Whether to be compliant or to be healthy seems like an easy question to answer

*I made a significant correction to this post today, so I’m moving it to the front page today.

— but it may not be that easy of a question for a patient of the current medical industry. Personally, I do like to be compliant and agreeable with other people but I also prefer to be healthy and agreeable rather than sick and agreeable. The terms compliant and non-compliant are used in the medical field when documenting how thoroughly a patient is following the recommendations of the medical team. However if the medical team’s recommendations are based on limited knowledge or incorrect information, then complying with the recommendations might not seem like a good idea to a patient. If an industry claims to not know what causes a disease or how to cure it then why should a patient be expected to believe that the same industry knows if a treatment will actually be adding to making the patient worse instead of helping them get better as is hoped? Some of their recommendations might be making the underlying, not well-understood, problem much worse.

The terms compliant and non-compliant may also be used in legal cases when there is conflict between a medical team’s recommendations and the parent’s decisions regarding the care of a child. Painful and possibly ineffective chemotherapy or other cancer treatments might be recommended to try to save a child’s life but if those treatments are just making the last few months, days, or years of the child’s life more miserable then who is being helped? The child and family are missing out on the quality  of life during their last days together and frequently with a significant financial cost. Paying for hope of a last chance cure at the cost of daily enjoyment seems like pretty expensive hope. The pharmaceutical industry’s profit margin may be helped but the child’s last days might be spent in more pain and nausea with less time to spend enjoying the company of their family.

Intravenous vitamin C has been used effectively against a variety of types of cancer at the Linus Pauling Institute for decades but vitamin C isn’t profitable because it can’t be patent protected. — A review article suggests there is some anti-tumor effects from the high dose intravenous vitamin C treatment but that it is not a miracle cure and is providing such a high dose, approximately 200 oranges worth twice a week, that it could be dangerous to a patient who had kidney problems. [8

Patents allow companies to charge higher prices for products because they are the only supplier. Generic products and natural products have market competition to help keep the price down for consumers.

A for-profit prison industry requires prisoners and tax-payer funding to finance their care and provide the profit, and a for-profit medical industry needs people to take medicine, whether they are sick or whether they are trying to prevent sickness. Requiring people to take maintenance medicine for chronic symptom control for years or for the rest of their life will add up to more profit for the medical industry over time compared to providing patients with effective preventive guidance or with a treatment that actually cures their underlying condition.

While I am fortunate not to have cancer I have been struggling with autoimmune and allergy symptoms for as long as I can remember and in my experience as a patient if currently available lab tests don’t reveal any diagnoses that are currently accepted within mainstream medical standards then your symptoms might be labeled psychosomatic – all-in-your-head physical symptoms that may be caused by mental stress or other emotional problems. That might be helpful for a patient who actually has psychosomatic problems but it isn’t very helpful for the long term treatment of a patient with an autoimmune disease.

Unfortunately though, in the current medical industry even if you receive an autoimmune diagnosis the cause is still considered unknown and immune suppressing chemotherapy drugs are frequently the only treatment available. However the good news is that the cause of some types of autoimmune disease has actually been discovered, but the news hasn’t made it into mainstream media or medical practice yet; and more good news, an effective therapy protocol has also been developed and life threatening chemotherapy drugs are not part of the medication protocol.

Severe migraine headaches every week were my worst health symptom, but I also had chronic fatigue and multiple muscle cramps similar to those described by patients with fibromyalgia, and I was sensitive to a variety of food and environmental allergens. I’ve only had a couple migraines since I tried the newly developed medication protocol. I spent a year and a half taking antibiotics every other day, and an angiotensin receptor blocker (olmesartan/Benicar) everyday, and avoiding vitamin D foods, supplements and sunlight everyday. This was not easy or comfortable, the antibiotics cause allergy like symptoms from the increased load of toxins that results from the remains of infected cells that healthy white blood cells were able to kill while on the combination of antibiotics and olmesartan, but the allergic symptoms were not as bad as having migraines that feel like a railroad spike pounding into your skull over and over for three days every week, never mind the muscle cramps, fatigue and other symptoms that I’d had off most of my life.

Not having weekly migraines and other daily symptoms was so wonderful that I wanted to share the good news but I found that it is difficult to get people to see past the mental block of “we don’t know what causes autoimmune disease or how to cure it.” — And we will never know what causes it or how to cure it if we keep ignoring the people who are making advances in figuring out what causes it and how to cure it.

