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October 04, 2016
Dr. Drottar`s promising Lyme and Morgellons remedy!
and animal Dewormer "Piperazin" for Lyme and Morgellons.
Read her story below....
I am a physician who is disabled after a thirty-year history with Lyme disease and Morgellons. My symptoms first began in my 20’s. I am a life-long camper and have had tick bites several times, but never had a bullseye rash or any obvious acute Lyme illness. I developed knee problems as a very young adult, but the doctors called it “chondro-malacia patellae” and said it was probably related to a childhood fall with damage to my cartilage.
I began to develop skin lesions that came & went in my late 20’s. By age 36, in 1991, I developed multiple minor physical ailments, including depression. I was treated for depression, under various diagnostic names, with numerous medications (sometimes 3 types at a time) over the next 23 years, with variable response. By 2001 I had chronic fatigue, persistent skin lesions, severe depression, poor word & name recall, and periods of mental confusion (“brain fog.”).
It wasn’t until I began to have significant spatial disorientation, that my friend convinced me to have a Western Blot Lyme test done at IGenix Lab in Palo Alto, CA. I had to see Lyme specialists in CA, in order to get adequate treatment, because my doctors in Portland felt my test “did not meet CDC criteria of 5 positive bands,” so therefore this was simply a type of Munchausen’s disease-seeking.
I had aggressive Lyme treatments over the next several years, including 7 months of IV antibiotic therapy, however my Morgellons symptoms simply worsened during that time. I began to have the persistent sensation of crawling insects with constant non-healing deep ulcerations, I had severe fatigue, endocrine dysfunction, hallucinations, delusions, and frequent brain fogs. I saw the fibers in several different forms. (I even had some extracted and analyzed by the local Naturopathic school.
Some were composed of simple keratin; gluco-polysaccrides like skin & nails.) I looked for answers everywhere. I used Chinese herbal medicine; I had acupuncture; I used specialty creams & ointments; I saw specialists of every type; I did numerous forms of physical & psychiatric treatments; I bandaged & treated my skin twice every day. I worked full-time on my recovery with very limited success. I was interviewed by our local TV station and spent a lot of time online communicating with other Morgellons sufferers.
In 2009, I began work with a new psychiatric nurse practitioner and we did some very beneficial therapy together. In 2010, I began seeing Dr. Steven Harris in Palo Alto, CA. I also joined a weight loss support program and lost 110 pounds over the next 2 years. I began to improve. The lesions lessened. The abnormal sensations stopped. The delusions and hallucinations seemed like distant dreams finally. The last medication that seemed to finally cure me was an anthelmintic medicine used in tropical countries, but controlled by the CDC here in the USA. They will only release it for use in BIOPSY-proven infections. I took the Diethylcarbazine 200 mg. twice every day for over 2 years.
It is available (without prescription) online from veterinary supply websites in Australia or Canada. It was used for heartworm prevention, but the dosing is too inconvenient. Fortunately, it has not been abandoned. I took this medicine until I had been symptom-free for at least 6 months. I have now been off it for over 3 years with NO recurrence. I have occasional skin rashes still, but no non-healing ulcerations. I have found that these seem to be related to a gluten allergy. I have been tested and show “anti-gliadin antibodies,” which document that this is a true intolerance.
I am off all psychiatric medications and treatment. I have found that regular outdoor exercise (gardening, walking, hiking) seems to cure any mood disorder, fatigue, or body aches. I am able to maintain a normal body weight now, although I must watch my food choices. I have residual cognitive impairments with poor short-term memory, and terrible recall of all proper nouns (names—any type of name!) However, that seems to make me pretty average for my current age group. ;-) I feel happy, free, and joyous! I am socially & physically more active than I have ever been.
I am enjoying life more than I have since my very early adulthood. I hope that all of you who suffer either of these difficult illnesses will be able to search out the proper help to achieve your own cures. Never give up looking, hoping, and searching: you only have your whole life to “get it right.”
-Beverly B. Drottar MD
February 28, 2015
Latest Lyme and Morgellons Info!
Article on latent chronic Lyme Disease
Relevance of chronic Lyme disease to Family Medicine
Is Morgellons only related to Lyme disease? Not convincent at all,
but we know about a relation to it over 10 years already!
February 12, 2014
LYME DISEASE BY SEXUAL TRANSMISSION?
Maybe sometimes but not always...
Stanford Woods Institute Researchers Found Ticks with Different Borrelia Types
Stanford Woods Institute for the Environment found Borrelia miyamotoi and B. burgdorferi
in ticks infected with one or both bacteria in nearly every park they examined. What a surprise!
News: Three Sudden Cardiac Deaths Associated with Lyme Carditis
August 28, 2013
CDC is waking up slowly: Lyme disease is more common than we thought?
