Biotoxin VIII: Absent Androgens

Biotoxin VIII: Absent Androgens

References:  Surviving Mold,  Jr Sex Medicine,

How many men do you know who say they are low on energy? And how many ads do you see touting the claim that they are “low T” and suggesting they get on more testosterone? Are you a bit skeptical that that may be the case? You should be, because many of those men, if not most, are Biotoxin Refugees, not “Gonadal Insufficiency” as modern medicine defines them.   They can get fixed by going upstream, in the majority of situations, to the root cause.   So just how does that happen?   Explain that “root cause”.  (First: Definition –  Biotoxin Refugee: they are sick from biotoxins and no one recognizes it and calls them crazy.  They are medically homeless and fleeing from a pervasive enemy.)

Here’s the skinny explanation. We are now in the phase of explaining the next layer of biotoxin illness, the hypothalamic and pituitary damage that arises from biotoxin’s effect on MSH (melanocyte stimulating hormone), VIP (vasoactive intestinal peptide), ADH (anti-diuretic hormone) and all the rest.   To recap, you inhale the biotoxin. That comes from the breakdown products of “black mold” which is code word for a complex mix of molds, bacteria, actinomycetes etc  . When the mid winter sun is angling across your room, you can see tiny bits of dust floating in the air. You breathe that in.   That floating stuff is what turns into the dust bunnies under your bed, and contains the substrates of biotoxin illness. The biotoxins all share a similar structure that makes them incredibly fat-soluble and damages cells by mucking up their energy production and DNA messaging. Your innate immune system recognizes them as foreign and sets off fire alarms in the form of “cytokines”, calling 911. But your adaptive system, the higher order immune system that makes antibodies and T-cells doesn’t “see” or “recognize” biotoxins in 25% of us. Those are the folks who get in trouble. The biotoxin sets off your bodies 911 system, and your adaptive system doesn’t know what to do. You flounder. That floundering takes the shape of downshifting POMC endocrine system: the 11 hormones made from one protein substrate. When you downshift 11 different hormones, you are going to have a broad array of dysfunction. No wonder hormone production takes a hit.

That’s the upstream skinny. So simply giving testosterone circumvents the real problem. Of course, folks feel better and function better for a short period of time. And then it fades. A higher dose of T then reboots the problem and your pituitary responds by making less and less LH, the hormone that drives T production. And it fades again. You have now accomplished a further down-regulation of your hypothalamus; the same place the biotoxin down regulated. And all the complex interplays of LH and pituitary/hypothalamic balance get forced out of balance.

We can’t get close to understanding all the interactions of our pituitary/hypothalamic hormones yet. Thinking that Testosterone replacement will fix our waning libido is true, only so far. There are several dozen other functions of T that aren’t so easily measured or experienced. I want to live long enough for the research to emerge that clarifies them all. As an example, STEP 11, 4 weeks from now will tell you how VIP normalizes MSH, lowers TGF-beta1 and raises VGEF. VIP is called Vasoactive Intestinal Peptide, but it does so much more, it’s hard to describe. Its name implies that it is involved just in the gut, because that is where it was first discovered. But its most important function is likely it’s balancing the POMC system, and bringing the orchestra of the hypothalamic opera into tune.

So, what specifically is being mucked up with androgens? Part of the explanation is around the enzyme aromatase. This enzyme is the last step of estrogen production, which is turning testosterone into estrogen. Aromatase gets up regulated in biotoxin illness. Testosterone disappears into estrogen. Giving more T results in more Estrogen until you get to the root problem.   The solution is not more T, it’s DHEA, the precursor to T. Most folks in their 40s and 50s have very low DHEA the precursor hormone to T and E. Giving that doesn’t seem to disrupt the whole system, and allows your body to proceed with balancing its hormones as it sees fit. We need to know more. That’s coming. Sooner would be better.

WWW.What will work for me. Well, I’ve now checked MSH and TGF-beta 1 in a handful of my clients with low T, and sure enough, they have all been low and all report basements that smell “musty”.   I’m not sure we can explain the whole story to them yet, but I’m certain this is a more satisfying track.

 

Pop Quiz

  1. We need testosterone for more than libido. T or F                                    Answer. Immune function is on the list and that may be part of the dysfunctional damage of biotoxins.

 

  1. Biotoxin refugees are?                                                                                     Answer: Folks with low energy, diffuse pain, lousy sexual function, diarrhea, trouble concentrating, mind fog…….(all the 31 symptoms of biotoxin illness) and no one wants to give them the time of day because the current medical model hasn’t learned biotoxin illness yet, so they are “homeless”.

 

  1. Replacing Testosterone is fraught with risk because?                             Answer: the enzyme aromatase is already up-regulated by biotoxins, and further exacerbated with extra T. Aromatase makes more estrogen from the T. So the T/E ratio gets all out of whack. The human body likes proper balance.

 

  1. The best way to fix low T is:   a) Replace it,   b) Give Clomiphene, c) Fix the biotoxin problem, d) Give DHEA e)   All of the above                                                                 Answer: Probably C needs to be number 1.   You do that by d). Your may use b) now and then.   Stay tuned, more to learn.

