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Does anyone already on t3 or NDT have experience of Dr Mark Spring?
please PM me if you have, thank you.
please PM me if you have, thank you.
sulamaye
in
Thyroid UK
4 months ago
Hello all
I have just been diagnosed with a “(since 2014)” added. I’m hoping to find some helpful tips and ideas from you all going forward. It will be lovely to be able to get advice from those that have already been there. I feel like I’ve been told yes it’s sub-clinical, here’s some thyroxine, now off you go
I have just been diagnosed with a “(since 2014)” added. I’m hoping to find some helpful tips and ideas from you all going forward. It will be lovely to be able to get advice from those that have already been there. I feel like I’ve been told yes it’s sub-clinical, here’s some thyroxine, now off you go
Kimmi01
in
Thyroid UK
4 months ago
Need recommendations for herbal supplements.
I'm 67 and have had anxiety since menopause. I don't do hrt and haven't taken natural supplements. My anxiety comes and goes and is exacerbated by histamine in pollen season and possibly low oestrogen ongoing. Constantly light headed and sob intermittently and can't make arrangements in advance as each
I'm 67 and have had anxiety since menopause. I don't do hrt and haven't taken natural supplements. My anxiety comes and goes and is exacerbated by histamine in pollen season and possibly low oestrogen ongoing. Constantly light headed and sob intermittently and can't make arrangements in advance as each
celticlady
in
Anxiety Support
4 months ago
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Blood Tests NOT T4
Hi all Just looking for a bit of a steer. I was diagnosed with Graves' Disease in 2021 but as of now not on any medication, i couldn't tolerate Carbimazole as it made me very unwell. My last tests in around June 2022 with my endocrinologist showed my graves disease antibodies were very weak and things
Hi all Just looking for a bit of a steer. I was diagnosed with Graves' Disease in 2021 but as of now not on any medication, i couldn't tolerate Carbimazole as it made me very unwell. My last tests in around June 2022 with my endocrinologist showed my graves disease antibodies were very weak and things
SnowQueenOne
in
Graves Disease Support
4 months ago
Endo appointment sorted.... But... 🤦♀️
Hi everyone ❤️ I've now received my endocrinologist appointment, it appears to be at the RVI Newcastle on April 2nd 9.20am..one problem, I can't get there for 9.20am🤦♀️ I have to catch a taxi to train station, then the first train from my end to Newcastle, then a taxi to the RVI... Then do it all
Hi everyone ❤️ I've now received my endocrinologist appointment, it appears to be at the RVI Newcastle on April 2nd 9.20am..one problem, I can't get there for 9.20am🤦♀️ I have to catch a taxi to train station, then the first train from my end to Newcastle, then a taxi to the RVI... Then do it all
birkie
in
Thyroid UK
4 months ago
Wheat Diet may Exacerbate Multiple Sclerosis Severity
Wheat diet may exacerbate multiple sclerosis severity, research finds - Jan 2024
by Natkritta Hüppe, Universitätsmedizin der Johannes Gutenberg-Universität Mainz https://medicalxpress.com/news/2024-01-wheat-diet-exacerbate-multiple-sclerosis.html
Highlights:
A research team at the University
Wheat diet may exacerbate multiple sclerosis severity, research finds - Jan 2024
by Natkritta Hüppe, Universitätsmedizin der Johannes Gutenberg-Universität Mainz https://medicalxpress.com/news/2024-01-wheat-diet-exacerbate-multiple-sclerosis.html
Highlights:
A research team at the University
Bolt_Upright
in
Cure Parkinson's
4 months ago
Update on unexpected cholesterol rise.
