How To Chelate With The Andrew Cutler Protocol

by | May 17, 2018 | 11 comments

How to Chelate with the Andrew Cutler Protocol

 

  1. The Andrew Cutler Protocol – Overview
  2. Chelating with DMSA
  3. Chelating with DMPS
  4. Chelating with ALA, Alpha Lipoic Acid
  5. Chelating with DMSA and ALA
  6. Chelating with DMPS and ALA
  7. Choosing and increasing dosages
  8. Dump Phase
  9. Supplements
  10. My experience with the Andrew Cutler Chelation
  11. What does mercury chelation have to do with ozone therapy?

1. The Andrew Cutler Protocol – Overview

 

IMPORTANT: Chelation can be performed only after ALL amalgam fillings and all other mercury sources have been removed. Chelating with amalgam leftovers can result in a mobilization and redistribution of mercury into the Central Nervous System. Please, ask your dentist for bite-wing x-rays to verify that you are truly amalgam free. 

Chelating with the Andrew Cutler Protocol involves the following three chelators:

  • ALA (Alpha Lipoic Acid), half life: 3 hours
  • DMSA (Dimercaptosuccunic acid), half life: 3 to 4 hours 
  • DMPS (Dimercaptopropane sulfonic acid), half life: 6 to 8 hours

DMSA and DMPS are prescription medications in many countries, which requires the consultation of a medical doctor. Please make sure you comply with your country’s laws before you start using these substances.

During the Andrew Cutler Chelation the chelators are taken in rounds of at least 63 hours in low oral dosages according to their half lives. After each round there is a break of at least three days. 

What this means in practice is described in detail on this page. 

Starting dosages range between 3 and 20 mg. 

A successful chelation can take 100 to 300 rounds, or 1 to 5 years. 

Table 1: Example of the constant succession of rounds and breaks during the Andrew Cutler program. 

ROUND 1 BREAK ROUND 2 BREAK  and so on … 
Day 1 Day 2 Day 3 Day 1 Day 2 Day 3 Day 1 Day 2 Day 3 Day 4 Day 1 Day 2 Day 3  

 

2. Chelating with DMSA

The purpose of DMSA is to lower mercury levels in the blood. In this way, it prepares the body for chelation with Alpha Lipoic Acid, which is the most important chelator.

DMSA is used during the first 3 months after the last mercury exposure, which in most cases is amalgam removal.  

Chelating with DMSA: things to remember

  • DMSA will clear mercury only out of the blood and the extracellular fluid. It cannot chelate mercury out of the brain or other organs.
  • DMSA can be taken 4 days after mercury exposure has ended. For example: If you had your amalgams removed on May 1st, you can start using DMSA on May 5th.
  • DMSA chelates mercury and lead.
  • DMSA can lower neutrophils which can lead to a flare-up of candida. 
  • DMSA has a half life of 3 to 4 hours.

Chelating with DMSA: What it looks like in practice. 

You pick one dosage and stick to that dosage over the entire round. You select either a 3-hour or 4-hour interval. If you choose 3-hour intervals, then a DMSA round looks just like an ALA round (see table 5 or 6 below).

Table 2: Example of a round with DMSA with 4-hour intervals:

DAY 1 DAY 2 DAY 3
12 am 12 am 12 am
4 am 4 am 4 am
8 am 8 am 8 am
12 pm 12 pm 12 pm
4 pm 4 pm 4 pm
8 pm 8 pm 8 pm

A 72 hours round with 4 hours intervals consists of 18 dosages. 72 hours / 4 hours intervals = 18. You can start a round at any random time. What is important that the intervals in between single dosages are always the same. 

 

3. Chelating with DMPS

The purpose of DMPS is to lower mercury levels in the blood. It prepares the body for chelation with Alpha Lipoic Acid, which is the most important chelator. 

DMPS is used during the first 3 months after the last mercury exposure has ended, which in most cases is amalgam removal.  