 

  1. Giving T without measuring MSH may be jumping the gun. T or F     Answer: Bingo, that’s this week’s take-home.

BioToxin VII: The Gluten Connection

References: NatureImmunityClinical and Devel ImmunSurviving Mold,

How many folks do you know who are gluten sensitive? You hear some people scoff at the idea but you also know quite a few folks that say they just feel better when they are off gluten. They don’t have celiac disease, at last most don’t. So, what’s up? Would you be surprised if you heard that biotoxins set off your innate immune response, and that sets up for the production of TH-17 immune cells, that tip you in the balance towards autoimmune disease? And gluten does that!
Step 4 in Shoemaker’s Surviving Mold Pathway is to get off of gluten/amylose for at least 3 months if you have antibodies to Gluten. This is the next phase of the Shoemaker protocol: sequentially and progressively cleaning up all the sources of persistent inflammation. And actually, he calls for you being off amylose. Amylose is about 30% of most white carbs. It is composed of long strings of glucose hooked together at the 1,4 positions on the glucose molecule, making for a long, linear chain. Amylopectin is the other component of most starches. It is branched and less dense in formation. Plants can store more energy as amylose. Curiously, it’s structure also binds iodine avidly, making for a dark color indicating the presence of amylose with iodine.
This is where future research is going to have a rich source of discovery. We don’t know all the details yet. What we do see is that lowered MSH (melanocyte stimulating hormone) and elevated TGF-beta 1 leads to unbalanced TH17 immune cells. These are the regulatory cells that march you down the path to autoimmune disease. And oddly enough, we see antibodies to gluten like IGg and IgA antibodies to gluten in biotoxin disease. That’s what leads you to step 4.

Get off of anything that stimulates inflammation. It’s not just wheat, it’s all amylose products like potatoes and rice too. All white carbs.

Now, your brain, your gut and your immune system all make a team, a triad. When you have inflammation in your gut, your brain doesn’t feel so good either. Biotoxins are setting off cytokines all over your body that are then blocking the leptin receptor in your brain, lowering your MSH. Without MSH to direct your immune system, your gut gets dysfunctional. Autoimmunity emerges.  Gluten wasn’t the first step, mold biotoxin set the table.

You thought your gluten sensitivity was set off by the changes made to wheat back in the 1950s when we tripled it’s chromosomes. I thought that. May not be the sole problem The underlying dynamic may be that your innate immune system is goofy because of biotoxins from molds. And you are in the 25-30% of folks sensitive to those biotoxins. If you live and work in clean environments, you might not ever feel the effects. You can eat bread and potatoes all day long. But add in biotoxins and your genetic susceptibility takes over.

We have tantalizing clues that this is what’s happening. Rock solid proof awaits. We do know that Hashimoto’s gets better with wheat avoidance. We do know that Crohns and Sjogren’s appear to be sensitive. Stay tuned.

WWW.What will work for me. I don’t eat much wheat anymore. We just don’t buy bread or potatoes. It becomes a lifestyle thing. Shoemaker asks the same as Functional medicine with wheat, 3 months without any. Now, that’s hard. For those who are sensitive, the rewards are there. I can’t wait for more science to figure out this connection more fully.

 

Pop Quiz

  1. Gluten irritates your gut and sets off autoimmune disease? T or F                          Answer: We used to say this was true. We now think that biotoxins lower your MSH that then makes your immune system unable to protect your gut. That’s the nuance.
  2. To have an effective challenge of being gluten free, you need to be off for how long? Answer: Three months
  3. If I put a drop of iodine into a cup of hot water with rice flour in it, it will instantly turn black, making for a great magic trick? T or F                                                  Answer: True. Amylose binds iodine avidly. It’s kind of fun. You can complete the trick with a tablespoon of green tea after your iodine turns the water black – if you want to really have fun with food chemistry tricks. Poof, clear again. Try it.
  4. Turning off amylose sensitivity is the first step in fixing the inflamed body, once biotoxin is removed from your body and your MARCoNs are cleaned up. T or F               Answer: That’s it. Now we embark on tackling all the sources of inflammation and calming your hot body down.
  5. Biotoxin illness spreads its trouble much further afield than I ever imagined. T or F                Answer: Just wait till we get to hormones! True, true, true.

 

 

 

 

 

glutathione

MARCoNs and Biotoxin Illness, Part VI

References: Surviving Mold, Biotoxin Journey, Weston Price Foundation, Truly Heal, What Doctors Don’t Tell You,

MARCoNs stands for MULTIPLE ANTIBIOTIC RESISTANT COAGULASE NEGATIVE STAPH. It grows in your nose, if and only if your immune system allows it. Coag Negative Staph is meant to be a simple commensal skin organism that everyone has. No big deal, right? I can culture it off your forehead, your arm, your leg. It’s a normal skin organism.

That changes with Biotoxin illness. Biotoxins, in the 30% of the population that are genetically unable to defend themselves sufficiently, (they just can’t “see” the toxin to make an antibody) make a flood of cytokines that damage the leptin receptor in your hypothalamus, not allowing you to make enough Melanocyte Stimulating Hormone (MSH). With low MSH, you can’t make a proper balance of T-reg cells that keep you defended against invading bugs. Like Staph epidermidis, Coag Neg Staph. MARCoNs takes up residence in your nose.

Then, something wicked happens. MARCoNs make two evil extra proteins, heavens knows why, that continue to suppress MSH. That enables them to keep up residence in your nose and sinuses. This “merry-go-round” persists endlessly in biotoxin illness, keeping your MSH Low. This has disastrous implications we will explore in future mailings. Bredesen projects that as many as 500,000 Americans with cognitive decline owe part of it to MARCoNs, so this is a big, big deal.

