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low ADH levels in blood.anybody had this with parkinsons
Hi. Has anybody with Parkinson's had an issue with getting up in the night to pee and then doc has tested blood and found low levels of AD H which is anti diruetic hormone. I don't think it has anything to do with Parkinson's but family member may have low levels of this ( awaiting blood test to see
Hi. Has anybody with Parkinson's had an issue with getting up in the night to pee and then doc has tested blood and found low levels of AD H which is anti diruetic hormone. I don't think it has anything to do with Parkinson's but family member may have low levels of this ( awaiting blood test to see
20fatcats
in
Cure Parkinson's
2 months ago
"treating PSA" vs "treating cancer" advice
Hi all, My dad was diagnosed with stage 4 metastatic prostate cancer over a year ago (history of his diagnosis is in my profile). When he was diagnosed he did triple therapy (docataxel, zoladex and nubeqa). He has now on zoladex injections (every 3 months) and nubeqa (darolutamide) tablets daily. Thankfully
Hi all, My dad was diagnosed with stage 4 metastatic prostate cancer over a year ago (history of his diagnosis is in my profile). When he was diagnosed he did triple therapy (docataxel, zoladex and nubeqa). He has now on zoladex injections (every 3 months) and nubeqa (darolutamide) tablets daily. Thankfully
Jdhanoa
in
Advanced Prostate Cancer
2 months ago
Roseway Labs
Hi, I’m hoping to increase my Levothyroxine dose ( my GP won’t and can’t be doing with trying to convince them). My question is will Roseway Labs be able to or do they need agreement by my GP? Do I need to show them my latest blood test to have an increase? And do I need to make an appointment with
Hi, I’m hoping to increase my Levothyroxine dose ( my GP won’t and can’t be doing with trying to convince them). My question is will Roseway Labs be able to or do they need agreement by my GP? Do I need to show them my latest blood test to have an increase? And do I need to make an appointment with
Bright-eyes
in
Thyroid UK
2 months ago
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Don't know where to start
After 4 years I still don't really know what I have.Initially diagnosed with Undifferentiated Inflammatory Arthritis, then discovered by accident that it had changed to Connective Tissue Disease and Lupus. I also discovered only yesterday that at some point I tested positive for ANA which I've never
After 4 years I still don't really know what I have.Initially diagnosed with Undifferentiated Inflammatory Arthritis, then discovered by accident that it had changed to Connective Tissue Disease and Lupus. I also discovered only yesterday that at some point I tested positive for ANA which I've never
Brychni
in
LUPUS UK
2 months ago
bleeding
Hi all I was taking clopidrell blood thinners from few years then I sadly kept heavy nose bleeds so I been taking 75 mg Asprin daily and I notice I have now bleeding gums ! Also got to repeat blood test for Gp I have low folate and low B12 so seeing Gp Thursday ! I have an app coming up for heamatology
Hi all I was taking clopidrell blood thinners from few years then I sadly kept heavy nose bleeds so I been taking 75 mg Asprin daily and I notice I have now bleeding gums ! Also got to repeat blood test for Gp I have low folate and low B12 so seeing Gp Thursday ! I have an app coming up for heamatology
Birdlady2021
in
MPN Voice
2 months ago
help to understand test results
After a year of monitoring my TSH due to a bout of subacute thyroiditis, initially suspected as thyroid cancer. I am now at a point where my GP feels medication may be required and have undertaken an extensive range of blood tests through the GP I have an appointment on the 4th July to discuss options
After a year of monitoring my TSH due to a bout of subacute thyroiditis, initially suspected as thyroid cancer. I am now at a point where my GP feels medication may be required and have undertaken an extensive range of blood tests through the GP I have an appointment on the 4th July to discuss options
Mac2013
in
Thyroid UK
2 months ago
Muzvare
I am a woman aged 53. Iwas diagnosed with lupus two weeks ago. However, I was not given any treatment. I got no advice on what to do next. I am supposed to go for blood tests in 3 months. Please any tips after diagnosis. I feel lonely with diagnosis and nothing said after that. Any tips on diet or
I am a woman aged 53. Iwas diagnosed with lupus two weeks ago. However, I was not given any treatment. I got no advice on what to do next. I am supposed to go for blood tests in 3 months. Please any tips after diagnosis. I feel lonely with diagnosis and nothing said after that. Any tips on diet or
Muzvare
in
LUPUS UK
2 months ago