The good old corrupt CDC...
Lyme rate is actually 10 times higher than reported by CDC
Tick-Borne Illness Could Be Worse Than Known Lyme Disease !
may not even know to look for new
bacteria subtype "Borrelia miyamotoi",
Oh well, not even Borrelia Burgdorferi is in most cases recognized by the usual Antibody-Crap.
July 13, 2013
NHI (National Health Institute) LISTS MORGELLONS AS RARE DISEASE!
Oh, come on, not again that old stuff...
March 22, 2013
LATEST MORGELLONS INFORMATION AND STATEMENT TO DR. STRICKER`S FAKE ARTICLE
glassy keratin filaments (actually hairs) really the cause of
Morgellons disease as stated in the latest article of Dr. Raphael
Stricker, MD? http://f1000research.com/articles/2-25/v1
Citation: Raphael B. Stricker, M.D., University of California at San Francisco. An investigation conducted by the University found that Dr. Stricker falsified data for a manuscript and a PHS-supported publication reporting research on AIDS. In the manuscript, Dr. Stricker selectively suppressed data that did not support his hypothesis, and reported consistently positive data whereas only one of four experiments had produced positive results.
The same happens now with his unprofessional keratin theory, rather I would say that the filaments itselfs are just filamentous organisms and not hairs (keratin). Of course this might be good for public relations for Morgellons, but it is not useful in acknowledge or treatment of Morgellons disease at all! I don`t claim that Morgellons is only caused by spirochetes, although my long term Morgellons survey (over 18,000 cases) show that many (approx. 70%) are really suffering from a positive proved spirochetal infection.
The remaining cases never had seropositive tests or Lyme symptoms at all, but shared other criteria such as surgeries, chemotherapies and various other diseases before contracting Morgellons later simply by skin contact. Yes indeed, Morgellons is contagious for immunocompromised people, because it might be an opportunistic fungus or protozoa!
Check my survey page: http://www.morgellons-research.org/morgellons/morgellons-inquiry2.htm
I would rather ask Dr. Stricker: why he did not ask his patients how they contracted Morgellons? Is it true that spirochetes are really involved in creating colored and rootless keratin filaments? And without any root how does one explain their growth? Keratin filaments cannot rather be blue, pink, green, yellow or red and twisted together, surviving for a long time (a few years) in the environment and causing re-infection.
Nor can keratin filaments release a liquid to penetrate the skin and cause further re-infection, which is clearly visible thru a microscope after one has touched contaminated papers or other objects! Morgellons filaments can be also found in fecies, the intestines, kidneys and urine and not just in the skin! Keratin filaments don`t move, change shape, or react to chemicals and hot and spicy odors, or create fuzz balls. Fungi or protozoa can do so (e.g. fungus balls) but not spirochetes!
What would Dr. Wymore, the forensic lab in Tulsa, and many other researchers say about this? Did they blatently overlook and fail to recognize what are simply keratin filaments, or supposed "hairs"?
Eventually many Lyme patients report symptoms
of increasing grey hair and rapid nail and hair growth (e.g. beard,
scalp, ear and nose hair etc.). An experienced Lyme specialist usually
has knowledge of these patterns. Even veterinarians with whom I`ve
spoken are aware of spirochete-associated bovine digital dermatitis (or
hairy heel wart disease) and longer glassy hairs, but not colored
moving fibers! Dr. Stricker is the only one who is now making a
connection between these well known "side effects" of spirochetes and
Could be, but this is so superficial
and irrelevant because spirochete cannot create colored
filaments and they are not black at all! In all probability Dr.
Stricker has not systematically investigated or listened to the
Morgellons afflicted at all (in order to make comparisons and draw
conclusions), despite many patients visiting him and paying dearly for
much needed help.
That is nothing new, but Lyme treatment alone cannot fully treat Morgellons and therefore Stricker and others from ILADS haven`t had much success in treating Morgellons or even complete success with treating long term Lyme disease. To spend upwards of 15,000 dollars, to be pumped up with many months of antibiotics or even with Ivermectin (dangerous stuff - kills brain cells!), without any logic or strategy behind the treatment...of course you might have some improvement, but to be cured completely and forever with antibiotics alone might be wishful thinking!
The fact remains that increased skin sheddings or glassy hairs (hyperplasia or hyperkeratosis) are only one of many side effects of a spirochetal infection and the primary focus should be on a subsequent secondary contagious mold or protozoa infection to which the body becomes susceptible after a spirochetal infection and the accompanying reduced immune function.