The real enemy with MARCoNs is the biofilm. Understanding biofilms has been a huge advance. In biofilms there is a community of organisms that appear to act in concert, not as individuals. They gang up and share their genetic material and create a soup of goop that protects them from the intrusion of white cells that could gobble them up, or antibiotics that could damage them. Something about MARCoNs and biotoxin illness encourages the development of a biofilm in your nose. It doesn’t necessarily cause any symptoms, so you can’t tell its there. But you won’t clear the MARCoNs if you don’t address the protective biofilm.

Hence, BEG spray. EDTA is the E in BEG and dissolves biofilms. B is for Bactran and G for gentamicin, two antibiotics that will kill staph. One spray each side three times a day for a month should do it, if you have oral Rifampin with it, or two sprays, three times a day without the rifampin. XClear, or xylitol nose spray for a week ahead of time will help break up biofilms too and is a good addition if you want to really get a running start. If you have trouble, read the Biotoxin Journey blog referenced above.

This opens the whole field of chronic sinusitis. Sinus infection is the number one reason for antibiotic use in America today, and the majority of folks who get more than one course of antibiotics have a fungal infection instead/in addition. It appears that infected sinuses and infected teeth are all one community. Shoemaker has shown that a lot of infected teeth also have MARCoNs in them. Weston Price, back in the 1920’s and 30’s showed that you don’t clear root canals of their infection because the bacteria burrow into the interstices of the teeth and the dentin canals of the teeth. Weston Price put infected teeth into rabbits and found that the rabbits got the same disease as the human tooth donor. Was he dealing with MARCoNs? And now we are learning that ozone therapy can cure sinusitis by instilling ozone gas into sinuses, better than many other methods. Ozone works by unknown mechanisms, presumably by turning on better oxygen flow in white cells, making them into little Ninja tigers. But it seems to work. The literature to support this is in Chinese and Russian and Italian. American’s have been a bit behind the curve at researching ozone. My read is that there appears to be a convergence of understanding of new methods and mechanisms of disease, aching for more collaborative research.

WWW.What will work for me. This is mesmerizing because it is so new and so confoundingly different from anything traditional medicine has taught. I’m following Shoemaker’s protocol to the T. He has been a genius at elucidating a pathway to cure biotoxin illness. Getting rid of MARCONS is step three in his pathway. He data base (8,000 patients) is huge and shows that 80% of folks with biotoxin illness have MARCoNs and 60% are methicillin resistant. BEG spray for a month works. My experience with about 100 agrees with him. But I want to keep my eyes open for real methods that work. This ozone thing might bear fruit. Let’s stay tuned.

 

Pop Quiz:

  1. MARCoNs is a rare bacteria. T or F                                                    Answer: Trick question. It’s rare in healthy folks, but 30% of the populations is vulnerable to biotoxin illness and with that, they have a 60% chance of getting MARCoNs.
  2. MARCoNs is a normal skin bacteria turned devil in your nose? T or F                    Answer: Bingo. Right on the money
  3. If you have biotoxin illness, you won’t get better unless you eradicate MARCoNs. T or F Answer: Bingo, Right on the money
  4. Root canal teeth may have MARCoNs infections, just like sinuses, connecting sinus and teeth infections. T or F                                                                   Answer: Whoa, True and head turning.
  5. Bacteria from infected teeth were shown to transmit disease to rabbits by whom and when? Answer:  Weston Price, dentist extraordinaire, from the 1920s. He didn’t know about MARCoNs or biofilms, but he was all over the complications of it
glutathione

Biotoxin V: How do I Get Rid of Biotoxins?


References: Biotoxin Journey

You now know that biotoxins circulate endlessly in folks whose immune system can’t “see” the toxin and label it. You know that merry-go-round involves the toxin entering through your nose lungs most of the time, or ingested, or stung, or absorbed. From there the toxin sets off all sorts of cytokines in toll-receptor proteins all over your body. These cytokines descend on your primitive lizard brain, your hypothalamus, and essentially damage the leptin receptor that is the entry point to proper functioning of your POMC (pro-opiomelanocortin) system, that is foundational to your pituitary and most of your hormones.

The net effect of this blockade of the leptin system and POMC system are that you reduce the output of MSH, melanocyte stimulating hormone, which might be considered the “mother of all hormones” as it is so upstream from much of your endocrine system. You have trouble concentrating and remembering. You have a head ache. Your muscles ache. All your symptoms are nonspecific. All your traditional lab tests are normal.

Now, the toxins circulate through your body and eventually find their way to your liver, which politely and promptly dumps them into your bile. From your bile the toxin ends up in your gut. In your gut, it passes down to your colon, where, without an antibody label on it (because your immune system can’t see it) you reabsorb it. The Merry-Go-Round. The toxin circulates endlessly.

And that is the key! That is how we can rid you of it. Cholestyramine (CSM) is an old fashioned cholesterol drug, invented to soak up bile acids in your gut, which was supposed to lower cholesterol as a secondary effect. Turns out that strategy to reduce blood cholesterol was an ineffective remedy. But it is a potent binding agent nevertheless. It binds almost every biotoxin brilliantly while it is in your gut. The shapes of biotoxins make them quite fat soluble, so they pass through membranes easily so binding them is the only way off the merry-go-round. A second drug called cholesevalam (Welchol) also works, but takes 2-3 times the time to do it. It’s a good back up for folks who get too constipated with CSM. It is used as a blood sugar drug in diabetes.