Lida Mattman is a research scientist who conclusively showed that Rheumatoid arthritis is caused by a bacteria but that breakthrough hasn’t reached the patient yet. Some types of bacteria can survive in a modified form within the interior of some types of human cells. The form is hard to grow in normal agar gel cultures but Lida Mattman developed techniques that are able to culture the cell wall deficient microbes. She discusses the pathogens that cause Lyme’s Disease and Lou Gehrig’s Disease and other stealth pathogens at the Autoimmunity Research Foundation’s Chicago Conference, March 12, 2005, in this video link: (video, at ~19:30 she recommends not visiting people who had just suffered a coronary/heart attack in person at the hospital, just send a card, as evidence has shown that a infectious but unidentified pathogen is involved in some coronaries and therefore probably also in cerebral strokes which occur in the same way – but she probably doesn’t really mean not to visit your loved ones. She gets a laugh from the crowd as she shared a story about getting a sample to test after her husband had a coronary – so she probably did visit him but the point may also be that we don’t know what we don’t know and it might be dangerous, at least to the immune compromised).

Some types of pathogens, including the virus that causes HIV/AIDS, have forms that can actually enter human cells and survive and grow within the cell. This sets up an inflammatory condition with overactive white blood cells that may be looking for the infection but instead attack other healthy tissue – ‘auto-immune’ – attacking self. Lida Mattman found cell wall deficient bacteria involved in Rheumatoid Arthritis and Lyme’s Disease and other diseases. The bacteria that causes tuberculosis also has a form that can live within cells. The textbookofbacteriology.net site uses the term faculative intracellular parasite in their description of the pathogen that causes tuberculosis. [7]

The specialized pathogens developed ways to disguise the infected cells from healthy immune cells. The angiotensin receptor blocker medication olmesartan is normally given once a day for high blood pressure but for the auotimmune treatment protocol it is given three to four times per day every six to eight hours in order to keep the levels steady all day and night because the infected cells hide by developing angiotensin receptors – blocking the receptors takes away the disguise. I think – this is my rough understanding of how the medication helps in the protocol developed by Trevor Marshall, a biomedical engineer. Blocking the angiotensin receptor disguise somehow allows the healthy immune cells to identify and kill the infected cells instead of continuing to ineffectively attack other healthy tissue (such as finger joints in Rheumatoid arthritis or lung tissue in sarcoidosis).

Correction, (9/16/2015): The part about the angiotensin receptor blocker medication was wrong. The medication olmesartan (Benicar) is not only acting as a angiotensin receptor blocker (which can help reduce the production of inflammatory cytokines which cause pain and fatigue and can help prevent fibrotic tissue from forming). It also acts as an agonist, an activator, of the vitamin D receptors (VDRs). By activating the VDRs the medication is allowing the healthy immune cells to do their normal functions. The pathogens had developed a variety of ways to block the vitamin D receptors in order to ‘hide’ by disabling the immune cell’s normal immune functions that are controlled by the active VDR. It transcribes over 1000 genes that are involved not only in calcium balance but also in cancer metastasis and many other functions. MPKB: Science behind olmesartan (Benicar).

Prof. Marshall is not a medical doctor but he is a biomedical researcher who did not choose to be compliant when he was diagnosed with sarcoidosis and was told that he probably only had a year and a half left to live – over a decade ago. Instead he developed  his specialized medical protocol and then sought and received orphan drug approval by the U.S. FDA so that olmesartan/Benicar can be prescribed for use with the antibiotic Marshall Protocol in addition to it being able to be prescribed for its normal use for treating high blood pressure. Using the blood pressure medication three to four times per day may increase the risk of feeling light headed when standing up quickly but taking it 3-4 times per day doesn’t cause the blood pressure to drop 3-4 times lower than normal. (I did have to catch my balance occasionally and fainted once or twice while taking olmesartan three times per day for a year and a half. Fainting is weird but fifteen years of migraines is worse.)

A three day migraine or chronic arthritic degeneration seems worse to me than feeling light headed when standing up quickly – and the medication protocol isn’t needed for the rest of life as many medications are prescribed for patients with chronic illnesses. While the protocol reduces symptoms after a year or two on the medications, an autoimmune patient might need to follow Trevor Marshall’s protocol for a year or two more than once over their lifetime because autoimmune diseases tend to flair up and go in remission with the patient’s overall level of health or stress or environmental toxin load – there really is a lot we don’t know about autoimmune disease. Having good and bad times, remissions and relapses, may be common in autoimmune disease because just a few remaining infected cells may linger over the years and then multiply again during a stressful or otherwise unhealthy time of life.