Chelating with DMPS: things to remember

  • DMPS works very similarly to DMSA.
  • According to Dr. Cutler, DMPS is not significantly more effective than DMSA, but most people tolerate it better than DMSA.
  • DMPS will clear mercury only out of the blood and the extracellular fluid. It cannot chelate mercury out of the brain or organs.
  • DMPS can be taken 4 days after mercury exposure has ended. In other words, if you had your amalgams removed on May 1st, you can start using DMPS on May 5th.
  • Some people develop allergic reactions to the drug, which show up as rashes. 
  • DMPS is considerably more expensive than DMSA. 
  • DMPS chelates mercury and arsenic.
  • DMPS has a half life of 6 to 8 hours.

Chelating with DMPS: What it looks like in practice.

You pick one interval and dosage and stick to that interval over the entire round. So if you pick a 6-hour interval, you should keep that until the end of the round. Same if you pick a 8-hour interval. Do not change dosages mid-round. 

Table 3: Example of a round with DMPS with 6-hour intervals. 

DAY 1 DAY 2 DAY 3
12 am 12 am 12 am
6 am 6 am 6 am
12 pm 12 pm 12 pm
6 pm 6 pm 6 pm

A 72 hours round with 6 hours intervals consists of 12 dosages. 72 hours / 6 hours intervals = 12. You can start a round at any random time. What is important that the intervals in between single dosages are always the same. 

 

Table 4: Example of a round with DMPS with 8-hour intervals. 

DAY 1 DAY 2 DAY 3
12 am 12 am 12 am
8 am 8 am 8 am
4 pm 4 pm 4 pm

A 72 hours round with 6 hours intervals consists of 9 dosages. 72 hours / 8 hours intervals = 9. You can start a round at any random time. What is important that the intervals in between single dosages are always the same. 

 

4. Chelating with ALA

Alpha Lipoic Acid is the most important chelator.

One can successfully chelate mercury with ALA alone. DMSA and DMPS are optional. 

It’s the only one of the three agents which is able to penetrate the blood-brain barrier (BBB) and pull the mercury out of your Central Nervous System (CNS) and from the inside of your organs. You start chelating with ALA three months after the last mercury exposure.

Example: if you had your amalgams removed on Feb 1st, the earliest you can start chelating with ALA is May 1st. 

Chelating with ALA: things to remember

  • ALA chelates mercury and arsenic.
  • ALA has a half-life of 3 hours. This means that it must be taken every 3 hours, DAY and NIGHT.  During the night, it’s possible to extend the intervals twice to 4 hours since the metabolism slows down when we sleep. During the day, you have to go back to 3-hour intervals.

Chelating with ALA: What does it look like in practice?

You pick one dosage and keep that same dosage over the duration of the entire round. A round consists of minimum 63 hours. 

Table 5: An example of a 63-hour round with ALA.

FRI SAT SUN MON
  12 am 12 am 12 am
  3 am 3 am 3 am
  6 am 6 am 6 am
  9 am 9 am  
  12 pm 12 pm  
  3 pm 3 pm  
6 pm 6 pm 6 pm  
9 pm 9 pm 9 pm  

A 63 hours round with 3 hours intervals consists of 21 dosages. 63 hours / 3 hours intervals = 21. This example is ideal for people who work during the week or go to school. A 63 hours round as displayed above allows to start a round on Friday evening and finish Monday morning. 

 

In this article I mostly choose 72-hour rounds simply because a) longer rounds are in general preferable to shorter ones; and b) if you want to always alternate 3 days on and 3 days off, then 72-hour rounds and 72-hour breaks make for a simple and clear schedule.

Table 6: An example of a 72-hour round with ALA. 

