Yes my main goal for thyroid treatment, good LDL cholesterol. I've been on thyroid meds now for almost 10 years. I don't remember my original labs.@Vince, I know you have benefited for years on thyroid treatment, so I thought I'd run some questions by you. I ran panels and per Defy, am a candidate for T3 treatment. Per my labs, I think I am borderline (have to do rT3 ratio calculation to justify treatment). In any case, I tried T3 for a bit and stopped. In fairness, I was also treating with cream, which in retrospect, was pushing my testosterone levels way over the top. So, I am not sure if the bad experience was T3, test, or both. I am considering stabilizing my test levels and trying T3 again. Questions:
Thanks for sharing!
- What did you labs look like prior to starting treatment?
- What subjective benefit did you notice once you started?
- Along those lines, did you notice any benefit outside of energy/mental clarity?
- What objective benefit have you noticed
- ie, have you seen improvements in other areas such as cholesterol, testosterone, etc.?
Can you speak to subjective benefits (example, traditionally, people associate thyroid with energy/mental clarity; did it help your libido? Mood? Did it facilitate your TRT goals?).Yes my main goal for thyroid treatment, good LDL cholesterol. I've been on thyroid meds now for almost 10 years. I don't remember my original labs.
I go to a Lipidologist and get very thorough cholesterol panels.
Great Post. I will be talking to my PA about thyroid and cortisol on my next visit. thank you!I am a final year med student and have been replacing my hormones for multiple years. I post this because I want to raise awareness that it is not just testosterone. One thing I frequently notice, is that many males are really fixating on testosterone (e.g. whether adding HCG or different doses of anastrozole would make a difference, etc.), however upon asking them about their body temperature, blood pressure, pulse, and other signs and symptoms, it is often evident, that they are deficient in thyroid or adrenal hormones.
Frequently, after discovering low testosterone levels, many males go on TRT and feel somewhat better. Often, however, their energy levels (and other symptoms) do not improve as they wished. Many then tend to raise their dosage of testosterone -often repeatedly. Doing this, some symptoms improve (e.g. energy, mood) and therefore to them, it seems obvious that they were still deficient and simply have not raised their dosage high enough. But if thyroid or adrenal hormones are deficient, injecting all the testosterone in the world, will not make someone feel (or function) much better. For example, both libido and body hair are two things generally ascribed to testosterone. But if levels of thyroid hormones or cortisol are low, libido will be as well, even if testosterone levels are high. The same holds for body hair.
Unfortunately, the overreplacement of any hormone is tempting because it might ”feel good” and does often indeed improve some symptoms (esp. energy levels). However, the overreplacement of any of the major hormones (e.g. cortisol, thyroid hormones, testosterone) will almost always improve energy levels and mood, which will almost always improve symptoms. Therefore, every single one of the major hormones can be (ab)used as a stimulant and “masking-agent”. However, over the long run any form of overreplacement -whether intentional or not- carries more risks than benefits and likely comes with a tradeoff of health and longevity in the future for an increase in wellbeing and performance in the present.
Instead of over-replacing and abusing a single hormone in high and unphysiological doses, it would be much healthier, safer, more natural, and more effective to add one or more other hormones in small and physiological doses.
While treating adrenals can be dangerous if not done properly, treating thyroid hormones is quite safe and easy to do (comparably speaking) and for many males, it can make a world of a difference and bring them back alive -sometimes even more than TRT.
Thyroid hormones are the most prescribed medication on the planet. Despite there being millions of people with thyroid issues, the vast majority of them are not treated adequately (i.e. in 99% of people T4 monotherapy is used). This holds back millions of people from living far better lives and from contributing what they otherwise could. In my opinion, the therapy of choice should follow this order:
NDT > T3/T4 > T4 > T3
What about dosage?
dosages needed vary widely depending on patient needs, cortisol levels, ability to derive T3 by deiodination, thyroid sensitivity, IGF1 levels, and esp. the endogenous residual output by the individual's own thyroid gland.
A reasonable, generic protocol to start thyroid replacement is the following:
- T4: 50mcg-200mcg (average: 120mcg; once per day)
- NDT: 1–2.5 grains (average: 1.5 grains; twice per day)
- T3: 40–80mcg T3 (average: 60mcg T3; split into at least 3 daily doses)
Principle: Starting with 25% of the presumed target dose and then gradually increasing the dosage over a 2 month period.
Implementation: Starting out with 0.25 grains of NDT (or 20–25% of the presumed target dose) → increase by 0.25 grains every 14 days until the average target dose of 1.25 or 1.5 grains/day is reached (about 0.25 grains less in the summer).
I wrote an article on how to properly replace thyroid hormones and because this post is already quite long and there are many other topics to delve into, if you are interested you can read more on some of these topics:
How To Replace Thyroid Hormones - An Ultimate Guide
- Improving thyroid hormones naturally
- Thyroid hormones require adequate levels of cortisol
- A low-carb diet can impair thyroid status at multiple levels
- Why T4 is not the therapy of choice
- Temporary use of high-dose T3 can reverse thyroid resistance
- Permanent treatment with T3-only?
- Dosage
- Timing
- How to start therapy
- Thyroid treatment in individuals with low levels of cortisol
I hope you find value in it. If you have any questions, feel free to leave your questions below!
My libido has always been strong. I did fix my thyroid before I started trt. I believe at least for me, trt was more beneficial then thyroid meds.Can you speak to subjective benefits (example, traditionally, people associate thyroid with energy/mental clarity; did it help your libido? Mood? Did it facilitate your TRT goals?).
Thanks again.
