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High T4
Hi Greygoose, I've seen your reply to Helen'shubby. Just wondering about my T4 and T3 . I'm awaiting new test results but my last test showed T4 at 22.4 ( 7.5- 21.1) ( 109.56%) FT3 4.9 (3.8-6.8) (36.67%) TSH is always undetectable B12 351 (110- 914.0) I am supplementing now (nature provides 3000mcg daily
Hi Greygoose, I've seen your reply to Helen'shubby. Just wondering about my T4 and T3 . I'm awaiting new test results but my last test showed T4 at 22.4 ( 7.5- 21.1) ( 109.56%) FT3 4.9 (3.8-6.8) (36.67%) TSH is always undetectable B12 351 (110- 914.0) I am supplementing now (nature provides 3000mcg daily
Shellian
in
Thyroid UK
5 months ago
Biotin and ESR/CRP Testing
Good evening. I have been taking supplements - AdCalD3 (of course!), Vit K2, VitB complex magnesium glycerine/malate and fish oil - fairly religiously since starting on pred. To help with hair/skin/bone thinning, I have also taken collagen and biotin. I was alarmed to discover tonight that biotin can
Good evening. I have been taking supplements - AdCalD3 (of course!), Vit K2, VitB complex magnesium glycerine/malate and fish oil - fairly religiously since starting on pred. To help with hair/skin/bone thinning, I have also taken collagen and biotin. I was alarmed to discover tonight that biotin can
Burroughs123
in
PMRGCAuk
8 months ago
APS Symptoms
As many of you know I have been diagnosed with Sjogrens Syndrome, Lupus, Fibromyalgia in addition to APS. I was on Warfarin from 2015 - 2020 (following a clot on my brain) My target was 4 and below that I was unable to function. Migraines, every muscle hurt, could hardly walk etc. in 2020 my INR became
As many of you know I have been diagnosed with Sjogrens Syndrome, Lupus, Fibromyalgia in addition to APS. I was on Warfarin from 2015 - 2020 (following a clot on my brain) My target was 4 and below that I was unable to function. Migraines, every muscle hurt, could hardly walk etc. in 2020 my INR became
WendyWoo50
in
Hughes Syndrome APS Forum
8 months ago
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Vitamin and mineral supplements? My latest results
Hi all, I've just had my latest Blue Horizon results (see image) which I would welcome comments on, particularly regarding the vitamins and minerals I might need to supplement. All blood tests were done no later than 9.30am, no levo for 24 hours before. I've worked really hard this year on my diet, but
Hi all, I've just had my latest Blue Horizon results (see image) which I would welcome comments on, particularly regarding the vitamins and minerals I might need to supplement. All blood tests were done no later than 9.30am, no levo for 24 hours before. I've worked really hard this year on my diet, but
Forestgarden
in
Thyroid UK
8 months ago
Help please
Hello could someone look at my recent blood test please.Since my last post(I know it's been 2 years)I had scan, because of high ferritin which came back clear. All blood tests normal. GP says it's not thyroid! Been having symptoms of hyper and hypo, March I kept having metalic taste GP said it's burning
Hello could someone look at my recent blood test please.Since my last post(I know it's been 2 years)I had scan, because of high ferritin which came back clear. All blood tests normal. GP says it's not thyroid! Been having symptoms of hyper and hypo, March I kept having metalic taste GP said it's burning
mollyjo
in
Thyroid UK
2 months ago
Regenerus cortisol has flatlined, low ferritin but other results seem normal.Gastritis, ‘fizzing’ legs
I will post now and try again later to attach the results PDFs, as it won’t let me at the mo. [u]GP Tests :[/u] Ferritin 21 ( 13 - 150 ) Folate 4 ( 3.8 - 26 ) B12 514. ( 180 - 999 ) GP told me to improve ferritin with diet. I then had acute [u]gastritis[/u]. I’ve stopped omeprazole and will do
I will post now and try again later to attach the results PDFs, as it won’t let me at the mo. [u]GP Tests :[/u] Ferritin 21 ( 13 - 150 ) Folate 4 ( 3.8 - 26 ) B12 514. ( 180 - 999 ) GP told me to improve ferritin with diet. I then had acute [u]gastritis[/u]. I’ve stopped omeprazole and will do
Applethorpe
in
Thyroid UK
