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Factor X deficiency
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High Transferrin Saturation without optimal iron levels
Hello, I am currently trying to get my iron levels up and they are slowly creeping in the right direction. However. My latest bloods show that my TSAT is now too high at 65% (up from 39% two months ago), and ferritin at 70ug/L (up from 65ug/L.) Is this just something to monitor for now?
Hello, I am currently trying to get my iron levels up and they are slowly creeping in the right direction. However. My latest bloods show that my TSAT is now too high at 65% (up from 39% two months ago), and ferritin at 70ug/L (up from 65ug/L.) Is this just something to monitor for now?
Thywotsit
in
Thyroid UK
6 months ago
Just saw my first rheumatologist yesterday, very confused by diagnosis?
Can you have negative rheumatoid factor, negative CCP antibodies, no pain, stiffness, swelling or symptoms in the small joints (hands, feet etc) & it still be possible to have rheumatoid arthritis? All of my symptoms for the past 5 and 1/2 months seem to be classical PMR (before I started taking prednisone
Can you have negative rheumatoid factor, negative CCP antibodies, no pain, stiffness, swelling or symptoms in the small joints (hands, feet etc) & it still be possible to have rheumatoid arthritis? All of my symptoms for the past 5 and 1/2 months seem to be classical PMR (before I started taking prednisone
LarMarge6
in
PMRGCAuk
6 months ago
Pneumonia and collapsed lung after catching the ‘100 day cough’
For all you folks who have Lupus, please be careful of this ‘100’ day cough that is going around at the moment, as this is what caused me to end up in hospital. I was diagnosed with Lupus in February 2022. I’ve had a rough ride for the past few years, ending up in hospital every year for one thing
For all you folks who have Lupus, please be careful of this ‘100’ day cough that is going around at the moment, as this is what caused me to end up in hospital. I was diagnosed with Lupus in February 2022. I’ve had a rough ride for the past few years, ending up in hospital every year for one thing
Loopy1971
in
LUPUS UK
5 months ago
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Newbie and confused. Functional B12 deficiency?
Hi everyone, I am new here but I have been a member of the thyroid forum for many years. I've also just joined the Sjogren's and the lupus groups because some of my symptoms could be attributed to these though I have no diagnoses, and the Changing Faces group for my rhinophyma. I have Hashi's and thyroid
Hi everyone, I am new here but I have been a member of the thyroid forum for many years. I've also just joined the Sjogren's and the lupus groups because some of my symptoms could be attributed to these though I have no diagnoses, and the Changing Faces group for my rhinophyma. I have Hashi's and thyroid
grumpyold
in
Pernicious Anaemia Society
6 months ago
Fear brought on by test result” my chart”
I have gone into total melt down. Living alone and having multiple co morbidities is terrifying ! I was moved from my trusted GP to 2 part time gps, I used to have a cardiology check then f to f every year , not been seen now for three years. Also have various Rheumatoid arthritis diseases , biologics
I have gone into total melt down. Living alone and having multiple co morbidities is terrifying ! I was moved from my trusted GP to 2 part time gps, I used to have a cardiology check then f to f every year , not been seen now for three years. Also have various Rheumatoid arthritis diseases , biologics
Luludean
in
Atrial Fibrillation Support
5 months ago
Repost results
Im taking teva levothyroxine 100mcgThybon t3, 15mcg, split 3 x 5mcg dose Magnesium glycinate 650mg Vit D3,k2 mk-7, 5000iu Any advice very much appreciated 🌸🌸🌸🌸🌸🌸🌸
Im taking teva levothyroxine 100mcgThybon t3, 15mcg, split 3 x 5mcg dose Magnesium glycinate 650mg Vit D3,k2 mk-7, 5000iu Any advice very much appreciated 🌸🌸🌸🌸🌸🌸🌸
Geegee777
in
Thyroid UK
7 months ago
Advice on Iron levels
Serum Ferritin level blood test has come back showing at 15 ug/l - is this low? Doctor saying it is low normal rangeand not normally consdered as iron deficiency - but am presenting symptoms and thought range was 15.0 - 300.0 ug/L. Advise needed please.