Tuberculosis is a disease that has been shown to be caused by a type of bacteria able to live within human cells and the infection can be spread through air-borne respiratory droplets when actively sick patients cough or sneeze. The disease can remain dormant for years in healthy people and the sickness can be spread by people who never got sick themselves and therefore don’t realize that they are carriers. A continuing education session for health professionals recommends using Universal Precautions, in order to protect staff and to help prevent spread of infection between patients, health professionals are recommended to wear adequate masks and gloves and treat all patients as if they were potentially contagious because anyone might be a carrier of a dormant infection. The course, Infection Control and Prevention, Module 5, Element II: Mechanism of Transmission available at atrainceu.com [atrainceu.com] has more information about Universal Precautions.

“Every year, more than 9 million people worldwide develop TB and nearly 2 million people die from the disease. Tuberculosis is a bacterial infection caused by Mycobacterium tuberculosis and is spread in airborne droplets when people with the disease cough or sneeze. Most people with healthy immune systems infected with M. tuberculosis never become ill. However, the bacteria remain dormant within the body and can cause tuberculosis years later if host immunity declines.” – atrainceu.com, Infection Control and Prevention, Module 5, Element II: Mechanism of Transmission [atrainceu.com]

Tuberculosis, I learned recently, is also a type of infection that interferes with normal vitamin/hormone D metabolic pathways. The vitamin D receptor (VDR) plays a role in the ability of white blood cells to kill infected cells and cancerous cells. Some pathogens have developed ways to suppress the Vitamin D Receptor’s activity so white blood cells aren’t able to effectively resist the infection process. Other pathogens that have been shown to reduce the activity of the Vitamin D Receptor, in addition to the pathogen that causes Tuberculosis, include the mold Aspergillus, the viruses that cause Epstein-Barr chronic fatigue syndrome and HIV/AIDS, and the autoimmune diseases sarcoidosis, Crohn’s Disease, and Rheumatoid Arthritis. Elevated levels of 1, 25(OH)2D are seen with the bacterial infections: “Elevated 1,25(OH)2D appears to be evidence of a disabled immune system’s attempt to activate the VDR to combat infection.” [page 19, 1]

The Infection Control and Prevention course provides more information about Aspergillus. It is a fairly common mold that generally only becomes a problem for immuno-compromised individuals, [atrainceu.com], but interestingly those at increased risk also include people who have advanced cases of HIV/AIDS and those who have been on long term corticosteroid therapy (which acts similarly to having elevated levels of 1, 25(OH)2D, which is the active hormone form of vitamin D, and is actually not a vitamin. It is a seco-steroid based on a molecule of cholesterol). [2]

It seems to me that people with advanced cases of HIV/AIDs, whether they also have opportunistic aspergillosis or not, might like to know that taking olmesartan/Benicar daily and avoiding vitamin D foods, supplements and sunlight [1] might help their healthy white blood cells to be able to work more effectively again or might at least not add any negative symptoms that can occur when there is elevated levels of hormone D. The elevated hormone level itself is a health risk itself because it is telling the bones to release their stored calcium which can lead to osteoporosis of bones and calcification of soft tissue. The article [1]  doesn’t suggest that AIDS patients might be helped by Benicar because it is a review of research that has already occured article – research has shown that Benicar is helpful for autoimmune diseases like sarcoidosis but more research is needed to find out how the HIV and Epstein-Barr viruses and aspergillus mold suppress the Vitamin D Receptor and how to stop the down-regulation.

Our medical industry uses donated blood and organs that are screened for many diseases but they can’t screen for diseases that don’t officially have a known infectious agent. Dormant tuberculosis can cause carriers to become sick years after they were exposed and in all those years as a carrier the person might also have been a regular blood donor. Sarcoidosis patients who are in remission are allowed to donate blood and plasma yet there have been organ transplant patients who got sarcoidosis only after receiving the organ transplant. If the organ donor wasn’t known to have active sarcoidosis then the medical industry may not realize that the person might be a carrier of infected cells that could cause symptoms in a more immuno-compromised person. All organ transplant patients are purposely given immune suppressing medications in order to prevent the body’s own immune defenses from attacking the transplanted organ.

The longer autoimmune disease is treated as something without a known cause the longer we may be spreading it through contaminated blood and organ donations. The longer autoimmune disease is treated as something without a known cure the longer patients have to suffer reduced quality of life and shortened lifespans.

