Monday, March 18, 2019

Calling all Ehlers-Danlos Syndrome Sufferers: A New Option

The young teenage boy who sat with his mother and grandmother across from me in my treatment room was a mystery case to every doctor. They had traveled from another state to my clinic due to our focus on rare and "incurable" illness.

As I took an extensive case history, the boy would periodically vomit a bit into a trash can, one of the many symptoms he wanted fixed. All day, everyday, he would vomit a little or a lot, up to 42 times a day. Associated with this symptom was severe abdominal pain, causing him to cross his arm over his stomach and rock back and forth in misery.

All of the conventional medical tests from his previous doctors had ruled out all the usual causes, but had found nothing wrong.

Because of the fact that every test had come back inconclusive for anything, a normal finding in many of the patients we see, I took care to ask them for every possible oddity about his situation. About a half hour into the questioning the grandmother exclaimed, "Oh, you should show the doctor how you can stick out your tongue and touch your nose!"  The boy obligingly proceeded to not just touch his tongue to his nose, but laid his tongue on top of his nose! Omigosh, I said. The grandmother, seeing I was surprised told him to show me his other oddity, the ability to turn his head and look behind him. He proceeded to shockingly turn his head almost to the point that it appeared his head was on backwards.

This was the first, and best clue to the case. Up to this point his previous doctors were only focused on various possible infections, but to me it was a fantastic clue that I continued to pursue. Upon asking him, he proceeded to show me that he could reverse his elbows, wrist, and bend his thumb back to his wrist. I had it! From a clinical diagnosis, he likely had Ehlers-Danlos Syndrome, a supposedly "rare" condition that surprisingly affects millions worldwide. 

Armed with the knowledge of what I was dealing with, the treatment plan was adapted to his unique situation and for the next three weeks of daily treatments his abdominal pain and vomiting completely resolved. 

Almost ten years have passed since I treated that case of EDS and I have learned much more and developed much deeper treatments to help people with EDS symptoms, that stands a good chance of dramatically improving their quality of life, not to mention the longevity of their life, since people with EDS often have a shorter lifespan. 

A Call For Those Suffering from EDS
It is because of these new discoveries and innovations over the years that I have decided to do a Quality of Life Case Review of people with EDS who come to the Hansa Center for Optimum Health for our 3 week, all-inclusive program of care. This program is designed to provide you with the maximum applied effort to enable your body to repair or improve your functional biochemistry and to improve your muscle and ligament tone, not to mention optimizing heart function. This program of care is very comprehensive. The all-inclusive package is designed to accomplish a few things:
  1. To enable the doctors to take the time they need to really dig deep into your case without rushing. 
  2. To be able to combine all the best treatments and therapies in a synergistic way to enable the greatest potential for deep healing. Patients are usually in the clinic for 4-6 hours a day, Monday through Friday for the 3-week program of care.
  3. To eliminate the fear of running up a huge bill for all the various treatments and therapies.
  4. The program is designed so that the treatments and therapies greatly exceed the package price, so that you receive our maximum applied effort, as opposed to the maximum that insurance will cover. (We do not take insurance as our services are not considered "usual and customary" by insurance companies due to the large amounts of time that doctors spend with patients in each visit.)
What Needs to Be Addressed:

It should be understood that if EDS is simply a genetic issue then everyone would have the same symptoms. In reality EDS affects everyone differently, some just have a few mild symptoms, while others literally die from their symptoms. This tells us that given the most optimum functional biochemical and structural support the rapid decline in a person's body could be dramatically improved and possibly stopped. 

As it stands, very few doctors know anything more than to treat the pain and inflammation with high power prescriptions, and then send patients to physiotherapy...forever. We are not striving to help people with EDS because it is easy, but because of the profound suffering that we want to help relieve. The physiotherapy is often not possible for many people due to the extremely unstable nature of their joints, not to mention the fact that POTS (postural orthostatic tachycardia) prevents many from simply standing up! Something must be done to advance the knowledge of how to stablize things.

It is obvious that someone needs to address the Zebra in the room, and go deeper than symptom suppression. That is why we have brought all the best treatment ideas under one roof to address the totality of everything that is going wrong, not just your symptoms.

Our Approach

Believe it or not all of this must be assessed and addressed as needed within the 3 week program.