8 months ago
foods to eat for longevity
https://theenergyblueprint.com/foods-you-need-to-eat-for-longevity/?inf_contact_key=77e91c5d37fb88ad538161bb2cf2cb6ecc0558ed5d4c28cbfab114022b1ec50d Energy blueprint. Foods & Supplements You NEED TO EAT For Longevity and Energy | Dr. Michael Murray. This was really interesting. (Transcript has a few
https://theenergyblueprint.com/foods-you-need-to-eat-for-longevity/?inf_contact_key=77e91c5d37fb88ad538161bb2cf2cb6ecc0558ed5d4c28cbfab114022b1ec50d Energy blueprint. Foods & Supplements You NEED TO EAT For Longevity and Energy | Dr. Michael Murray. This was really interesting. (Transcript has a few
LAJ12345
in
Cure Parkinson's
9 months ago
Bloods advice pls -starting T3 combo
Morning everyone, hope you're good. 😁I'm getting ready to start t3 combo. There have been a few hiccups with thyroxine dosage/supply. So currently, my prescription of thyroxine has gone up to 87.5mcg, (was put down to 75 as they didn't stock 85) & 5mcg of T3. I just wanted to check in with you to
Morning everyone, hope you're good. 😁I'm getting ready to start t3 combo. There have been a few hiccups with thyroxine dosage/supply. So currently, my prescription of thyroxine has gone up to 87.5mcg, (was put down to 75 as they didn't stock 85) & 5mcg of T3. I just wanted to check in with you to
VEG71
in
Thyroid UK
9 months ago
Lorenzo's Oil Revisited
Chances are you don't take it. I investigated it thoroughly and even had a decent source secured. I only opted out when I was told it would nullify my medical insurance. Depending on whatever scientific report you read it either doesn't work, or stops/reverses progression if you start taking it before
Chances are you don't take it. I investigated it thoroughly and even had a decent source secured. I only opted out when I was told it would nullify my medical insurance. Depending on whatever scientific report you read it either doesn't work, or stops/reverses progression if you start taking it before
monkeybus
in
AMN EASIER
9 months ago
Teva levothyroxine solution, any positive results for anyone?
Hi Has anyone tried Teva levothyroxine solution, and had positive results compared to taking any levothyroxine tablets? To cut a very long story short, the 75 mcg Wockhardt tablets I take are causing terrible pressure all over body and excruiciating burning through top of my head. So bad I collapse.
Hi Has anyone tried Teva levothyroxine solution, and had positive results compared to taking any levothyroxine tablets? To cut a very long story short, the 75 mcg Wockhardt tablets I take are causing terrible pressure all over body and excruiciating burning through top of my head. So bad I collapse.
Razzydaz
in
Thyroid UK
7 months ago
I am now able to tolerate antibiotics again after my nerves healed
Hello! I just want to give this update about my situation. I hope people on here find this because my situation was a nightmare and I think this can help people who are confused and not sure what to do or if they'll ever be able to tolerate antibiotics again (TL;DR: you will be able to if you can heal
Hello! I just want to give this update about my situation. I hope people on here find this because my situation was a nightmare and I think this can help people who are confused and not sure what to do or if they'll ever be able to tolerate antibiotics again (TL;DR: you will be able to if you can heal
Whoa182
in
Pernicious Anaemia Society
6 months ago
TG6 , gluten ataxia, antibodies and a strict diet
I have been diagnosed with Idiopathic Cerebellum Ataxia for 6 years . My consultant recently arranged for a TG6 test at Sheffield hospital . The result came back as mildly positive ( 4.2 with 4.0 as normal ) As I understand it , a strict gluten free diet should remove antibodies from the body preventing
I have been diagnosed with Idiopathic Cerebellum Ataxia for 6 years . My consultant recently arranged for a TG6 test at Sheffield hospital . The result came back as mildly positive ( 4.2 with 4.0 as normal ) As I understand it , a strict gluten free diet should remove antibodies from the body preventing
cyclist49
in
Ataxia UK
13 hours ago
Could Gluten Intolerance lead to RLS?