The dose of cholestyramine is 9 grams, four times a day. That is typically one scoop of the standard preparations and the dose recommended by the FDA for cholesterol care.

There are some caveats. Folks who have Lyme will tend to have a flare of symptoms shortly after starting CSM (Herxheimer reaction). Collecting data like C3a and C4a and MMP9 before hand and with a flare will confirm the real perpetrator, and allow countermeasures ahead of time like pretreatment with a no-amylose diet, fish oil or pioglitizone which blocks PPAR receptors and reduces TNF-alpha production).

And in a month you are better. Did you get that? It seems impossibly complex when you read the above, but the cure is easy. One month, binding agent, fixed!

That is totally, unbelievable, factually true (20-40% of the time). But you have to watch the details. Can you get better if you are still living in a contaminated home? No. Can you get better if you have Merry-Go-Round #2 in your nose going on? No. Can you get better if your whole pituitary POMC system is screwed up? No. But those are all reduced likelihood events, and the subjects of coming weeks detail. Keep reading.

Notice, I didn’t mention any of ten other binding agents. You know why? Because Shoemaker has checked all of them against placebo controls and found none of them (charcoal, clay, zeolite,) to work like cholestyramine. So, don’t bother.

WWW.What will work for me.   This is a whole new field of medicine. The cure seems very simple but it has so many caveats that the devil is in the details. Cholestyramine is a magically simple drug, provided you have all your ducks lined up. In the meantime, I’m looking into ways to clean up basements and circulate air. My neighbor has had his basement being vented with an aerator that pushes out air and dries out basements better than dehumidifiers. I’m exploring one for myself.

 

Pop Quiz

  1.  The best way to excrete biotoxins is to snag them in your gut? T or F       Answer: True. You got it. You read the book. Nice work
  2. The best drug to do this is………?                                                                        Answer: Cholestyramine
  3. The right dose is…………..?                                                                                  Answer: One scoop or 9 grams
  4. Many binding agents bind mold toxins? T or F                                              Answer: Well, only one other works (Welchol) and it works at 1/2 to 1/3 the pace.
  5. Taking cholestyramine, one time a day will keep me protected?               Answer:   Nope. Seems to be a threshold of dose to work.   4 grams a day might be the lease you can take to be effective, and at least it keeps your constipation at bay. Ok, we didn’t mention it above but it is in the references.
Mold, Biotoxin Illness

Biotoxin Pathway IV: The Biotoxin POMC Merry-Go-Round

References: Nature, Biotoxin Pathway

You’ve been exposed to a biotoxin. You didn’t know it because you didn’t even know the building was damaged by water, or the brown discoloration in the bay your were fishing didn’t look all that weird, or the fish you ate tasted a little odd but not that awful. We now know that many organisms can set it off: Dinoflagellates: Pfiesteria and ciguatera, fungi like Stachybotrys and Chaetomium, Blue-green algae like Microcystis and Lyngbya, Spirochetes like Borrelia burgdorferi, Apicomplexans from Babesia microti, some gram positive bacteria like Coagulase negative Staph and anthrax, some spider bites like brown recluse spiders – lion fish, etc. The DNA fragments and protein fragments from “black mold” in water damaged buildings is likely the number one cause in America.

How do those toxins wreak their damage? Here’s how.

The various biotoxins set off your innate immune system. And in the 25-30% of us who are not able to mount an effective antibody response (adaptive immune system) the toxin gets “started” on the first merry-go-round. As it circulates through the air, (most commonly) you breathe it in through your nose and it soaks up into your taste/smell receptors at the tops of your sinuses, or through your lungs. Because your body cannot “see” it and make an effective antibody to clear it, the biotoxin circulates up to your brain where it gives your POMC system a whack. How exactly does this happen? The biotoxins bind to many toll receptor proteins” that set off cytokines, TGF-beta1 and split products of complement. There are dozens, if not hundreds of cytokines. These cytokines, in turn, being part of the innate immune system, set off MMP-9 in your blood, and in your brain, they block the Leptin Receptor. This is a critical junction receptor because there are many processes that run through it. Notably, POMC.  Pro-Opio-Melano-Cortoin.  POMC  is the precursor protein that can be chopped into 11 different hormones, depending how it is chopped up. If you can’t make POMC, you can’t make a lot of things. The O stands for Opio – and there is a down regulation on pain control. The M stands for Melano and that stands for Melanocyte Stimulating Hormone and the C stands for Cortin, all about energy homeostasis.  Folks affected end of tired, in pain, overweight and “sick”.

The biotoxin then circulates in your blood and your liver says, “let’s dump this junk” and into the bile it goes. In your bile, it proceeds to your gut and your colon, where it happily gets reabsorbed.   Back into your blood, up to your brain, back to your toll receptor proteins all over your body, back to your elevated TGF-beta one and MMP-9, back to your blocked leptin receptor. It’s like the horror show merry-go-round with the crazy clowns and the monster show. Round and round and round because your immune system can’t see it.