Keep in mind, the following are not necessarily in the order of treatment strategy that our doctors will employ from your first treatment to the last of treatment of your package.
  •  A key issue in EDS arises from the liver. The liver is supposed to produce Ceruloplasmin, the key transporter of copper to the body. Copper is required to produce Lysyl Oxidase. Lysyl Oxidase is deficient or absent in EDS. Primary liver support and strategic supplemental support of the body's production of Ceruloplasmin is paramount to any hope of improving EDS. (Ceruloplasmin blood tests cannot determine if it is activated ceruloplasmin or inactivated. Based on the overwhelming clinical evidence the CP is the inactivated form in EDS.)
  • Balance the ratio of copper to iron in the muscles, ligaments, and organs. Each ceruloplasmin molecule carries six atoms of copper into the body so that the body can manufacture all of the key copper-dependent enzymes that are deficient in EDS, such as:
    • Ferroxidase: a deficiency of this causes the tissues of the brain, muscles, and organs to overload with iron oxide to toxic levels causing all manner of problems. The overload of the tissues with this toxic form of iron is present in all EDS and is a major issue.
    • Lysyl Oxidate: an enzyme manufactured in the body from Lysine and hydroxylysine which that requires copper donated from ceruloplasmin in order to make healthy collagen through the cross-linking of collagen and elastin, the key problem areas in EDS.
    • Cytochrome C Oxidase: this copper-enzyme deficiency causes decreased energy in the muscles, neurons, and ultimately can cause demyelination of the nerves. So you can see that working out in physiotherapy is often a diminishing return since you need this enzyme to make exercise muscle gains.
    • Ascorbate Oxidase: a deficiency causes demineralization of the bones.
    • Dopamine-beta-Hydroxylase: deficiency causes reduced production of neurotransmitters and catecholamines, causing neurologic effects, temperature regulation problems, and vision problems.
    • Diamine Oxidase: (DAO) deficiency sets you up for histamine reactions to various foods in your diet. Without this enzyme you cannot break down histamine. Histamine blocks the production of ceruloplasmin (CP), creating a vicious cycle of problems all over the body because without the CP, copper cannot get transported from the liver to the many enzymes that require copper in order to work!
    • Superoxide Dismutase: another copper-dependent enzyme that is needed to protect the body from oxygen free radicals that progressively damage the tissues.
    • There are many others that could be listed, but this gives you an idea of how important repairing the body's ability to produce CP really is if any hope of improvement can be achieved.
  • Once activated ceruloplasmin (CP) production is restored, the circulating CP will begin to cause the toxic copper and toxic iron overload in the tissues to be liberated from within the connective tissues and from within the cells all over the body. Treatments and therapies must help the body quickly eliminate this liberated iron out of the body. Iron and copper are definitely needed by the body, but they should not be stored inside the cells to toxic levels. Your iron and copper blood tests are only showing what amount of iron is circulating in the blood, not what is stuck in the tissues. 
  • Dietary changes are important. Eliminate histamine-rich foods. Histamine naturally occurs in various foods, such as fermented foods, preserved meats, tomato, soy sauce, and much more. Histamine blocks the production of ceruloplasmin, therefore a low histamine diet is necessary until the body's functional biochemistry is repaired.
  • Dietary sources of iron, such as iron-enriched breads, beef, and iron supplements must be stopped. Remember, if you are anemic and have low iron levels, in EDS it is most often not truly an iron deficiency, it is a iron utilization problem, since all the iron you are taking is rapidly and inappropriately getting stored in the cells and tissues, due to the lack of the iron-regulating nature of ceruloplasmin. Once the ceruloplasmin is restored, the iron levels will once again return to normal in your blood. By the way, the much maligned H. Pylori bacteria that often wreak havoc on the stomach and small intestines actually is striving to help the body by blocking the absorption of more iron. Once the tissue iron toxicity issues and CP issues are resolved, the H. Pylori infection may fade into the microbial collective and cause no more problems.
  • CP converts the highly toxic ferrous iron into its non-toxic ferric iron form.
  • Mast cells, histamine (released by mast cells), and pro-inflammatory substances, such as PD2 which are also released inappropriately by mast cells, must be addressed at each step of the biochemical pathway to determine what the body needs in order for each metabolic step to function correctly. Without assessing the mast cell issues, there is no hope of getting the ceruloplasmin to work. Sensitivities will be addressed using tested Low-Dose Immunotherapy, Low-Dose Antigen Therapy, as well as other bioenergetic therapies.
  • There is often a lack of bio-available copper, which I mentioned is directly causing the iron overload and the enzyme deficiencies, that cause the muscle, ligament, organ disturbances seen in EDS. The body often has plenty of copper, but the copper is bound up in unusable forms, creating an essential deficiency, in other words it is not bio-available. The body requires nano-particle size minerals in order to absorb them. Nano-particle copper is most often created by plants, such as organic alfalfa, and organic dried apples, dried pears, and in organically fed animals in which case their liver is highest in copper. Of course liver also is a source of iron, however you will see later in this list of goals that the liver itself is needed and circulating iron is actually usually low to normal so the iron from the liver will often still benefit the body. The key here is also to liberate the stuck copper from the tissues so that it can be used. In doing so the CP will liberate the stuck, and toxic overload of iron as well. Supporting the kidneys with strategic remedies and therapies is important since the kidneys are the key mineral-regulating organs of the body.
  • In those with heart problems from their EDS, it is often a combination of things occurring. First the CP is cardioprotective, and without it the heart muscle and valves become essentially floppy and weak, like all of the other muscles of the body. The copper overload from the breakdown in the body's ability to attach it to the ceruloplasmin can cause arrhythmia. It also can cause heart conduction disturbances. Copper is also very electrically conductive, which is why we use it in the electrical cords that you plug into your house electrical outlets. Without the CP delivering copper to the enzymes and those enzymes working in the heart and muscles, there can be not good electrical conduction in the heart. 