Check these skin pictures to see what I`m talking about:
These side effects caused from spirochetes in the epithelial cells with its symptomatic and some information about new Lyme tests I am working on are what I explained a few months ago to one of Dr. Stricker and C. Casey associates, and it makes me wonder that the very next day Stricker posted his new article, misappropriating my information for what purpose only he can justify! I know careers could be spent crusading against bad information and plagiarism in emerging fields, but I`m tired and I don`t have time for all this P.R.!
Added June, 2013: After I wrote this statement that Stricker has no great knowledge about typical symptoms caused by spirochetes in the skin tissue, called also "dermato-borreliosis, including e.g. hyperplasia and hyperkeratosis, he posted quickly a new article to be not blamed. What a disgusting and dubious person...
Myself is not showing anymore signs of Morgellons fibers coming out of the skin, but I am still suffering slightly from Lyme skin symptoms. So what to say about that Dr. Stricker?
I`m trying to devote more of my limited time to working on what will actually find a more conclusive method of diagnosing Lyme and Morgellons illnesses, an alternative to and replacement for the ineffective antibody or antigen-specific-cytokines-release based testing available on the market today.
Now even ILADS claims to be working on new Lyme tests. Oh, isn`t that also a timely coincidence? This is so reprehensible because despite being long established ILADS hasn`t introduced anything truly original in regards to new Lyme tests or treatment to help the afflicted.
In the end you may say, "who cares" if all the work finally helps Morgellons sufferers? I do, as I (and others) have done all this hard work for so many years while the likes of Stricker jump in and focus on an irrelevant idea and make such false claims. This might be good for some discussion and perhaps in the future for Dr. Sticker`s portfolio, and in my opinion he just copied, manipulated and falsified data to benefit from it, as he did already before.
Anyway, all this might be actually not so helpful in furthering the understanding and treatment of Morgellons.
Unfortunately this is the acknowledgement I often receive from the very practitioners to whom I refer the desperate patients who contact me for help. Many others are more centered on an ever-increasing paycheck than in moving the understanding and treatment of these syndromes forward.
Another main problem is the fact that physicians haven`t sufficiently researched new methods and tests to preclude incorrect (or even delusionally based) diagnosis for Lyme or Morgellons symptoms, and that primary care MDs are limited by insurance companies and the denial of authorities to acknowledge Morgellons as a real disease!
Thus in order to themselves make a living, many private-pay MDs and of course myriads of quacks have taken now advantage of the sick in order to exploit their desperation because they have no connections or money and cannot receive proper medical care by regular physicians. All because Morgellons has been relegated to the stupid diagnosis of "delusional parasitosis" due to the fantastic and infallible CDC report.
Check also this article from
University of New Haven: Evidence Mounting that Morgellons Disease is
an Emerging Infectious Illness, Contrary to CDC Report http://www.newhaven.edu/515835/
It came out after I talked to Mark Eberhard from the CDC about this report. Scroll down to read it!
So many have committed suicide out of loneliness and desperation, and just for this reason, I would love to make a lawsuit against the CDC, the Center of "NO" Disease Control!
"It is neither this disease nor the afflicted which are the mystery,
but rather the authorities and the extremes to which they go to deny Morgellons exists."
March 13, 2013
LISA JACKSON (56), A MORGELLONS SUFFERER HAS PASSED AWAY ON SUNDAY, MARCH 10
Lisa was for many years a good friend of mine and she lived in California were she died from cancer now. She suffered from Morgellons and Lyme disease for so many years. Now her fight is over, and it is pretty clear to me that Lyme disease is causing cancer too! Rest in peace dear Lisa....
August 18, 2012
Talking to DR. Mark Eberhard from CDC about the CDC-Morgellons-Report
Read below some short excerpts from my friendly (even if it doesn`t look like) conducted discussion a few days ago with Dr. Mark Eberhard Director of the Division of Parasitic Diseases and Malaria (DPDM) Center for Disease Control (CDC) Center for Global Health (CGH). To keep it short I left out some of his answers praising himself and the good work of the glorious CDC, and some other small talk. He took some time to listen to me, maybe because he knew me already, or because he was just curious that someone called him from Germany. Who knows?
------------ Memory protocol ---------------
Marc Neumann: Concerning the Morgellons report by the CDC, there were however a lot of protests and many inconsistencies, in particular regarding the recognition or correct representation of this illness. Your name is mentioned also here in Germany in different articles, as allegedly you and some others represent this report in a way that makes most Morgellons patients look like delusional parasitosis patients (patients imagining parasites under or on the skin).