Serum Ferritin level blood test has come back showing at 15 ug/l - is this low? Doctor saying it is low normal rangeand not normally consdered as iron deficiency - but am presenting symptoms and thought range was 15.0 - 300.0 ug/L. Advise needed please.
Rolbo
in
Thyroid UK
7 months ago
What’s the protocol for GP actioning full iron panel?
It’s become apparent that my daughter’s ferritin levels are deficient and she’s going to put in a request to her GP for a full iron panel. I routinely read here that one shouldn’t supplement with iron based on a low ferritin reading alone but I’d like to know what the supporting information for this
It’s become apparent that my daughter’s ferritin levels are deficient and she’s going to put in a request to her GP for a full iron panel. I routinely read here that one shouldn’t supplement with iron based on a low ferritin reading alone but I’d like to know what the supporting information for this
J972
in
Thyroid UK
7 months ago
advice needed please re iron and thyroxine
hi there, I’d really appreciate some advice. I’ve been on Thyroxine for a number of years and have been fine, I’ve just been told that I have Anaemia and have started on Ferrous Fumarate tabs 210 mg. I’ve started to feel tearful and anxious this last week and wonder if the iron is affecting my thyroid
hi there, I’d really appreciate some advice. I’ve been on Thyroxine for a number of years and have been fine, I’ve just been told that I have Anaemia and have started on Ferrous Fumarate tabs 210 mg. I’ve started to feel tearful and anxious this last week and wonder if the iron is affecting my thyroid
Poppyqueen
in
Thyroid UK
7 months ago
Advice needed please about liquid Levothyroxine side effects
Hello, I wrote a post about a month ago saying my adult son was unable to get liquid levothyroxine as it was out of stock. He was taking the brill Pharma brand and tolerated it really well. The chemist managed to source Teva liquid levothyroxine three weeks after we asked for a repeat prescription
Hello, I wrote a post about a month ago saying my adult son was unable to get liquid levothyroxine as it was out of stock. He was taking the brill Pharma brand and tolerated it really well. The chemist managed to source Teva liquid levothyroxine three weeks after we asked for a repeat prescription
Annie567
in
Thyroid UK
7 months ago
More Challenges to Overcome!
Some of you may recall that for some years, I've frequently experienced ectopic beats. They've been calmed down with a lowish dose of a beta blocker (Propranolol) and don't usually give me too much cause for concern......until about a week ago when they re-emerged, but with a different manifestation
Some of you may recall that for some years, I've frequently experienced ectopic beats. They've been calmed down with a lowish dose of a beta blocker (Propranolol) and don't usually give me too much cause for concern......until about a week ago when they re-emerged, but with a different manifestation
Kendrew
in
PMRGCAuk
5 months ago
Persistant cough
hi everyone I haven’t posted for a while it was about my persistant cough. I now have had this cough for over a year now it has gradually got worse over the past few months. Coughing day and night. People come up to me in the street becauthey think I’m choking. My GP has treated me with antibiotics and
hi everyone I haven’t posted for a while it was about my persistant cough. I now have had this cough for over a year now it has gradually got worse over the past few months. Coughing day and night. People come up to me in the street becauthey think I’m choking. My GP has treated me with antibiotics and
Mudmaker
in
MPN Voice
5 months ago
Ramipril
I thought I would share with you my experience of a cough due to ramipril in case it helps someone else as I didn’t believe it would cause such an awful cough. I was prescribed ramipril after having a HA in July last years. No side effects at all. I got an awful cold in November which also came with
I thought I would share with you my experience of a cough due to ramipril in case it helps someone else as I didn’t believe it would cause such an awful cough. I was prescribed ramipril after having a HA in July last years. No side effects at all. I got an awful cold in November which also came with
trafar
in
British Heart Foundation
6 months ago
Suspected Pernicious Anemia - what next?
