@mostlylurking said in Just found out I have reactive hypoglycemia. What now?:
@yerrag said in Just found out I have reactive hypoglycemia. What now?:
@yerrag said in Just found out I have reactive hypoglycemia. What now?:
Mercury displaces oxygen from any to all of the four binding sites in hemoglobin for oxygen, and reduces the ability to transport a key substrate, oxygen, from being used optimally with sugar for mitochondrial respiration, from which we produce energy.
I have a little different perspective regarding how my mercury affects my health, probably based on my own personal experiences and research. This does not mean we are not both correct.
I look at it this way:
Mercury causes severe oxidative stress (perhaps via what you just wrote?) Thiamine is used to quench the oxidative stress. But then thiamine stores get depleted and it becomes deficient. Also, the body's glutathione cycle gets overwhelmed and reduced glutathione becomes deficient and cannot recover.
I'm not sure if I have to question whether the stress brought upon my mercury toxicity is oxidative stress, as my experience with it, where I experience hypoxemia and hypoxia leads me towards producing less energy. This failure to energize maximally and optimally is a reductive stress as it is a failure in oxidative processes, and this down regulation in energy production leads to many imbalances. Instead of the rusting away of oxidative stress, where tissues are destroyed an an active manner, tissues deteriorate, in a passive manner, with less nutrients delivered so to speak. Mercury, by merely reducing oxygen supply, does enough harm already.
Now, I am not sure if mercury acts like lead and iron as they are involved in lipid peroxidation chain reactions, which indeed produce a lot of oxidative stress.
But I suspect that it doesn't. As looking back, I believe I had both mercury toxicity and lead toxicity at the same time but if mercury produces reductive stress and if lead causes oxidative stress, the kinda balance each other out in masking the effects of both these stresses. It was after I successfully removed mercury from my system that the oxidative stress from lead toxicity was unmasked. As I then began to experience an increase in my blood pressure.
As I felt the oxidative stress from lead required my body's primary antioxidants to be used continually to counter the oxidative stress. Since albumin is the primary antioxidant in the ECF, I was using up albumin as it gets oxidized when it acts as an antioxidant. But albumin has other uses, and because it was heavily being used, my blood was always low in volume, as albumin is needed to hold on to salt, and salt attract water from the non-blood ECF into the ECF in blood in the form of plasma. With low blood volume, the body compensate by increasing blood pressure to ensure enough blood goes around the body, especially vital organs.
That said, it still does not make thiamine less useful, as it is possible a lot of NADPH is needed to produce ROS that is used by neutrophils and macrophages and eosinophils as white blood cells go an an endless recurring loop in trying to rid the body of lead, which remains stubborn in not getting phagocytized and excreted away. It may be that I would need more thiamine than the RDA to make up for the heavy use of thiamine to produce NADPH in the pentose phosphate pathway.
It is my understanding that the mercury cycles between being in circulation and being more safely parked in storage, possibly in the bones, but also possibly in the fat, including the brain. Occasionally, something stirs the mercury out of storage which causes the body to have to deal with it again via thiamine, selenium, and probably the glutathione cycle. Because I do not have full understanding (who does?), I do not know if thiamine (or selenium) could actually bond so firmly to the mercury to be able to escort it out of the body in some small degree. There are reports of selenium + NAC working extremely well.
A lot of substances are said to such as vitamin C. Alpha-lipoic acid as well. Then there is cilantro and there is some clays. I'd rather not waste my time putting much in them. The few that I've tried I've given up mainly because I don't have the confidence they would work, and I believe in going the long haul if I have the xonfidence. Without confidence, I wouldn't want to see my time wasted seeing something not working.
Side note: thiamine is used to chelate lead successfully so I suppose it may be able to do likewise with mercury to a very small degree. (Please note the issue of zinc depletion). Dr. Lonsdale spoke of the ability of TTFD to chelate lead.
I would rather place a bet on Emeramide. Thiamine would be better for where it is has its strengths.
Thanks for the correction! I don't retain names well, and you'll find me posting in the manner of "a doctor I don't remember the name of" occasionally. Rather than dig up his name and lose my trend of thought, I'd much rather continue writing to keep what I had mentally organized in my mind intact to be able to write out my thoughts. I was referring to DMSA when I said DMSO in my previous post.
Good news! I was hoping that is what you meant to write.
You write very well.
Thank you. Being in such forums, we all get the chance to improve on our writing.
I'm sorry that the IV chelation didn't work as well on you as it did me. I had mercury successfully removed, not just because hair and nail tests proved to its success, but my greatly improved resistance to flu, which had been a great thorn, and my greater endurance in running long distances proved it. As to the use of Emeramide, I used 20g of it last year, not for mercury toxicity, but for lead.
Your immune system improvement does point to successful removal of toxin load. I survived organophosphate poisoning in 1994 via detoxing that included 60+ EDTA IV chelations. But EDTA does not chelate mercury. But it worked on lead, cadmium, arsenic, etc. That doctor knew about thiamine; I was swallowing 16 big b-complex caps/day (=1600mg thiamine hcl). So I recovered. But the mercury was still in my body.
I'm glad thiamine was able to tide you by. Your efforts at chelating mercury may yet see success with Emeramide. But I still think you would have succeeded with the use of DMSA. There may be some confounding variable involves that your doctor failed to take into account. And I hate to be in the unfortunate position of running into a naturopath that doesn't know what he's doing.