18 days ago I posted that id had an unexpected rise in my cholesterol level, despite no change to diet etc. However I did change to taking my atorvastatin in the morning rather than night time, due to concern it was causing insomnia. Well I started taking it at night again, and now my cholesterol is
18 days ago I posted that id had an unexpected rise in my cholesterol level, despite no change to diet etc. However I did change to taking my atorvastatin in the morning rather than night time, due to concern it was causing insomnia. Well I started taking it at night again, and now my cholesterol is
APC65
in
British Heart Foundation
4 months ago
New blood results
Just like to put my latest results here, I’ve been totally worn out lately and I have an appointment tomorrow with my Gp, my fatigue is now off the scale, all I want to do is sleep. I’m really struggling with my Ferritin levels even though I take an Iron supplement and I eat well, I would be really
Just like to put my latest results here, I’ve been totally worn out lately and I have an appointment tomorrow with my Gp, my fatigue is now off the scale, all I want to do is sleep. I’m really struggling with my Ferritin levels even though I take an Iron supplement and I eat well, I would be really
Kimkat
in
Thyroid UK
4 months ago
newly diagnosed hyper, started carbimizole more covered in rash
hi just joined today. So last summer I was sweating profusely and getting out of breath. I thought it was due to weight gain so enquired to my gp about wegovy! He declined saying bmi wasn’t high enough and sent me for full bloods and discovered my thyroid was overactive (38 with normal range being 12
hi just joined today. So last summer I was sweating profusely and getting out of breath. I thought it was due to weight gain so enquired to my gp about wegovy! He declined saying bmi wasn’t high enough and sent me for full bloods and discovered my thyroid was overactive (38 with normal range being 12
Kiki_76
in
Thyroid UK
4 months ago
Post Menopausal Dizziness & Anxiety
I'm 67. I went through menopause at 50 using herbal supplements-not too many problems with hot sweats but noticed an increase in anxiety but managed a stressful job . Fast forward to now, I feel light headed and off balance nearly all the time-pollen season is worse due to histamine so I have to watch
I'm 67. I went through menopause at 50 using herbal supplements-not too many problems with hot sweats but noticed an increase in anxiety but managed a stressful job . Fast forward to now, I feel light headed and off balance nearly all the time-pollen season is worse due to histamine so I have to watch
celticlady
in
Menopause and Perimenopause Support
4 months ago
Medscape article on RLS
Restless legs Medscape Medscape is the leading online global destination for physicians and healthcare professionals worldwide, offering the latest medical news and expert perspectives; essential point-of-care drug and disease information; and relevant professional education and CME. This is
Restless legs Medscape Medscape is the leading online global destination for physicians and healthcare professionals worldwide, offering the latest medical news and expert perspectives; essential point-of-care drug and disease information; and relevant professional education and CME. This is
thorp
in
Restless Legs Syndrome
4 days ago
More advice please
Hi everyone, Further to my previous posts, I saw private Endo last week who won’t prescribe T3 until Short Synacthen test is done for borderline low cortisol of 248 and reverse t3 blood test done to confirm poor t3 conversion (???). I have been told today by his secretary (after arranging the tests
Hi everyone, Further to my previous posts, I saw private Endo last week who won’t prescribe T3 until Short Synacthen test is done for borderline low cortisol of 248 and reverse t3 blood test done to confirm poor t3 conversion (???). I have been told today by his secretary (after arranging the tests
Koababy20
in
Thyroid UK
2 months ago
Low B12 and ferritin questions
Over the past year I have had frequent respiratory infections and when not ill, I am always exhausted. I often need to stay in bed on my days off recovering. Alongside the exhaustion and frequent infections I have dealt with nausea and gastric problems which I always thought were due to IBS. I faint
Over the past year I have had frequent respiratory infections and when not ill, I am always exhausted. I often need to stay in bed on my days off recovering. Alongside the exhaustion and frequent infections I have dealt with nausea and gastric problems which I always thought were due to IBS. I faint
bakedbean5007
in
Pernicious Anaemia Society
7 days ago
To Trial or not to Trial?