After watching the video about what can cause Parkinson’s that was posted on this website, I started thinking about inflammation, and inflammation of the body and gut. I found this website from the gluten free society who have found correlation between gluten and rls. My husband who has had RLS for
After watching the video about what can cause Parkinson’s that was posted on this website, I started thinking about inflammation, and inflammation of the body and gut. I found this website from the gluten free society who have found correlation between gluten and rls. My husband who has had RLS for
Sandalsforever
in
Restless Legs Syndrome
3 days ago
Switching to Metavive- Last results
Good morning!I am 42 years old , and mother of 2. I was diagnosed with Hashimoto thyroiditis, in 2019, between two pregnancies. I've been on Eutirox 75mcg/day since 2020, and fluctuate fron hyper to hypothyroidism since then, weught loss and gain, fatigue... I change my life style, gluten free diet
Good morning!I am 42 years old , and mother of 2. I was diagnosed with Hashimoto thyroiditis, in 2019, between two pregnancies. I've been on Eutirox 75mcg/day since 2020, and fluctuate fron hyper to hypothyroidism since then, weught loss and gain, fatigue... I change my life style, gluten free diet
Mireiame
in
Thyroid UK
17 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
19 days ago
Idiopathic ataxia or unknown cause.
Hi all. I urge anyone who has not yet been diagnosed with a particular type of ataxia , so idiopathic of unknown cause, which means they do not know what is causing it. To contact Sheffield and see if you can participate in a new study into gluten ataxia. Although a gluten free diet will not cure ataxia
Hi all. I urge anyone who has not yet been diagnosed with a particular type of ataxia , so idiopathic of unknown cause, which means they do not know what is causing it. To contact Sheffield and see if you can participate in a new study into gluten ataxia. Although a gluten free diet will not cure ataxia
penelope2
in
Ataxia UK
22 days ago
gluten free
hi , Have been thinking I might try gluten free diet ,been reading how it can help with Fibromyalgia symptoms . Does anyone follow a gluten free diet and has it helped.
hi , Have been thinking I might try gluten free diet ,been reading how it can help with Fibromyalgia symptoms . Does anyone follow a gluten free diet and has it helped.
Thornthorpe
in
Fibromyalgia Action UK
24 days ago
Ttc with high tpo antibodies
I have had 3 miscarriages in the last couple of years. 1 spontaneous 2 mmc. Always around 6 to 7 weeks. I was given aspirin and progesterone on the last pregnancy but it didn't work. After my 3rd mc I had lots of investigations done and it showed I had high TPO antibodies. Everything else was normal.
I have had 3 miscarriages in the last couple of years. 1 spontaneous 2 mmc. Always around 6 to 7 weeks. I was given aspirin and progesterone on the last pregnancy but it didn't work. After my 3rd mc I had lots of investigations done and it showed I had high TPO antibodies. Everything else was normal.
Stevienicksfangirl
in
Thyroid UK
30 days ago
Improving diagnosis, and management of Gluten Ataxia.
🙂People in the UK Improving diagnosis and management of Gluten ataxia Ataxia UK, Coeliac UK, and the Sheffield Hospitals Charity have awarded funding to Professor Marios Hadjivassiliou and colleagues at the Sheffield Ataxia Centre, for a research project to help improve the diagnosis and management
🙂People in the UK Improving diagnosis and management of Gluten ataxia Ataxia UK, Coeliac UK, and the Sheffield Hospitals Charity have awarded funding to Professor Marios Hadjivassiliou and colleagues at the Sheffield Ataxia Centre, for a research project to help improve the diagnosis and management
wobblybee
in
Ataxia UK
1 month ago
Help to understand bloods etc
Hi I am new to the forum but was diagnosed with Hashimotos in Jul 23 with these blood results Thyroperoxidase Ab IU/ml - 181 T4 (free) pmol/L - 15.6 TSH mIU/L - 5.1 I have been on Levothyroxine Sodium 25mcg Tab since Jul 23 and my TSH is now 1.9. My doc is now only using this to check my progress
Hi I am new to the forum but was diagnosed with Hashimotos in Jul 23 with these blood results Thyroperoxidase Ab IU/ml - 181 T4 (free) pmol/L - 15.6 TSH mIU/L - 5.1 I have been on Levothyroxine Sodium 25mcg Tab since Jul 23 and my TSH is now 1.9. My doc is now only using this to check my progress
Samfonz
in
Thyroid UK
1 month ago
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