The quotet statement is often abused by people who mistaken the physiological doses with the declined refence range that is the average of a very unhealthy population.in high and unphysiological doses,
Yes, surely the effects of endogenous levels are different compared to the same results achieved via exogenous hormonesTotally agree, and Im not a big fan if high doses as well, once I step over my sweet spot on anything I feel bad. Also I think its not just about replacing hormones, but optimising and fixing health issues like what Im trying to do regarding my NAFLD.
However one clarification:
The quotet statement is often abused by people who mistaken the physiological doses with the declined refence range that is the average of a very unhealthy population.
Also when one is on exogenous hormones often it is needed to achieve higher serum concentrations to get the same effect like if you were on endogenous production, at least for testosterone and FT3.
What level of scientific support is there for statements like this? Clearly it doesn't hold at the molecular level when bioidentical hormones are used. But intuitively the idea makes sense when you consider hormone levels being out of sync with normal feedback mechanisms.Yes, surely the effects of endogenous levels are different compared to the same results achieved via exogenous hormones
Unfortunately not much. However, what we can say is that at the level of the hypothalamus the releasing hormones (e.g. GnRH, CRH, etc.) are also transmitted into the nervous system. Furthermore, various tissues have receptors for stimulating hormones (e.g. LH-receptors in the adrenal glands, TSH receptors on fibroblasts, etc.) and if there is suppression at the level of the hypothalamus these additional pathways are shut off which should result at least in a tiny measurable differenceWhat level of scientific support is there for statements like this? Clearly it doesn't hold at the molecular level when bioidentical hormones are used. But intuitively the idea makes sense when you consider hormone levels being out of sync with normal feedback mechanisms.
You're preaching to the choir when it comes to concerns about HPTA suppression. It's this reasoning that leads me to try to restore a reasonable level of upstream activity under TRT—with kisspeptin, GnRH, enclomiphene and such. Although subjective and anecdotal, my results support the hypothesis that suppression isn't necessarily benign.... However, what we can say is that at the level of the hypothalamus the releasing hormones (e.g. GnRH, CRH, etc.) are also transmitted into the nervous system. Furthermore, various tissues have receptors for stimulating hormones (e.g. LH-receptors in the adrenal glands, TSH receptors on fibroblasts, etc.) and if there is suppression at the level of the hypothalamus these additional pathways are shut off which should result at least in a tiny measurable difference
Have you tried semaglutide (ozempic)? It also kickstart hypothalamic pathways - esp. if "damage" to hormonal axes was done by undernutrition/overtraining etc.You're preaching to the choir when it comes to concerns about HPTA suppression. It's this reasoning that leads me to try to restore a reasonable level of upstream activity under TRT—with kisspeptin, GnRH, enclomiphene and such. Although subjective and anecdotal, my results support the hypothesis that suppression isn't necess
I'm not familiar with semaglutide. I see that it's used to raise insulin and reduce blood sugar. A cursory search doesn't turn up much more information. It's noted that "Semaglutide directly accessed the ... hypothalamus but did not cross the blood-brain barrier;.."[R] Can you provide any references on its ability to "kickstart hypothalamic pathways"? I'd like to know more.Have you tried semaglutide (ozempic)? It also kickstart hypothalamic pathways - esp. if "damage" to hormonal axes was done by undernutrition/overtraining etc.
Well, it should not be too hard to find. Google "GLP-1 and LH/FSH" or "GLP-1 and POMC neurons". It actually does cross the blood brain barrier as there is a receptor for it. Furthermore, it can act on brain stem and hypothalamic areas at the circumventricular organsI'm not familiar with semaglutide. I see that it's used to raise insulin and reduce blood sugar. A cursory search doesn't turn up much more information. It's noted that "Semaglutide directly accessed the ... hypothalamus but did not cross the blood-brain barrier;.."[R] Can you provide any references on its ability to "kickstart hypothalamic pathways"? I'd like to know more.
The first one that comes up doesn't sound promising:... Google "GLP-1 and LH/FSH" ...
I came off testosterone using semaglutide. My T levels doubled twice within 4 weeks. I am now somewhere in the 500s. A friend of mine had diet-induced low T. Using semaglutide without dietary changes his LH/FSH multiplied and T levels doubled.The first one that comes up doesn't sound promising:
In contrast to the animal literature, our data demonstrate that acute GLP-1 administration does not affect reproductive hormone secretion in healthy men.Effects of Glucagon-like Peptide-1 on the Reproductive Axis in Healthy Men
AbstractContext. Glucagon-like peptide-1 (GLP-1) potently reduces food intake and augments glucose-stimulated insulin secretion. Recent animal data suggestacademic.oup.com
So your saying semaglutide can actually increase T ? And it’s safe ???? Can you explain more. What if I have no issues in insulin and don’t have diabetes?I came off testosterone using semaglutide. My T levels doubled twice within 4 weeks. I am now somewhere in the 500s. A friend of mine had diet-induced low T. Using semaglutide without dietary changes his LH/FSH multiplied and T levels doubled.
Also, your study is exactly the problem: It does not affect it in HEALTHY men, whose reproductive axis is fully functioning. But in people with hypothalamic or pituitary forms of hypogonadism it does indeed help (esp. if dieting, stress, low body fat) are at the root cause
Given that your low T is of hypothalamic origin (mainly POMC-neurons mediated), then yes. Yes, it is far safer than almost all other drugs out there, as it is basically a benign hormone (acting on GPCR instead of nuclear receptors as do steroid hormones). Also, it is certainly worth a try and there is almost no risk to that other than the cost of getting the drugSo your saying semaglutide can actually increase T ? And it’s safe ???? Can you explain more. What if I have no issues in insulin and don’t have diabetes?