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Newbie and blood tests
Good morning all, I've been borderline underactive thyroid for a year or so. I was never told my levels and they aren't on my GP app. I've been retested recently and have a TSH level of 6. I also have a TSH receptor level of 0.3. I have a few symptoms.. Tiredness Brain fog Cold all the time Thinning
Good morning all, I've been borderline underactive thyroid for a year or so. I was never told my levels and they aren't on my GP app. I've been retested recently and have a TSH level of 6. I also have a TSH receptor level of 0.3. I have a few symptoms.. Tiredness Brain fog Cold all the time Thinning
HubbaBubbaLover
in
Thyroid UK
1 month ago
Thoughts on blood test ? (Quite new to T3 meds)
Any thoughts regarding my latest bloods please? I take 100 mcg T4 and 20mcg T3. My symptoms are nausea and brain fog. (I have an Underactive Thyroid). Free T3 5.1 pmol/L (in range) (3.10-6.80pmol)L THS 0.01 pmol/L (out of range) (range 0.27-4.20mIU/L) Free T4
Any thoughts regarding my latest bloods please? I take 100 mcg T4 and 20mcg T3. My symptoms are nausea and brain fog. (I have an Underactive Thyroid). Free T3 5.1 pmol/L (in range) (3.10-6.80pmol)L THS 0.01 pmol/L (out of range) (range 0.27-4.20mIU/L) Free T4
Heyhop
in
Thyroid UK
1 month ago
Fatty liver in biopsy but not scans
Hiya, I’m just curious if anyone has had a similar experience where their liver biopsy results shows signs of fatty liver but ultrasounds/CT show an enlarged liver but no fatty liver signs. I’m wondering if this means it’s extremely early stages maybe?
Hiya, I’m just curious if anyone has had a similar experience where their liver biopsy results shows signs of fatty liver but ultrasounds/CT show an enlarged liver but no fatty liver signs. I’m wondering if this means it’s extremely early stages maybe?
Chaucer89
in
British Liver Trust
6 months ago
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Autoimmune condition
Hi everyone. The results from my ANA and ENA came back with a broad diagnosis of connective tissue disease. They've ruled out lupus. This plus the thyroid stuff is going to be fun to deal with 😅. The Coeliac disease test was inconclusive because my GP forgot to advise me to have bread for at least 4
Hi everyone. The results from my ANA and ENA came back with a broad diagnosis of connective tissue disease. They've ruled out lupus. This plus the thyroid stuff is going to be fun to deal with 😅. The Coeliac disease test was inconclusive because my GP forgot to advise me to have bread for at least 4
MauveMouse
in
Thyroid UK
1 month ago
How high is high phosphorous??
I just got labs back. I was happy to see the crazy good numbers. Even with 2 hours3 days a week. only. MY creatinine went down from almost 7 to 5.89. My bun, pth, potassium all went down and are in range. Calcium in range. Glucose in range. A1C 5.3. the only number that was bad was phosphorous which
I just got labs back. I was happy to see the crazy good numbers. Even with 2 hours3 days a week. only. MY creatinine went down from almost 7 to 5.89. My bun, pth, potassium all went down and are in range. Calcium in range. Glucose in range. A1C 5.3. the only number that was bad was phosphorous which
Bassetmommer
in
Kidney Dialysis
6 months ago
little advice from fellow Coeliac’s
hi Was wondering if any other coeliac out there has had similar experience/symptons? I got diagnosed with Coeliac disease about 4 years ago I follow the diet, have separate toaster, chopping board etc I’ve been suffering with terrible upper tummy and back passage cramps, blood and yellow mucus
hi Was wondering if any other coeliac out there has had similar experience/symptons? I got diagnosed with Coeliac disease about 4 years ago I follow the diet, have separate toaster, chopping board etc I’ve been suffering with terrible upper tummy and back passage cramps, blood and yellow mucus
RJane83
in
Gluten Free Guerrillas
1 month ago
Latest blood tests
Hi everyone, I posted a while ago about getting all my underactive thyroid symptoms back, joint pains, fatigue, anxiety and others. I’d had test results saying my TSH was low, but the dr was saying that it was satisfactory. I managed to speak to another dr and she ordered full blood tests. My results
Hi everyone, I posted a while ago about getting all my underactive thyroid symptoms back, joint pains, fatigue, anxiety and others. I’d had test results saying my TSH was low, but the dr was saying that it was satisfactory. I managed to speak to another dr and she ordered full blood tests. My results
Button83
in
Thyroid UK
1 month ago
Any info on the drug Dapaglifozen?
