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'promosm' ❤️

Love the sound of this project. I’m not a woman but I’m gay and feel closer to NB than a man. I have been dismissed constantly since I first started to feel unwell with what I now know is hypothyroidism. They put me through years of mental health ‘treatment’ which meant that I was never listened to again and never tested again past an early TSH test and then nothing else for ten years. Surprise surprise I didn’t get better! I had my horrific symptoms labelled as ‘somatic’ which still makes it nearly impossible to be listened to by any doctor and I have had everything from broken legs to infections blamed on my imagination and it takes me around 4-5x more appointments compared to straight cis males I know before anyone does anything which is torture when I absolutely hate being anywhere near these people now. They usually get listened to straight away and have referrals or prescriptions whereas I get pushed out the door.

I think that Doctors really don't want to know the Free T3 lab value, because they prefer to believe that T4 MAGICALLY converts to T3 and also... they really don't know what to do if T3 is low. 😉

Reverse T3 isn’t even discussed. Also a patient either pituitary issues might have low TSH, T3, T4 all at once. Reverse T3 when high can block the effectiveness of T3 so needs to be treated with only T3. Raising T4 in patients that have too much or higher Reverse T3, will increase Reverse T3 and decrease the effectiveness of T3.

thank you

The endocrinologist are trained in dieabetis

All doctors need to learn. Doctors are not trained in thyroid and we suffer we are the forgotten sick

Can I get t3 with thyroid cancer I’m on leveroxin thes feeling s are aful

I live in UK. I was diagnosed in 1998/9, in my 40's. I was told that I could only be given T4 synthetic, Levo. I tried sourcing my own T3, asked my GP to help with a trial of the T3. He told me that T3 is an illegal drug which he would not help me with and which I was never to mention again in his presence! Go figure? I know more than he does! I have never been well since diagnosis, I cannot lose weight and believe me I have tried very hard. But I can gain at a terrific speed at times. Hypoo thyroid is gradually killing me I believe!

Thank you very much Doctor Bianco for this informative and interesting presentation.👏👏👏 As a man living without a thyroid for already 6 years and having struggled with T4 therapy alone, I want to confirm that reducing T4 and adding T3 twice a day has improved the symptoms a lot. I have not found the right proportion for me yet because I still have some symptoms, but I am sure that now I am on the right path. The only thing I am concerned about is keeping TSH at least closer to the lower range. T3 actually suppresses TSH a lot, which, in its turn, as far as I know, can negatively affect T4 to T3 conversion. What if TSH is slightly lower than the below range? Is going to effect seriously on T4 T3 conversion? or going to have some important long term effects on a patients health?

I think for the dose of t3 it's not enough to think only on bodysize. Patiënts with poor deodinaise maybe need more.

I agree with @blondebeauty. My GPs are totally incapable of understanding how the thyroid works and the blood tests that do not give an accurate picture of what is wrong. I have had to do my own medical research - generally from holistic doctors in the USA who identified the fact that the LIVER converts T4 to T3. If there is a live problem, like my NAFLD, it does not work efficiently to do that but the blood tests will NOT show this. Also, high stress levels, Cortisol, affects the Hypothalamus which sends the instruction to the Pituitary gland to make TSH! Not even Endocrinologists seem to understand this!!! I have a huge goitre that is choking me but my GP is reluctant to send me for TESTS, preferring to rely on a basic blood test for TSH. How's that for our NHS system? I'm in despair any my Anxiety levels are sky high. All they want to do is suppress me with brain chemicals for anxiety - which will make my liver even more toxic and even less able to make T3!!! Not even Private Endocrinologists seem to understand the links between the liver and high Cortisol. I don't know where to turn for help but refuse to take mind-altering anti-anxiety drugs which don't work anyway. My anxiety is due to STRESS concerning my Thyroid goitre and the reluctance of my GP to find the reason for my goitre. The final thing for me will be to have surgery which I believe is very dangerous! Meanwhile my life is HELL with strong anxiety symptoms for 10 hrs a day that shake my body, nauseate my stomach and make it jittery as well as strong palpitations which make my BP worse.