6 MONTHS SINCE MISCARRIAGE - TRYING TO CONCEIVE
Hello, I am 26 year old and got pregnant for the first time last year around august and miscarried in October therefore, almost 2 months. After that, my periods my have been irregular and so my period cycle. I have also gained weight that is triggering my PCOS. I have been trying to get pregnant for
Hello, I am 26 year old and got pregnant for the first time last year around august and miscarried in October therefore, almost 2 months. After that, my periods my have been irregular and so my period cycle. I have also gained weight that is triggering my PCOS. I have been trying to get pregnant for
qz123
in
Fertility Network UK
2 months ago
looking for diagnosis
Have had a tough last 2 years with elevated liver enzymes, bad fatigue, headaches initially balance problems and now a constant headache and forehead artery is sore along its length. Beginning of last year i had the temperal ultrasound but not conclusive. Into my 3rd week of constant headaches which
Have had a tough last 2 years with elevated liver enzymes, bad fatigue, headaches initially balance problems and now a constant headache and forehead artery is sore along its length. Beginning of last year i had the temperal ultrasound but not conclusive. Into my 3rd week of constant headaches which
Oztrax
in
PMRGCAuk
2 months ago
Doctors /drugs and blood results
I recently posted I'd had a knee replacement 1st march . I've had 2 before no problem . This time my Rls has gone mad . I've had all the normal drugs and been on bupromorphine for 3 to 4 yrs no problems . Been great. Until this operation . I also have hurt the tendons etc in the same leg on my outer
I recently posted I'd had a knee replacement 1st march . I've had 2 before no problem . This time my Rls has gone mad . I've had all the normal drugs and been on bupromorphine for 3 to 4 yrs no problems . Been great. Until this operation . I also have hurt the tendons etc in the same leg on my outer
Palamino
in
Restless Legs Syndrome
2 months ago
New to group
Hi it’s taken six months of agony however today after last round of blood tests I am starting steroids tomorrow. I am very nervous especially as I have glaucoma, the doctor said I have no choice I must take the steroids. Anyone else taking meds with glaucoma? He also warned I could feel very strange
Hi it’s taken six months of agony however today after last round of blood tests I am starting steroids tomorrow. I am very nervous especially as I have glaucoma, the doctor said I have no choice I must take the steroids. Anyone else taking meds with glaucoma? He also warned I could feel very strange
Sunshine8888
in
PMRGCAuk
2 months ago
Intrinsic factor jump from 1.1 to now 18.8 high
hello All, so I received my blood test results today for intrinsic factor and it is 18 high over the limit of 1.1. in February I was at 1.1. does anyone have any suggestions on why such a jump. I have been injecting b12 for 1.5 months now. would that have changed anything? my CBC was really good hemoglobin
hello All, so I received my blood test results today for intrinsic factor and it is 18 high over the limit of 1.1. in February I was at 1.1. does anyone have any suggestions on why such a jump. I have been injecting b12 for 1.5 months now. would that have changed anything? my CBC was really good hemoglobin
JesusMercy60
in
Pernicious Anaemia Society
2 months ago
Different Types of MS
I was reading a post on another online group earlier today and realized I really needed this for clarity. Maybe you do too. Robbie Multiple sclerosis (MS) is a chronic disease that affects the brain and spinal cord. It is thought to be an autoimmune disease. This means that the body's immune system
I was reading a post on another online group earlier today and realized I really needed this for clarity. Maybe you do too. Robbie Multiple sclerosis (MS) is a chronic disease that affects the brain and spinal cord. It is thought to be an autoimmune disease. This means that the body's immune system
robster1
in
My MSAA Community
2 months ago
Hashimoto’s Dr’s Reply - help needed please
Bloods above - is anyone able to help me with a response to this letter please? I have asked for my levo to be put back up to 150 and they have refused - I have previously posted that I regularly don’t get meds I can take, brands are changed regularly - they often give me meds I have reactions to so
Bloods above - is anyone able to help me with a response to this letter please? I have asked for my levo to be put back up to 150 and they have refused - I have previously posted that I regularly don’t get meds I can take, brands are changed regularly - they often give me meds I have reactions to so
D911
in
Thyroid UK
2 months ago
Silent Reflux and B12 Deficiency- Any Link?
