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Blood-coagulation factor XIII
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Johns Hopkins adjusted clinical groups system score mean under nhs?
I see this on record Johns Hopkins adjusted clinical groups system score of ACG 5. What does it mean how does it impact me in any way.? I have started asking for blood tests and my GP has not been happy about it. Surgery has never been keen to blood tests though this seems to have popped up on record
I see this on record Johns Hopkins adjusted clinical groups system score of ACG 5. What does it mean how does it impact me in any way.? I have started asking for blood tests and my GP has not been happy about it. Surgery has never been keen to blood tests though this seems to have popped up on record
thyroidsymtoms
in
Thyroid UK
1 month ago
Discharged by rheumy!
I went to my appointment yesterday, full of tales of woe about all my various health problems this year which caused a delay in my tapering. I'm on half a mg pred. He said my blood tests were all fine. I've had no recurrence of any GCA symptoms. My hip and shoulder stiffness (which is constant and not
I went to my appointment yesterday, full of tales of woe about all my various health problems this year which caused a delay in my tapering. I'm on half a mg pred. He said my blood tests were all fine. I've had no recurrence of any GCA symptoms. My hip and shoulder stiffness (which is constant and not
Broseley
in
PMRGCAuk
1 month ago
Metrical psalms
Ref to statins I've been taking Atorvastatin for approximately 15yrs ! unaware of muscle damage/ weakness but was aware of muscle pain which I didn't have I also take thyroxine 50mcgs daily. I became aware of my inability of going up stairs without having to lever myself up on the bannisters because
Ref to statins I've been taking Atorvastatin for approximately 15yrs ! unaware of muscle damage/ weakness but was aware of muscle pain which I didn't have I also take thyroxine 50mcgs daily. I became aware of my inability of going up stairs without having to lever myself up on the bannisters because
metricalpsalms
in
British Heart Foundation
1 month ago
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Time between Afib trigger & episode
Hi all, I've very recently been diagnosed with Afib (thanks, Apple Watch for highlighting the problem I'd never heard of) and have been to the GP/hospital since February to get a proper diagnosis. So far all my results are showing normal (blood pressure, Echo, blood tests, that sort of thing). ECG did
Hi all, I've very recently been diagnosed with Afib (thanks, Apple Watch for highlighting the problem I'd never heard of) and have been to the GP/hospital since February to get a proper diagnosis. So far all my results are showing normal (blood pressure, Echo, blood tests, that sort of thing). ECG did
MrBinks
in
Atrial Fibrillation Support
1 month ago
New diagnose - GMG
Was diagnosed with FM January 2020, never got a follow-up because of COVID-19, just increasing the medication from GP. Previous winter 22-23 was BAD!!! Didn't leave the house, almost all the winter in bed. Horrible pain, itching that hurts, shaking, and on and on...Till began to slur words, chock on
Was diagnosed with FM January 2020, never got a follow-up because of COVID-19, just increasing the medication from GP. Previous winter 22-23 was BAD!!! Didn't leave the house, almost all the winter in bed. Horrible pain, itching that hurts, shaking, and on and on...Till began to slur words, chock on
Polly-S
in
Fibromyalgia Action UK
1 month ago
My question is about the best way of getting a diagnosis of scleroderma or of discounting it?
I was diagnosed recently with Raynaud's disease which can get quite painful, but is manageable. I have GORD and a small hiatus hernia. However I do get abdominal pain and have asthma exacerbated by allergies. I have just had a CT scan and was told the pain is probably musco-skeletal, plus I have an atrophied
I was diagnosed recently with Raynaud's disease which can get quite painful, but is manageable. I have GORD and a small hiatus hernia. However I do get abdominal pain and have asthma exacerbated by allergies. I have just had a CT scan and was told the pain is probably musco-skeletal, plus I have an atrophied
strongmouse
in
Scleroderma & Raynaud's UK (SRUK)
1 month ago
In shock, TSH from 20.3 to 0.103!
