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My symptoms are not as dramatic as yours, but I’m having the same ones! I’m so sorry you are going through this. It’s hell on earth.

Raw eggs offer so much more than cooked eggs. There are people healing from mycoplasma infections using up to 10 raw eggs a day. My hair texture completely changed overnight. Thanks for the reminder to get back in my eggs!

His protocol is a one size fits all and it may help a few people by luck but it’s better to follow people that really understand specific genetic mutations and supplement accordingly.

I just did TEI and waiting on results. Excited to get some help as mineral balancing and tei is way over my head. Anyone know how long it usually takes to get results back?

I tried fredd’s Protocol for a few months and got worse. My mutations in COMT is what I suspect caused the awful side effects. I do know it’s helped a lot in cfs community. Sterling Hill has a great understating of all of this if anyone cares to research her work.

Me too? Folinic acid can be terrible for MTHFR mutations and cause more of a methylation block. It would put certain people in an even more state of folate deficiency. That’s why everyone’s genes need to be ran first.

Yeah well the long sentences are because I also suffer from brain fog. And cfs. I’m lucky if I can the info from my head to paper. But listen, you guys need to be focusing on more than just TEI. If you take the wrong supplement for your mutations, u can really mess yourselves up. Just...

As clear as I can be, I’m very knowledgeable in cortisol and it’s uses. I’ve even done circadian t3 to push my cortisol up. Unfortunately just a high dose of cortisol with thyroid doesn’t work for me. Trust me, I’ve tried.

I was curious how many here have had their genetic profile ran? I did 23 and me around five years ago and I go back to it quite a bit as they learn more and more. I was really focused for a while on my methylation system. It would be interesting to see what genes those of us that have been...

I know this is old but I’m sorry I missed this. Helen what would you advise for someone like me. I had really messed up cortisol (super high after stopping ssri) and failed dexamethasone suppresion test. They actually thought I could have cushing’s. It was the suppression test that led me to...

That’s great to hear your fatigue improving! Mine is severe, I’m on disability for it as my heart valve got weakened. I cannot exercise at all and at times early on was bedridden. What Med did you take?

That’s awesome. I have a lot of autoimmune showing up like lupus and sclerodoma. So I feel like my immune system is totally messed up. I totally agree, I always get super excited when I try something new and get an immune response. I used to get cold sores constantly, and since pssd I have...

Helen do you know of the symptom of never catching colds or gettig viral infections is th1 or 2? Ever since pssd I don’t EVER get sick. Definitely unbalanced but I can’t figure which way.

It helped me a little with brain fog but I didn’t notice much else. I bought a machine. Probably didn’t give it enough time.

“A Jedi” is not one of my symptoms unfortunately. Anhedonia lol

From my understanding agonists activate the receptor, so yes they do do something to the receptor? I don’t understand the implication here?

And what was the Med that caused the damage?

Yeah I hear that a lot with people not responding to alcohol anymore. What tca were you taking?

I am way more sensitive to alcohol in terms of low tolerance now. But sometimes next day after I will have improvements in symptoms. Benzos make me feel awful and just blah. Opiates make me feel better in some regards, so I use kratom a lot.