I have decided not to trial. Going to just do the Venetaclax & Obin protocol. I’m just not in the mood for the extra appointments and brain damage that invariably comes with them. I’m waiting for a start date. Had the bone marrow biopsy and endless other tests this week - decided not to peek at the
I have decided not to trial. Going to just do the Venetaclax & Obin protocol. I’m just not in the mood for the extra appointments and brain damage that invariably comes with them. I’m waiting for a start date. Had the bone marrow biopsy and endless other tests this week - decided not to peek at the
SunnyCA
in
CLL Support
4 months ago
Day 2 or Day 5 transfer? Help!!!
Hi Guys!!! I need to hear from anyone that had experience with a day 2 transfer. Im definitely not new to ivf, I have had 3 egg retrievals ( the last one was yesterday) and 5 embryo transfers so far in the space of 4 yrs, all unsuccessful..... I have actually never seen a positive pregnancy test 😩 I
Hi Guys!!! I need to hear from anyone that had experience with a day 2 transfer. Im definitely not new to ivf, I have had 3 egg retrievals ( the last one was yesterday) and 5 embryo transfers so far in the space of 4 yrs, all unsuccessful..... I have actually never seen a positive pregnancy test 😩 I
Islandgrl
in
Fertility Network UK
4 months ago
Interesting article about the effects of Covid19 on your blood
Having caught Covid19 a short time after my allo SCT and with my anaemia ongoing, I was interested to see this article. This is not CLL specific but worth a read. "[i]Several studies have reported, in COVID-19 patients, hematological abnormalities. Most of these alterations are associated with a higher
Having caught Covid19 a short time after my allo SCT and with my anaemia ongoing, I was interested to see this article. This is not CLL specific but worth a read. "[i]Several studies have reported, in COVID-19 patients, hematological abnormalities. Most of these alterations are associated with a higher
Jm954
Administrator
in
CLL Support
4 months ago
recommendations for nhs endo please?
Hi forum friends I went to my gp Friday to see what help I might get re my thyroid now and also if I might see a haematologist re high serum iron but low ferritin (28 …5-204) I didnt get many answers as he concentrated on a current kidney issue I have so he’s booked me another face to face 30/1 to
Hi forum friends I went to my gp Friday to see what help I might get re my thyroid now and also if I might see a haematologist re high serum iron but low ferritin (28 …5-204) I didnt get many answers as he concentrated on a current kidney issue I have so he’s booked me another face to face 30/1 to
Starseed56
in
Thyroid UK
4 months ago
Secondary hypothyroidism
Can anyone please tell me where free t4 should be at for secondary hypothyroidism. Should it be in mid range to upper third? Mine was 1.01 in a range of 0.76 to 1.46. I feel very hypo.
Can anyone please tell me where free t4 should be at for secondary hypothyroidism. Should it be in mid range to upper third? Mine was 1.01 in a range of 0.76 to 1.46. I feel very hypo.
Dryski
in
Thyroid UK
4 months ago
Ferritin results
Hi, I had my blood test results back today and my serum ferritin is 30ug/L. No TSAT. Results tho. I've been prescribed ferrous sulphate 200mg. Not sure what 30ug/L means though can anyone enlighten me?
Hi, I had my blood test results back today and my serum ferritin is 30ug/L. No TSAT. Results tho. I've been prescribed ferrous sulphate 200mg. Not sure what 30ug/L means though can anyone enlighten me?
Ragdoll1
in
Restless Legs Syndrome
20 days ago
live blood analysis …migraines
Around 7 years ago following blood tests for TATT and various other ailments, it was found that I had a low B12 (156) and GP agreed to prescribe the usual injections… loading dose and then 3 monthly. After lots of research on this site and through trial and error I finally settled on SE every 2 weeks
Around 7 years ago following blood tests for TATT and various other ailments, it was found that I had a low B12 (156) and GP agreed to prescribe the usual injections… loading dose and then 3 monthly. After lots of research on this site and through trial and error I finally settled on SE every 2 weeks
Countrylou
in
Pernicious Anaemia Society
4 months ago
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