DAY 1 DAY 2 DAY 3
 12 am 12 am 12 am
 3 am 3 am 3 am
 6 am 6 am 6 am
 9 am 9 am 9 am
 12 pm 12 pm 12 pm
 3 pm 3 pm 3 pm
6 pm 6 pm 6 pm
9 pm 9 pm 9 pm

A 72-hour round consists of 24 dosages, or 8 per day: 72 hours / 3 hours intervals = 24 dosages.

 

5. Chelating with DMSA and ALA

The usual course of action is that people first get their amalgams removed, then chelate with DMSA or DMPS for 3 months to lower mercury blood levels, and after that add ALA. 
 
But: If three or more than three months have passed since your last mercury exposure (in most cases in the form of amalgam fillings), you can start chelating with the combination of DMSA and ALA right away. 
 
Example: If you had your amalgam fillings removed two years ago but you are learning about this protocol only now, you don’t have to chelate with DMSA first. You can immediately start with a combination of DMSA and ALA or ALA alone. 
 
Practically speaking, in such a case it makes more sense to first start with just ALA to gauge one’s reaction and to see if there is a reaction at all. Then, once you have found a manageable amount of ALA for you, you can add DMSA at the same or half the dosage.
 
The ratio of ALA and DMSA is not very important for the success of the program. Ratios of around 1:1, 2:1 or 1:2 are common. 
 
When DMSA and ALA are combined, you choose the half-life of 3 hours. That way, both compounds are taken together at the same time.
 

Table 7: An example of a 72-hour round with DMSA and ALA. 

DAY 1 DAY 2 DAY 3
 12 am – DMSA and ALA 12 am – DMSA and ALA 12 am – DMSA and ALA
 3 am – DMSA and ALA 3 am – DMSA and ALA 3 am – DMSA and ALA
 6 am – DMSA and ALA 6 am – DMSA and ALA 6 am – DMSA and ALA
 9 am – DMSA and ALA 9 am – DMSA and ALA 9 am – DMSA and ALA
 12 pm – DMSA and ALA 12 pm – DMSA and ALA 12 pm – DMSA and ALA
 3 pm – DMSA and ALA 3 pm – DMSA and ALA 3 pm – DMSA and ALA
6 pm – DMSA and ALA 6 pm – DMSA and ALA 6 pm – DMSA and ALA
9 pm – DMSA and ALA 9 pm – DMSA and ALA 9 pm – DMSA and ALA

A 72-hour round consists of 24 dosages, or 8 per day: 72 hours / 3 hours intervals = 24 dosages. The exact starting time is irrelevant, it can be also 1:34 pm on any day of the week. What is important is the constant intervals of 3 hours between the single dosages. 

 

6. Chelating with DMPS and ALA

The usual course of action is that people first get their amalgams removed, then chelate with DMSA or DMPS for 3 months to lower mercury blood levels, and after that add ALA. 
 
But: If three or more than three months have passed since your last mercury exposure (in most cases in the form of amalgam fillings), you can start chelating with the combination of DMPS and ALA right away. 
 
Example: if you had your amalgam fillings removed two years ago, but you are learning about this protocol only now, you don’t have to chelate with DMPS first. You can immediately start with a combination of DMPS and ALA or ALA alone. 
 
Practically speaking, in such a case it makes more sense to first start with just ALA to gauge one’s reaction and to see if there is a reaction at all. Then, once you have a manageable dosage of ALA, you can add DMPS at the same or half the dosage.
 
The ratio of ALA and DMPS is not very important for the success of the program. Ratios of around 1:1, 2:1 or 1:2 are common. 
 
When DMPS and ALA are combined, ALA is taken every 3 hours and DMPS every 6 hours.
 

Table 8: An example of a 72-hour round with DMPS and ALA.