Hey, Can you please make a similar video on Hyperthyroidism????

I’m a Caucasian female of high income and I fought for a decade to finally get my thyroid functioning optimally seeing dozens of doctors your assumptions are ten thousand percent correct. Guess what fixed my thyroid? T3 only I have a conversion problem and my body converts t4 into mostly rt3. T4 only works for nobody. Endos need to wake the hell up and realize that t4 is an inactive storage hormone and most people are highly inflamed and don’t convert levo/synthroid into t3 properly. Wake the hell up and start giving a t4/t3 combo to treat hypothyroidism

Thank you 🙏

Dr Reena is so easy to listen to. And easy to understand. Thanks for this great interview.

I am in UK and (after 25 years of problems with just levothyroxine only) I managed to convince endo consultant to put me on combined therapy (20mcg liothyronine and 125mcg levothyroxine). Still not handed over to GP... Lab tests requesting T3 tests constantly ignored by the lab despite consultant requests... so T3 adjusted on my subjective feeling rather than blood levels Feeling a lot better

‘That didn’t go anywhere’ in reference to the poor patients who were trying to fight back against being forced to take a medication that meant they had reduced cognitive function and still had symptoms… 😔 What is wrong with doctors if they thought they could just ignore what their patients were saying?! While I find this infuriating I really needed to see this right now because I’m going through this myself. I’m so unwell and only getting worse but they will only give me T4 which always ends up being too high compared to the T3 level that I need to be able to think properly. It’s horrible and there’s not many options to do anything about it…

Glad that person asked why it’s still even possible for nhs doctors to treat thyroid patients so badly and how they can get away with repeatedly ignoring them and not investigating their symptoms and then if they do, not ordering the extensive testing required to rule out every possible explanation. It’s barbaric and has to stop before any other people lose any more of their lives unnecessarily.

Totally understand refusing to mention anything to do with mental health for fear of it being used against you. I spent over a decade trying to figure out what was wrong and now I have so many mental health misdiagnosis that they automatically ignore me before I even get in the door. It’s so stifling to be so powerless over your own health at a time when you are so unwell and need help the most. People say just change doctors but I don’t know how to find another local GP and there’s no guarantee that they would be any better.

Interesting guy, sounds like he went through many things I did. Well apart from finding a good doctor that didn’t insist I was fine or mentally ill. 🙄 Covid gave me horrific eye problems too which no doctor or optician would even believe and I found the medical gaslighting more damaging than the actual virus as I was made to feel like a hypochondriac all over again after a lifetime fighting doctors for an explanation for my health problems and only ever being made worse which caused enough damage without the untreated hypothyroidism on top. 😪

I second that, amazing job Mr. Arthur! We are proud of you!

Well done Mr. Arthur! Thank you for your dedication to this! 🙏🏼♥️♥️♥️

The tsh is higher in colder weather not the time of year because when it is cold in Australia it is warmer in the Ststes.

My thyroid cancer was completely cured by #DRONYENEKE on TH-cam i came across series of comment from different individual that he has helped cure different kinds of diseases and virus contact him today he will set you free from your health challenges don't listen to what the hospitals are saying there is healing powers in natural herbs

Can you provide a detail video about scoring of thypro questionnaire hindi version

I wonder how successful parathyroid auto-transplantations are. It seems to be quite difficult.

Can you provide the link for downloding the Thypro questionnaire english version

Excellent, informative presentation, explained many insecurities I had about the surgery decision I was considering. Thank you.

every symptom is what i've got, i guess this video may have made me realize, i never heard of it before but always so pale with bloodshot eyes and never been near subtances

i'm one of the few people who in the 1990s was taught "we gotta go through it!" from his book in primary school

Interesting

A bit presumptuous to assume that if you have had a full thyroid function test it is because you are are more intelligent, middle class white woman. Whilst I am intelligent and none of the latter. You simply have to advocate for yourself and try to have a basic understanding of the physiology of your ailment. Also in regards to ethnicity many forget that “Black Caribbean” is bogus as we tend to be genetically multi-ethnic and are also prone to European disease. Many folk of Caribbean are more likely to get a full lipid panel test when they speak of fatigue, gastric issues, arthralgia, and are put on a statin (regardless of BMI and diet) than be tested for low thyroid function. Then they have lifetime of degraded health due to the side effects of statins.