Hello, I am very glad to have found this forum as I have been researching B12D and PA a lot recently. I became familiar with the society’s website and found it so helpful. I am 29F in the US and I suspect I have Pernicious Anemia. This is what I know so far (sorry in advance if this post rambles on)
Hello, I am very glad to have found this forum as I have been researching B12D and PA a lot recently. I became familiar with the society’s website and found it so helpful. I am 29F in the US and I suspect I have Pernicious Anemia. This is what I know so far (sorry in advance if this post rambles on)
Marlowekat
in
Pernicious Anaemia Society
6 months ago
Achilles tendonitis and damage due to antibiotic side effect - odd icy sensation?
I have had RA for nearly 10 years, currently on Benepali and Metotrexate injections. Rheumatoid factor 74 and Anti-cpp 600 in 2014 and generally do not score above normal for blood CRP tests (interesting anomaly) even when ultrasound in clinic reviews shows inflammation. As well as small joint hand
I have had RA for nearly 10 years, currently on Benepali and Metotrexate injections. Rheumatoid factor 74 and Anti-cpp 600 in 2014 and generally do not score above normal for blood CRP tests (interesting anomaly) even when ultrasound in clinic reviews shows inflammation. As well as small joint hand
Braecoon
in
NRAS
6 months ago
Can't increase my iron levels
Hi all, I posted in February 2023 my low iron results and started taking 200 Ferrous Sulphate daily then. My iron results after 3 months were Ferritin 39 (20-204) Serum iron 18.6 (4.4-27.9) Feb 23 was: serum iron 11, ferritin was 29. So not a huge improvement. But now, a year on, even worse! Despite
Hi all, I posted in February 2023 my low iron results and started taking 200 Ferrous Sulphate daily then. My iron results after 3 months were Ferritin 39 (20-204) Serum iron 18.6 (4.4-27.9) Feb 23 was: serum iron 11, ferritin was 29. So not a huge improvement. But now, a year on, even worse! Despite
Suzanneharb
in
Thyroid UK
7 months ago
Reassurance please
Hi, I have a diagnosis of an autoimmune thyroid condition. Went privately as NHS tests all within range on tests. Waiting on further bloods, which has been difficult to get done, so I can have follow up appointment with private GP for thyroid treatment. Appointment in July. In the interim I did see NHS
Hi, I have a diagnosis of an autoimmune thyroid condition. Went privately as NHS tests all within range on tests. Waiting on further bloods, which has been difficult to get done, so I can have follow up appointment with private GP for thyroid treatment. Appointment in July. In the interim I did see NHS
Fizzwhizz
in
Thyroid UK
6 months ago
Feel like giving up.
For unknown reasons other than we think Rituxumab is not working for you any more my medication was changed to Kevzera (Sarilulmab) in November. The work up checks were done and good to go apart from a Chest X Ray as I hadn't had one for a while. A shadow area was found on my lung with suspected
For unknown reasons other than we think Rituxumab is not working for you any more my medication was changed to Kevzera (Sarilulmab) in November. The work up checks were done and good to go apart from a Chest X Ray as I hadn't had one for a while. A shadow area was found on my lung with suspected
3LittleBirds2
in
NRAS
6 months ago
Pernicious anaemia
Hi the result of my intrinsic factor came back positive and I start loading doses on Monday The results were written a little strangely though Intrinsic Factor antibodies 12.0 U/ml Negative=<7 Equiveocal= 7-10 Positive > 10 Looking on other websites the results are given in different measurements
Hi the result of my intrinsic factor came back positive and I start loading doses on Monday The results were written a little strangely though Intrinsic Factor antibodies 12.0 U/ml Negative=<7 Equiveocal= 7-10 Positive > 10 Looking on other websites the results are given in different measurements
mully
in
Pernicious Anaemia Society
6 months ago
Anyone Know About Silent Reflux
Following on from my experience of asthma flare up I'm wondering if like Cade in his post about breathing problems whilst exercising, if I could have silent reflux. It was shortness of breath that led me to seek medical treatment, and even though I had no wheezing or cough the hospital concluded it was
Following on from my experience of asthma flare up I'm wondering if like Cade in his post about breathing problems whilst exercising, if I could have silent reflux. It was shortness of breath that led me to seek medical treatment, and even though I had no wheezing or cough the hospital concluded it was
Sparklingsunshine
in
Thyroid UK
6 months ago
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