That’s merry-go-round (MGR) one. MGR two goes as follows. With a damaged alpha MSH secondary to blocked POMC, your immune system becomes even more blinded. A perfectly innocuous bacteria that grows on your skin, called Coagulase Negative Staph (I can grow it off anyone’s skin, anywhere) can invade into your nose and take up residence. Curiously, it seems to pick up antibiotic resistance from who knows where. We call it MARCONs: multiple antibiotic resistant Coag Negative Staph. It secretes two proteins, called A and B, which cleave MSH, further reducing MSH. With low MSH, MARCONs can keep hanging out in the “biofilm” in your nose. That’s MGR number two. The biofilm in your nose is a good hiding place for it to persist. You can’t clear it on your own. So it perpetuates itself.   MGR #2. Round and round.

Two merry-go-rounds that are both self perpetuating, and never-ending. I mean, years. The biotoxin can circulate endlessly, and the MARCONs can persist endlessly. Many folks continue to be exposed to the biotoxin, reinforcing the merry-go-round by juicing it up. They symptoms are odd enough and strange enough, and delayed enough, that the association with the source isn’t immediately clear. So on, and on it goes. And where it stops…nobody knows.

Well, you now know. We can stop this continuous cycle. That’s coming next week.

WWW:What will work for me. I’ve seen people sick for 10 years who come in having seen 10 doctors. So these merry-go-rounds are nuclear powered. They can go forever if not interrupted. And the level of their disruption is a real wake up call. I want you to know the steps it takes to clear them. But the first step is a clear, visual image in your brain of the two merry-go-rounds. Next week, we start dismantling them and pulling off the horses, one by one.

Pop Quiz

  1. Biotoxins can come from many sources but the most common, as best we know come from…?                                   Answer: Water damaged buildings and mold..

 

  1. Biotoxins attach to what in many cells all over your body?           Answer: Toll receptor proteins
  2. The net effect of biotoxin invasion is to set off all sorts of what signaling?         Answer:   Cytokine activation.   Possibly dozens or more different ones. So far we can measure MMP-9 and TGF-Beta1 but there are likely many more.

 

  1. What is Merry-go-round #1.             Answer: the endless circulation of toxin through your blood, into your brain, out by the bile into your gut and back into your blood via your small bowel and colon. Back to your brain. And again and again.

 

  1. And what allows MGR2 to get started?             Answer: Low MSH that allows the invasion of MARCONS into your nose.   MARCONS makes two proteins from its hiding place in biofilms in your nose. Those two proteins cleave MSH, leading to continued suppression of your immune system and further lowering of MSH. Round and round and round. That’s MGR2.
glutathione

Biotoxin Illness Part III: The Role of Glutathione

References: Toxins (2014)SciWorldJr,

So, you know about your immune system having two layers, the innate or lizard system, and the adaptive or precise mammalian system. A good analogy is like a bomb going off by a terrorist. Your city reacts with a curfew, 911 is activated, the police clear the streets, sirens are wailing. This is your innate immune system – “all hands on deck, but who is it that we are fighting?”. Nonspecific, system wide, reactive. Then, surveillance cameras pick up a suspicious character and his license plate is put out there with a sketch of what he looks like. Then his picture shows up from the driver’s license bureau. This is slower, your adaptive system, but it has precision and accuracy.

What are you using to clear the toxin, once you know what it is? The answer is glutathione. Glutathione is simply three amino acids tagged together but they have sulfur atoms in them, making it able to soak up loose electrons. Every cell in your body has it. It’s your natural defense, in effect, part of your 911 mop up system. It’s sort of like your fire hose cooling off the burning embers of the fire. And as you age you make less of it. Dramatically less.

Turns out, it is a critical player in Biotoxin illness. It enables your body to tag and dispose of mold toxins. The paper we review this week details how we make glutathione through a delicate dance with Nrf signaling and the protein GST or Glutathione S transferase (GsT) . There are 7 GsT types inside a cell, and the first and most common has many genetic variants. Half the adult population has a polymorphism that is dramatically less active. This has been associated with oxidative stress all over the body, most notably in the brain with Alzheimer’s. Mold toxins wreak some of their havoc by down regulating the level of glutathione production. And as we age, our levels of glutathione drop dramatically.

Well, well! If that’s what mold toxins do, what would happen if we gave glutathione to someone with all the symptoms of biotoxin illness, and positive markers of biotoxin disease? Here are two stories. A middle aged woman with three years of asthma symptoms not responsive to typical asthma therapy and cleared of asthma by the traditional medical system becomes symptomatic again. Treatment with one gram of IV glutathione for three days completely reverses her symptoms. In fact, her oxygen saturation surged from 95% to 98% within 10 minutes of treatment.
A second story. Multiple insect stings. A mid seventies women with over 15 hornet stings, treated with traditional Benadryl with only partial success. Insect stings are known to be another entry into the Biotoxin pathway. Two treatments with 1 gram IV glutathione result in dramatic and almost immediate, complete recovery.

Did you get that? Now, you can’t take oral glutathione easily as it is digested in your stomach like any other protein. And not everyone has access to IV glutathione. (It is just 3 amino acids long). But you can take it in “liposomal form” which is widely available in Supplement stores and on the net. And, more importantly, you can take N-acetyl cysteine or NAC and give yourself the rate limiting cysteine combination. NAC is a revolutionary supplement that has been around for 40 years. 40 years ago it revolutionized Tylenol overdoses. Prior to NAC, a Tylenol overdose was a guaranteed death sentence or liver transplant. NAC is so powerful that folks with Tylenol overdoses are now sent home from the hospital with NAC to take a couple of times a day. No wonder NAC makes Bredesen’s supplement list for Alzheimer’s prevention.