DAY 1 DAY 2 DAY 3
12 am – ALA 12 am – ALA 12 am – ALA
  3 am – DMPS and ALA   3 am – DMPS and ALA   3 am – DMPS and ALA
  6 am – ALA   6 am – ALA   6 am – ALA
  9 am – DMPS and ALA   9 am – DMPS and ALA   9 am – DMPS and ALA
12 pm – ALA 12 pm – ALA 12 pm – ALA
  3 pm – DMPS and ALA   3 pm – DMPS and ALA   3 pm – DMPS and ALA
  6 pm – ALA   6 pm – ALA   6 pm – ALA
  9 pm – DMPS and ALA   9 pm – DMPS and ALA   9 pm – DMPS and ALA

A 72-hour round consists of 24 ALA dosages and 12 DMPS dosages. ALA is taken every 3 hours, DMPS is taken every 6 hours. The exact starting time is irrelevant, it can be also 2:14 am on any day of the week. What is important are the constant intervals of 3 hours and 6 hours. 

 

7. Choosing and increasing dosages

A recommended starting dosage is 3 mg to 20 mg. Some may need to go as low as 1 mg. Others can start with more than 20 mg.
 
Mercury chelation results in the controlled mobilisation of one of the most dangerous neurotoxins known to men. As a consequence symptoms can worsen or new symptoms can emerge during the protocol.
 
Dosages of the chelators are chosen in a way that symptoms during chelation remain manageable. You should be able to perform daily tasks while on round. If you feel unable to function, your dosage is too high.
 
In such a case, abort the round, wait at least 3 days and then start a new round at a lower dosage.
 
Alternatively, one can shorten the interval between the dosages. This often results in a more comfortable chelation experience.
 
Example: instead of taking ALA every 3 hours, you can take it every 2.5 hours.
 
Shorter intervals are allowed, longer ones are not (except twice at night).
 
At the beginning one should proceed with caution. The goal is to find the dosage where there is a reaction but it is tolerable. Until that dosage is found, one can increase by doubling the amount with each round.
 
Never change the dosage mid-round. Always wait for a new round to start on a higher (or lower) amount.
 
Once you have found the initial dosage for you, you stay there for several months before increasing by maximum 50%.
 
Example:
 
Round 1: 3 mg ALA.
No reaction. Neither on or off round.
 
Round 2: 6 mg ALA
No reaction. Neither on or off round.
 
Round 3: 12 mg ALA
No reaction. Neither on or off round.
 
Round 4: 25 mg ALA.
A distinct but still manageable reaction: improved fatigue on day 1, worse on day 2 on round. Pronounced irritability during the break.
 
Stay on the same dosage, 25 mg ALA, during rounds 5 to 12.
 
On round 12 there is as good as no discernible reaction in symptoms.
 
Round 13: 38 mg ALA (25 mg + 50% = 38 mg)
Again, there is a distinct but manageable reaction.
 
Continue doing rounds with 38 mg until there are no more reactions. Then increase again by maximum 50%.
 
Repeat this process again and again until you reach the maximum dosage of 3 mg of ALA per kg of body weight. So if you weigh 60 kg, your maximum dosage is 180 mg ALA.
 
It can take several years to reach one’s maximum dosage. 
 

8. Dump Phase

The dump phase is a time period during mercury chelation when there is either no improvement or even a worsening of symptoms. It sets in around 2 to 4 months after starting chelation (or after amalgam removal). It shows its peak at around 6 to 9 months into chelation and can last several months.
 
Once the dump phase has passed, you’ll find that with continued chelation there will be a consistent improvement of your symptoms. The dump phase is only observed during mercury chelation. No other toxic metal shows this pattern.
 
It’s recommended that you chelate through the dump phase. Most people decide to reduce their chelator dosage during that time. 

This is an approximate illustration of what I went through during the first months of chelation. I started the AC program in September 2013, experienced an improvement in symptoms during the first 2 to 3 months, after which progress seemed to have stalled. By March/April 2014 I was doing very poorly with new, troubling symptoms setting in. I was feeling so bad that I had stopped chelating during that time. This was, unbeknownst to me at that time, the peak of the dump phase. Dr. Cutler maintains that the dump phase is something that most people go through while detoxing mercury. 

