Now, I remember there was a post about this recently where someone said she thought one of the authors might have been Swedish...I think this might be it. The article itself is from a Canadian thyroid site, but there is a reference to a study where one of the names is Danish. If someone knows which post I am referring to, please link to it here.
Anyway, here is the article; personally, I have to say it's one of the best I've read so far because it basically recognises that we are all different so have different needs:
THANK YOU ,VERY INTERESTING ARTICLE not sure I fully understood every thing but it confirmed a lot of my experience and theories in the parts i did comprehend
Unfortunately, if in the UK, I doubt the 'authorities' will change their attitude and become 'more updated' about how best to treat hypo patients untill they are on an optimum dose and also allow the prescription of NDTs (if necessary) to those who cannot recover on levo or T3 or T3/T4.
They withdrew NDTs (which has been prescribed (or given) worldwide since 1892 but unfortunately the Association made False Statements about this to have it withdrawn instantly n the UK. They wouldn't give an answer to the Scientist/doctor who sent them the following and every year for three years, they never did respond.
Thousands of hypo sufferers recovered on this product:-
I was told on here after I posted my thyroid results. I chose NDT, as I wanted something more natural/less Big Pharma. Since Dr P went off the scene, I self-medicate.
Oh, the reference to my endo is based on my hopeless endeavour to see if the NHS would pay for NDT. She was only interested in my cholesterol and trying to get me on statins. So, I guess it's carry on self-medicating.
They don't now prescribe NDT - which was always an alternative and many doctors prescribed it until its withdrawa.l due to their False Statemets. You can read below one of TUK's Advisers responded :-
Every year for three years before Dr Lowe's demise, they never did respond. Neither do they listen to patients many who have been fourced to source their own.
We should be given prescriptions for whatever resolves our clinical symptoms. It shouldn't be down to cost. If we have more consultations with doctors than we need, surely relieving symptoms will be cost-effective.
Yes there are some great articles coming from this author out of Canada so welcome to see and would love to know more about this person! Love the metaphors!
Elegantly written and I couldn’t have come across it at a better time. I found the section on having T3 as the cause of insomnia to be especially enlightening. Oh, the horrors of night awakenings and not be able to go back to sleep! It’s so dreadful and now I finally know of a fix! Thanks so much for sharing!
Thank you so much for posting this, I learned so much.
What a great article with insight into D1 D2 and D3. The only thing about test results are that some labs may not process the tests within an interval where the rises of hormones will normally occur. If there is a delay in the test processing may be this may not reflect accurately the daily or hourly fluctuations of the hormones in the system.
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Studies on TSH for those on combined T3 T4 therapy 
T4 and T3 optimal 3 hours after thyroid meds, I feel great, but suppressed TSH is throwing a spanner in the works.
T4 & T3 combination therapy... day 9... awesome! 
How to decide whether to try NDT or T4+T3 combination therapy?
I read that it isn't advisable to take thyroxine with suppressed TSH and T4! 