I suspect that my own load of mercury is/was(?) pretty high due to the dangerous way my amalgams were removed. If mercury is firmly parked in storage in the body it does not show up in hair and nail tests. Many believe that it is safer to allow it to stay in storage than to stir it up with chelation which pulls it back into circulation. That said, I myself have undergone at least 3 EDTA IV chelation series totaling over 100 IVs in all. I wouldn't do it again though.
I think I lucked out then having a good biological dentist working together with a good naturopath to ensure nothing slips thru the cracks. I was entirely dependent on their expertise then.
It is now understood that physicians who chelate people should always ascertain their thiamine status before chelating them because chelating a thiamine deficient person can kill them. It is also believed that EDTA IV chelation works better if thiamine is supplemented too. I was chelated in 2014 for lead, nobody bothered about thiamine, and I developed a severe case of rheumatoid arthritis.
No wonder you are strongly spreading the news on thiamine. Thanks to you, we are learning. I may try megadosing to see if I can find a way out of my Parkinsonian symptoms, which I got from my having used cinnamon bark oil wrongly a year ago.
In the ongoing trials for approval of Emeramide, the approval for mercury toxicity is the sole intent though, as to include other heavy metals such as lead risks further delay of approval.
But I can understand your caution in waiting it out for FDA approval. Even with FDA approval, there is no guarantee as effects vary by the wide variety in context.
In my case, I was very sick for the entire year from using the Emeramide I bought from Fandachem of China, but I never thought I got an inferior grade of Emeramide. It is fake only because it did not come from the inventor's company but making Emeramide isn't rocket science. I can even say you can make it if you had a small lab with simple equipment like some Pyrex distilling flasks and beakers and some Bunsen burners. And a good handle on chemistry. For that reason, I felt I am getting a very high quality generic substance. If we can buy antibiotics from India, even Rapamycin, with confidence, there is no reason why I would need to wait for FDA to approve formally Emeramide and be held hostage to a bureaucracy known for its corruption and regulatory culpability to conspire with special interests that profit from making the US (and to a leaser degree the world) their milking cow since the Flexner Report came out a century ago. From that point on, wide scale racketeering was employed making the government its enforcer and accomplice using the legal system to transform medicine into legalized snake oil for a population made into a market for blockbuster drugs and vaccines designed to intoxicate people from birth.
Going back to topic, I got sick by encountering a perfect storm of my own making when I used Emeramide as I was not yet fully recovered from acute bronchitis (which I caused unwittingly by taking cinnamon bark orally in a a manner that caused my lungs to be irritated and filled with mucus with the ability to expectorate it disabled). The detox process involving Emeramide caused more mucus to be produced, worsening my ability to breathe. This further deprived me of oxygen and the downstream effects slowly developed and it led to heart failure and I needed to be revived and placed in an ICU intubated. I was still strong enough to only stay at the ICU for two days though, and when I was released from the hospital, I didn't think I would find myself returning for another stay 5 months later. In short, it was that bad.
You've been through the mill. Me too.
I am now certain that I will be fully recovered. All the signs point to it. But the takeaway here is that I should have let my lung to recover fully before doing my lead detox with Emeramide. The stress of undergoing a healing crisis during the lead detox was too much to bear when I was still recovering from acute bronchitis. I was too excited to begin to detox lead with Emeramide that I lost sight of healing first from my condition of acute bronchitis.
Lesson learned and thankful.
Mercury causes high oxidative stress, high reactive oxygen species. I believe that this caused my low glutathione level that I had for many years. High oxidative stress depletes thiamine. Thiamine lowers oxidative stress, if you have (supplement) enough of it; my own glutathione level has normalized since taking high dose thiamine hcl, which I think proves that my oxidative stress level now has enough thiamine to deal with it.
a link or two about oxidative stress and thiamine:
https://www.sciencedirect.com/science/article/abs/pii/S0197018613000120
https://www.sciencedirect.com/science/article/abs/pii/S0197018601001206?via%3Dihub
Maybe. And you could very well be right.
There's new research that points to the main cause of mercury issues as being selenium deficiency. I added 200mcg of selenium to my supplement regime and my doctors remarked that my blood tests showed my health is improved.
Rethinking treatment of mercury poisoning: the roles of selenium,acetylcysteine, and thiol chelators in the treatment of mercury poisoning:a narrative review
Severe elemental mercury poisoning managed with selenium and N-acetylcysteine administration
The discussion about mercury poisoning here is pertinent to the topic of hyperglycemia (I think) because heavy metal poisoning increases oxidative stress which depletes thiamine and causes thiamine deficiency which derails glucose metabolism.
Thanks for sharing. I will catch up with this. Except for using it for daily supplementation with other b-vitamins, and when I needed to lower lactic acid in blood to lower acidity in cases of high serum acidity (to make room for blood to contain more CO2), I have little immediate need yet to megadose with thiamine.
It is my understanding that thiamine is required for oxidative metabolism to work properly. If there is a thiamine deficiency, the process gets derailed and the end product is lactic acid (the issue you describe above). If thiamine is available for the process, the end product is carbon dioxide which is very important for the body.
Ray Peat on carbon dioxide
Elliot Overton on energy metabolism and the benefit of high dose thiamine
Have been meaning to read Derrick Lonsdale's book, but I still have yet to finish any of Ray Peat's four books.
Dr. Lonsdale's book is very expensive, but a good read and I found it helpful. His articles are posted (for free) here. Here is a good one to start with.
I spend some time going thru the material you shared. It's eye-ooening to say the least.
Thanks!