Hello! I was diagnosed with low B12 following a blood test in December last year, on injections but only had 3 of the 6 loading doses then was moved on to one every three months due to severe side effects that worried my GP. Had my first of the 3 monthly ones a few weeks ago and all went well. I saw
Hello! I was diagnosed with low B12 following a blood test in December last year, on injections but only had 3 of the 6 loading doses then was moved on to one every three months due to severe side effects that worried my GP. Had my first of the 3 monthly ones a few weeks ago and all went well. I saw
Hidden
in
Pernicious Anaemia Society
2 months ago
hypothyroid
Hi all, New here and need some advice So, I first went on levothyroxine (50mg) back in April after running the London marathon. Fast forward 6 weeks to my initial blood test to see if the TSH had resolved itself, it was 0.3. Since then I’ve been feeling ridiculously fatigued and so unwell. So I
Hi all, New here and need some advice So, I first went on levothyroxine (50mg) back in April after running the London marathon. Fast forward 6 weeks to my initial blood test to see if the TSH had resolved itself, it was 0.3. Since then I’ve been feeling ridiculously fatigued and so unwell. So I
CAB92
in
Thyroid UK
2 months ago
Running low on iron
I have been put on Ferrous Sulphate but I can’t use it. My blood test for ferritin is 44 ug/L & it is only that high because I ate red meat I did do in desperation because the test last year was 10ug/L. I am vegetarian & I have great difficulty eating meat it seems to be hard to process for me. Anyhow
I have been put on Ferrous Sulphate but I can’t use it. My blood test for ferritin is 44 ug/L & it is only that high because I ate red meat I did do in desperation because the test last year was 10ug/L. I am vegetarian & I have great difficulty eating meat it seems to be hard to process for me. Anyhow
spinela7
in
Pernicious Anaemia Society
2 months ago
TG6 and gluten ataxia
I was diagnosed with Idiopathic Cerebellar Ataxia in 2018 and had all the usual tests which proved negative . My neurologist in Aberdeen recently managed to arrange a TG6 blood test in Sheffield . The result was 4.2 U/ML , and a result >4 is positive.I have none of the usual symptoms of celiac disease
I was diagnosed with Idiopathic Cerebellar Ataxia in 2018 and had all the usual tests which proved negative . My neurologist in Aberdeen recently managed to arrange a TG6 blood test in Sheffield . The result was 4.2 U/ML , and a result >4 is positive.I have none of the usual symptoms of celiac disease
cyclist49
in
Ataxia UK
2 months ago
Is thyroid causing my symptoms?
Hi all, I’m looking for some advice about my blood test results and whether thyroid issues could be the cause of my symptoms. Also if anyone can recommend a doctor in Cardiff / South Wales I’d really appreciate it. I’ve spent years trying to manage and believing (being told) my symptoms are due to anxiety
Hi all, I’m looking for some advice about my blood test results and whether thyroid issues could be the cause of my symptoms. Also if anyone can recommend a doctor in Cardiff / South Wales I’d really appreciate it. I’ve spent years trying to manage and believing (being told) my symptoms are due to anxiety
Legomami
in
Thyroid UK
2 months ago
Wow the GP experience is real…
I was recently privately diagnosed with autoimmune Hashimoto’s by a (NHS) endocrinologist with autoimmune Hashimoto’s. I was diagnosed via bloods and a scan, and there is a significant family history of Hashimoto’s. There was also a record of increasing TSH etc due to employer health checks. I think
I was recently privately diagnosed with autoimmune Hashimoto’s by a (NHS) endocrinologist with autoimmune Hashimoto’s. I was diagnosed via bloods and a scan, and there is a significant family history of Hashimoto’s. There was also a record of increasing TSH etc due to employer health checks. I think
N5girl
in
Thyroid UK
2 months ago
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