hello, I posted a while ago as I was getting so concerned at the rate my TSH was increasing, I had increased my levothyroxine gradually to 175mg with no improvement, the last bloods and drs appointment I had I was given instructions to increase to 200mg which I believe is the limit for my weight. by
hello, I posted a while ago as I was getting so concerned at the rate my TSH was increasing, I had increased my levothyroxine gradually to 175mg with no improvement, the last bloods and drs appointment I had I was given instructions to increase to 200mg which I believe is the limit for my weight. by
Emma1986x
in
Thyroid UK
1 month ago
Active B12 29 (37.5-150)
These are my student daughter's results. She is at uni in Edinburgh and struggling to find g.p. practice to take her on. She has an iron panel coming too but sample haemolised so have to redo it. These are first blood tests and she is not taking any supplements. Please advise on thoughts and next
These are my student daughter's results. She is at uni in Edinburgh and struggling to find g.p. practice to take her on. She has an iron panel coming too but sample haemolised so have to redo it. These are first blood tests and she is not taking any supplements. Please advise on thoughts and next
AKatieD
in
Pernicious Anaemia Society
1 month ago
Medichecks ferritin results and ranges
Hi all. I don't have a thyroid issue (this has been ruled out), but someone on the PAS forum suggested I post a query on here to see if anyone could shed light on this issue. Having accessed my GP records late last year I discovered I had a long-standing ferritin deficiency, as defined by NICE guidelines
Hi all. I don't have a thyroid issue (this has been ruled out), but someone on the PAS forum suggested I post a query on here to see if anyone could shed light on this issue. Having accessed my GP records late last year I discovered I had a long-standing ferritin deficiency, as defined by NICE guidelines
KBird01
in
Thyroid UK
1 month ago
Testing for Intrinsic Factor - borderline results
Hello to you all on this precious platform, thank you for saving my sanity on many occasions. I was diagnosed with pernicious anemia 10 years ago. My elder sister, following a lengthy battle with her GP was diagnosed a couple of years ago and given loading doses followed by 8 week top-ups. We both
Hello to you all on this precious platform, thank you for saving my sanity on many occasions. I was diagnosed with pernicious anemia 10 years ago. My elder sister, following a lengthy battle with her GP was diagnosed a couple of years ago and given loading doses followed by 8 week top-ups. We both
Discombobulated247
in
Pernicious Anaemia Society
8 months ago
On ending
Just over 2 months ago I had 2value.replacements mechanical op went very well unfortunately my after care didn't go all that well .Iam having to go to doctors 2 times a week.for blood tests to get warfine dose right and this week alone 2 hospital appointments.which is far way don't have car and patent
Just over 2 months ago I had 2value.replacements mechanical op went very well unfortunately my after care didn't go all that well .Iam having to go to doctors 2 times a week.for blood tests to get warfine dose right and this week alone 2 hospital appointments.which is far way don't have car and patent
Craig53
in
British Heart Foundation
1 month ago
New to Levo, question about TSH aim
I've been taking Levo 50mg per day for 3 months, and just had the first blood test result back. My TSH is at 2.85, and they are saying that I should stay on this dose and get tested again in a year. The last test before I started medication (January) my TSH was 8.6, T4 12.8. Both were done first thing
I've been taking Levo 50mg per day for 3 months, and just had the first blood test result back. My TSH is at 2.85, and they are saying that I should stay on this dose and get tested again in a year. The last test before I started medication (January) my TSH was 8.6, T4 12.8. Both were done first thing
tattiescone
in
Thyroid UK
1 month ago
Further advice needed from you lovely people.....Please
Some of you will remember my recent post about my private blood test results and a scan which showed I have a very small thyroid......... Test results shown above, all vits and mins were ok. On advice from some of you knowledagable people, I increased my Levo by 25mg and informed my Gp and endocrinologist
Some of you will remember my recent post about my private blood test results and a scan which showed I have a very small thyroid......... Test results shown above, all vits and mins were ok. On advice from some of you knowledagable people, I increased my Levo by 25mg and informed my Gp and endocrinologist
