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How do I update my bio?
My bio on Health Unlocked website needs updating. How do I do that? I can't seem to update my bio from 2023. I'm interested in adding PSAs and testosterone quarterly blood tests from 2023 and 2024. My good new is that my PSA has been 0.01 "nearly undetectable" for more than a year. My MO said don't
My bio on Health Unlocked website needs updating. How do I do that? I can't seem to update my bio from 2023. I'm interested in adding PSAs and testosterone quarterly blood tests from 2023 and 2024. My good new is that my PSA has been 0.01 "nearly undetectable" for more than a year. My MO said don't
happycamperguy
in
Advanced Prostate Cancer
25 days ago
Stop Ibrance?
My HB and Platelets have been bad for a while. Mainly because I haven' eaten anything. I am now eating again and feel much better (I had other reasons), but she has ordered me back for new blood tests and wants me to change to Xeloda. I want a chance to get my appetite back up and eating normally before
My HB and Platelets have been bad for a while. Mainly because I haven' eaten anything. I am now eating again and feel much better (I had other reasons), but she has ordered me back for new blood tests and wants me to change to Xeloda. I want a chance to get my appetite back up and eating normally before
SwedishSissi
in
SHARE Metastatic Breast Cancer
25 days ago
Compensated Cirrhosis - Sudden Extreme Increase in Liver Stiffness - Under Treatment, Blood Tests Normalized
During annual medical tests in Feb 2024: - Saw elevated Liver Enzymes, Hi bilirubinFibroscan (ordered by Dr) Stage 2 Fatty Liver, LSM 12.59, Early eosphageal varices, normal platelets (low end of normal) - Compensated Child-A Cirrhosis - Diabetic, high Cholesterol, hi triglycerides Hypertension: All
During annual medical tests in Feb 2024: - Saw elevated Liver Enzymes, Hi bilirubinFibroscan (ordered by Dr) Stage 2 Fatty Liver, LSM 12.59, Early eosphageal varices, normal platelets (low end of normal) - Compensated Child-A Cirrhosis - Diabetic, high Cholesterol, hi triglycerides Hypertension: All
ZeroInfiniti
in
British Liver Trust
25 days ago
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Ana vs ENA
Hello, After many years of joint pain and 5+ years of eye troubles, I was given a series of blood tests including autoantibodies. I've come back positive three times now for dsdna autoantibody (the second two tests simply being repeats). The numbers (I think) were fairly low positives - between 48 and
Hello, After many years of joint pain and 5+ years of eye troubles, I was given a series of blood tests including autoantibodies. I've come back positive three times now for dsdna autoantibody (the second two tests simply being repeats). The numbers (I think) were fairly low positives - between 48 and
Soph160
in
LUPUS UK
25 days ago
Taking NDT but still tired
1. NDT doses - take 1 pill at 6 a.m. - take 1/2 pill at 2 p.m. 2. Supplements - take a bottle of Orthomol Vital F daily - 2 brazul nuts daily Hello I had removed my thyroid gland 12 years ago and I've been taking NDT manufactured from Thailand(THYROID-S) since 2017. But since about 3 - 4 years
1. NDT doses - take 1 pill at 6 a.m. - take 1/2 pill at 2 p.m. 2. Supplements - take a bottle of Orthomol Vital F daily - 2 brazul nuts daily Hello I had removed my thyroid gland 12 years ago and I've been taking NDT manufactured from Thailand(THYROID-S) since 2017. But since about 3 - 4 years
shiny92
in
Thyroid UK
25 days ago
new member
Hi. My name is Emchar. I am waiting for diagnosis of possible Sjögrens or other issues related to swollen salivary glands and dry mouth and Raynauds. My Rheumatologist is not sure and has done further blood tests and is sending me for Ultrasound scan. I also have Pernicious Anemia diagnosed 2013. Obviously
