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Amylase test
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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
2 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
3 months ago
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
4 months ago
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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
3 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
9 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
9 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
The joy of the unclear diagnosis 😂
This is a verrrry long post!! If anyone actually reads to the end you have my full respect I’m a returning member to the forum. I used to be active when I was being treated for severe asthma. I used to routinely end up in hospital for basic chest infections, and struggled with chest aching and tightness
This is a verrrry long post!! If anyone actually reads to the end you have my full respect I’m a returning member to the forum. I used to be active when I was being treated for severe asthma. I used to routinely end up in hospital for basic chest infections, and struggled with chest aching and tightness
saltyskies
in
Lung Conditions Community Forum
1 year ago
ADVICE PLEASE
Does this mean a cancer,as it is borderlineBone profile Full blood count Liver function tests Serum amylase level Tumour Markers Urea and electrolytes
Does this mean a cancer,as it is borderlineBone profile Full blood count Liver function tests Serum amylase level Tumour Markers Urea and electrolytes
pettyt65
in
Thyroid UK
1 year ago
Mottled skin on stomach
Has anyone had this? I don't have any other symptoms of pancreatitis except for slightly raised amylase however I do also have acid reflux that's improving on PPIs.The mottling is mild and sometimes not visible but seems to have started at the same time I started with reflux.
Has anyone had this? I don't have any other symptoms of pancreatitis except for slightly raised amylase however I do also have acid reflux that's improving on PPIs.The mottling is mild and sometimes not visible but seems to have started at the same time I started with reflux.
Jaby86
in
Chronic Pancreatitis Support
1 year ago
Mottled skin on stomach
I know it can related to pancreatitis but I don't have any other symptoms but it's definitely something that I have noticed since having reflux for the past 2 months.I have an ultrasound on my abdomen on Friday as my
amylase
results from a blood
test
were slightly raised so they are checking for any
I know it can related to pancreatitis but I don't have any other symptoms but it's definitely something that I have noticed since having reflux for the past 2 months.I have an ultrasound on my abdomen on Friday as my
amylase
results from a blood
test
were slightly raised so they are checking for any
Jaby86
in
Acid Reflux Support
1 year ago
chronic pancreatitis?
hello, please note I have an existing rare autoimmune disease called Adult Onset Stills Disease of rheumatology speciality. I fear I may have chronic pancreatitis or autoimmune pancreatitis due to symptoms however the locum GP who rang me to discuss raised amylase in my blood tests is referring me for
hello, please note I have an existing rare autoimmune disease called Adult Onset Stills Disease of rheumatology speciality. I fear I may have chronic pancreatitis or autoimmune pancreatitis due to symptoms however the locum GP who rang me to discuss raised amylase in my blood tests is referring me for
Hidden
in
Chronic Pancreatitis Support
1 year ago
Thwarted again !
I have just seen a new gp, who was actually rather lovely compared to the AH who was the last one.I actually saw him for my back pain and did mention rls. Now, what he wants to try is 10 mg amitrytamine (bah, can't spell it !)in the morning, 1000 mg of naprogesic and 25mg of pregabalin in the morning
I have just seen a new gp, who was actually rather lovely compared to the AH who was the last one.I actually saw him for my back pain and did mention rls. Now, what he wants to try is 10 mg amitrytamine (bah, can't spell it !)in the morning, 1000 mg of naprogesic and 25mg of pregabalin in the morning
Oscarcat63
in
Restless Legs Syndrome
29 minutes ago
Tirosint Sol ampules
Hi Since I moved to Dorset from Ireland I have had problems getting meds on an Irish prescription because the UK doctors won’t prescribe it. I can get my Thybon Henning 20 from Germany but the T4 tirosint is in capsules and I was allergic to they for some reason. They say only gelatine and glycerin
Hi Since I moved to Dorset from Ireland I have had problems getting meds on an Irish prescription because the UK doctors won’t prescribe it. I can get my Thybon Henning 20 from Germany but the T4 tirosint is in capsules and I was allergic to they for some reason. They say only gelatine and glycerin
jand123
in
Thyroid UK
3 hours ago
Advice please
I thought I was going mad at first, my RLS is horrendous and affecting me at work. Poor and very little sleep, getting confused and making mistakes, forgetting information. The RLS was starting early on a morning and nothing I could do to relieve it. I was taking too many cocodomoI out of desperation
I thought I was going mad at first, my RLS is horrendous and affecting me at work. Poor and very little sleep, getting confused and making mistakes, forgetting information. The RLS was starting early on a morning and nothing I could do to relieve it. I was taking too many cocodomoI out of desperation
Coopersmum
in
Restless Legs Syndrome
3 hours ago
Mercury pharma
Help,panic mode ! Went to pharmacy and no Mercury pharma thyroxine,say I will have too just take another brand cannot tolerate teva.My gp always request Mercury pharma for me and have had it for years.Have they gone out of bisnuss as cannot get there web page up to contact them.
Help,panic mode ! Went to pharmacy and no Mercury pharma thyroxine,say I will have too just take another brand cannot tolerate teva.My gp always request Mercury pharma for me and have had it for years.Have they gone out of bisnuss as cannot get there web page up to contact them.
susiebow
in
Thyroid UK
3 hours ago
Doctor
I am wondering if anyone has come across a Dr Zachariah in Horsham? I am looking for thyroid and adrenal glands. Please PM me as I would be interested to hear experiences. Thank you! PS As a side note, I was prescribed the 20mcg T3 after asking not to have the 10mcg capsules - thank you to everyone
I am wondering if anyone has come across a Dr Zachariah in Horsham? I am looking for thyroid and adrenal glands. Please PM me as I would be interested to hear experiences. Thank you! PS As a side note, I was prescribed the 20mcg T3 after asking not to have the 10mcg capsules - thank you to everyone
AppleOrchard
in
Thyroid UK
2 hours ago
How much T3 do you keep as backup?
I have to order a repeat T3 prescription in the next couple of day from a private GP at a lab and as I will be going away from home for approx 3 months I will have to request a large amount. It made me think that I should probably keep a reasonably large bank of T3 since running out could be very nasty
I have to order a repeat T3 prescription in the next couple of day from a private GP at a lab and as I will be going away from home for approx 3 months I will have to request a large amount. It made me think that I should probably keep a reasonably large bank of T3 since running out could be very nasty
inthedoldrums
in
Thyroid UK
18 hours ago
Vitamin B6 in B Complexes
Seeking advice on Vitamin B6 in B Complexes. Background: Diagnosed hypothyroid since the late 1990's; switched to T3 liothyronine only since about 2014 because levothyroxine didn't help me . Diagnosed with Parkinson's (finally!) in early 2023. Currently under the care of a movement disorders specialist
Seeking advice on Vitamin B6 in B Complexes. Background: Diagnosed hypothyroid since the late 1990's; switched to T3 liothyronine only since about 2014 because levothyroxine didn't help me . Diagnosed with Parkinson's (finally!) in early 2023. Currently under the care of a movement disorders specialist
chrysalis56
in
Thyroid UK
1 day ago
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