WWW.What will work for me. Well, I take NAC in my daily supplement list. If I was still an emergency physician, I would find a way to study glutathione for folks with nasty insect stings. But I’m now adding IV glutathione to my treatment regimen for everyone with Biotoxin illness. The jury is out about randomized, placebo controlled trials. But considering that glutathione is in you already, just less because you are old, means you and I should consider paying attention to our glutathione levels as we age.

Pop Quiz

  1. Glutathione is my natural antibody booster. T or F                                          Answer: False. Nothing to do with antibodies as that is the adaptive, more precise immune system. So called “glut” is your innate immune system’s fire hose. Just calming things down.
  2. As we age we make more glutathione. T or F                                                    Answer: Again, false. Testing to see if you actually red the article. Much, much less.
  3. Biotoxin illness down regulates your production of glutathione. T or F       Answer. Ok, we will give you a true
  4. There is a simple supplement that gives you the amino acid pieces to make your own glutathione. And it is called……………..                                                                 Answer: NAC or N-acetyl cysteine
  5. We all make pretty much the same amount of glutathione. T or F                 Answer: surprisingly false. There are 7 different forms of glutathione converting enzyme inside the human cell, and the first and most dominant one comes in form that is much less active in 50% of us. Why, we don’t know. But every protein has many slight alterations that we inherit in our gene mix called polymorphisms. That happens to be one that is curiously dysfunctional.

Biotoxin Illness Part II: How the Weird Symptoms Come About

Biotoxin Illness II: The Weird Symptoms and How They Come About

References: Surviving MoldDr Thomas,

To understand the “weird” and protean symptoms of Biotoxin Illness, you need to first understand how it comes about. The toxins enter the body in many ways, probably mostly through breathing in via lungs or nose, but also through tick bites or insect stings, or even skin surface contact. In the case of molds, it’s not the spores growing but the proteins and DNA fragments of dead mold organisms that set off the problem. And it’s not just mold but also all the other organisms that live in water damaged buildings like actinomycetes, mycobacteria, and their proteins and DNA.
All that “gunk” is foreign to the human body. And we react to it. Now, our immune system has two layers. Our “innate” system is very primitive and reactive. It just fires off and sets off indiscrete reactions. It sends out chemicals to call in troops to help it out and starts a cascade of reactions called the complement system. It doesn’t have any long lasting memory. That is the “adaptive” system that develops specific antibodies and has memory.

The innate system is programmed into you, and is responsible for telling your “friend or foe”. That’s the problem with mold. 24% of us can’t recognize the biotoxin. It’s as if we can’t see it, or have dark glasses on. Two percent of us are downright blind and have an immune system that is totally clueless. In those folks the mold toxin stays in the body, and keeps circulating again and again in a cycle from blood, to liver, to excretion in the bile, to reabsorption in the bowel back into the blood where there is another whack at the brain. The damage to your brain comes about because of non-discript secretion of chemical messages that circulate everywhere, but in dysfunctional levels, all because of the innate immune system activation. These biotoxins are by and large fat soluble, so the brain is a natural destination.

It’s that programming you can measure for and test. Every cell in your body has labelling proteins that your innate immune system knows makes you you. Those are called HLA alleles or haplotypes. They are what we measure when we test you for a transplant to make sure we put in an organ that looks close enough to you to pass muster. Folks sensitive to mold have a variety of alleles that just don’t see the mold toxins. Their immune recognition is kaput, and the toxin just persists and persists.
The subsequent action of the innate immune system is to proceed to damage your brainstem, your bodies hormonal gearbox.

Now you will understand why the symptoms are weird. We are disturbing a very primitive immune system. So, your doctor does some standard tests and finds nothing. You tell her/him that you have: diarrhea, abdominal pain, persistent fatigue, numbness, extreme thirst, disorientation, metallic taste, watery eyes, congested sinuses, shortness of breath, weakness, body aches, headache, sensitivity to light or sound, Trouble learning new info, dizziness, cough,
impaired memory, difficulty with word finding,heightened skin sensitivity
tingling/pins and needles. If you have 7 of these, it’s a slam dunk.

This leads you to see doctor after doctor and nothing is found. But you walk into a water damaged building, and in 5 minutes, you feel sick. That is the cardinal symptom of biotoxin illness.

WWW.what will work for me. My ears are getting tuned to recognizing the desperate tone of voice of folks who have seen many physicians and been told they are fine. We need to all learn this stuff. It’s a journey of discovery that will change much of the way we do medicine. It will be a department at the local medical school in time.

Pop Quiz

 

  1. Your innate immune system is very specific and focused. T or F                         Answer. False as false can be. Very diffuse and non-specific.

 

  1. Folks susceptible to mold illness have an over reactive immune system. T or F         Answer: Both T and F. Because their antibody system can’t label and mark the toxins, they keep circulating and setting off the innate immune system, creating a cycle of damage.

 

  1. Can you name three symptoms from the list above that someone you know may have and hasn’t found an answer?                                                   Answer: Just look. It’s happening to folks all around us

 

  1. The toxins in mold that make all this mess are easily identified. T or F                  Answer: False. We really don’t have a clue yet what they are. In Pfisteria we have identified it. But most other illnesses, it’s a field waiting for research and clarity.

 

  1. Until we know how to identify the toxins, what is the first logical step?                 Answer: do a simple screening test to see if their is signs of damage, and then test the home and workplace (school) to see if there is ongoing exposure. You can’t get better if you are in a dangerous place.