Hi. My name is Emchar. I am waiting for diagnosis of possible Sjögrens or other issues related to swollen salivary glands and dry mouth and Raynauds. My Rheumatologist is not sure and has done further blood tests and is sending me for Ultrasound scan. I also have Pernicious Anemia diagnosed 2013. Obviously
EmChar
in
LUPUS UK
25 days ago
Rheumatogy appointment
hi recently referred to Rheumatologist for symptoms of Rheumatic condition. I had swollen salivary glands 2 years dry mouth so trouble eating; Reynauds phenomenon; aching muscles; fatigue. GP concerned about symptoms and negative ANA but queried staining/pattern. Appointment last Friday with Rheumatologist
hi recently referred to Rheumatologist for symptoms of Rheumatic condition. I had swollen salivary glands 2 years dry mouth so trouble eating; Reynauds phenomenon; aching muscles; fatigue. GP concerned about symptoms and negative ANA but queried staining/pattern. Appointment last Friday with Rheumatologist
EmChar
in
LUPUS UK
25 days ago
what now failed R223
‘what now’ failed R223 My husband this week because of low Hb 83 had a blood transfusion + iron infusion. He has suffered ‘Proctitis’ rectal bleeding since having radiotherapy 2019 and although complaining to Oncologist, GP, Gastroenterologist had endoscopy (found Barrett’s disease and has difficulty
‘what now’ failed R223 My husband this week because of low Hb 83 had a blood transfusion + iron infusion. He has suffered ‘Proctitis’ rectal bleeding since having radiotherapy 2019 and although complaining to Oncologist, GP, Gastroenterologist had endoscopy (found Barrett’s disease and has difficulty
Janhpr
in
Advanced Prostate Cancer
25 days ago
Advice re levothyroxine dosage
HelloI would be very greatful for advice regarding my next move re Levothyroxine dosage. On 10 May 2024 began 100mcg levothyroxine after titrating up following blood tests and still experiencing symptoms since Jan 24. Did finger prick test on 20 June (test taken at 7.30 am, fasted and no levo 24 hours
HelloI would be very greatful for advice regarding my next move re Levothyroxine dosage. On 10 May 2024 began 100mcg levothyroxine after titrating up following blood tests and still experiencing symptoms since Jan 24. Did finger prick test on 20 June (test taken at 7.30 am, fasted and no levo 24 hours
pastashapes
in
Thyroid UK
25 days ago
Myelofibrosis- GVHD graft, versus, host, disease.
Hi, thanks for accepting me onto your site. My name is Gary, I am 64 years old and was diagnosed with Myelofibrosis in July, 2024. It all started when I began to feel lethargic and very tired, I had no inspiration to do anything. I was a taxi driver and was only managing to work one or two days a week
Hi, thanks for accepting me onto your site. My name is Gary, I am 64 years old and was diagnosed with Myelofibrosis in July, 2024. It all started when I began to feel lethargic and very tired, I had no inspiration to do anything. I was a taxi driver and was only managing to work one or two days a week
FreemanSaviors
in
MPN Voice
25 days ago
Myelofibrosis - GVHD - graft, versus, host, disease
Hi, thanks for accepting me onto the site. My name is Gary, I am 64 years old and was diagnosed with Myelofibrosis in July, 2024. It all started when I began to feel lethargic and very tired, I had no inspiration to do anything. I was a taxi driver and was only managing to work one or two days a week
Hi, thanks for accepting me onto the site. My name is Gary, I am 64 years old and was diagnosed with Myelofibrosis in July, 2024. It all started when I began to feel lethargic and very tired, I had no inspiration to do anything. I was a taxi driver and was only managing to work one or two days a week
FreemanSaviors
in
MPN Voice
25 days ago
8 years undiagnosed - possible hypothyroidism?
