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t3 Sources
Hi All have been happy and healthy on T3 for the last number of years however my reliable source has discontinued manufacturing and my hypo is back in a big way and both NHS and private docs are just useless and cannot access nor prescribe t3 - could anyone be so kind to point me in the direction of
Hi All have been happy and healthy on T3 for the last number of years however my reliable source has discontinued manufacturing and my hypo is back in a big way and both NHS and private docs are just useless and cannot access nor prescribe t3 - could anyone be so kind to point me in the direction of
Happy37yes
in
Thyroid UK
4 months ago
advice on synacthen test
for anyone who has been following my story they will know I’ve been having medication issues and I am now taking T3 only. Still having issues with weight gain. Spoke to my endocrinologist last week and she has agreed the increase to 40mcg. This was after she had suggested trying a small dose of levothyroxine
for anyone who has been following my story they will know I’ve been having medication issues and I am now taking T3 only. Still having issues with weight gain. Spoke to my endocrinologist last week and she has agreed the increase to 40mcg. This was after she had suggested trying a small dose of levothyroxine
ScriptMaz
in
Thyroid UK
2 months ago
How to choose doctor
Hi. I’m thinking of going private to get treated for Hashimoto’s but I’m not sure whether to and if so who to go to. I was self medicating with T3 but was told that my heart attack in January was down to taking too much. I’ve since come off it and feel awful. I don’t know whether to go back to
Hi. I’m thinking of going private to get treated for Hashimoto’s but I’m not sure whether to and if so who to go to. I was self medicating with T3 but was told that my heart attack in January was down to taking too much. I’ve since come off it and feel awful. I don’t know whether to go back to
DownAndDesperate
in
Thyroid UK
4 months ago
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help with results please
I’d be grateful if anyone could help with results please. I’m on combined therapy 50mg T4 and 35mg T3 TFT 0.02 (0.35-4.94) FT3 4.5 (2.4-6.00) FT4 8.1 (9.00-19.00) B12 433 (187-883) Vit D 126.1 >50 Thank you :)
I’d be grateful if anyone could help with results please. I’m on combined therapy 50mg T4 and 35mg T3 TFT 0.02 (0.35-4.94) FT3 4.5 (2.4-6.00) FT4 8.1 (9.00-19.00) B12 433 (187-883) Vit D 126.1 >50 Thank you :)
Bollieforme
in
Thyroid UK
4 months ago
advice please- protein shakes
I know we shouldn’t take other tablets or vitamins close to thyroxine, but is a meal replacement shake made from pea protein okay to drink an hour after thyroxine? is that different to vitamins as it’s food? Also, do we really have to avoid soya? I can’t have diary and most other protein shakes
I know we shouldn’t take other tablets or vitamins close to thyroxine, but is a meal replacement shake made from pea protein okay to drink an hour after thyroxine? is that different to vitamins as it’s food? Also, do we really have to avoid soya? I can’t have diary and most other protein shakes
Goinginsane1
in
Thyroid UK
4 months ago
When to take iron with T3 multi-dosing.
I'm writing this post again as I didn't get many replies and my private Dr hasn't replied. I'm trying to work out when to fit in taking iron (Three arrows) with my T3 doses. I am taking T3 as per my private Dr's schedule which is 3 times per day and 6-7 hours apart. I'm wondering whether to switch to
I'm writing this post again as I didn't get many replies and my private Dr hasn't replied. I'm trying to work out when to fit in taking iron (Three arrows) with my T3 doses. I am taking T3 as per my private Dr's schedule which is 3 times per day and 6-7 hours apart. I'm wondering whether to switch to
PinkSkittles
in
Thyroid UK
4 months ago
How to get an accurate T3 reading with bloods?