 

Explaining Biotoxin Illness

References: Surviving Mold,

We are all familiar with bacterial illness. We have experienced sore throats, or skin infections, or sinusitis and have been diagnosed and treated with antibiotics. We have also seen traumatic illness, and have had X-rays and casts or stitches for cuts. We understand metabolic illness with thyroid and sugar and other metabolic parameters. But biotoxin illness? Even the spell checker tries to correct me and call it biotin illness. I mean, BIOTOXIN. This is a whole new field of medicine that will become part of internal medicine or family medicine in the future. For now, it’s just being elucidated and clarified. Here goes my stab at it. This will likely take several weeks to make it a clear story.
In introducing this topic, one has to give credit to Ritchie Shoemaker as the first to understand the new field, the paradigm shift. He was a family physician in Pocomoke, Maryland who persisted in believing his patients who said their were ill in the midst of a pfiesteria bloom on the Pocomoke river. The CDC and Johns Hopkins both came to town for the mystery illness and could not name anything to explain the sick folks symptoms. Dr Shoemaker is now clinically retired but actively teaching new physicians to understand the huge new field through his web site, www.survivingmold.com. One of his patients had terrible diarrhea with the mystery illness. He gave her cholestyramine, an old fashioned cholesterol drug now known to be useless for cholesterol and used mostly to control loose bowels in folks with funny guts. She got better in two days. Not just her stool was better, but her fatigue, her brain fog, her aches and pains – all went away. And then, other patients also got better with cholestyramine.
So, what is biotoxin illness? It is a constellation of symptoms brought on by toxins made by a variety of sources. We are still finding them. Mold in water damaged buildings is likely the most common, with about 30-50% of American buildings being damaged with measurable mold detritus. It’s not the mold spore, but the fragments and protein of many different molds, actinomycetes, volatile organic compounds (VOCs), inflammagens and other yet to be identified components that set off the syndrome. Other causes include aforementioned pfiesteria, a water based dinoflagellate. Lyme disease, spider bites, eating Lion Fish, red tides, the antibiotic CIPRO, multiple wasp stings, beruli ulcer, and probably many more. In weeks to come, we will explain how it may be that some 500,000 Americans are getting Alzheimer’s with mold toxin as a participant.
Most folks are likely fine until they have some trigger that sets them off. Some antecedent event makes them more vulnerable. And they have to be capable of being vulnerable. Turns out roughly 24% of us are genetically “vulnerable”. Our immune systems are unable to see and tag those toxins that will make us ill. We can even measure and find those folks with HLA testing, the same testing you do to see your self identifying proteins that make you you when you need to get a organ transplant. There are patterns Dr Shoemaker has identified that represent the vulnerable and susceptible. The rest of us, 70% are capable of seeing mold toxins and have no trouble getting rid of them. Then there are 2% of us that are catastrophically sensitive.

And what does this illness look like? Simply stated, they check out at ok by typical modern medicine. They express fatigue, brain fog, joints pains, rashes, diarrhea, cough and so many other symptoms that their doctors dismiss them as psychiatric. The house of medicine calls it fibromylagia, or chronic fatigue. And if I told you that 80% of chronic fatigue folks had mold in their urine, would you sit up and pay attention? This needs to be a whole new branch of medicine. Every doctor should know it. It affects 25% of us.

WWW.what will work for me. I’m trying to wrap my head around this way of thinking. It’s a whole new field. If you stick with me, I’m going to keep defining it for you, and learning it for my self. I feel like someone turned on the lights. I’ve tested about 50 people with unexplained fatigue and illness. I’m batting 90% mold as best I can tell. Biotoxin illness. Even my spell checker doesn’t recognize the word.

Pop Quiz

  1. Biotoxin illness is caused by rare bacteria or weird molds? T or F                       Answer: No. It’s is caused by the immune reaction to proteins and broken bits of DNA, or to foreign compounds that alert our innate immune system in a human that doesn’t have the genetic ability to adapt. (Lion fish, red ted, ciguatera, pfiesteria, mold, CIPRO, beruli ulcer, wasp stings….and probably many more)

 

  1. Most of us get sick to these biotoxins when exposed. T or F                              Answer: False. Fully 70% of us have immune systems that see the toxins, tag it, excrete it, done.

 

  1. We can get a simple blood test to measure our risk of biotoxin illness. T or F           Answer: Well, if you consider transplant tissue typing a simple test, sure. But right now it costs some $ 600 bucks and takes a week to get back.

 

  1. Mold illness may play a role in many common illness, like Alzheimer’s.                 Answer: True. But unfair. We haven’t gotten to that yet. Just a hint.

 

  1. So you mean to tell me that that whacko person who walked into our church and said, “I can’t stay here, this place is bad for me,” wasn’t whacko?                     Answer: Hang your head in humility. They were likely one of the 2% who are exquisitely sensitized. Be grateful you don’t live in their skin. And make sure your home is not water damaged.

Juicing is Dangerous for You

Juicing is Dangerous.

References: Advances in NutritionAppetiteEating on the Wild Side,

I get asked all the time about juicing or “smoothies”. Most of the smoothies are described as rich combinations of green vegetables, or yogurt, or fruit. Then, I had someone describe to me how their blood sugar went up almost to 1,000 with a seemingly innocuous concoction. What’s going on that can make that happen?

