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Ultrasound and Vitamin D
Hello. I posted on here last week looking some advice on my latest blood tests. I have had and underactve thyroid for almost 3 years but have been experiencing all of the symptoms that I had prior to being diagnosed (and taking Thyroxine - I have always been on 50mg). I have just received blood results
Hello. I posted on here last week looking some advice on my latest blood tests. I have had and underactve thyroid for almost 3 years but have been experiencing all of the symptoms that I had prior to being diagnosed (and taking Thyroxine - I have always been on 50mg). I have just received blood results
Flo1000
in
Thyroid UK
3 months ago
Plant-based raw food diet eases symptoms of SLE, Sjögren’s: Report
More research needed into diet's role in autoimmune disease Three women with the autoimmune conditions systemic lupus erythematosus (SLE) and Sjögren’s syndrome saw their symptoms ease after starting a diet rich in plant-based raw foods, according to a recent case series report. The diet included
More research needed into diet's role in autoimmune disease Three women with the autoimmune conditions systemic lupus erythematosus (SLE) and Sjögren’s syndrome saw their symptoms ease after starting a diet rich in plant-based raw foods, according to a recent case series report. The diet included
lupus-support1
Administrator
in
LUpus Patients Understanding and Support
3 months ago
Methylene Blue
Has anyone used or considered Methylene Blue in very low dosages for their Parkinson's? Franciso Gonzalez-Lima of the University of Texas, Austin is an expert on its advantages for treating neurological diseases. Mercola did an interview with him on the subject. Mercola does not promote synthetic drugs
Has anyone used or considered Methylene Blue in very low dosages for their Parkinson's? Franciso Gonzalez-Lima of the University of Texas, Austin is an expert on its advantages for treating neurological diseases. Mercola did an interview with him on the subject. Mercola does not promote synthetic drugs
Trailing
in
Cure Parkinson's
1 year ago
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zoldronate risk factors?
Hi , risedronate has only worked on my spine and not my hips for the last 2 years. hips at 16% risk, t_score -3.6. albeit I have not been taking enough vit D over the last 2 years. I have upped my vit D now, my calcium intake is fine. Zoledronate has been mentioned but I am wary of the risk of zoldronate
Hi , risedronate has only worked on my spine and not my hips for the last 2 years. hips at 16% risk, t_score -3.6. albeit I have not been taking enough vit D over the last 2 years. I have upped my vit D now, my calcium intake is fine. Zoledronate has been mentioned but I am wary of the risk of zoldronate
lindyloo2018
in
Bone Health and Osteoporosis UK
3 months ago
zoledronate risk factors ?
Hi , risedronate has only worked on my spine and not my hips for the last 2 years. hips at 16% risk, t_score -3.6. albeit I have not been taking enough vit D over the last 2 years. I have upped my vit D now, my calcium intake is fine. Zoledronate has been mentioned but I am wary of the risk of zoldronate
Hi , risedronate has only worked on my spine and not my hips for the last 2 years. hips at 16% risk, t_score -3.6. albeit I have not been taking enough vit D over the last 2 years. I have upped my vit D now, my calcium intake is fine. Zoledronate has been mentioned but I am wary of the risk of zoldronate
lindyloo2018
in
NRAS
3 months ago
Help with latest blood test results and Vit D3 advice
Hello everyone,I would really appreciate any advice regarding my latest fasting blood tests, done before taking my Levothyroxine tablet. I am still on 75mcg Levothyroxine since diagnosed with Hashimoto's in 2010. After my latest post, around Nov 2022, I followed the advice I was given and started taking
Hello everyone,I would really appreciate any advice regarding my latest fasting blood tests, done before taking my Levothyroxine tablet. I am still on 75mcg Levothyroxine since diagnosed with Hashimoto's in 2010. After my latest post, around Nov 2022, I followed the advice I was given and started taking
Griffin43
in
Thyroid UK
3 months ago
Getting tested after taking any supplements...
Hi there, I found this information after worrying that I have lost my mind due to GP responses, on top of all of my very B12 like symptoms, Inc. Neurological. How I felt was gradual at first and more like fatigue and gastic upsets, intermittent mild tingling, over the last few years, but last year my
Hi there, I found this information after worrying that I have lost my mind due to GP responses, on top of all of my very B12 like symptoms, Inc. Neurological. How I felt was gradual at first and more like fatigue and gastic upsets, intermittent mild tingling, over the last few years, but last year my
Suffering_sunny
in
Pernicious Anaemia Society
3 months ago
vitamin deficiencies
I had most of my sigmoid removed because of diverticulitis five years ago. My question is my surgeon said that it should not affect my vitamin or mineral intake because the sigmoid doesn’t involve that. Got on finding that it most certainly does I get a B12 injection because I’m a vegetarian so that
I had most of my sigmoid removed because of diverticulitis five years ago. My question is my surgeon said that it should not affect my vitamin or mineral intake because the sigmoid doesn’t involve that. Got on finding that it most certainly does I get a B12 injection because I’m a vegetarian so that
Gardeningbuff
in
Bowel Disease Support
3 months ago
Temp going up and down all day
Hi folks, I recently received the results of my 2.6cm nodule and it was thankfully benign. Such a relief. tey did say I had a few nodules and that they were on both sides. I have been following all your advise and tips and immediately started vit d, b21, b complex, iron, and a probiotic. I also take
Hi folks, I recently received the results of my 2.6cm nodule and it was thankfully benign. Such a relief. tey did say I had a few nodules and that they were on both sides. I have been following all your advise and tips and immediately started vit d, b21, b complex, iron, and a probiotic. I also take
madeline05
in
Thyroid UK
3 months ago
still confused about my iron results
I’ve now redone my iron panel with medichecks and have similar results to last time. I can’t work out why my ferritin continues to drop. And what I can do about it as I know I need higher ferritin levels for optimum thyroid hormone function. …………………………… Ferritin……….Iron……….. Trans. Sat………..TIBC……….