  • Tuberculosis: annually worldwide, 9 million infected and 2 million deaths, [atrainceu.com]
  • Epstein-Barr virus (EBV): According to the Centers for Disease Control about 90% of adults have antibodies against EBV, suggesting a current infection or history of exposure. The disease can be spread before a person has active symptoms and the virus can remain in a latent/inactive phase for years and can become active again at any time. [cdc.gov]
  • HIV/AIDS virus: According to the Centers for Disease Control there are about 50,000 people in the U.S. infected with HIV/AIDS each year and there are about 1.2 million people currently in the U.S. with an HIV/AIDS infection. About 12.8% of them may not be aware of their disease status. [cdc.gov]
  • Aspergillosis: According to the Centers for Disease Control the exact prevalence of opportunistic aspergillosis is unknown because it is not required to be reported in the U.S. however it is a common type of fungal infection found in organ transplant patients with a cumulative incidence of 19% over twelve months during a 2001-2006 study. It may also be a problem for up to 15% of patients with cystic fibrosis and 2.5% of patients with asthma, which represents 4.8 million people worldwide, 400,000 of whom might have a more severe form of aspergillosis.  There are 1.2 million people estimated to have aspergillosis as a complication of their tuberculosis disease and there may be 70,000 people who have aspergillosis as a complication of their sarcoidosis disease. [cdc.gov]
  • Sarcoidosis: According to a study of U.S. Navy personnel, “Sarcoidosis Among U.S. Navy Enlisted Men, 1965-1993,” the rate of disease incidence dropped over the time period but was significantly more of a risk for enlisted men who were assigned to aircraft carriers. The study was made at the request of a veteran who wondered if his case of sarcoidosis might have been due to an environmental contaminant.  “Although 70% of case-patients and 66% of controls had ever served on ships, 26% of case-patients and 17% of controls had ever served specifically on aircraft carriers.” (case-patients, n=1121) [3] *Living within the confined quarters of a ship or aircraft carrier may have affected risk of sarcoidosis infections if the disease can remain dormant similarly to tuberculosis. Exposure to the blood or body fluids of a seemingly healthy person might be able to be a source of latent infection for an immuno-compromised individual if the disease is carried within infected white blood cells.
  • Crohn’s Disease: I haven’t found statistics regarding the prevalence of this type of inflammatory bowel disease but the Mayo Clinic site at least mentions that an infectious agent might be involved: [4] Unfortunately they also recommend vitamin D and calcium supplements to help counteract the risk of osteoporosis if steroid therapy is used. [5] This would be bad if the patient actually has elevated levels of hormone D (1, 25(OH)2D) because levels above 42 pg/ml are a signal for calcium to leave the bones which ultimately increases the risk of osteoporosis and calcification of soft tissue. “In fact, there is ample evidence that elevated 1,25(OH)2D leads to bone loss. Brot et al. [53] found that elevated levels of 1,25(OH)2D were strongly associated with decreased bone mineral density and content, and increased bone turnover. When levels are above 42 pg/ml 1,25(OH)2D stimulates bone osteoclasts. This leads to osteoporosis, dental fractures and calcium deposition into the soft tissues [54]. Vanderschueren et al. [55] found that a combination of high 1,25(OH)2D and low 25(OH)D is associated with the poorest bone health.” [1] Adequate magnesium is very important when elevated calcium levels are a problem because it helps the kidneys to excrete excess calcium.
  • Rheumatoid Arthritis: Infection is also mentioned as a possible cause of Rheumatoid Arthritis on the Mayo Clinic site. [6]

That is an incomplete list of statistics but the point was that many people may be affected by pathogens that have developed ways to manipulate our immune system’s normal Vitamin D Receptor metabolism.

Trevor Marshall doesn’t recommend that people who are using his protocol with the help of their physician worry too much about what specific pathogens might be the cause of their own abnormal vitamin D/hormone D levels. Comparing the level of the inactive vitamin D, 25 (OH) D, with the level of the active hormone D, 1, 25 (OH)2D, can suggest infection when the inactive form is low but the active form is normal or elevated. Healthy individuals can remain at 30 pg/ml of the hormone while they are getting plenty of sun exposure and dietary supplies of the vitamin form. Elevated levels are not normal. Elevated levels during active autoimmune disease can be in the 100s while the vitamin level remains low and tends to remain low even when large dose supplements are taken regularly.

The problem is that the infection process has inhibited breakdown of the active hormone and/or causes over production of the enzyme that converts the vitamin into the hormone form so all the large dose vitamin is being converted into the active hormone form which wouldn’t be noticed if only the vitamin level was being measured by the lab – as is the routine currently. The hormone level is a more unstable form that is more expensive to process. The mainstream medical recommendation is based on the theory that the enzyme that can convert the vitamin into the hormone is under careful control by the kidneys, which may be true for healthy people but might not be true for someone with sarcoidosis or Rheumatoid arthritis.

