Anyone with Ehlers Danlos and chronic pain flare ups find a solution?

notmcas

@Ecstatic_Hamster Couldn't you dissolve the cbd+thc in tocopherols and avoid the whole suppository? My girlfriend does say it helps quite a bit during a flare up. Pregnenolone seems useful, I assume dosed a few times a day. I'm a bit more nervous about naltrexone, she is reliant on barbiturates for bad flare ups but doesn't seem to experience serious withdrawl since she's careful. And naltrexone isn't really solving the underlying issues?

@notmcas said in Anyone with Ehlers Danlos and chronic pain flare ups find a solution?:

I'm surprised that they'd give you such trouble at a total of 236. Mine was 300 and my doctor wouldn't even consider thyroid despite my tsh being ~3 and I'm still young. I was able to game tests by upping selenium, vitamin A, and taurine pretty high but they still just call it a fluke and won't consider any kind of thyroid which I bet would lower it. My dad has the same issue of high cholesterol and temps around 95-96 and doc is constantly threatening statins and yelling at him, his tsh is about 3.8. Did you have to have an over range tsh to get thyroid?

I suspect that they were just itching to find justification to put me on something; I'm 74 and all I take that is prescription is my NP Thyroid by Acella.

"Mine was 300 and my doctor wouldn't even consider thyroid despite my tsh being ~3 and I'm still young."
This clearly points to a problem with hypothyroidism. If your doctor won't consider prescribing a good desiccated thyroid product like NP Thyroid, you probably should be looking for a better doctor. Asking your local pharmacists which doctors are prescribing NP Thyroid by Accella would shorten your search. Your father probably has the same problem so would also benefit from your effort to find a competent doctor.

Ray Peat on hypothyroidism
Read this one first.

"Did you have to have an over range tsh to get thyroid?
No, I don't. My tsh has always been around .01-.001. TSH really isn't a helpful test. The range is way to broad on the test. TSH is short for "thyroid stimulating hormone" which is released by the pituitary. My current endocrinologist said he had seen that almost zero TSH before and said he would ignore that part of the test and rely more on my symptoms.

Read this one by Ray Peat for better understanding.

I added 200mcg of selenium last summer and the numbers on my blood tests noticeably improved. Selenium is needed to convert T4 into T3 via the diodinases.
"Selenium plays a crucial role in TH metabolism due to its location in the catalytic site of the three deiodinases [76]. Since the thyroid gland, with its capacity to store selenium, maintains a high concentration of this element, it is not easy to evaluate the immediate benefits of dietary selenium supplementation on selenium-containing enzymes [77]. Nonetheless, clinical data suggest that selenium deficiency is associated with an increased risk of a high anti-thyroid antibody titer, whereas selenium supplementation decreases thyroid peroxidase antibody titer, which could allow routine selenium supplementation as an additive tool to permit a reduction in the levothyroxine dose required for hypothyroidism therapy or to prevent progression of subclinical hypothyroidism [78–80]."

I was very low in selenium because of my mercury toxicity. Mercury causes problems with selenium.

notmcas

@mostlylurking That's interesting, I'd like to see her do a selenium test too. She reacts very bad to shots so maybe it's a consideration of heavy metals. For me I wanted to get something like NP Thyroid or even just levothyroxine since I actually think I convert pretty good I just cannot tolerate fasting without my temp bottoming. My doctor will not even consider it unless tsh goes above 5 though so I'd basically have to game it by fasting a while or consuming too much iodine or whatever trick to get it over the threshold for a test...

@notmcas said in Anyone with Ehlers Danlos and chronic pain flare ups find a solution?:

My girlfriend does say it helps quite a bit during a flare up. Pregnenolone seems useful, I assume dosed a few times a day. I'm a bit more nervous about naltrexone, she is reliant on barbiturates for bad flare ups but doesn't seem to experience serious withdrawl since she's careful. And naltrexone isn't really solving the underlying issues?