This column has reviewed the science of changing an apple to apple sauce, then juice before. Barbara Rolls and her team at Penn State observed 58 random volunteer adults for a meal once a week over 5 weeks. Each volunteer was provided a precise “preload” of calories weighing exactly 226 grams with 125 calories in it; aka, one really nice apple. After 15 minutes, they eat whatever they wanted for their meal.

This is what they found. Eating a whole, solid apple resulted in a 15% reduction of calorie intake. That is a 62-calorie reduction for the entire meal. That would be interesting enough by itself. You can lose weight by having an apple 15 minutes before a meal! (62 calories a day is 1800 calories a month or 6 pounds a year.)

But wait, it gets better. Here is the heart of the juicing question. When they changed the apple into applesauce with the same weight, calories, rate of ingestion, timing, resulted in eating 91 calories less overall. Then change the calories into juice. It became 150 calories less.. Applesauce reduced total meal calorie consumption a tiny bit, compared to juice which had virtually no reduction in calories.

The final sword in the experiment was to add fiber added back into the apple juice. Now it becomes a drinkable product, aka juicing. You erase the positive effect of eating a whole apple before a meal. The drinkers did compensate for their calories in the meal, but they did not reduce their total overall calories like eating a whole apple did. It’s interesting that juice, with or without fiber had the same effect. Being liquid just doesn’t register in your brain, no matter the fiber content. Did you get that, juicing erases the message to your brain about content of food.

Our brains and physiology are quite complex. Part of a meal is the actual process of “eating” it. Chewing our food makes a difference in how much food we eat. Stretching it out over time makes a difference. The waiting of 15 minutes before the meal may have been part of the impact. We call that part the cephalic phase during which your body starts to get ready to digest and process food. Managing your cephalic phase sounds like heavy science. Or maybe it’s just plain heavy weight gain.

Here’s my take on it. Eating the whole fruit delivers fiber with the sugar and slows the process of absorbing the sugar dramatically. Mechanically grinding up an apple, or any vegetable, is far more efficient than chewing in terms of mechanically disrupting the cell wall and releasing the sugars inside. When you drink it, you get a burst of glucose delivery to your gut. This results in a burst of insulin release. This results in a burst of LDL production to ship fat to your fat cells instead of energy to your brain and muscles. You thought you ate 800 calories for your meal but your body is saving some of it to fat, because of the insulin burst. Hence, you eat more.

Moral of the story: juicing changing the way you get nutrients: the speed, the mechanics of chewing, the rate of glucose rise all are disrupted. You gain weight.
Now, if you are averse to vegetables and you can’t get them any other way……and aren’t overweight. I’ll relent. If your smoothie is just kale and asparagus and yogurt, I’ll concede. But throw in an apple or a banana, and my skepticism goes up. The heart of the matter is that today’s apple is really much more endowed with sugar than nature’s original apple. Malus Sikimensis, the Himalayan apple is the worlds original, and has a very bitter/sour flavor, sort of like a crab apple. We have changed it into a Golden Delicious, with 1% of it’s original phytonutrients and 10 times its sugar. Hmmm.

www.What will work for me. Eat the whole food. Chew. Sit. Wait. Talk. Enjoy. Visit. The calories you drink are the calories you store. Repeat after me. The calories you drink are the calories you store. Plain and simple.

Pop Quiz

  1. Juicing is really healthy for me?                                                                               Answer: Please reread this column
  2. I hate vegetables. If I juice them, I can get some down. Is that ok?                  Answer: if you keep the high glycemic fruits out of it, you are getting some fiber this way, but be careful if you are trying to lose weight.
  3. The calories I drink are…………                                                                                 Answer:                        The calories I store. (smoothies)
  4. The calories I drink are …………….                                                                            Answer: The calories I store (beer).
  5. The hormonal effect of food is more important for weight control than the quality of the food. T or F                                                                                                                  Answer: True. That’s the secret behind this message. Smoothies make glucose be delivered too fast, turning on insulin. Insulin is your storage hormone. The exact same food, delivered slowly and with fiber built in makes for a different metabolic product.

 

 

Upcoming Seminar: The End of Alzheimer’s

Save the Date  Oct 14th, Saturday Morning

“The End of Alzheimer’s”

NO-ONE Should Ever Get This Awful Disease

Yes, that is possible, for you and for your loved ones.

And it is reversible if we catch you early enough.

Dale Bredesen has proven it, and we will explain his methods.  You will learn the details of how you can protect yourself, what life style changes you can make, how you can measure your success, what lab tests you can order and what supplements you should be adding.  We will detail the various pathways by which our brains get injured, resulting in Alzheimer’s.  You will leave knowing at least 10 specific things you can start doing today to keep your brain healthy and vibrant into your 90s.

Dr John Whitcomb and MD Custom Pharmacy are collaborating to bring you this important information.

Saturday Morning:  Oct 14Th 4th.   4 hours and we will feed you lunch.  2 lectures and an hour of questions and answers.  Then, a demonstration luncheon on how you should be eating.

To Register:  Call MD Custom Pharmacy   262-373-1050

Place:  Beautiful Redeemer Church on Townline Road in Sussex (Just south of Townline and Lisbon Road Stop Light.  We will start at 8 am with coffee and greeting.

Price:  $ 35 for the first early registrants.  $ 45 in the last week.  We can only seat a limited number so please call now and save your spot.