  • Synchronization of the brain and the heart is dramatically poor in EDS. Simply correcting the CP activation and biochemical pathways is not enough to get the dual-processors of your body to synchronize correctly. My innovation, NeuroCardial Synchronization, is designed to correct the synchronization of the heart and brain, and often corrects the tone of the heart and valves, as well as the rhythm of the beats and the maintaining of normal blood circulation. POTS (Postural Orthostatic Tachycardia Syndrome) often resolves in this process.
  • All of the nutitional building blocks to healthy production of all of this is needed in order to now produce the necessary and sustained amounts of CP. The body in a CP-deficient state is depleted in Magnesium, food-form Vitamin E, A, and C (not Ascorbic Acid which is the most common synthetic form of Vitamin C that destroys the ferroxidase activity of ceruloplasmin!), and Omega 3 fatty acid. Cod liver oil is a great source of these vitamins and fatty acid. Strategic liver support is needed to improve its overall function. Blessed Thistle capsules can be beneficial, but a key product is freeze-dried, organic or grass-fed, no antibiotic, no hormones beef liver. Dandelion greens, and roots if you can get them from a clean source, can be highly beneficial for the liver. In our protocols we have many other products that we can use to test your body to see which is best for your particular liver issues.
  • Glyphosate from Round-Up herbicides is known to chelate (deplete) manganese, another key mineral related to the liver functioning in that it is required to make glutathione which is necessary for liver detoxification. Glyphosate also chelates copper from the soil, from the plants, and from our body. Again, without copper you cannot make activated ceruloplasmin. Without ceruloplasmin delivering its six atoms of copper to the body you cannot regulate the iron, nor can your body manufacture the enzymes necessary to make Lysyl oxidase and all the other enzymes missing in EDS. Without these enzymes your muscles, ligaments, and connective tissues become floppy, elastic, and weak.
  • Non-GMO foods are not safe when considering their amount of glyphosate, since unlike organic foods, non-GMO is still drenched with Round-Up herbicides. Eliminating all foods that are not organic is critical...forever. Glyphosate from RoundUp binds to the same receptors as the highly needed amino-acid, glycine. Detoxing the Glyphosate is highly important, while at the same time supplementing the body with glycine. As you can tell all of this protocol must be strategically applied in the right order and with the right timing.
  • An interesting finding we have seen in our clinic is that some of the ligament laxity improves as we improve the light-metabolism of the body. Light of various wavelengths is now seen as a nutrient to the body. Indeed it is light that adds energetic bonds to molecules in the body to get from one molecule to the next step in its pathway, in combination with the appropriate enzyme. Biophoton, light generated in the body, by the body, is the glue that holds the electrons in their orbit around the nucleus of the atoms. Biophotons can be seen as the software that is playing or projecting through the hardware of the DNA and RNA to create the correct molecules needed to maintain our structure and function. To not address problems in the light metabolism of the body is to miss a critical component, since everything we are doing is striving to restore longterm function without having to continually prop up the body with ever failing bandaids. Our innovative therapy, NeuroPhotonic Therapy addresses this light metabolism and has resulted in same day improvements in the decreased range of motion that is possible in a previously hyper-mobile joint, something unheard of with any other therapy.
  • Total body fascia release therapy is important to stop the body from essentially leaking energy out into the atmosphere. You need to be able to hold your energy within your body. When the fascia membrane is stuck, energy bleeds out of the body and the body is like an old cell phone battery that wont hold a charge anymore. The heart is the electromagnetic generator of the body, generating over 5000x more energy that the entire nervous system. The combination of copper-dependent enzymes, such as Cytochrome C Oxidase, which is responsible for the heart muscle and other muscles ability to make energy, and the energy leaking out anyway through the multiple fascia restrictions make it nearly impossible to have enough energy just to do the most basic functions inside the body and in your daily life. 
  • Optimization of the biochemical Heme pathway must be addressed in order to produce the detoxifying Cytochrome P450 and Cytochrome A and to maintain good blood formation and oxygenation of the tissues.
  • Psychiatric disturbances occur in EDS due to the CP, iron, and copper issues. Symptoms often include depression, neurotic behaviors, disorganization of personality, and occasionally intellectual deterioration. Various neurofeedback methods are applied to help repattern the brain waves to get out of the electrochemical loop that EDS caused.
  • Not least of all, the various forms of collagen, types I-V need to be assessed for what the body needs to enable correcting the formation and production of healthy collagen. It goes without saying that until proper copper metabolism is restored, along with the activation of ceruloplasmin, that the formation of normal collagen and elastin cannot occur. Conversely, the stage is set for healthy collagen and elastin to be formed when all of these issues have been successfully addressed. 
  • Genetics are the blueprint, however the blueprint is the hardware, in computer terms. However the software is able to bipass the DNA and can still encode the RNA for the production of what the body needs. Surrounding the DNA are 4 million epigenetic switches that can be flipped to also create the necessary components of the body. Our system of testing called Fractal Frequency Modulation (FrFM) is designed to cause a sift all the way from the macro (larger tissues) to the micro (smallest energetic components), since you truly cannot shift one without necessarily shifting the other. By changing form you change function. EDS is a fractal incoherence and FrFM strives to restore fractal coherence all the way down to the software. 
  • If the desired effect is achieved with the above, then and indeed throughout this whole process the structural alignment and entire musculoskeletal system alignment and function must be addressed and maintained. This is achieved through non-rotational, non-force, aligning of the joint complexes. 
  • A wide range of supportive therapies are applied, such as lymphatic drainage therapy (ST8), Therapeutic massage therapy with various healing ointments on oils, BEMER mat therapy to increase microcirculation, PEMF to essentially pump the cells to increase cell detoxification and reduce pain, Biomat to increase the liquidity of the gelatinous dysfunction lymph fluid. Low-level laser applied at specific frequencies to enhance tissue/cellular performance.
  • Lastly, time is needed to watch how the body handles each day's treatments and therapies. Daily, one-hour doctor visits allow adjustments to what we are doing, based on what road blocks pop up in the body's biochemical pathways.