Personal Impact

My own was hormone D level was 55 pg/ml recently which is within the range considered normal but it is towards the high end of the range. It has remained around that level even while limiting dietary sources and exposure to sunlight. The vitamin level was below 10 which is low, above 20 to 30 is the low end of the normal range for the vitamin form of D. So do I have low levels, normal levels or elevated levels?  My endocrinologist’s recommendation that was sent with the vitamin D/hormone D lab report was to start taking vitamin D and calcium in order to help reduce osteoporosis risk but if all levels over 42 pg/ml are causing calcium to leave my bones already then adding extra vitamin D is more likely to add to the infection risk. The use of Benicar and reduced intake of vitamin D and sun exposure is mentioned in this review article about Vitamin D and infection: [1]

My own medical history includes an episode of Epstein-Barr virus/mononucleosis during college and more recently a diagnosis of Grave’s Disease, which is an autoimmune thyroid condition related to Rheumatoid Arthritis in that bone marrow cells become labeled with a thyroid receptor and infiltrate the thyroid gland. The thyroid can become overactive and overproduce thyroid hormone and sometimes the bone marrow cells become mislabeled in a slightly different way and infiltrate the fatty area behind the eye sockets and cause the eyeballs to protrude. 

Professional Impact:

I would like professional guidance about abnormal vitamin/hormone D metabolism iin infection for myself and family and for feeling comfortable about counseling nutrition clients. Without knowing both the vitamin and hormone D levels of a client I can’t really know whether a low vitamin D level alone means the client isn’t getting enough of the nutrient or sun exposure or whether they might have an underlying infection that hasn’t been diagnosed. But without the professional ‘evidence-based’ guidance from the mainstream medical industry I can’t really recommend alternative strategies to a client legally. A professional code of ethics encourages us to do no harm in the health industry but during the earlier phases of medical research it can be more difficult to figure out what might be helpful and what might be harmful.

*I may add to this later but I’m going to try to post it now because I’m having trouble saving it. 2:12pm post was successful, update added, and at 10:54pm.

9/16/2015 correction added. A type of gastro intestinal bacteria, Prevotella copri, has been found to be more prevalent in the GI tracts of people with rheumatoid arthritis.  Intestinal bacteria linked to rheumatoid arthritis (Nov. 5, 2013).

This post is continued on the next two posts:

/Disclosure: This information is provided for educational purposes within the guidelines of fair use. While I am a Registered Dietitian this information is not intended to provide individual health guidance. Please see a health professional for individual health care purposes./

The Arthritis Foundation, Juvenile RA and minocycline

Close-mindedness can be hard on oneself, other people and for the planet.


I got irate last night reading a free magazine but I kept going and found some helpful information and even reinforcement of my recommendation for use of antibiotics for an autoimmune condition. The complimentary magazine that arrived was, Arthritis Today, Advice from the Experts You Trust, which is published by the Arthritis Foundation. Their motto is, “Take Control, We can help”. The cover story is about a medically disabled 26 year old veteran, Mike Jackson, whose photo makes me think cannabinoid deficit not ibuprofen deficit – although ibuprofen does help reduce breakdown of endogenous cannabinoids. He suffered through ten years of military service with osteoarthritis and was given cortisone shots and ibuprofen and later on shoulder surgeries.

I would have given him green leafy vegetables and nutmeg, beans, nuts and seeds, and ibuprofen. The magazine does have an article about cooking with quinoa for gluten avoidance and four recipes that use cocoa powder.

The gluten article mentions that only an estimated 5% of people with celiac disease have been diagnosed. There is a lab test for aiding in diagnosis. Primary symptoms include bloating, digestive pain and constipation is frequently an issue. Joint pain has also been found to be a symptom because the overactive white blood cells from the intestines can travel and cause problems elsewhere in the body.
/Speculation/ Celiac disease may be an autoimm

Another nutrition article discusses portion control when using healthy fats or foods that are rich sources like walnuts (1/4 cup sv size) or avocado (one sixth of an avocado sv size). “Go to ArthritisToday.org/MA12 to learn more about the differences between good and bad fats.” I went – I don’t agree with the article’s grouping of all saturated fats as equally “bad” as trans fats. That is a very brief article with a brief list of a few foods and a few risks or benefits. The portion control article was more accurate.

