And if you wonder: Well yes, there actually IS something that all of us can do about it:

The rapidly-growing, third-major endocrine society in the world, the IHS (International Hormone Society), co-founded by Dr. Thierry Hertoghe from Belgium, who treats patients from all over the world in his practice located in Brussels, and who is, among other things, president of the World Society of Anti-Ageing Medicine, actually fights FOR us all; for labwork not based only on the TSH and on misleading reference ranges, but at least as much on symptoms and clinical signs, and therapies that do not treat us with synthetic T4 only, which keeps most of us ill and fat, but with natural hormones (like Armour), and by also taking into account other hormonal and nutritional deficiencies, and toxins.

The more people join (it’s free), the more weight our demands for this kind of much more adequate treatment will have. The more people join, the better the chances are also to fend off legal attacks against doctors who try to help us, like the one recently against Dr. Skinner in the UK (see http://www.tpa-uk.org.uk/skinner_hearing_transcripts.php), and like the one (unfortunately successful) against Dr. Peatfield, also from the UK, who BTW authored the book “Your Thyroid and How to Keep It Healthy: The Great Thyroid Scandal and How to Survive It”. Quod erat demonstrandum.

Because if we let the medical establishment (including the pharmaceutical companies) have their way, other doctors who might be inclined to help us will be scared off to do so, because they risk their license to practice and therefor their only means for earning their lives.

Thanks to Dr. Hertoghe (main witness of defense), the testimony of Dr. Skinner’s patients and the weight of the IHS behind them, Dr. Skinner was allowed to continue practicing, despite him not following the generally accepted guidelines for treating hypothyroidism in the UK (only with a TSH > 10!).

So please make your voice heard and vote for your treatment of choice by joining the IHS! http://intlhormonesociety.org/) The IHS is not funded by any pharmaceutical group, and I’m also not financially involved in it in any way. I am just a patient of Dr. Hertoghe like many of us. And I have to testify that after 10 years of being left untreated, being treated according to a wrong diagnosis, being undertreated and refused treatment, Dr. Hertoghe ended my misery and gave me back my life.

So please help yourself and all your fellow patients, so that more doctors like Dr. Hertoghe become the majority, not the exception, available to all, be they insured privately, publicly or not at all (Dr. Hertoghe has been training some 700 physicians in his own practice during the last years, and gives seminars etc. to about 1000 physicians a year).

Let’s make a difference!

The real problem here is that Medicare Part D was legislated by Congress, who by definition are the worst ones to be deciding our health care. Plenty of aspects of the Part D formulary do not make sense.

Case in point: the anti-emetic promethazine (Phenergan) is not covered under Part D. This is because it is a Part B benefit when used for nausea and vomiting after chemotherapy. But, since it is not covered under Part D, the popular cough syrup Phenergan with Codeine (promethazine with codeine) is also NOT covered under Medicare at all (part B or D). Congressional intelligence at its finest.

OK here is what I was discussing today with my mother and my doctor when he told me I would have to have a LAB TEST EVERY 3 MONTHS to get a prescription for a drug they know I am going to have to take the REST OF MY LIFE.

The most important aspect of this is that there is a statistic that says that 1 in 7 women of menopausal age plus has this problem, and in iodine-deficient areas the numbers rise to something like 1 in 3.

That makes hypothyroidism no longer an ABnormality but a STANDARD STATE for women of our age. (Although many of us were hypothyroid all our lives that doesn’t refute this argument, but only enhances it.)

It is robbery and abuse to force us to get a prescription to buy our meds every three months – meds that we need to live and work in a society that now REQUIRES us to work.

Our numbers are so huge that I believe we can get these laws changed if we organize and get started. We can also change these ridiculous prejudices against Armour if WE say en masse that WE, who have to be on this stuff just to stay ALIVE, want it.

I think we can do it. Of course you are elected to get it started. I don’t know what the h*** I’m doing although I have helped with campaigns in the past.

I wonder if we have to do this state to state – or are there federal laws that govern this?

I have no health insurance at the moment! Can you imagine what an expense getting a lab test is every month in addition to the doctor’s visit and the meds???

It’s just completely criminal.

Anyhow let me know what you want me to do to help. We HAVE to do this. These laws are SEXIST.