I hope you can see a logical plan throughout this outline. It is a lot, but keep in mind that it often takes more words to describe the what's and why's of the protocol than it actually takes in application in the treatment room.

We are aware that not many other doctors are researching real solutions for EDS. We can make no success guarantees, any more than any other doctors, however the above shows you we are doing quite a bit more than your doctor is likely doing. This is a completely non-invasive, non-pharmaceutical approach.

When what you are doing is intolerable, and doing nothing is not an option, doing something different may be the best plan.

We hope to speak to you soon to discuss how we can dramatically increase your quality and longevity of life. Share

Friday, March 1, 2019

Histamine and Mast Cells: Issues and Solutions

By Dr. David A. Jernigan

Do you envy people who can eat anything they want, wear perfume or cologne, and are exposed to daily scents without reacting? Antihistamines are a crutch that can get you some relief, however they do not fix anything. The luxury of having the ability to think clearly, eat anything, be pain free, and be essentially symptom free without having to take something is impossible, you may be thinking.  I am here to tell you it is now possible, but like most complicated illnesses it requires sensitive testing and treatments tailored to the specific biochemical issues that are blocked in your unique body. 

Good luck finding a doctor who really understands much beyond simple first and second line pharmaceutical answers that often don't work for many people. 
  
Everyone has heard of allergies, histamine, and especially antihistamines, but less people have heard of mast cell activation, mastocytosis, and histamine intolerance. Even fewer have heard of genetic SNP mutations that are jamming up the biochemical pathways. If you have researched mast cells and mutations, then you probably have been surfing the internet looking for deeper answers because of your hypersensitivities...not just physically, but emotionally and mentally!  
Two of my family members were born with this problem and after 25 years of treating some of the toughest cases and researching real solutions, I have learned much about the regulation of histamine and the biochemistry of these pathways. I have a passion for helping people move way beyond just symptom relief. My wife has been my "muse." She had extremely high blood histamine levels, causing severe issues for years that kept her  isolated from the world!  I researched endlessly to find new solutions, trying one treatment after another until finally developing a new way to treat it. Since then, all of her symptoms have resolved. At one point she only had 6 foods she could eat. Now she can eat anything and the world is no longer the threat it used to be! 

If you are reading this, you likely know that histamine intolerance cannot be corrected with simple antihistamine drugs or by taking DAO supplements. These can help the symptoms, but are just masking or bypassing the real problems and do not offer lasting correction.

Like so many other serious illnesses, there is no at-home protocol and you must be tested and treated in the clinic. Trust me, it would be way easier and more lucrative for me to say, "Buy my amazing anti-histamine remedy" like so many other internet doctors. 

What I developed, that finally worked, is a new concept in all of medicine called Fractal Frequency Modulation™ (FRFM). The theory behind FRFM detects fractal asymmetries down to the level of the genes, enabling our doctors to target strategic treatments to the exact issue, providing the body with the building blocks and restorative frequency information to restore fractal symmetry, not just physically in the tissues, but also in the body's electromagnetic regulatory system as well. 

The picture attached to this article is medical science's latest understanding of the true fractal nature and complexity of human DNA. From the organs and tissues to the software that runs the body, it all can be seen as physical and energetic fractals. Health is the manifestation of fractal symmetry throughout the body. Disease by any name is the result of fractal asymmetry.

FRFM has now helped many people. Just last week, a mother and son, who had already traveled several times from another state to the Hansa Center,  for the best treatments we could offer at the time, became symptom free this week, using the new abilities of FRFM! Their severe headaches, joint and muscle pain all went away...not from masking the symptoms, but from finally opening up the blocked metabolic pathways, restoring fractal symmetry.

The only way to address the complex illnesses of this day and age, is to correct the many possible combinations of problems, and provide the body with the ability to finally start producing the many enzymes involved in methylation, neurotransmitter function, cytokines, and histamine regulation. 

This article is quite extensive, but suffice it to say that histamine related problems can create an incredible range of symptoms. It might be one chronic symptom or many symptoms. If you would like to be tested and treated at the Hansa Center for Optimum Health, in Wichita, KS, contact us at the number listed at the bottom of this article. Healing is most often a process, not an event. 

Your unique issues can be likened to a complex combination lock on a bank vault door, behind which your health is being locked up. To make things tougher the combination is changed dynamically in response to incorrect attempts to unlock it, getting more complicated with each incorrect entry. In my mind, FRFM seems to access the body's computer system to help the doctor stop guessing, stop doing incorrect treatments, and progressively, over daily treatments for 1-3 weeks, get the vault door to your health to open. 

Fractal Fequency Modulation can be used on any illness, not just for the issues discussed here.

You don't need to read this exhaustive article on the intricacies of histamine-related issues if you already know you want to come get started with FRFM, but if that option is not available for you, then reading about avoiding the known aggravating factors and the possible beneficial remedies itemized in this article, will be of definite benefit.

Difference and Similarities of Histamine Issues

Mast Cell Activation Syndrome, Histamine Intolerance, and Mastocytosis all have unique causes and yet share many of the same symptoms. Mast cells are found in connective tissue, containing small granules (small little packets) that are rich in histamine.  The most well known is histamine, but others include leukotrienes (which also play a role in allergies), serotonin, ATP (your body’s primary energy currency), inflammatory cytokines such as TNF-alpha and interleukin-4, reactive oxygen species (like H2O2, which help kill off foreign invaders), and enzymes like tryptase.
Mast cells carry all these compounds around in the bloodstream, selectively releasing their contents when triggered. Triggers include binding with two or more IgE molecules (the “hypersensitivity” immunoglobulin, characteristic of true allergies), physical injury, or pathogenic microbes. 

When mast cells release all their contents at once, that’s called anaphylaxis, and it can be life-threatening.

Mast Cell Diseases

Histamine Intolerance is when a person cannot efficiently break down histamine from the body, as well as naturally occurring histamine contained in various foods. Histamine intolerance can also involve deficiencies of key enzymes normally produced by the body, such as Diamine Oxidase and Histamine N-Methyl Transferase. This can also be complicated by various genetic mutations.
Mastocytosis is when a person has too many mast cells due to genetic mutations. This can be cutaneous (skin only—also called urticaria pigmentosa) or systemic (in other forms of connective tissue also, especially the stomach and intestinal linings). Cutaneous mastocytosis is diagnosed by skin biopsy, while systemic mastocytosis is diagnosed via bone marrow biopsy.
Mast Cell Activation Syndrome (MCAS) looks very similar to mastocytosis, but in this case the person has a normal number of mast cells. Their mast cells are just hyper-responsive, meaning they release their contents with very little stimulus.

Symptoms and Testing for MCAS

Symptoms common to MCAS include itchiness, easy bruising, lightheadedness, diarrhea, intestinal cramping, nausea and vomiting, brain fog, headaches and migraines, fatigue, food and chemical sensitivities. All symptoms worsen in response to certain triggers, different for each patient, but they tend to be things like high histamine foods, chemical exposure, hormone fluctuations (like before menses), exertion, temperature changes, and stress. Sometimes the triggers are the fillers or additives in medications.
MCAS is determined by meeting three criteria: 1) presenting with the symptoms above, without a diagnosis of systemic mastocytosis or a previous episode of anaphylaxis, 2) increase in serum tryptase (one of the enzymes contained in mast cells—it should be in the cells, not in the bloodstream), or increase in other mast cell mediators like histamine; and 3) improvement with treatment with mast cell stabilizers. (mentioned below) 

Now we can bypass the weeks of waiting for lab tests to come back, and apply the powerful FFM testing which is all done inside each office visit.