Full size - https://ibb.co/chkSycC 34 / M Iron is normal, ferritin was 90 ug/L last time checked Hello, I've had severe health problems for around 8 years now and have been through many hospital departments and tests and no one can still quite figure out what's wrong with me. I've effectively been
Full size - https://ibb.co/chkSycC 34 / M Iron is normal, ferritin was 90 ug/L last time checked Hello, I've had severe health problems for around 8 years now and have been through many hospital departments and tests and no one can still quite figure out what's wrong with me. I've effectively been
CursedLemon
in
Thyroid UK
26 days ago
latest results
Have had Normagesic amnesia for many years never treated. Approximately 2 years ago was started on loading doses for B12 deficiency and 3 monthly for a year then stopped. Despite requests to continue these have been denied. Have type 2 diabetes and all neurological problems in feet and legs always attributed
Have had Normagesic amnesia for many years never treated. Approximately 2 years ago was started on loading doses for B12 deficiency and 3 monthly for a year then stopped. Despite requests to continue these have been denied. Have type 2 diabetes and all neurological problems in feet and legs always attributed
Nonameme
in
Pernicious Anaemia Society
26 days ago
Thyroid Nodules - Advice Please 🙏
I'm new here and it's my first time posting. It was noticed I had a large nodule on my thyroid while having a CT scan for an unrelated issue 5 weeks ago. I can feel a large lump on the right hand side of my neck which is also visible and an ultrasound scan has since confirmed there are several nodules
I'm new here and it's my first time posting. It was noticed I had a large nodule on my thyroid while having a CT scan for an unrelated issue 5 weeks ago. I can feel a large lump on the right hand side of my neck which is also visible and an ultrasound scan has since confirmed there are several nodules
StaffyMam
in
Thyroid UK
26 days ago
Partial thyroidectomy
Hi I'm based in the UK, 1st time posting. I've been advised to have a partial thyroidectomy by an ENT consultant following a Thy3 test result. It's going to happen soon, I am being fast tracked for surgery, pre-op in 2 days. Found the lump in March but it may have been there for some time. Its about
Hi I'm based in the UK, 1st time posting. I've been advised to have a partial thyroidectomy by an ENT consultant following a Thy3 test result. It's going to happen soon, I am being fast tracked for surgery, pre-op in 2 days. Found the lump in March but it may have been there for some time. Its about
Kallew1
in
Thyroid UK
26 days ago
FBC interpretation
I live in France and so therefore cannot obtain private blood test results for Folate, B12, and Ferritin without catching a ferry and returning to the UK which I am too ill to do at present. I do however have a full blood count from a few months ago. My questions is can anybody on this site help me
I live in France and so therefore cannot obtain private blood test results for Folate, B12, and Ferritin without catching a ferry and returning to the UK which I am too ill to do at present. I do however have a full blood count from a few months ago. My questions is can anybody on this site help me
Brightness14
in
Thyroid UK
26 days ago
AST to ALT ratio has become greater than 1 after decades of elevated levels
My ALT and AST have been elevated for decades. For second time in a row now, my AST has becomevhigher than ALT ; they are currently in 60ish range. A very nice article i read on the DiRitiis ratio from around 2013 says my new current ratio of 1.1 suggests fibrosis and ir bad prognosis to cirrhosis
My ALT and AST have been elevated for decades. For second time in a row now, my AST has becomevhigher than ALT ; they are currently in 60ish range. A very nice article i read on the DiRitiis ratio from around 2013 says my new current ratio of 1.1 suggests fibrosis and ir bad prognosis to cirrhosis
SkinNBones
in
British Liver Trust
26 days ago
+100 Days post transplant
Well I've made it to the first mile post, I can't believe it's 100 days since my SCT, I cannot thank my brother too much for being my donor. I still have low blood counts and had a BMB 3 1/2 weeks ago for the Dr's to check what's going on, three of the 4 counts showed either 100% or very nearly of donor
Well I've made it to the first mile post, I can't believe it's 100 days since my SCT, I cannot thank my brother too much for being my donor. I still have low blood counts and had a BMB 3 1/2 weeks ago for the Dr's to check what's going on, three of the 4 counts showed either 100% or very nearly of donor
Flyingsteamer
in
MPN Voice
26 days ago
Thyroid help!
Alright it’s been a while since I posted. I had my baby in July last year and since I’ve not been taking care of myself and forgetting my levothyroxine most mornings after sleepless nights. About 8 weeks ago I switched taking my Levo in the morning to the evening as I had more time while baby was asleep
Alright it’s been a while since I posted. I had my baby in July last year and since I’ve not been taking care of myself and forgetting my levothyroxine most mornings after sleepless nights. About 8 weeks ago I switched taking my Levo in the morning to the evening as I had more time while baby was asleep
GinaR86
in
Thyroid UK
26 days ago
TSH declining whilst on carbimazole
hi, I was diagnosed with Graves’ disease and I am currently taking 10mg carbimazole 4 days a week and 5mg 3 days a week. I have been taking for around 20 months now and whilst my T3&T4 levels have been in normal range for ages, my TSH has only recently been detectable( after about 16 months) Anyway
hi, I was diagnosed with Graves’ disease and I am currently taking 10mg carbimazole 4 days a week and 5mg 3 days a week. I have been taking for around 20 months now and whilst my T3&T4 levels have been in normal range for ages, my TSH has only recently been detectable( after about 16 months) Anyway
Hylan23
in
Thyroid UK
26 days ago
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