Vitamin E and progesterone work in similar ways.
Ray Peat on vitamin E and progesterone, interviews

Has your girlfriend removed all polyunsaturated fats (PUFA) from her diet? The body stores PUFA in the fat cells for years. Taking some niacinamide (smaller doses, several times/day) help with the PUFA problem.
Ray Peat on Niacinamide, written work
Ray Peat on niacinamide and free fatty acids, interviews

@notmcas said in Anyone with Ehlers Danlos and chronic pain flare ups find a solution?:

That's interesting, I'd like to see her do a selenium test too. She reacts very bad to shots so maybe it's a consideration of heavy metals. For me I wanted to get something like NP Thyroid or even just levothyroxine since I actually think I convert pretty good I just cannot tolerate fasting without my temp bottoming. My doctor will not even consider it unless tsh goes above 5 though so I'd basically have to game it by fasting a while or consuming too much iodine or whatever trick to get it over the threshold for a test...

Does your girlfriend have any silver fillings?

NP thyroid (a prescription natural desiccated thyroid product) would work better for anyone, I think. Synthetic T4 is really lousy stuff. Personal opinion. Your doctor sounds clueless. Trying to "game the test" really is a terrible idea. If you are not happy with the doctor, (I wouldn't be from what you've said here) you should find a better one. Think of doctors as shade tree mechanics (that's probably an insult to shade tree mechanics).
See this Ray Peat article

notmcas

@mostlylurking She has not removed all PUFA but doesn't have silver fillings. I think mold might have been a big contributor since she's lived in moldy homes and has flare ups before rain or after snow melt. I'm not sure what to do for mold toxicity at this point though. It was why I was considering the flowers of sulfur as per ray's suggestion for candida or fungal infections.

For the doctor issue, I mean I've tried another and a few online doctors. They basically say if tsh is not above say 4.5 or 5 they will not consider any treatment. Even when I asked my primary care if I could pay out of pocket for a thyroid test he got angry with me and said I didn't need that and prescribed me statins that I refused. I guess I could try an endo?

@notmcas Ask your local pharmacists which doctors prescribe NP Thyroid by Acella. It is a very common medication. It is the one pharmacists use to fill prescriptions for desiccated thyroid that do not specify the brand; it is used for the "generic" catagory.

You need to find a reasonable doctor. Read the Ray Peat Thyroid article. Take it to heart. Understand that there really are doctors who understand hypothyroidism, you just have to find one. You need a good doctor that is willing to test you every 6-8 weeks for several months in order to optimize your medication amount (my own took 9 months).

@notmcas said in Anyone with Ehlers Danlos and chronic pain flare ups find a solution?:

She has not removed all PUFA but doesn't have silver fillings.

PUFA is estrogenic and toxic. It is making her sicker. She needs to understand this and banish all of it from her diet. Taking small doses of niacinamide throughout the day would be helpful.
Ray Peat on PUFA written work
Ray Peat on PUFA audio

Has she EVER had silver fillings? Did she have any when she was a child? Was she ever around when a mercury thermometer was broken or in the building where it happened? Was she ever around when a fluorescent light tube or bulb was broken?

I lived through many years of being super sensitive to mold. It would make me almost catatonic. I'm not that way anymore. Removing all toxins from her environment (including pufa) will be helpful. Getting her high estrognen down and under control will be helpful. These things will take some of the burden off of her immune system so that it will be better able to function more normally.

Is she vaccinated? For covid?

@notmcas said in Anyone with Ehlers Danlos and chronic pain flare ups find a solution?:

For the doctor issue, I mean I've tried another and a few online doctors. They basically say if tsh is not above say 4.5 or 5 they will not consider any treatment.

This is the mind set of doctors in the United States who cow-tow to the American Thyroid Association. They have hijacked the industry. I believe it's criminal what they are doing. Their policies massively increase the number of lucrative (really sick) customers for the American Medical Industrial Complex.

Which country are you located in? If in the US, which state?

Have you considered a Functional Doctor? Or a doctor that practices Orthomolecular medicine?

Find a Doctor via the NP Thyroid/Acella website

Have you asked your local pharmacists which doctors in your area prescribe NP Thyroid by Acella? I still contend that this is the fastest way to find a doctor that has some clue about treating hypothyroidism.

notmcas

@mostlylurking she’s gotten the first vaccine, and I’ll just say it did not go well. I didn’t get it but schools were forcing it and all that. She’s never gotten silver fillings as far as she knows.