Causes and Associations of MCAS

MCAS can show up as a concomitant condition with POTS, with Lyme, and with CIRS (Chronic Inflammatory Response Syndrome), a biotoxin-related illness, often caused by mold exposure. I also often see symptoms consistent with MCAS associated with multiple chemical sensitivity.
Melanocyte-stimulating hormone (MSH), usually low after exposure to water-damaged buildings, helps to modulate the allergenic immune response when levels are adequate and even causes mast cells to undergo apoptosis, or programmed cell death. The lack of sufficient MSH and histamine's influence on inflammation, in the presence of CIRS, may be part of the reason why CIRS and MCAS are related.

Treatments for MCAS

I am not a fan of avoidance diets, preferring rather to help the body fix the problem. Of course, until you get the root issues fixed, avoiding known triggers is a must! 

In addition to a low-histamine diet, (see below) there are both pharmaceutical and natural approaches. Pharmaceuticals include anti-histamines and anti-leukotrienes, as well as mast cell stabilizers. Natural mast cell stabilizers include quercetin and vitamin C. All of these options only "manage" the symptoms.

At the Hansa Center for Optimum Health, our doctors can do sensitive testing of your body  using Fractal Frequency Modulation testing using the actual human recombinant enzymes, Histamine N-methyl transferase, MAO-A and B, MTHFR, Aldehyde Dehydrogenase, Diamine oxidase, and others in the metabolism of histamine and inflammatory pathways via Fractal Frequency Modulation to work to enable the restoration of your body's ability to produce these enzymes or help the body balance them. These tests can identify unique tailored treatments  that can work each biochemical step on the pathways by which histamine gets out of the body. 

I highly suggest genetic testing, such as 23andMe to determine potential problems with these pathways, however it is not necessary to have this if you come for FRFM testing and treatment.
Of course, if MCAS is secondary to biotoxin exposure or Multiple Chemical Sensitivity, the offending chemicals must be removed from your life. The real treatment is detoxification and addressing the causes. FRFM is how this is addressed by the doctors at the Hansa Center for Optimum Health.


Histamine Intolerance Syndrome

There are not many issues that can cause so many problems in virtually every area of the body than Histamine Intolerance (HIT). HIT can be caused by all of the same issues in various degrees as listed above regarding MCAS, especially with the deficiency of the body's production of the primary enzymes.

HIT is a specialty of its own, since there is so much to know. The following are just the bullet points outlining everything you would want to know about HIT.

Histamine Intolerance has been called a "Pseudo-Allergy," because many of its symptoms appear to be allergies when in fact they are not truly IgE-mediated, Type-1 hypersensitivity reactions typically seen in those suffering with allergies.

It is likely that some level of histamine intolerance is aggravating the condition of any person suffering from the many chronic, degenerative or inflammatory illnesses. Without our BRS testing to help guide our doctors, it would be very difficult to navigate a person to resolution. Thankfully we can often rapidly find and address many of the possible causes, though it is definitely a lengthy process to dig deep enough to figure out all the various things that have created this systemic issue and how to then facilitate the body's restoration of how it handles histamine.

This article will also provide you with the information of things you need to avoid in your diet, as well as medications, and even natural supplements that might be promoting the overproduction of histamine.

Before you say, "This isn't my problem" please read this article thoroughly and possibly print it out for your doctor so that they can try and help you.



What is the difference between Allergies and Histamine Intolerance?

• Allergies are an IgE mediated, histamine response to an allergen, i.e., pollen or cat dander.

Histamine Intolerance (HIT) is a toxic response by the body due to the excessive accumulation of endogenous or exogenous histamine from an inability of the body to efficiently breakdown histamine and hypersensitivity of cell antigen receptors.



Histamine Intolerance is caused by:

– The Over production of Histamine

– The decreased ability of the body to breakdown histamine

– Decreased Diamine Oxidase (DAO) enzyme production in the body

– Histamine is broken down by oxidative deamination by DAO (former name: histaminase)

–Decreased Histamine N-Methyl Transferase (HNMT) enzyme production in the body which is needed to breakdown histamine.

–Histamine is broken down by ring methylation as a result of histamine-N-methyltransferase (HNMT)

See how many systems and symptoms can be caused by HIT




Symptoms of Histamine Intolerance (HIT)

• Histamine serves various functions in our body. This is why histaminosis may trigger a wide range of symptoms, affecting different organ systems.

• People suffering from HIT may display highly diverse symptoms. Every person has individual weak spots, which may be afflicted earlier than other parts in the body. Sufferers may be troubled by many of the following symptoms, either simultaneously or alternately

• Some afflictions are chronic or very frequent, others may only occur sporadically. The symptoms are so varied that the people affected by HIT often do not suspect a single trigger


HIT and Gastro-intestinal and Urinary Symptoms

• Irritable stomach or an irritable bowel respectively. A direct connection between food intake and the symptoms is often difficult to discern. This is due to the fact that the ingredients of ingested foods are only slowly absorbed by the body during the bowel transit time, which may last several hours, so that problems may only manifest themselves with a considerable delay.

• Eating aged or leftover foods, or those with high histamine content, may trigger abdominal cramps and severe diarrhea within 15-30 minutes.

• Histamine increases the motility of the bowel movements, so that the bolus passes the intestines faster than normal, which impairs the absorption of nutrients because of the short retention time.

• More rarely also constipation or constipation alternating with diarrhea

• Heart burn, acid reflux (increases HCl)

• Symptoms similar to gastric flu (gastroenteritis)

• Histamine plays a role in the regulation of the circadian rhythm and acts as neurotransmitter. Histamine stimulates the production of melatonin.

• High levels of histamine (as well as high melatonin) in the body may lead to a wide range of neurological symptoms. Neurological symptoms are in particular pronounced with a HNMT enzymopathy. Headache, fatigue, sleep disturbance may also be typical symptoms of a DAO enzymopathy.