Article on glucosamine was helpful about which chemical form may provide more relief. A 2005 Cochrane Review of trials regarding effectiveness of the supplements found that glucosamine sulfate (GS) trials had more consistantly positive results than trials that used glucosamine hydrochloride (GH). That makes perfect sense to me, although the article mentions that “Oliver Grundmann, PhD, . . .  says it isn’t clear why the two have different effects.” Our average diet is lower in sulfur containing foods than chloride or chloride containing additives. Chloride can interfere with the thyroid gland in a way similar to bromide and fluoride. So thanks for complimentary magazine – I have early symptoms of osteoarthritis but I don’t think it was ever added as an official diagnosis yet as I have been actively fighting the degeneration for over a decade with the regular use of magnesium, glucosamine, and Methylsulfonylmethane (MSM) among other things. Veterinarians use MSM regularly.[arthritis-msm-supplements.com/msm_for_horses_dmso.htm]

This quote fills me with wrath:

“Even if methotrexate leads to ‘clinical remission’ (defined here as no more than three swollen joints) in RA, a new study shows the joints might still be eroding.” – Shahreen Abedin,     Source: Annals of the Rheumatic Diseases, Nov. 7, 2011

The suggestion is to add more DMARD’s in addition to the methotrexate and if there are any slow healing wounds then the article next to it suggests that following the aggressive immune suppressants with skin-graft surgery would make that wound healing problem go away. Reminder – DMARD is a fancy acronym meaing we are using some chemotherapy drugs in an off label use – not for cancer. And the article on the next page encourages parents to use an aggressive mixtures of the immune suppressing drugs in their young children with a diagnosis of Juvenile Rheumatoid Arthritis.

“Disease-modifying antirheumatic drugs (DMARDs), as the name suggest, are drugs designed to modify the course of rheumatic diseases.” (Gee, vasculitis is part of the group of diagnoses that DMARDs are recommended for. and Minocycline is actually on the list with the note that it is not currently approved for arthritis by the FDA.) Article, “What you need to know about DMARDs”

Why is Benicar plus antibiotics and avoiding excess vitamin D, calcium and free glutamates such a horrible treatment suggestion compared to drugs that make one’s hair fall out. Should four year olds be bald – no.

Two young girls diagnosed with Rheumatoid Arthritis were 2012 Arthritis Walk National Honorees along with Mike Jackson. Unlike osteoarthritis which I think has to do with a genetic susceptibility to problems with disruption of nerve and muscle signals that result in the degeneration over time, Rheumatoid Arthritis has been proven to be related to cell wall deficient bacteria by research scientist, Lida Mattman. I posted links and a little more about her work, 2/17/2012: [https://transcendingsquare.com/2012/02/17/cell-wall-deficient-pathogens-l-forms/]


An excerpt that I posted within that article:

“Dr. Hoekstra’s mentor, Lida Holmes Mattman, Ph.D., also of Wayne State (now professor emeritus of biology), confirmed the causal role of P. acnes in a laboratory experiment. Dr. Mattman extracted the bacteria from the synovial fluid (which lubricates joints) of human arthritis patients, and injected it into chicken embryos. The chicks then exhibited symptoms of rheumatoid arthritis. When she treated the chicks with antibiotics known to disable P. acnes, the disease disappeared.”

Original Source: Lida H. Mattman, Ph.D., Cell Wall Deficient Forms–Stealth Pathogens, 2nd Edition, CRC Press (1993), CRC Press, 2000 Corporate Blvd. N.W., Boca Raton, FL 33431. I found the excerpt posted within a Lyme’s disease article: [shoptown.com/Dean/ALS2Lyme.htm] [4]

I knew a preschool child with juvenile rheumatoid arthritis whose mother was curious about the possibility of alternative treatments but she was never able to talk her Medicaid doctor into trying antibiotics instead of methotrexate. She did find moderate use of vitamin D and calcium foods and increased magnesium foods helpful for reducing the number of bad days her child experienced. I don’t know how they are doing now. I don’t think Minocycline would help an adult with osteoarthritis but it would be likely to help the two little girls with Juvenile RA more than Methotrexate would in the long run. Immune suppression will not support the healthy white blood cell’s ability to find the cells that have been colonized by the cell wall deficient forms of the Propioni acnes bacterium.

In the case of rheumatoid arthritis, a hallmark of conventional medical treatment is the use of steroids, which can provide symptomatic relief, but no cure. The danger here, cautions Dr. Hoekstra, is that such drugs “give a free and clear run to the bacteria involved (Propioni bacterium acnes). If such a patient is ever to subdue this microorganism, they must have a competent immune system, and to have this, they must be off the steroids.”[link #4]

Gluten intolerance and celiac disease can have overactive white blood cells causing damage in the joints and  in osteoarthritis damage to joints results over time. Genetic differences may be triggering more food allergen recognition in white blood cells in sensitive people. So elimination diets can help identify which foods are better to limit for life and to consider as treats. Over use of the trigger foods can increase coagulation of the allergen protein clumps in joints and inflammation damage occurs over time.

The girls with Juvenile RA on the other hand may be sensitive briefly during disease flair up when there are too many white blood cells for other reasons (P. acnes) and they start reacting to more foods and other external allergens but get rid of the infection and the food sensitivities would gradually go away as the intestines healed and the number of white blood cells returned to a normal number. So avoiding gluten or other flair up foods while treating the underlying cell wall deficient bacterial infection might eventually lead to fewer flair ups with less severe symptoms and the treats might become a normal food to use again.