I’ve now redone my iron panel with medichecks and have similar results to last time. I can’t work out why my ferritin continues to drop. And what I can do about it as I know I need higher ferritin levels for optimum thyroid hormone function. …………………………… Ferritin……….Iron……….. Trans. Sat………..TIBC……….
Mazes
in
Thyroid UK
3 months ago
t3 Monotherapy
Hello everyone, I have been a reader of the forum for a while now and it is nice to know so many other people are struggling with un-resolved thyroid problems. This forum was the first place where I thought wow, these guys get it. I have hypermobile ehlers danlos syndrome, I was diagnosed with MS
Hello everyone, I have been a reader of the forum for a while now and it is nice to know so many other people are struggling with un-resolved thyroid problems. This forum was the first place where I thought wow, these guys get it. I have hypermobile ehlers danlos syndrome, I was diagnosed with MS
Jimjamio
in
Thyroid UK
3 months ago
Zinc supplement
I have NASH cirrhosis which is compensated and T2 diabetes. I am 68 years old, struggling to stick to a healthy eating plan. I take B12 and a vitamin D supplement. Is it safe for me to take a zinc supplement? I would appreciate any advice in relation to this. Many thanks and I hope everyone is keeping
I have NASH cirrhosis which is compensated and T2 diabetes. I am 68 years old, struggling to stick to a healthy eating plan. I take B12 and a vitamin D supplement. Is it safe for me to take a zinc supplement? I would appreciate any advice in relation to this. Many thanks and I hope everyone is keeping
Robert1220
in
British Liver Trust
3 months ago
Megaloblastic anaemia
Hi, I was diagnosed with megaloblastic anaemia yesterday. My gp, sent over a prescription for Cyanocobalamin 1mg/1ml solution for injection ampoules. My pharmacy and other pharmacies don't stock it. I left a note for my doctor with the receptionist to ask for possibly a different brand or type. I'm new
Hi, I was diagnosed with megaloblastic anaemia yesterday. My gp, sent over a prescription for Cyanocobalamin 1mg/1ml solution for injection ampoules. My pharmacy and other pharmacies don't stock it. I left a note for my doctor with the receptionist to ask for possibly a different brand or type. I'm new
fatfatfat
in
Pernicious Anaemia Society
3 months ago
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
3 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
3 months ago
Feeling dreadful but doc says results are fine!
Hi there, I was diagnosed with underactive thyroid back in July 2020. I was prescribed 25mg levothyroxine which was increased to 50mg after 6 months. Shortly after starting levothyroxine I started getting stiffness in my neck and shoulders along with pain in my hips and groin - the only way I can
Hi there, I was diagnosed with underactive thyroid back in July 2020. I was prescribed 25mg levothyroxine which was increased to 50mg after 6 months. Shortly after starting levothyroxine I started getting stiffness in my neck and shoulders along with pain in my hips and groin - the only way I can
FlamingoPenguin
in
Thyroid UK
3 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
3 months ago
bloods following bariatric surgery.
very quick question lovely knowledgeable peeps. My daughter had bariatric surgery 2years ago. Done really well with weight loss. However despite taking recommended supplements is suffering hair loss, being cold, ratty tempered, tearful and extremely fatigued. Did Medichecks advanced woman blood test.
very quick question lovely knowledgeable peeps. My daughter had bariatric surgery 2years ago. Done really well with weight loss. However despite taking recommended supplements is suffering hair loss, being cold, ratty tempered, tearful and extremely fatigued. Did Medichecks advanced woman blood test.
Auders
in
Thyroid UK
3 months ago
Suppression of TSH but low T4/T3 levels whilst taking Levo/Lio Combo
A few years ago, my thyroid results were looking a lot better but NHS GP over the last 2 years has told me to reduce my dosage twice (because of the 'risks' of overtreatment). I'm now on 100mcg levothyroxine (75mcg supplied by GP and topped up by myself) and 25mcg liothyronine (self-sourced). I now don't
A few years ago, my thyroid results were looking a lot better but NHS GP over the last 2 years has told me to reduce my dosage twice (because of the 'risks' of overtreatment). I'm now on 100mcg levothyroxine (75mcg supplied by GP and topped up by myself) and 25mcg liothyronine (self-sourced). I now don't
Louise1610
in
Thyroid UK
3 months ago
Update after Endo
Good morning, I'm just writing this as an update to anyone who may be interested in my seemingly-odd case... My Endo appointment went well. (Or so I thought but if you're learning from this post, please read the comments!) She believes I have Graves disease, despite the antibodies indicating Hashimotos
Good morning, I'm just writing this as an update to anyone who may be interested in my seemingly-odd case... My Endo appointment went well. (Or so I thought but if you're learning from this post, please read the comments!) She believes I have Graves disease, despite the antibodies indicating Hashimotos
Opposite
in
Thyroid UK
3 months ago
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