I’m in MA. I will try that approach, hopefully they’ll at least let me try some. I tried with thyroid online doctors and they refused under 5tsh too. I’ve actually felt pretty good on some NDT I ordered but I just don’t trust those non prescription products to be good.

@notmcas said in Anyone with Ehlers Danlos and chronic pain flare ups find a solution?:

@mostlylurking she’s gotten the first vaccine, and I’ll just say it did not go well. I didn’t get it but schools were forcing it and all that. She’s never gotten silver fillings as far as she knows.

I’m in MA. I will try that approach, hopefully they’ll at least let me try some. I tried with thyroid online doctors and they refused under 5tsh too. I’ve actually felt pretty good on some NDT I ordered but I just don’t trust those non prescription products to be good.

OK. The "vax" may well be exacerbating her problem. The FLCCC has protocol that may be helpful.

The pharmacists aren't going to let you "try some". But they will be happy to tell you which doctors are ordering prescriptions of NP Thyroid for their patients that practice medicine in your area.

@notmcas said in Anyone with Ehlers Danlos and chronic pain flare ups find a solution?:

she’s gotten the first vaccine, and I’ll just say it did not go well. I didn’t get it but schools were forcing it and all that.

Here is a link to Dr. Peter McCullough's protocol:
Dr Peter McCullough: How to Detox Spike Protein from Body (November 2023)

I am not a doctor and this is not medical advice.

notmcas

@notmcas Thank you, I can't say that the vaccine has made her any worse really since before it. But someone else was very affected.

I more meant that maybe a doctor could give a trial dose. But I think you have to be an MD to prescribe both NDT and synthroid. I will try through the Acella doctors or pharmacy though, maybe my dad get get it at least since his temps and pulse are so obviously low.

@notmcas Do you want to get well? A trial dose is not going to be helpful. It takes months of titrating the dose up to your optimum dose. You need a doctor who is familiar with treating people with desiccated thyroid who understands the procedure. It would be very helpful if you understood the procedure. So please read the Ray Peat articles that I posted earlier. The Broda Barnes book would also be helpful reading.

notmcas

@mostlylurking Yes, I just thought that with a trial dose I could prove to the doc that my "dangerous cholesterol" would improve with some thyroid. I know I have to keep taking it at least until I detox from pufa and my diet is good, it's more to convince them to allow me to keep using it. I did reach out to a functional doctor for us both so fingers crossed.

@notmcas said in Anyone with Ehlers Danlos and chronic pain flare ups find a solution?:

Yes, I just thought that with a trial dose I could prove to the doc that my "dangerous cholesterol" would improve with some thyroid. I know I have to keep taking it at least until I detox from pufa and my diet is good, it's more to convince them to allow me to keep using it. I did reach out to a functional doctor for us both so fingers crossed.

If you are dealing with a reasonably informed doctor (who has the sense to prescribe desiccated thyroid), he will know from your first test (assuming it has similar numbers as the ones you posted here) that you have hypothyroidism and that treating the hypothyroidism will normalize your cholesterol. The medical industry has known at least since the 1940's that this is the case; that hypothyroidism results in high cholesterol and treating hypothyroidism normalizes cholesterol. If the doctor is reasonably informed and already uses desiccated thyroid to treat his patients, you won't have to do anything but let them run a full panel thyroid test. That test will convince the doctor. Who else do you think you need to convince so you can keep getting treatment? Go read the Ray Peat article.

from the linked article:
"Barnes experimented on rabbits, and found that when their thyroid glands were removed, they developed atherosclerosis, just as hypothyroid people did. By the mid-1930s, it was generally known that hypothyroidism causes the cholesterol level in the blood to increase; hypercholesterolemia was a diagnostic sign of hypothyroidism. Administering a thyroid supplement, blood cholesterol came down to normal exactly as the basal metabolic rate came up to the normal rate. The biology of atherosclerotic heart disease was basically solved before the second world war."