Some people can be gluten intolerant genetically and some can be gluten intolerant while having sensitive digestive problems for other reasons. Just like lactose intolerance some people have it for life and some only have it after a digestive sickness.

Juvenile RA means one is born with problems. I was never able to breathe well and was covered with eczema blotches during my infancy. Born with problems from birth will really reduce life expectancy when methotrexate is chosen, but even with generally good control the later degeneration is somewhat inevitable as the CWD bacteria continue to parasitize preferred organs and tissue types. Based on the life cycle of the T. cruzi and T. brucei in a chronically infected human then 20 years plus 15 years is the expected timeline for early cardiac or CNS symptoms to start appearing. The spirochetes of syphilis have been linked to megalomania / obsessive compulsive tendencies in the later stages of the disease. At age 45 almost 46 I am actually doing pretty well if my mother’s Rocky Mountain Spotted Fever was lingering in her system.

This is not a pleasant thought but wouldn’t treatment options for a 2 and 4 year old that didn’t involve eventual hair loss be a prettier thought?

So as defined earlier the goal of therapy with DMARDs is to achieve ‘clinical remission’ or to get the pain narrowed down to only three swollen joints – or fewer – but not necessarily all the way to zero. And so swollen painful areas are considered a normal part of clinical remission and, worse, the irreversible degeneration was found to be ongoing even during this wonderful state of ‘clinical remission’.

A potential side effect of many of the immune suppressing drugs is osteoporosis.

I enjoyed the article with tips for packing for a major move with less pain (more organized = less work = less pain) near the end of the magazine – I think I will enroll in the Arthritis Foundation and continue getting their magazine. I do have one toe with loss of range of movement where an old injury had occurred.

Update: After examining both feet, the broken toe actually isn’t that different from the other foot’s toe now. Early calcification is reversible with a change in diet and hormonal balance.

Their motto “Take Control, the Arthritis Foundation can help.” I did find some helpful info, recipes and other tips that will assist me in my continued battle to control my chronic degenerative condition. First impressions can close a mind, going back for a second look can open doorways and minds. I don’t have to agree with everything to find value in some things.

Disclaimer: Opinions are my own and the information is provided for educational purposes within the guidelines of fair use. While I am a Registered Dietitian this information is not intended to provide individual health guidance. Please see a health professional for individual health care purposes. Thanks.

Cell Wall Deficient Pathogens – L-Forms

Rheumatoid arthritis and other autoimmune diseases are actually the body’s attempt to find and kill human cells that had been colonized by pathogenic bacteria or fungi. At the microscopic level single celled organisms can exist in forms that are as different as the baby tadpole to the fully grown frog. During times of better health of the host the parasitic pathogen can change forms and hide from the better armed immune system within a few infected cells. During times of sickness, when there may be a flair up of the chronic symptoms, the colonies of cell wall deficient microbes multiply within the infected host cells and the host cells divide. Eventually the number of infected cells increase to another level of the pathogens life cycle and the host cells can split open and release pathogens that have the outer wall again which might increase risk of spreading the infection to other hosts.L-forms are referring to a “Life-form” stage of bacterial growth in which the bacterium can lose its outer wall and start growing within the interior of a human cell or other host cell. The following article by Amy Proal goes into extensive detail about the history of research in the field of autoimmune disease and cell wall deficient pathogens. http://bacteriality.com/2007/08/18/history/

Lida Mattman, a pioneer in the field of L-form microbes, is pictured at her microscope. She died at age 96 in 2008.  Obituary: http://www.lymenet.de/literatur/lida_mattman.htm

Sue Massie is a mother who found that Lyme’s disease was a problem for her husband, herself and their 6 children. She shares her family’s medical journey – they all were sick with low grade chronic symptoms. Dr. Mattman is quoted near the bottom of the article regarding the potential risk of infection from physical contact with a human carrier of Lyme’s disease (Borrellia burgdoferi):

“Dr. Mattman believes that touching can spread Lyme disease. The Lyme spirochete can actually occur in tears, and therefore can be transmitted to hands, which contaminates doorknobs, pens, people shaking hands, etc. This appears to be consistent with the observation that whole families often culture positive for Lyme and present with symptoms.” http://www.springboard4health.com/notebook/health_lyme_disease.html