 

9. Supplements 

Dr. Andrew Cutler called the following supplements the “Core Four”. They are the most important supplements to take during chelation. Minerals and vitamins speed up recovery and allow the body to fix the damage mercury has caused. 

1. Vitamin C*, 2 to 5 grams per day. Or more if bowel tolerance allows. 

2. Magnesium, up to 1,000 mg per day. Take it in smaller dosages of 150 to 200 mg with meals and before bed time. 

3. Zinc, 25 to 50 mg per day

4. Vitamin E, up to 1,000 IE per day. 

* A word of caution about Vitamin C. This is a personal note of mine and is a strict deviation from the Cutler protocol. I have successfully chelated without supplementing with Vitamin C (or zinc or Vitamin E). The reason I did that was because I reacted badly to it and to most other supplements. As I later found out this was due to oxalates. Dr. Cutler maintains that the idea of oxalates causing problems is nonsense. After visits to ER and numerous doctors, I had to find out that he was dead wrong about it. Vitamin C can convert to oxalates in the body. If there are significant oxalate stores present, taking Vitamin C in large dosages can be highly detrimental to one’s health, even without kidney problems.  

There are also many other supplements which are recommended. The most popular ones are Adrenal Cortex and B Vitamins. According to Dr. Cutler anything that will lessen symptoms and make chelation more bearable should be taken. This includes pharmaceuticals and even psychotropic drugs. 

 

10. My experience with the Andrew Cutler Chelation

From September 2013 until February 2018, I chelated with the Andrew Cutler protocol in order to remedy a chronic mercury poisoning. Except for a 1.5 month break in March/April 2014, I chelated continuously during that time, only taking the minimum 3-day breaks in between rounds. 

During that period I have performed over 211 rounds from 3 days to 78 days in length. I have reached dosages of up to 400 mg ALA. In order to be officially finished, I would need to chelate for another 30 days. But I consider myself as basically being mercury-free at this point.

At the end of 2014 I have completed a one-on-one online / phone course with Dr. Andrew Cutler.  After having successfully passed the exam, I was issued a certificate.

This, plus my 4 year ACC experience, makes me a certified Cutler expert. 

11. What does mercury chelation have to do with ozone therapy? 

Why am I writing about chelation at all here? Isn’t this an ozone website?

I am of the opinion that a large number of people who do ozone treatments for infections like Lyme or inflammatory conditions like MS, really may be dealing with a misdiagnosed mercury poisoning. Ozone is not able to remove mercury. 

Unless mercury is detoxed properly, antibiotics or even ozone therapy, may not work as intended.

Hence, getting rid of this most insidious of toxins is of paramount importance on the way to health.

Although I had to find out that Andrew Cutler was wrong about a number of things, the most important one being oxalates (more on that in a future article), I do believe that when it comes to mercury removal his approach is the only scientifically sound and is the safest way to remove the toxic metal from deep stores like brain, liver, or adrenals.

 

Recommended reading: “Amalgam Illness”, Andrew Hall Cutler, PhD

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11 Comments

  1. Lawrence Liodice
    Lawrence Liodice on May 18, 2018 at 12:36 pm

    Hi Paola,
    Congrats on completing the Cutler program. I have completed 150 rounds and feeling a lot better but I am not done.
    I thought the ALA dose at completion was 200mg not 400mg according to Dr Cutler. Is there a reason you took the max dose to 400mg?
    Best,
    Larry

    Reply
    • paola d
      paola d on May 18, 2018 at 1:49 pm

      Hi Lawrence,
      according to Cutler one has reached one’s maximum dosage at 3 mg x body weight in kg.
      According to this my maximum dosage was around 220 mg ALA.
      But Cutler was also once asked if one can go above that. There was one person who asked him if it was ok to go as high as 600 mg and Cutler said yes. So, I decided to push it, too, and that is why I went as high as 400 mg. But this was just because I wanted to see how high I can go and to speed things up.