Please don't assume that if you stop eating PUFA and change your diet your hypothyroidism will magically disappear. Even if it all hinged on the PUFA content of your body (it doesn't), it takes at least four years for your body to detox the pufa that's already stored in there, assuming you don't eat any more of it.

notmcas

@mostlylurking I’m okay to take it indefinitely, my only worry is that I’ll only get it prescribed once it hits over 4.5 tsh. Mines just under 3 and rising every half year. I’m very responsive to food though, I’ll go from 96.8 to 98.6 with a sweet meal, when I tried an online ndt it was more normalized but I don’t trust the product. I’ll discuss with a functional doctor. I actually know quite a few people with diagnosed hashimotos who’re only given something like 25mcg of levothyroxine… and obviously continue to have bad hypo symptoms. I suggest they ask for ndt but most people seem to thing nothing would work of the levo doesn’t

Peatly

@notmcas said in Anyone with Ehlers Danlos and chronic pain flare ups find a solution?:

@mostlylurking she’s gotten the first vaccine, and I’ll just say it did not go well. I didn’t get it but schools were forcing it and all that. She’s never gotten silver fillings as far as she knows.

I’m in MA. I will try that approach, hopefully they’ll at least let me try some. I tried with thyroid online doctors and they refused under 5tsh too. I’ve actually felt pretty good on some NDT I ordered but I just don’t trust those non prescription products to be good.

I came across this article recently.
https://www.midwesterndoctor.com/p/the-hidden-link-between-hypermobility

@notmcas said in Anyone with Ehlers Danlos and chronic pain flare ups find a solution?:

I’m okay to take it indefinitely, my only worry is that I’ll only get it prescribed once it hits over 4.5 tsh. Mines just under 3 and rising every half year. I’m very responsive to food though, I’ll go from 96.8 to 98.6 with a sweet meal, when I tried an online ndt it was more normalized but I don’t trust the product. I’ll discuss with a functional doctor. I actually know quite a few people with diagnosed hashimotos who’re only given something like 25mcg of levothyroxine… and obviously continue to have bad hypo symptoms. I suggest they ask for ndt but most people seem to thing nothing would work of the levo doesn’t

Go research "hypothyroid symptoms" on line. Make a written list of your hypothyroid symptoms for your reference and take it with you to your doctor's appointment. Tell the new doctor about them. It would not be a smart idea to talk to the new doctor about your past "self medicating" and your experiences with it; it won't tell the doctor anything and they won't like the idea at all. It might get you thrown out of their office. Don't blather on about how sugar raises your temperature. Just tell them all your horrible no good very bad hypothyroid symptoms. Do NOT self medicate for a minimum of 2 weeks before you go to get your blood drawn. Do NOT take any biotin for 2 weeks before you get your blood drawn. And get the full thyroid panel of testing. Hold out for the product with the active T3 included; I like NP Thyroid by Acella. Educate yourself. Read the Ray Peat articles about hypothyroidism.

This site has good information. It hosts many of Ray Peat's articles. Read up. Learn about how the test is not calibrated correctly and how to understand the test results. If your free T3 is not in the upper part of the "normal" range and you're still symptomatic, ask the doctor to increase your medication dose.

If the new doctor refuses to let you have a thyroid med with T3 in it, walk out of there and go find a new doctor who will. Synthetic T4 doesn't work for most people.

@Peatly Interesting article, thanks for posting. That photo of the person's thumb touching their wrist area brought back memories; I was like that when I was younger. I'm healthier now since I addressed my estrogen dominance and my hypothyroidism and my need for more thiamine, etc. I tried to see if I could still touch my wrist with my thumb; not even close.

notmcas

@mostlylurking I'm already trying to get in contact with a functional doctor. But my girlfriend feels in a pretty bad state right now. She normally takes an SNRI that keeps her body pain tolerable but it seems like it's not working well anymore, I'm not sure if it's adrenal fatigue or something like that, her serotonin on a blood test is basically zero. I wanted to know out of the supplements which one made a quick difference for you to feel less body pain and flare ups, the high dose thiamine?