Ive asked a similar question before, regarding blood testing for T4/T3 and realised for years I was having a blood sample done a few hours after I had taken my Levo upon waking up. People on here then said to have the bloods done that morning before taking T4, to get a more accurate reading. Since then
Ive asked a similar question before, regarding blood testing for T4/T3 and realised for years I was having a blood sample done a few hours after I had taken my Levo upon waking up. People on here then said to have the bloods done that morning before taking T4, to get a more accurate reading. Since then
Ooohmatron
in
Thyroid UK
25 days ago
slow release liothyronine
Like many people on here I miss the wise opinion and knowledge of Diogenes enormously. I know he was working on the formulation of a slow release liothyronine which was in clinical trial. Does anyone have an update on this? is it any closer? In the meantime I am tempted to try sustained release compounded
Like many people on here I miss the wise opinion and knowledge of Diogenes enormously. I know he was working on the formulation of a slow release liothyronine which was in clinical trial. Does anyone have an update on this? is it any closer? In the meantime I am tempted to try sustained release compounded
Mollyfan
in
Thyroid UK
4 months ago
Parathyroid levels
I have not been feeling too great and have had my thyroid checked, t4 and t3 are now all normal and back to my 175 a day. Still not been well really bad tummy aches, back ache, really struggling with aches in my muscles etc. Had more blood tests lately, they said to check bones. Doctor rang yesterday
I have not been feeling too great and have had my thyroid checked, t4 and t3 are now all normal and back to my 175 a day. Still not been well really bad tummy aches, back ache, really struggling with aches in my muscles etc. Had more blood tests lately, they said to check bones. Doctor rang yesterday
lynpalmer
in
Thyroid UK
27 days ago
toxic metal test results
I’m not sure if people on here can give their thoughts on my provoked urine test please? I’ve never had one done before Many thanks if so.
I’m not sure if people on here can give their thoughts on my provoked urine test please? I’ve never had one done before Many thanks if so.
CornishChick
in
Thyroid UK
4 months ago
Are my remaining symptoms perimenopause?
I've just done bloods after 13 weeks on a stable dose (150mcg T4 & 30mcg T3) which are as follows: TSH: 0.007 T4: 18.7 (12-22) 67% T3: 6 (3.1 - 6.8) 78% My vits are low but also stable since I quit gluten, I will work on them. Folate: 12.2 (>7) Vit D: 67 (50-250) Ferritin: 77 (30-150) Recent female
I've just done bloods after 13 weeks on a stable dose (150mcg T4 & 30mcg T3) which are as follows: TSH: 0.007 T4: 18.7 (12-22) 67% T3: 6 (3.1 - 6.8) 78% My vits are low but also stable since I quit gluten, I will work on them. Folate: 12.2 (>7) Vit D: 67 (50-250) Ferritin: 77 (30-150) Recent female
WitchingHour2point0
in
Thyroid UK
5 months ago
time to try T3
Hypothyroid - 20 years always on T4 but same brand Mercury Pharma, currently taking 150mcg. Like everyone I private test to get T3 T4 have paid in the past to see private endocrinologists and am reasonably well informed (mainly through this forum). I don’t suffer as badly as many people do but maybe
Hypothyroid - 20 years always on T4 but same brand Mercury Pharma, currently taking 150mcg. Like everyone I private test to get T3 T4 have paid in the past to see private endocrinologists and am reasonably well informed (mainly through this forum). I don’t suffer as badly as many people do but maybe
Sususulio
in
Thyroid UK
4 months ago
T3 Trial continued
Medichecks 20 March 2024 History:
Hypothyroid (after RAI in c2004)
Spent 2023 improving folate, B12, Vit D although ferritin still poor. Came off PPIs and now take Gaviscon twice daily. Gastritis issues ongoing though. Officially a poor converter (dud DIO2) so really wanted to try T3 Gluten
Medichecks 20 March 2024 History:
Hypothyroid (after RAI in c2004)
Spent 2023 improving folate, B12, Vit D although ferritin still poor. Came off PPIs and now take Gaviscon twice daily. Gastritis issues ongoing though. Officially a poor converter (dud DIO2) so really wanted to try T3 Gluten
Rambling9
in
Thyroid UK
4 months ago
Is an Alkaline Phosphate level of 71 (UK) good?
Is an Alkaline Phosphate level of 71 (UK) good? Was put on steroids to deal with newly diagnosed PMR and they fell by 20 units in 2 weeks!
