Hi Laszla
In the article, Jen Gunter says she would do blood testing in certain circumstances:
"But to be a poor absorber, we need a definition. Do we say that someone with an estradiol level of 70 pg/ml (257 pmol/L) on a 100 mcg patch is a poor absorber, or are they just at the low end of the bell curve (because someone has to be at the low end of the bell curve, that is how distribution curves work)? It's impossible to say without studies of so-called poor absorbers matching levels with symptoms.
If someone were in menopause, meaning no period for the past 12 months and on a 100 mcg patch and is still having terrible hot flashes or sleeping poorly (nocturnal hot flashes might be under recalled) or symptoms I would expect to resolve with estrogen, I would consider doing a one-time estradiol level to make sure it’s at least around 50 pg/ml. If it’s lower, she may be a poor absorber, but because absorption can be erratic and the test results have a margin of error, I would not give her more of what she isn’t absorbing; I’d likely suggest switching to a different transdermal system or to oral therapy. If her estrogen level were in an expected range, I’d look for other causes of her symptoms and other therapies. I still might even suggest a different estrogen delivery system to see if that worked better because, as I already noted, levels may not tell us what is happening at the cell level."
***END QUOTE
I was floored to learn that I had been prescribed a drug with a known potential for non-absorption and I had not been given a blood test when I failed to respond to treatment. For 1.5 years, on top of the menopausal symptoms, I experienced constant bleeding which my doctor attributed to estrogen. He wanted to reduce my estrogen dose and I begged him not to. During that time, I had two biopsies and numerous scans. Even when my endometrial thickness went down to 0.4 mm, my doctor didn't question whether I had a problem with absorption. He said a thin endometrium is normal in menopause. If I wasn't happy about the bleeding, I could have a Mirena. He didn't provide me with any other options.
It wasn't until my hair fell out and he could see my scalp that he said I looked like my estrogen was low and ordered a blood test. He was supposed to be a menopause specialist. It was the first time I questioned the competency of my treating physician and felt unsafe.
In hindsight, the bleeding was due to the lack of estrogen absorption. I had been taking progesterone for a year and a half. While all of this was going on, I was on the waiting list of a menopause clinic. I had to wait 18 months for an appointment.
My new doctor wanted me to try a different transdermal regimen. Blood tests confirmed I was not absorbing. Fortunately, the experiments only lasted 4 or 5 months. But during that time, I didn't get more than 5 hours sleep per night, waking from multiple episodes of night sweats.
I think I've spent most of my time on MHT not absorbing estrogen. I worry that my bones have suffered as a result. I had a DEXA scan in August and I have an appointment in November to go over my results.
In terms of costs to the healthcare system, it would have been cheaper to give me a few blood tests than the multiple biopsies and scans I received.
The system may work for the majority of woman, but the rest of us suffer needlessly.