• Noise sensitivity, search for tranquility and uneventfulness, vulnerability for sensory overload

• susceptibility to stress, impaired ability to withstand stress, feeling of burnout (feeling of mental and nervous exhaustion and breakdown)

• Clearing of throat in stress situations

• Tension, nervousness, jumpiness (also without external cause), restlessness, tingling sensation, feeling of caffeine overdose

• Muscle twitching, tremor, clenched jaws, grinding of teeth (bruxism), worn down teeth

• Symptoms similar to those of poisoning with a mild neurotoxin

• Melancholia, sadness, weepiness, depressive moods, depressions (often without visible cause)

• Temporary loss or impairment of the sense of smell



• Cardiac arrhythmias

Palpitation (stronger heart beat caused by a release of adrenaline)


HIT and Endocrine System

• Dysmenorrhea (menstrual cramps),

• Development disorder, failure to thrive


HIT and Immune System

• increased susceptibility for inflammations, inflamed areas

• Sore throat

• Hoarseness

• Flu-like symptoms without defined onset of disease, prolonged malaise, pain in the limbs

• Sinus infection (sinusitis): frontal sinusitis, maxillary sinusitis, inflammation of other sinuses such as sphenoid or ethmoid sinuses

• Constant swelling painful lymph nodes

• Tonsillitis, adenoid vegetation (adenoid hyperplasia), possible surgical removal of tonsils. (The tonsils serve the immune defense. Their removal may further acerbate the increased susceptibility for infectious diseases.)

Autoimmune illness. Inflammation of connective tissue: tissue underneath the skin with inflammatory pain or tenderness

• Painful feeling of inflammation, heat or pressure in the head, chronic (non-bacterial) inflammation of the brain (chronic encephalitis)

• Painful/burning bladder, desire to void, frequent urination (similar to bacterial bladder infection)

Conjunctivitis, irritated reddened eyes, itching of the eyes.

• Misted, impaired vision

• Soft-tissue rheumatism: e.g. pain in the tendons or joints, back pain: the back muscles hurt similar to a strained muscle/muscle ache (muscular rheumatism, inflammation of a muscle)

• Periodic toothache, inflammation of the gums or wisdom teeth

• Herpes simplex labialis (oral herpes, cold sores) or symptoms similar to herpes (e.g. badly healing skin cracks)


HIT and Skin

• Excessive sweating, attack of sweating, night-time sweating, perspiring hands/feet, hot flashes

Flushing of face following meals (flush), heat build-up, facial skin feels slightly irritated

• Skin blemishes, acne, pimples, blackheads, overproduction of sebaceous gland, oily skin

Atopic eczema, Atopic dermatitis, Itching (e.g. itchy scalp, itchy vaccination scars)

• Physical irritation such as scratching, strokes or heat triggering flashes/rash or itching

• Upper arms covered in little red spots/pimples, partially keratinised or purulent (impaired keratinisation), perhaps in connection with pollen allergies?

• Hands with burning/aching inflammation/blisters/nodules/calluses

• Sun allergy: the skin goes very quickly red in the sun, but the sunburn disappears on the following day.

• Dry lips

HIT and Respiratory Symptoms

Perennial rhinitis, swelling of nasal mucous membrane, runny nose (rhinitis, rhinorrhea) especially after food intake, also independent from type and histamine content of food, possibly aggravated by cold/smoke/smog/smells

• Blowing the nose may lead to nosebleed (because of increased permeability of the blood vessels)

Aphtha lesions of the oral mucosa, which become small yellow-white holes/wounds that hurt and will not heal for days and sometimes months. In addition to the oral mucosa, some papillae on the tongue may hurt like an aphtha.

• Chronic cough, constant tickly throat, dry cough, bronchitis, irritated bronchia

• Constant clearing of the throat, particularly in stress situations

• Sputum: viscid mucus to expectorate, frequent clearing of throat, perhaps also breathy vocal cords, particularly after sumptuous meals (similar to cystic fibrosis)



HIT and Fluid Regulation Symptoms

– Swollen eyelids

– Leg swelling

– Abdominal bloating.


Possible Miscellaneous HIT Symptoms

• Sensitivity to EMF pollution, WiFi, etc.

• Sensitive to Geopathic stressors

• Sensitive to Enviropathic stressors


DAO vs HNMT (The two pathways your body has to break down histamine)

Diamine Oxidase enzyme (DAO) expression is restricted to specific tissues; the highest activities are shown for small intestines, ascending colon, and for placenta and kidney. DAO is responsible for scavenging extracellular histamine (i.e., after ingestion of histamine-rich food) after mediator release.

• Histamine N-Methyltransferase enzyme (HNMT) is widely expressed in human tissues; the greatest expression is in kidney and liver, followed by spleen, colon, prostate, ovary, spinal cord cells, bronchi, and trachea. HNMT is regarded as the key enzyme for histamine degradation in the bronchial epithelium. HNMT can convert histamine only in the intracellular space of cells.




Sources of Histamine and the cellular release of Histamine

• Foods containing histamine

• Mast cell dysregulation releasing excessive histamine

• Mental/Emotional Stress

• Allergies (endogenous or exogenous antigens)

• Physical stress

• Medications

• Geopathic Stress

• EMF/Enviropathic stress

• Inflammation


Examples of Medications that influence histamine levels

• Non-steroidal anti-inflammatory drugs (ibuprofen)

• Antidepressants (Cymbalta, Effexor, Prozac, Zoloft)

• Immune modulators (Humira, Enbrel, Plaquenil)

• Antiarrhythmics (propanolol, metaprolol, Cardizem, Norvasc)

• Aspirin – Histamine liberator

• Amitriptylene – DAO blocker

• Valium – DAO Blocker

• Lasiks – DAO Blocker

• Codeine – Histamine Liberator

• Augmentin – DAO Blocker

• Chloroquinine – DAO Blocker and Histamine liberator

• Quinine – Histamine liberator

• All X-ray contrast – Histamine liberator

• Metoprin – HNMT blocker

• Opiates (Heroin/Morphine…) – Histamine liberator

• Thiamine/Vit B1 – Histamine liberator



• Histamine release increases during the periods of panic attack, especially when the adrenergic, “fight or flight” response is at its peak.

