you advise how to stop as I am concerned about stopping it suddenly. I have capsules not tablet so am unable to break in half. many thanks for your advice.
DylanA
in
Thyroid UK
16 hours ago
New T3 Supplier Please
Hi Everyone, I posted earlier about my T3 supplier and have been advised by mods to consider change to Tiromel instead as better availability. I would really appreciate details of recent suppliers for this, by DM only please as per group rules. Thank you and keep well everyone. Gillian
Hi Everyone, I posted earlier about my T3 supplier and have been advised by mods to consider change to Tiromel instead as better availability. I would really appreciate details of recent suppliers for this, by DM only please as per group rules. Thank you and keep well everyone. Gillian
startagaingirl
in
Thyroid UK
20 hours ago
Re: ?D102 test
Hiya! Does anyone know, please: 1) If the D102 test is the one that tests for the gene related to t4 to t3 conversion? 2) I looked at Regenerus Labs and on the test it says: “DI02 Support telephone consultation…Recommended: Contact practitioner before placing order” does anyone know what this
Hiya! Does anyone know, please: 1) If the D102 test is the one that tests for the gene related to t4 to t3 conversion? 2) I looked at Regenerus Labs and on the test it says: “DI02 Support telephone consultation…Recommended: Contact practitioner before placing order” does anyone know what this
JoJoloveschocolate
in
Thyroid UK
21 hours ago
latest bloods
I’m on a journey with t3 it’s taking a while. Latest bloods reflect 15mcg taken in one dose and 50mcg levothyroxine I think I need to increase levo but on 75 I was slightly over medicated I felt. A reply on here suggested 62.5mcg as middle road which makes sense to me but pills are tiny and crumbly
I’m on a journey with t3 it’s taking a while. Latest bloods reflect 15mcg taken in one dose and 50mcg levothyroxine I think I need to increase levo but on 75 I was slightly over medicated I felt. A reply on here suggested 62.5mcg as middle road which makes sense to me but pills are tiny and crumbly
Mag999
in
Thyroid UK
22 hours ago
T3 private source
I wonder is it possible to source T3 outside of UK as you can with NDT? Been on NDT a few years but this latest batch doesn’t seem to suit like it usually does. Please PM me if know of a reliable source. Thank you.
I wonder is it possible to source T3 outside of UK as you can with NDT? Been on NDT a few years but this latest batch doesn’t seem to suit like it usually does. Please PM me if know of a reliable source. Thank you.
Veritate
in
Thyroid UK
2 days ago
Was hoping for some advice please
Didn't really receive any advice from my previous post https://healthunlocked.com/thyroiduk/posts/151062372/help-please After dropping from 125mcg Levo to 100mcg and retesting after 9 weeks, my T4, very surprisingly, is still quite high in range and I think I still feel overmedicated. As with last
Didn't really receive any advice from my previous post https://healthunlocked.com/thyroiduk/posts/151062372/help-please After dropping from 125mcg Levo to 100mcg and retesting after 9 weeks, my T4, very surprisingly, is still quite high in range and I think I still feel overmedicated. As with last
Jefner
in
Thyroid UK
2 days ago
Short synacthen test. Any restrictions recommended re medicines please
I have a short synacthen booked via endocrinology NHS.As I use inhaler for COPD, I have been advised not to use it after 4pm the day before. Other than this, everything else, including food, as normal. Does anyone know if this is the only medication I should stop. Thanking you
I have a short synacthen booked via endocrinology NHS.As I use inhaler for COPD, I have been advised not to use it after 4pm the day before. Other than this, everything else, including food, as normal. Does anyone know if this is the only medication I should stop. Thanking you
DandyButch
in
Thyroid UK
2 days ago
am I now over medicated?
I have increased my Levo to 50 mcg and 5 mcg T3. It has been 8 days now. I have stabbing pains all over my body, my palms are burning hot, I am hot and itchy forearms. Feel awful. My joints in knees, ankles and wrists are stiff especially my thumbs. Endo is on leave for 3 weeks. Am I now over medicated
I have increased my Levo to 50 mcg and 5 mcg T3. It has been 8 days now. I have stabbing pains all over my body, my palms are burning hot, I am hot and itchy forearms. Feel awful. My joints in knees, ankles and wrists are stiff especially my thumbs. Endo is on leave for 3 weeks. Am I now over medicated
Redforme
in
Thyroid UK
2 days ago
Is there concerning interactions with cytomel/T3?
Hey folks Was wondering, are there any potentially dangerous interactions that me/people should bê aware of ? Wondering as i deal with some stuff,só i take some chemicals, as for example i take tropisetron an 5ht3 antagonist /nicotinc receptor agonist, Tudca/Udca (bile acids) but also others as sometimes
Hey folks Was wondering, are there any potentially dangerous interactions that me/people should bê aware of ? Wondering as i deal with some stuff,só i take some chemicals, as for example i take tropisetron an 5ht3 antagonist /nicotinc receptor agonist, Tudca/Udca (bile acids) but also others as sometimes
Mobilepirate
in
Thyroid UK
2 days ago
dreaded GP request for bloods
Well there it is. It took longer than I expected I must say - around 7 years since I started my (real) thyroid journey, and about 5 since I last spoke to a GP about it, but the call has finally come. No more T3 until they have bloods. Of course I have bloods, but they almost all show me being over
Well there it is. It took longer than I expected I must say - around 7 years since I started my (real) thyroid journey, and about 5 since I last spoke to a GP about it, but the call has finally come. No more T3 until they have bloods. Of course I have bloods, but they almost all show me being over
Murphysmum
in
Thyroid UK
2 days ago
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