      Best,

    • GREG THOMPSON
      GREG THOMPSON on June 11, 2018 at 8:06 pm

      Thank you for thorough review and your personal experience. I am curious to find out what else Dr.Cutler was wrong about?

    • paola d
      paola d on June 13, 2018 at 10:37 pm

      Hi Greg,

      the oxalate part has actually quite wide ranging consequences.
      I am planning on writing about this in my next articles.

      Best,

  2. Pavol Sebo
    Pavol Sebo on June 13, 2018 at 7:30 am

    Hello Paola,

    I congratulate you from my whole heart that you made it so far with the mercury chelation! I can only hardly imagine, how you feel after all that poison is out of your system.

    I am Pavol from Slovakia with CML leukemia. We communicated a bit in the past…

    I had several 10-20-40 pass treatments ad Dr. Lahodny’s last year. First it helped tremendously, but after around 4 times the improvements started to become marginal. Then the Dr. had the idea of trying his chelation infusion of 2000mg EDTA and 100mg DMSA and when I felt strong and immediate improvement in the remaining tinnitus I was having I understood that it was all the time about heavy metal toxicity. . .

    I started in august with EDTA, took that as suppositories till november and it helped me greatly and improved my wellbeing very much, however I felt, it wasn’t moving a lot of mercury compared to other toxins. So I started with DMPS in november. It went well for some weeks with 4x5mg – 4x10mg and even 4x15mg a day and I felt it was working. Then my body became a kind of overburdened or I guess the autonome detox pathways started working, as white fat spots started going out through my skin and I finally, after long years, started being able to sweat even at low intensity trainings. My sweat also started to smell bad :>

    But it didn’t stop at that. My heartbeat reacted with palpitations and the whole body got irritated badly and I wasn’t able to sleep, when I tried to come back to the DMPS rounds. I just wasn’t able to tolerate not even 4x4mg of DMPS daily and even needed to give the body several weeks of rest phases and now I settled on around 1-2mg of DMPS 4times daily, as my system doesn’t tolerate more. I figured out from forums and Amalgam Illness that I probably got into the dump phase…

    Yet, here is my question. I want to ask you, because I didn’t find it anywhere in Cutler’s work. What is your proven by experience and working intestine mercury absorbent of choice? The thing is that over the course of oral chelation I experienced that a lot of the mercury that doesn’t leave the body with urine, ends up in the gut. And when I take something that I used before to kill candida colonies in the past and I had no reactions to it, in the last months it caused dramatic worsening of my condition as I felt that anything candida killing causes the newly formed colonies that grew and bound up the unexpelled mercury to burst up and release large amounts of mercury into the blood that a during the time before DMPS just werent’there. I know as a fact that before I had my bowels in good shape as I was eating (and still am) a ketogenic diet, I drank a lot of water kefir and I had no bad reactions to for instance turpentine with castor oil which I used for sporadic bowel flushes… But now, even when I tried the stupid chlorella, dr. Klinghard pushes so much, I needed a whole week to recover from the damage the mobilized mercury caused.

    I normally use a mix of bentonite, zeolite or activated charcoal with psyllium, but I don’t have the impression that it helps much. Especially, when I add diatomaceous earth I feel, that it kills some candida and releases some by it bound mercury as I feel a low level of toxicity a few hours later.

    I will never touch anything silica based again and don’t even think about NDF as not only chlorella caused a redistribution burst, but stinging nettle extract as well.

    Currently I am in a resting phase after the last DMPS round where I was able to take 4x1mg over a few days until my palpitations started again and I had to go off. I also need much longer breaks now for me to be able to tolerate circulating mercury again. The white fat spots and the bad smell of the sweat also nicely indicate how much the body is pushing currently out. What bothers me is mostly the unsolved gut mercury cumulation :<

    I will greatly appreciate any input on gut mercury brushing from your side.