  • A link to the book by Lida H. Mattman, Ph.D in Immunology from Yale University, “Cell Wall Deficient Forms: Stealth Bacteria“: http://www.lymebook.com/cell-wall-deficient-forms-mattman
  • A book review about Lida Mattman’s book, Cell Wall Deficient Forms: Stealth Bacteria:
    From Book News, Inc.
    Mattman (immunology, Nelson Medical Research Institute, Warren, MI) explores pleomorphic forms of bacteria and fungi, which are inconvenient to deal with but allow a much more precise identification of a pathogen and diagnosis of disease. She provides information to help researchers determine the organisms that should be added to the childhood vaccine, especially for boys; the bacterium found in its pleomorphic state in direct smears of synovial fluid of rheumatoid arthritis cases; the chronic disease for which an acid-fast organism is routinely found in smears of 72-h blood cultures in any routine medium; the bacterium that has a life cycle in the human erythrocyte as complex as that of Plasmodium malaria; the common pathogen of which the L form can permanently damage mammalian myocardium; and other microbes. No dates are noted for previous editions. Book News, Inc.®, Portland, OR http://www.personalconsult.com/articles/lymecellwalldeficiency.html
  • Excerpt from the book “The Top Ten Treatments for Lyme Diseasehttp://www.lymebook.com/marshall-protocol:  “In the past, sarcoidosis patients have received only minimal benefit from antibiotic therapy. But Dr. Marshall discovered that, upon reduction of 1,25-D levels, sarcoidosis patients can actually be cured with antibiotic therapy.”

Coinfections are a frequent problem within autoimmune disease sufferers. Sarcoidosis patients have had a variety of different species of pathogens cultured from blood samples. A weakness in immune strength may leave some people more susceptible to be a host for the types of pathogens that can survive in the L-form and colonize within human or other host cells. The good news is that the same treatment plan helps the human’s immune system to recognize the infected cells and reduce the infection without chemotherapy or other immune suppressing medications.

Benicar is a medication used in the Marshall Protocol, the treatment plan developed by Trevor Marshall, a biomedical engineer who worked on finding treatment for his own case of sarcoidosis.

Benicar acts to block the Angiotensin Receptor on cell surfaces. It may help the host defense by removing the disguise of “self” that the colonized cells may be using to confuse the healthy uninfected white blood cells. The overactivity of white blood cells is the characteristic response of autoimmunity that adds to long term degeneration. Previous medication strategies have been to suppress the overactive response. The use of Benicar every 6 hours maintains a constant inhibition of the Angiotensin Receptor that may help the healthy WBC identify the sick ones. Another benefit of Benicar therapy would be to reduce wasting of magnesium resources by the kidneys.

Excerpt from “The Stealth Pathogen Theory”  http://www.shoptown.com/Dean/ALS2Lyme.htm:

In the case of rheumatoid arthritis, Dr. Hoekstra has found that virtually all the patients he has studied have had significant amounts of a bacteria called Propioni bacterium acnes. “This is the genus and species of the organism we believe is responsible for propagating and perpetuating this disease,” says Dr. Hoekstra. “It is a very common bacteria in an altered state of being–it’s cell wall deficient.”

 The bacteria was first identified and described in 1981 by G.A. Denys at Wayne State University in Detroit, Michigan. “This bacteria is passed transplacentally, from mother to fetus, and this may be responsible for rheumatoid arthritis showing up in generations in a single family,” says Dr. Hoekstra.

 Why this bacteria is prevalent in seemingly all cases of rheumatoid arthritis is not clear; overuse of antibiotics may be a factor encouraging its growth. “The use of antibiotics is one of the most potent ways of inducing cell wall deficiency; bacteria seem to do this as a survival mechanism.”

 In other words, when a bacteria is transformed into a cell wall deficient form, it assumes different characteristics from the whole or native type of microorganism it used to be, Dr. Hoekstra explains. “The organism remains intact except it loses its cell wall and its antigenic characteristics, enabling it to function as a cellular chameleon.” When it loses its antigenic signature, the bacteria is able to mask itself against destruction by the immune system’s antibodies which can no longer recognize it as an antigen (foreign protein).

 Dr. Hoekstra’s mentor, Lida Holmes Mattman, Ph.D., also of Wayne State (now professor emeritus of biology), confirmed the causal role of P. acnes in a laboratory experiment. Dr. Mattman extracted the bacteria from the synovial fluid (which lubricates joints) of human arthritis patients, and injected it into chicken embryos. The chicks then exhibited symptoms of rheumatoid arthritis. When she treated the chicks with antibiotics known to disable P. acnes, the disease disappeared.

Disclaimer: Opinions are my own and the information is provided for educational purposes within the guidelines of fair use. While I am a Registered Dietitian this information is not intended to provide individual health guidance. Please see a health professional for individual health care purposes.