• Histamine factors into the fight or flight because H3 histamine receptors in the brain promote the most "wakeful" firing pattern. In fact a sudden rush of histamine in the brain could contribute to a schizophrenic episode.

• Histamine is involved in panic events by causing a closing of the airways in the lungs. When released in the lungs, histamine causes the airways to swell shut in an attempt to close the door on offending allergens and keep them out. Panic attack periods are known for the sense of weight or contraction on the lungs.

Effects of Sleep on Histamine

• Sleep--It has been shown that histaminergic cells have the most "wakeful" firing pattern of any neuronal type. They fire rapidly during waking, and completely stop firing during sleep.

• The cell bodies of neurons which release histamine as a neurotransmitter are found in the posterior hypothalamus, in various tuberomammillary nuclei. From here, these histaminergic neurons project throughout the brain, to the cortex through the medial forebrain bundle.

• Antihistamines, substances that block the H1 histamine receptors improve sleep.

Destruction of histamine releasing neurons, or inhibition of histamine synthesis leads to an inability to maintain vigilance.

Influence of Histamine on Sex

• Histamine is released as part of sexual arousal from mast cells in the genitals, and histamine release has been connected to the sex flush in women.

• The female orgasm can be facilitated by supplemental folic acid along with niacin, which will increase histamine release.

• Men with high histamine levels may suffer from premature ejaculations.



Four types of histamine receptors in the body (H1, H2, H3, H4)

H1 Receptors

• Ileum contraction

• Modulate Circadian rhythms

• Itching

• Systemic vasodilation

• Broncho-constriction (allergy-induced asthma)

• pain and itching due to insect stings

• Are the primary receptors involved in allergic rhinitis symptoms and motion sickness.

• Initiates release of intracellular stores of Ca2+ and opens Voltage gated Calcium channels.

H2 Receptors

• speed up sinus rhythms

• Stimulation of gastric acid (HCl) secretion

• Smooth muscle relaxation

• Inhibit antibody synthesis, T-cell proliferation and cytokine production

H3 Receptors

• Presynaptic autoreceptors

H4 Receptors

• Found primarily in bone marrow and white blood cells. It is also expressed in the colon, liver, lung, small intestine, spleen, testes, thymus, tonsils, and trachea.

• Mediate mast cell chemotaxis. Histamine was shown to mediate signaling and chemotaxis of mast cells via the H4 receptor. This mechanism might be responsible for excessive mast cell accumulation in allergen sensitive tissues.



Problems with Antihistamines

• Most over-the-counter antihistamines only block the H1 and/or H2 receptors

– The excessive histamine is still circulating so it can be forced more to the H3 and H4 receptor pathways

– H3 and H4 receptors are more related to Headaches, nausea, vomiting, vertigo, circadian rhythm problems, arousal, insomnia, appetite issues, memory problems, learning, and body temperature problems.

Methods to address Histamine Intolerance

Eliminate foods high in Histamine (temporarily or long term)

• BRADE allergy desensitization with NeuroPhotonic Therapy (Available at the Hansa Center only)

• Eliminate medications that block DAO or HNMT, or that liberate histamine from the cells.

• Use BRS to identify remedy support the biochemical pathways to enable the body to produce DAO and/or HNMT.

• Restore probiotics, fecal microbiome transplants.

Supplement diet with Diamine Oxidase (DAO), such as Hist-DAO (Xymogen)

• Treat Mental/Emotional (HPA axis) stress issues with BRS testing.

• Stabilize IgE mediated prostaglandin activation of mast cell release of histamine. (gamma linolenic Acid…Evening Primrose oil, Borage Oil, Black Currant Seed oil.)

• Oxford University Peptide shots (Amino acid shots) to block the histamine receptors at the cellular level.

Oxford University Peptide Injections

• An antigen must first be attached to cell surface receptors on mast cells. This triggers a response that often includes the release of histamine. Most allergies involve the release of histamine and other pro-inflammatory substances.

• The Oxford Peptides (U.S. = Amino Acid Injections) physically block the receptors so that antigens cannot attach to the cell receptors, therefore no histamine is released by the mast cells.


Antihistamine Supplements 

• HistDAO (Xymogen)

• HistoCal (NutriWest)

• Allermac (Jernigan)

• Resveratrol

• Turmero

• Whole System Histozyme (Nutriwest)

• Total CMO (NW) (autoimmune)

• Phoenix (Dr. Recommends)

• Isopathic Phenolics

• All homeo categories, Dairy, Beautox,

• Vitamin C

• Vitamin E

• Sulfur (MSM)

• Essential fatty acids (GLA)

• Bromelain

• Boswellia (Frankincense)

• Pancreatic enzymes (Digest, Total Enzyme, Carbo-zyme, Amylase)

• R-lipoic acid

• Glucosamine hydrochloride

• Proanthocyanidins (Plant pigments)

• N-Acetyl Cystiene

• Allergic reactions typically have an adrenal component. Cortisol, is a strong anti-inflammatory agent. For this reason proper adrenal function plays an important role in mediating the histamine release and inflammatory reactions that produce the symptoms experienced with allergies.

• A vicious cycle occurs with adrenal fatigue and the tendency to having allergies. The more histamine that is released the harder the adrenals have to work to produce more cortisol, thereby the more fatigued the adrenals become, which increases allergic reactions in a vicious circle.

Interactions of Nitric Oxide and Histamine

• Increasing Nitric oxide will down-regulate the release of histamine. (NO Saliva test strips; treat with Neo-40, NOx…)

• Histamine stimulates NO synthesis and release.

• Too much NO increases histamine as the body strives to bring down the high NO. (Be careful when treating low NO that new symptoms are not created by causing the over production of NO.)