    With thanks and regards,
    Pavol

    Reply
    • paola d
      paola d on June 13, 2018 at 10:36 pm

      Hi Pavol,

      according to Dr. Cutler the reabsorption of mercury through the gut is so low, that it is not clinically relevant.

      But I don’t quite understand what you mean with things like “4 x 4mg”. Chelators need to be taken according to a very strict schedule in rounds of at least 63 h duration. If this is not done, one risks redistribution of mercury and a worsening of the condition.

      I also don’t understand this: “10-20-40 pass treatments”.

      According to Dr. Cutler killing off of candida does not lead to the release of mercury either.

      I hope this helps.

      Best,

  3. Pavol Sebo
    Pavol Sebo on June 14, 2018 at 10:03 am

    Hello Paola.

    Thank you for the answer.

    I started with regular 10-pass treatments, which means alltogether 10x200ml of blood was ozonated. Then we went even for 20-pass resulting in alltogether 4L of blood being ozonated. 1 time we tried even 8L in one session, but there was no noticeable gain compared to the 4L procedure. The greatest oxygenizing and leukocyte reducing effect was achieved with the 4L doses. However, it was always just a symptom management tool and not a cause removing/solving process. Yet I am happy, that I experienced the causal role of heavy metals through that experience and could finally start removing the real cause of my leukemia with chelation.

    4x4mg I meant that over the chelation round of at least 3 days I was taking 4mg of DMPS every 6 hours. Even if now I was able to tolerate only 1mg doses and even then, after two days of taking, the palpitations and inability to fall asleep came.

    Regarding candida. This is another weakness or absence of Cutler’s experience including leaky gut. It is scientifically proven, that Candida Albicans is the main organism, that develops in tissues, especially the gut, where mercury toxicity is present. It lives to bind the mercury, store it in it’s membranes and it makes itself immune to the immune system. Over 2016-2017 when I was rebuilding my gut with butyrate, water kefir and a ton of candida colonies went out of me, I experienced only mild mercury toxicity released from the candida die off. I was also drinking lots of the Schweitzer formula which is a genious pathogen killer for blood penetration, after I had my gut in good shape and no candida was leaving and no toxicity occured either.

    However after a few months on DMPS, where supposedly 80% of the mercury should be leaving the body through the kidneys in urine and the rest gets processed by the liver and should leave through the gut, when using just a small dose of the Schweitzer formula, I experienced a tremendous outburst in circulating mercury toxicity even if I was on OFF round for around 3 weeks already. It was days of feeling warmth and hottness all over my body and my cheeks, days of strong palpitations and days of headache. It was 100% for sure released mercury from the gut, where some new candida grew as a means of binding the newly settled mercury, which wasn’t previously there.

    It took me almost two months to recover from that single outburst. Thatswhy I am searching for a proven and working absorbent/binder to take care of the secondary effects of mercury chelation, because the reabsorbtion through the gut is a real and painfull thing :< Maybe, in healthy gut it is absorbed little, but as it causes all of the degenerative diseases of the intestine and the leakage, one quickly sees, that the topic is much more complex than Cutler presented.

    http://amalgam.org/education/scientific-evidenceresearch/mercury-food-intolerances-connections-ulcerative-colitis-ibs-crohns-skin-conditions/

    With kind regards,

    Pavol

    Reply
    • Veronika
      Veronika on July 26, 2018 at 6:50 pm

      Hi Pavol,
      please send me an email on nikinicolle@seznam.cz, I´m from the Czech republic, we can discuss this issues more in our native language 🙂

  4. Richard
    Richard on July 29, 2018 at 5:11 pm

    How many years ago did dentists stop using amalgams in fillings?

    Reply
    • paola d
      paola d on August 1, 2018 at 10:19 pm

      Hi Richard,
      amalgam fillings are still legally used in most countries.
      Best,

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