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Blood-coagulation factor XIII
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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
20 days 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
20 days 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
20 days ago
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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
20 days 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
20 days 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
20 days 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
CBullen
in
Thyroid UK
20 days 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
20 days 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
20 days 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
20 days ago
Update on FIL -Venetoclax as a Monotherapy, Pancytopenia and Myelodysplasia
Hi everyone I have been meaning to post an update for months but things have been changing so rapidly, every day would have been a different story. So we did get to see a specialist who did a BM biopsy and recommended Venetoclax as a Monotherapy as his BM was 50% CLL. We were told it wasn't chemo
Hi everyone I have been meaning to post an update for months but things have been changing so rapidly, every day would have been a different story. So we did get to see a specialist who did a BM biopsy and recommended Venetoclax as a Monotherapy as his BM was 50% CLL. We were told it wasn't chemo
JoeMcDote
in
CLL Support
20 days 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
20 days ago
Blood test: T3 normal, still feel exhausted on 20 mcg Liothyronine
Thanks for everyone that has been helping me so far, however I had the T3 blood test at the hospital on Wednesday and found out this morning that my T3 is normal, so is TSH and T4, has anyone got any ideas what's happening and why I am so exhausted; I had vit.B12, Iron and vit. D3 test last October and
Thanks for everyone that has been helping me so far, however I had the T3 blood test at the hospital on Wednesday and found out this morning that my T3 is normal, so is TSH and T4, has anyone got any ideas what's happening and why I am so exhausted; I had vit.B12, Iron and vit. D3 test last October and
Denise500
in
Thyroid UK
20 days ago
Hypo or Hyper thyroid
hi, I am being treated for a hyperactive thyroid, I take 20mg of carbimazole a day, my issue is I have no symptoms of a hyper thyroid only blood tests are coming back high. I am over weight by 2.5 stone, I am tired, constipated, my hair has thinned, my eyebrows have thinned and when I look these symptoms
hi, I am being treated for a hyperactive thyroid, I take 20mg of carbimazole a day, my issue is I have no symptoms of a hyper thyroid only blood tests are coming back high. I am over weight by 2.5 stone, I am tired, constipated, my hair has thinned, my eyebrows have thinned and when I look these symptoms
Kenntess
in
Thyroid UK
21 days ago
Should I go back on 1 or 2 mg prednisone due to fatigue?
Hello friends! After a four year term of GCA, while doing a very slow taper of prednisone l have been off of prednisone for several months. Occasionally if I’m very fatigued I take a 1 mg. I have been very fatigued for the last few days and I’m wondering if I should maybe go back on a daily 1 mg
Hello friends! After a four year term of GCA, while doing a very slow taper of prednisone l have been off of prednisone for several months. Occasionally if I’m very fatigued I take a 1 mg. I have been very fatigued for the last few days and I’m wondering if I should maybe go back on a daily 1 mg
Snerd
in
PMRGCAuk
21 days ago
My Estimated GFR - eGFR
Some of you may recall when I was on diuretics (Furosemide) last year in an attempt to reduce the lymphatic fluid discharge from the macerated wounds on my foot (a result of "that we must not mention" Toe) my eGFR plummeted from 69% to 35% (distinctly worrying). A few months after they were stopped
Some of you may recall when I was on diuretics (Furosemide) last year in an attempt to reduce the lymphatic fluid discharge from the macerated wounds on my foot (a result of "that we must not mention" Toe) my eGFR plummeted from 69% to 35% (distinctly worrying). A few months after they were stopped
MichaelJH
Heart Star
in
British Heart Foundation
21 days ago
Should I take a higher dose of levothyroxine?
I was diagnosed with sub clinical hypothyroidism in September last year, from a routine blood test, doctor called and said she had sent over a prescription to the chemist but did not ask me if I had any symptoms at all. I took the tablets but they were then upped to 50mcg in the new year, both times
I was diagnosed with sub clinical hypothyroidism in September last year, from a routine blood test, doctor called and said she had sent over a prescription to the chemist but did not ask me if I had any symptoms at all. I took the tablets but they were then upped to 50mcg in the new year, both times
TinaBW
in
Thyroid UK
21 days ago
Looking for a job
I am only 51 and have been diagnosed with OPCA (results on blood tests pending). Can you advise me on what jobs to apply for? Need a work from home job, obviously :) have over 30 years of office experience (but my handwriting and speech are shocking....) Help and advice needed ... i get bored too easily
I am only 51 and have been diagnosed with OPCA (results on blood tests pending). Can you advise me on what jobs to apply for? Need a work from home job, obviously :) have over 30 years of office experience (but my handwriting and speech are shocking....) Help and advice needed ... i get bored too easily
BoneyEm1972
in
Ataxia UK
21 days ago
Superficial peroneal nerve pain in ankle
Just found this group for chronic pain, wondered if anyone has suffered with chronic ankle pain.I broke my ankle 13 years ago and always had pain after, had plate and 10 screws taken out then an arthroscopy to take scar tissue out. Still in pain. Was eventually told it was nerve damage and too late
Just found this group for chronic pain, wondered if anyone has suffered with chronic ankle pain.I broke my ankle 13 years ago and always had pain after, had plate and 10 screws taken out then an arthroscopy to take scar tissue out. Still in pain. Was eventually told it was nerve damage and too late
Oraney
in
Pain Concern
21 days ago
Xtandi did not work.
Hi all, I'm new to this board but would love some feedback. My father, 80, has been dealing with prostate cancer for a few years. He had initially had radiation plus Lupron injections. His PSA started rising again a few years ago and he wound up on Lupron regularly. His PSA has been slowly rising
Hi all, I'm new to this board but would love some feedback. My father, 80, has been dealing with prostate cancer for a few years. He had initially had radiation plus Lupron injections. His PSA started rising again a few years ago and he wound up on Lupron regularly. His PSA has been slowly rising
Estivez71
in
Advanced Prostate Cancer
21 days ago
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