Lupus sufferer already on the usual drugs Mycophenolic , Steroids ,Quinine etc
Lupus sufferer already on the usual drugs Mycophenolic , Steroids ,Quinine etc
Will1408
in
LUPUS UK
1 month ago
PSA Rising
Had surgery in November 2021. Gleason 4+3...Post surgery PSA was 0.01. Positive margin (1 millimetre). PSA has risen from 0.1 to 0.06 in 24 months. Doctor says I should do nothing. Until it hits 0.2. Next test is June 2024. Any advice will be appreciated.
Had surgery in November 2021. Gleason 4+3...Post surgery PSA was 0.01. Positive margin (1 millimetre). PSA has risen from 0.1 to 0.06 in 24 months. Doctor says I should do nothing. Until it hits 0.2. Next test is June 2024. Any advice will be appreciated.
Whatnext2019
in
Advanced Prostate Cancer
6 months ago
Advice Greatly Appreciated
Good Day, I would sooooo appreciate a response/advice/opinions.... I was recently advised by my GP (family doctor) that I have cirrhosis. This is of course terrifying...I apparently had sever fatty liver in July 2021 but I was sadly not informed of this. I would have turned it around immediately.
Good Day, I would sooooo appreciate a response/advice/opinions.... I was recently advised by my GP (family doctor) that I have cirrhosis. This is of course terrifying...I apparently had sever fatty liver in July 2021 but I was sadly not informed of this. I would have turned it around immediately.
Confused2024
in
British Liver Trust
6 months ago
underactive thyroid
getting numb feeling in my face arm and leg. Headache itchy skin and tired out light headed. My gp sent me for mri. Everything is fine. I have had an underactive thyroid for 25 years My blood pressure is also low I take 100 levothyroxine. Does it need increasing ???? Blood tests 3 rd June ! Any
getting numb feeling in my face arm and leg. Headache itchy skin and tired out light headed. My gp sent me for mri. Everything is fine. I have had an underactive thyroid for 25 years My blood pressure is also low I take 100 levothyroxine. Does it need increasing ???? Blood tests 3 rd June ! Any
Carlphilip1958
in
Thyroid UK
1 month ago
Mr Geoff Lloyd
Diagnosed in 2010 with advanced PC. Prostatectomy in 2011 followed by the "all clear". PSA refused to disappear and so RT followed. PSA still present and PC nodules found in my lung in 2021. I then had a 6 session course of chemotherapy and have been on Abiaterone and Demoxosone drugs ever since.Nodules
Diagnosed in 2010 with advanced PC. Prostatectomy in 2011 followed by the "all clear". PSA refused to disappear and so RT followed. PSA still present and PC nodules found in my lung in 2021. I then had a 6 session course of chemotherapy and have been on Abiaterone and Demoxosone drugs ever since.Nodules
Churchman123
in
Advanced Prostate Cancer
6 months ago
Interesting article on why women get higher levels of autoimmune disease
Two versions: [i][/i] [i]
Stanford Medicine-led study shows why women are at greater risk of autoimmune disease
[/i] [i][/i] [i][/i] [i]Research throws light on the mystery of why women are much more prone to autoimmune disorders: A molecule made by one X chromosome in every female cell can
Two versions: [i][/i] [i]
Stanford Medicine-led study shows why women are at greater risk of autoimmune disease
[/i] [i][/i] [i][/i] [i]Research throws light on the mystery of why women are much more prone to autoimmune disorders: A molecule made by one X chromosome in every female cell can
TSH110
in
Thyroid UK
1 month ago
💤 sleep
I've always been a good sleeper but following the stroke triggered by brain aneurysm surgery. I've been regularly finding myself waking at 1-2am thinking it's the morning and time to get up. I'm living in a rehab unit so there are always staff around to reorientate me to the time but it's an annoying
I've always been a good sleeper but following the stroke triggered by brain aneurysm surgery. I've been regularly finding myself waking at 1-2am thinking it's the morning and time to get up. I'm living in a rehab unit so there are always staff around to reorientate me to the time but it's an annoying
GardenElf
in
Brain Aneurysm Support