Jillymo
in
Thyroid UK
1 month ago
FasFasting before blood test
hi, following my last post, my gp has agreed to add B12, ferritin etc to my annual thyroid review. I've been told here to not take my usual morning dose before the test;however, looking online most medical websites say its not necessary to fast. Anyone care to clarify for me please. thanks
hi, following my last post, my gp has agreed to add B12, ferritin etc to my annual thyroid review. I've been told here to not take my usual morning dose before the test;however, looking online most medical websites say its not necessary to fast. Anyone care to clarify for me please. thanks
Doats
in
Thyroid UK
1 month ago
PMR since July 2018 and down to 1mg. Enter GCA
My Bio is pretty well up to date, until a week ago. Quick summary of things is: I'm ok, vision ok, diagnosed with GCA, and I've gone from 1mg (nearly done...or so I thought) to 60mg. Now on my third day of 60mg and waiting on new bloods I did today and a call from the consultant tomorrow to discuss
My Bio is pretty well up to date, until a week ago. Quick summary of things is: I'm ok, vision ok, diagnosed with GCA, and I've gone from 1mg (nearly done...or so I thought) to 60mg. Now on my third day of 60mg and waiting on new bloods I did today and a call from the consultant tomorrow to discuss
pata63
in
PMRGCAuk
1 month ago
Confusing Lab Test Results
I had a recent PMR flare that necessitated my temporarily going up from the 5mg I had tapered down to to a much higher dose. 20mg for 2 weeks, followed by 15mg for one week and then a drop to 10mg, where I have stayed for almost a month before I resume DL’s slow 5 week taper. Fortunately, my increased
I had a recent PMR flare that necessitated my temporarily going up from the 5mg I had tapered down to to a much higher dose. 20mg for 2 weeks, followed by 15mg for one week and then a drop to 10mg, where I have stayed for almost a month before I resume DL’s slow 5 week taper. Fortunately, my increased
Donna5658
in
PMRGCAuk
1 month ago
Interpreting blood tests
I've been on ADT for 4 months in preparation for RT and then HDR BT. I have localised G8 with an initial PSA of 8.1 Prior to commencing ADT, my PSA inexplicably dropped to 4.94 but then rose to 5.37 within 2 months. Anyway, here are my test results before starting ADT; These are Aussie measurements
I've been on ADT for 4 months in preparation for RT and then HDR BT. I have localised G8 with an initial PSA of 8.1 Prior to commencing ADT, my PSA inexplicably dropped to 4.94 but then rose to 5.37 within 2 months. Anyway, here are my test results before starting ADT; These are Aussie measurements
Mike58
in
Advanced Prostate Cancer
1 month ago
Silent Reflux? Is yours scary?
Initially I could just be having a drink of water from a bottle and suddenly spray the water straight back out of my mouth. No warning. No previous symptoms either. After a scan and blood tests that were fine, in a week it stopped. 3 months down the track, the left hand side of tongue and under tongue
Initially I could just be having a drink of water from a bottle and suddenly spray the water straight back out of my mouth. No warning. No previous symptoms either. After a scan and blood tests that were fine, in a week it stopped. 3 months down the track, the left hand side of tongue and under tongue
MeeMawMea
in
Acid Reflux Support
1 month ago
B vits
I think I need to start taking b vits again as feeling very foggy brained, apathetic etc. I stopped as ineggus b complex seemed to be exacerbating a pain under my right rib. I stopped taking them and the pain ceased. I tried one tablet again last week and the pain returned. I’ve had a chest x ray and
I think I need to start taking b vits again as feeling very foggy brained, apathetic etc. I stopped as ineggus b complex seemed to be exacerbating a pain under my right rib. I stopped taking them and the pain ceased. I tried one tablet again last week and the pain returned. I’ve had a chest x ray and
Fizzwhizz
in
Thyroid UK
1 month ago
experiences with seasonal changes?
If you have taken thyroid hormone replacement for some time and your levels are pretty much settled please can you share your experiences with seasonal changes? Do you find you need to reduce/increase your doses seasonally? What signs apart from blood test results indicate this if so?
If you have taken thyroid hormone replacement for some time and your levels are pretty much settled please can you share your experiences with seasonal changes? Do you find you need to reduce/increase your doses seasonally? What signs apart from blood test results indicate this if so?
Regenallotment
in
Thyroid UK
1 month ago
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