Is an Alkaline Phosphate level of 71 (UK) good? Was put on steroids to deal with newly diagnosed PMR and they fell by 20 units in 2 weeks!
Gioielli5
in
PBC Foundation
4 months ago
Not feeling the Heat like I usually do!!!
Hi all For years, I've really felt the heat during the summer months but, this summer, I'm actually feeling quite comfortable, which is great and I'm certainly not complaining. I have change my thyroid meds, at the end of last year, so several months ago. I was on Levothyroxine 150mcg daily but GP
Hi all For years, I've really felt the heat during the summer months but, this summer, I'm actually feeling quite comfortable, which is great and I'm certainly not complaining. I have change my thyroid meds, at the end of last year, so several months ago. I was on Levothyroxine 150mcg daily but GP
JMN2017
in
Thyroid UK
29 days ago
Help with my test results please
Hi All I would like help with my latest blood tests results PLEASE and guidance of what to do next ??? I have Autoimmune Hashimotos 27 years ! So to keep this short I’ve recently ( past 3 months ) changed from Armour Thyroid ( took for 5 years ) to Tirosint ( I’m lactose intolerant ) previous
Hi All I would like help with my latest blood tests results PLEASE and guidance of what to do next ??? I have Autoimmune Hashimotos 27 years ! So to keep this short I’ve recently ( past 3 months ) changed from Armour Thyroid ( took for 5 years ) to Tirosint ( I’m lactose intolerant ) previous
joskie
in
Thyroid UK
2 months ago
New blood results
Hello everyone Just received new blood results and if anyone can give advice I would be very grateful! Taking 125mcg Levo that was taken at 08.30 Sunday morning.Also split my 12.5mcg T3 dose one at 08.30 and the other half at 21.30 on the Sunday.Took my bloods at 08.00 the following day Monday Going
Hello everyone Just received new blood results and if anyone can give advice I would be very grateful! Taking 125mcg Levo that was taken at 08.30 Sunday morning.Also split my 12.5mcg T3 dose one at 08.30 and the other half at 21.30 on the Sunday.Took my bloods at 08.00 the following day Monday Going
jacobite33
in
Thyroid UK
4 months ago
I am lost, should I seek a second opinion?
hi, this will be a bit of a long one sorry. I am really confused and don’t know whether to accept my gps answer or go private for a second opinion. My issues started more noticeably in October last year when I started heavily bleeding and having long periods and very short periods of time of not bleeding
hi, this will be a bit of a long one sorry. I am really confused and don’t know whether to accept my gps answer or go private for a second opinion. My issues started more noticeably in October last year when I started heavily bleeding and having long periods and very short periods of time of not bleeding
Han99m
in
Thyroid UK
20 days ago
Berberine and iron?
Hi, So glad to have found this wonderful forum! I am a 74 year female who recently started taking pregabalin for RLS. I just got back my ferritin level and it is 12. I will order some iron and would like to know how many mg is a good dose. Also, I started taking niacin 500mg daily for my cholesterol
Hi, So glad to have found this wonderful forum! I am a 74 year female who recently started taking pregabalin for RLS. I just got back my ferritin level and it is 12. I will order some iron and would like to know how many mg is a good dose. Also, I started taking niacin 500mg daily for my cholesterol
glorious-granny
in
Restless Legs Syndrome
4 months ago
Seeing an MPN Specialist tomorrow!
I have an appointment at Stanford with an MPN Specialist tomorrow. Going on 5 years with ET+CALR and currently taking aspirin and 2 pills of Hydrea daily AND 90mcg of Pegasys once a week. We are in a transitional period right now and I will eventually just be taking Pegasys and aspirin. Took my 4th dose
I have an appointment at Stanford with an MPN Specialist tomorrow. Going on 5 years with ET+CALR and currently taking aspirin and 2 pills of Hydrea daily AND 90mcg of Pegasys once a week. We are in a transitional period right now and I will eventually just be taking Pegasys and aspirin. Took my 4th dose
Zeppelin11
in
MPN Voice
1 year ago
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