• Several factors increase levels of NO in the body: Allergies (histamine), poor iron status, hypoxia (oxygen deficiency), estrogen dominance and Carbon Monoxide exposure.


Dietary Recommendations and Histamine (While eliminating high-histamine foods from your diet is a great idea, diet alone is NOT a long term correction for the underlying HIT problems. You must work with your doctor to correct the enzymatic and histamine metabolic pathways.

• Avoid or reduce eating canned foods and processed or ready made meals.

• Avoid or reduce eating ripened and fermented foods (older cheeses, alcoholic drinks, products containing yeast)

• Histamine levels in foods vary, depending on how ripe, matured or hygienic the foods.

• As much as it is possible, only buy and eat fresh products.

• Don’t allow foods to linger outside the refrigerator – especially meat products



• Alcohol, primarily wine, champagne and beer

• Pickled or canned foods – sauerkraut. pickles, mayonnaise, olives

• Matured cheeses, including goat cheese

• Cured/Smoked meat products – salami, ham, sausages, bacon, salami, pepperoni, lunch meats and hot dogs

• Shellfish

• Beans and pulses – chickpeas, soy beans, peanuts

• Nuts – walnuts, cashew nuts, cashews, and peanuts

• Chocolates and other cocoa based products

• Avocados, eggplant, spinach, and tomatoes

• Most citric fruits, apricots, prunes, dates, figs, raisins

• Wheat based products

• Vinegar

• Processed and Ready-made meals

• Salty snacks, sweets with preservatives and artificial colorings

• Soured foods: sour cream, sour milk, buttermilk, sour dough bread

Foods that are Histamine Liberators

• Most citric fruits – kiwi, lemon, lime, pineapple, plums…

• Cocoa and chocolate

• Nuts

• Papaya

• Beans and pulses

• Tomatoes

• Wheat germ

• Additives – benzoate, sulphites, nitrites, glutamate, food dyes


Drinks that are Diamine Oxidase (DAO) Blockers

• Alcohol

• Black tea

• Energy drinks

• Green tea

• Mate tea


Antihistamine Herbs and Spices

• Amaranth seeds

• Anise

• Basil

• Berberine

• Carraway

• Chamomile

• Chili powder

• Cinnamon

• Clove

• Curry powder

• Echinacea

• wild oregano

• Fennel

• Fig

• Ginger

• Ginkgo

• Grapefruit

• Nutmeg

• Passionflower

• Tarragon

• Tumeric

• Skullcap

• Thyme

• Yarrow

• Papaya

• Reishi Mushroom

• Stinging nettle


Foods Low in Histamine

• Freshly cooked meat, poultry (frozen or fresh)

• Freshly caught fish

• Cooked eggs

• Gluten-free grains: rice, quinoa, corn, millet, amaranth

• Fresh fruits: mango, pear, watermelon, apple, kiwi, cantaloupe, grapes

• Fresh vegetables (except tomatoes, spinach, avocado, and eggplant)

• Dairy substitutes: coconut milk, rice milk, hemp milk, almond milk

• Cooking oils: olive oil, coconut oil

• Leafy herbs

• Herbal teas


Effects of Low Histamine (Histopenia)

• Histapenia (Low Histamine): It is found that 30-40 % of people with schizophrenia have low whole blood histamine levels and are over-methylated.

• People with low histamine tend to have more severe mental disorders and hallucinations, paranoid thoughts with less pronounced obsessions, despair, depression, low libido, anxiety, nervous legs and grandiosity.

• People with low histamine often have a multitude of food allergies and environmental allergies but they do not typically have seasonal allergies.

• Approximately 25% of bipolar patients have low histamine levels.


Biochemistry of Histopenia

• Low “Whole blood histamine”

• Low blood zinc

• Low basophils

• Elevated levels of serotonin, dopamine, and norepinephrine.

• Elevated copper, which is a brain stimulant and destroys histamine; causing brain dopamine levels to rise; copper then oxidizes catecholamines such as dopamine thus propagating neurotoxin formation. This causes paranoia and hallucinations in younger individuals, but depression may predominate in the older ones.


Conventional Testing for Histamine Intolerance (HIT): (Not all of these test must be performed to diagnose HIT.)

  • Histamine Determination, Whole Blood
  • Serum Tryptase levels are persistently above 15 ng/mL
  • 24-hour, Urine histamine metabolite, PGD2
  • 11-β-prostaglandin F2 alpha
  • These tests are now replaced by Fractal Frequency Modulation that was developed at the Hansa Center for Optimum Health by David A. Jernigan, D.C.

For over 20 years the Hansa Center for Optimum Health, in Wichita, Kansas has specialized in the restoration of health for people with previously unresponsive and chronic illnesses of virtually all types. Over 85% of people come from other states and countries. If you have done everything you and your doctor know to do and are still struggling, contact our wonderful Patient Care Coordinator, Kara, at patientcare@hansacenter.com, for information on the exciting new treatments we have developed at the Hansa Center for Optimum Health. For additional info, visit our website at www.HansaCenter.com. Call 316-686-5900 ext. 1 to schedule your visit.

This article is for educational purposes. Before implementing any supplements/remedies always consult with your healthcare professional. Due to the complexity of the human condition there remains the possibility of symptoms getting worse. Again, discuss the ideas presented here with your health care professional before beginning, and stop, or get support, if your condition worsens. This information is not intended to treat, cure, diagnose, or mitigate any disease or illness, and has not been evaluated by the FDA. The Hansa Center does not treat named diseases, but seeks to restore the body's optimum structural and functional integrity so that the body can rapidly heal itself. 

*Due to the exhaustive time spent per day with each patient, and poor repayment history of insurance companies, we unfortunately cannot accept insurance assignment. We do participate in Care Credit, and accept all major credit cards. We will gladly accept insurance when our elected officials revamp the health insurance industry to cover all results-based care. We encourage you to vote with this in mind. Please call 316-686-5900 ext. 1, for current pricing for our economically-priced, All-inclusive 2-3 weeks intensive packages of care.
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