6 months ago
Teesside Lupus Group
Hello everyone Just to let you know that our Lupus group has started having morning and afternoon meetings in the area. Anyone interested in joining our meetings please contact me. We are based in the North East. Lets meet for a chat and coffee. Keep on keeping on xxx
Hello everyone Just to let you know that our Lupus group has started having morning and afternoon meetings in the area. Anyone interested in joining our meetings please contact me. We are based in the North East. Lets meet for a chat and coffee. Keep on keeping on xxx
Pipido36
in
LUPUS UK
1 month ago
PSA Risen in Last 6 months
Have been on here a week ago, explaining that my husband (who was diagnosed 10years ago) has now been diagnosed with Gastroporesis, so not eating much due to constant nausea and vomiting. We are due to see his Urologist in 2 weeks time, so had the dreaded PSA blood test. It had been almost undetectable
Have been on here a week ago, explaining that my husband (who was diagnosed 10years ago) has now been diagnosed with Gastroporesis, so not eating much due to constant nausea and vomiting. We are due to see his Urologist in 2 weeks time, so had the dreaded PSA blood test. It had been almost undetectable
Hidden
in
Advanced Prostate Cancer
6 months ago
PSA Rising
Asking for a friend of my father this time. He had surgery in december 2022 and everything was removed including glands. Gleason 4+5. His PSA has risen från 0.1 to 0.14 in 12 months. His doctor says to do nothing until it hits 0.2. But shouldn’t he do more? Maybe he doesn’t have advanced cancer yet.
Asking for a friend of my father this time. He had surgery in december 2022 and everything was removed including glands. Gleason 4+5. His PSA has risen från 0.1 to 0.14 in 12 months. His doctor says to do nothing until it hits 0.2. But shouldn’t he do more? Maybe he doesn’t have advanced cancer yet.
TheTopBanana
in
Advanced Prostate Cancer
6 months ago
91% of lupus patients report using steroids to manage symptoms
Global survey highlights urgent need for treatments with fewer side effects About 91% of lupus patients report they are currently taking or had been using oral steroids to manage their symptoms, according to a global survey of more than 7,700 patients. The World Lupus Federation (WLF) released findings
Global survey highlights urgent need for treatments with fewer side effects About 91% of lupus patients report they are currently taking or had been using oral steroids to manage their symptoms, according to a global survey of more than 7,700 patients. The World Lupus Federation (WLF) released findings
lupus-support1
Administrator
in
LUpus Patients Understanding and Support
1 month ago
After Transplant
I had my transplant 9 weeks ago I can’t believe the difference it has had. I sleep all night, no boiling up in the night, my breathing is better I use breathe so loud I think it was all the fluids inside me I was struggling to breathe I feel like I’m 20 years old again and I’m 50 . My mind is so much
I had my transplant 9 weeks ago I can’t believe the difference it has had. I sleep all night, no boiling up in the night, my breathing is better I use breathe so loud I think it was all the fluids inside me I was struggling to breathe I feel like I’m 20 years old again and I’m 50 . My mind is so much
lonmallin50
in
British Liver Trust
6 months ago
Do I Poke The Bear?
I had my B12 jab last week, I get these every 2 months and am grateful to have them. I've suffered B12 issues since childhood, have dim memories of blood tests and B12 jabs back in the day. I changed surgeries in the early 90's due to moving and have been with this practice ever since. So I'm not sure
I had my B12 jab last week, I get these every 2 months and am grateful to have them. I've suffered B12 issues since childhood, have dim memories of blood tests and B12 jabs back in the day. I changed surgeries in the early 90's due to moving and have been with this practice ever since. So I'm not sure
Sparklingsunshine
in
Pernicious Anaemia Society
1 month ago
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