There is a 💯% cure to thyroid and I got my cure from Dr iyaremoses on TH-cam remedies and till now I'm completely cured is a good thing to share my experience..

There is a 💯% cure to thyroid and I got my cure from Dr iyaremoses on TH-cam remedies and till now I'm completely cured is a good thing to share my experience..

Permanently cured with dr iyaremoses herbal medicine on youtube#driyaremoses.

I had a marked change in my TSH level in 2021 having been on the same dose of thyroxine without any problems for over 25 years. The only difference in 2021 was that I had the Covid vaccines.

I just got blood test back for my yearly blood test. I have had both vaccines as well as the booster. I am in AZ. My Tsh levels have been the same since I had my thyroid killed almost 14 years ago. This blood work came back so upsetting. My TSH levels showed 39.50 high sensitivity. My blood sugar A1c was 9.5 all my test results were way up. I am greatly concerned about all this. I am generally healthy but I am exhausted and cold and losing my hair. Will this rectify itself over time? I feel this is all due to the vaccines. I have had reactions in the past to the pneaumonia shot.

Where are part 2 and 3

Where is part 2 and 3

Wow thank you Dr Jenkins and The Thyroid Trust… Hopefully with more listening to patients and understanding thyroid disease, things can improve for the 10% of patients that don’t respond on just thyroxine T4 alone…

This information is gold.

I have read about people feeling better on t3 only

By coincidence my husband and I have received weird blood test results this week following double vaccination with the AZ vaccine. My TSH has shot up after previously being stable on the same dose of thyroxine for over 20 years. My husband has become borderline overactive! In same week my brother told me he's just been diagnosed with vitiligo which is of course often related to thyroid disease - again he received double dose of the AZ vaccine. Given most of the general population don't have regular blood tests it makes me wonder how much autoimmune disease may eventually emerge and be put down to coincidence.

love this guy

I think he also didn’t mention looking back at prior TSH levels obtained when someone was feeling fine with no symptoms of hypothyroidism (a baseline value). I know my TSH levels from years ago were in the 1.9 range & I was diagnosed & feel incredibly better after starting Levothyroxine for a TSH of 4.55. Thanks for the talk, especially the info about taking Levothyroxine at night 🙂

Dr Renee is a real gem and thank you Thyroid Trust for this webinar.

Thyroid hormone T4 is a totally inactive storage hormone. DI01 converts 30% to T3, DI02 converts 70% to the active hormone. If you are a carrier of one of these gene defects you need to take pure T3 only or a combination of T4/T3. TSH is irrelevant once on T3 medicine as it will be suppressed as TSH is just a signal for the pituitary to tell the thyroid gland to make T4. Frankly if you have been suffering from hypothyroidism for years with no relief on high doses to T4 you obviously need to switch to T3. Get the gene test done NHS Endocrinologists have to give you a prescription. You'll have to pay for it privately but it's worth it because T3 is unaffordable unless you are rich.

Can you put the links for the surveys here?

I am 71 year old. My tsh is 5.0 & my ft3 & ft4 is normal. I made control on IBS, osteoporosis. I am suffering from Hashimoto thyroid for last 22 years. I am not gaining weight , but not reducing. I am on gluten ,sugar, dairy,soya,corn, Maidha free diet for last 2 years. Sometime I got disturbed with IBS with taking all these precautions.I am taking 62& half Thynoram tab every day. Is my dose if higher.?Can you guide me. My weight is 70 kg. Thank you.