I would like to mention at this point that this does not reflect my own opinion after I read this CDC report correctly. I think somebody just wants to misunderstand this report purposely and intentionally spread the opposite what this report actually reflects. Or is it perhaps just a matter of the vast information flow offered on the Internet, or the copy+paste mentality and the common laziness or inability to read and understand what is written somewhere. This could be actually a modern cognitive illness (perhaps ADHD?) caused by the Internet, and it will make us even more stupid than we were before then! Many cannot use their brain anymore due to this information overload!
Dr. Mark Eberhard: (Laughs...) Maybe, but it is so not completely correct that we would have maintained such a thing in the report--we left everything open ended, without branding people as definitely delusional.
Marc Neumann: Well, it is out there now, however, and, unfortunately, leads to the diverse opinions of some incorrect and indifferent physicians and lousy story hunters, who take only one side of the story like lemmings, without, for instance, having had direct contact with any actual Morgellons patients and treating physicians to gather real facts.
Dr. Mark Eberhard: I really feel sorry that something went wrong or been abused somehow due to some misinterpretations of the CDC report. It is clear to us that there is something going on actually, but as yet, we simply do not know clearly what the actual cause of this Morgellons illness could be.
Marc Neumann: Well, the fact is, that now after publication of this superficial report, all the debunkers state exactly the opposite, because the CDC left all quite uncertain in this report, right? And this uncertainty may mean for most readers: We do not have clear findings, thus patients are probably all delusional and that there is no need to treat them.
Dr. Mark Eberhard: As I have said, I feel sorry for these misinterpretations. If we would know the actual cause, we would describe it all differently. Actually, we relied mainly on the investigation of Kaiser Permanente.
Marc Neumann: You do not know what's causing it, but aren`t you ignoring some related facts too? I think you will be aware already that many world-wide sufferers kill themselves because they received no real medical assistance, and now more than ever Morgellons is being ignored due to this unclear CDC statement, which sounds a little bit ironic to me, as approximately two-thirds of all Morgellons patients, including myself, also suffer from proven Lyme disease. Do you know this fact either, or do you want to ignore this intentionally too?
At least these patients should not be rejected by physicians and should be tested and treated for Lyme disease, independently of the Morgellons syndrome. With this general ignorance of facts, even regular Lyme patients have to fight daily and are very often declared as simulators, fakers or hypochondriacs by this miserable and inhumane medical system. It all just has to do with money. No money actually means, you get no further help and you have to die! How much is a human life actually still worth in the U.S. nowadays? Ten cents, or even less? On the top of that, how can one assign an investigation to this corrupt Kaiser Permanente hospital chain? It might be the same as asking Satan for support then!
Dr. Mark Eberhard: However, the case is closed for the CDC at the moment, that's all I can say about it right now.
Marc Neumann: Come on, what's closed? Nevertheless it still has to do with human lives, does it not? I mean, your own citizens and taxpayers, whom are left on their own with this illness. Do you know that the whole world looks on the CDC report, and this does not give a good picture to the rest of the world. Especially that the U.S. wants to refuse medical assistance to its own citizens suffering from Lyme or Morgellons disease. With due respect, we are talking meanwhile about a pandemic, if you don't know this yet either! I do not call you just because of a local hay fever outbreak, and I just don't run my site for the past seven years now to support U.S. and worldwide sufferers just for pure fun. This would however, actually be the task of the medical system, don't you think so?
Dr. Mark Eberhard: I can understand that and thank you for your good work, but nevertheless I must repeat myself and say that the case is closed for the CDC.
Marc Neumann: Sorry, but not for me, and I do believe that huge dark clouds will cross the CDC in the future, as the case is still not closed for many! Does the CDC have a real interest in clearing this case up at all and to help their fellow citizens? Anyway, is the CDC still paid by tax funds or not? The CDC even promotes with this unclear report those who are believing in all these wild conspiracy theories, like Chemtrails, Nano-robots, Illuminati and population reduction, etc. After all, do you believe in those?
Dr. Mark Eberhard: No, definitely not! (Both laugh...)
Marc Neumann: But anyway, after the Tuskegee Syphilis experiments in Alabama and Guatemala, which were led even by the U.S. health authorities which have been abused African-American and Central-American men as human lab rats, I could actually be more predisposed to believe in a newer, improved and quiet variant of a spirochete-based bioweapon as result of this study! For what was this Tuskegee experiment led 40 years long, then? Where and which are the actual results of these despicable studies?
Isn`t it a shame for US, that these poor people have never, ever received medicines and even the local physicians were threatened with license withdrawal, if anyone would try to help these people. Isn`t it precisely the same story running now also with Morgellons sufferers, not anymore locally but globally? Is this all pure coincidence, or the already long-known procedure of U.S. authorities, in order to suppress the truth in the usual stupid way, just by ignoring and manipulating everything?
Dr. Mark Eberhard: In addition I cannot say anything about!
Marc Neumann: Really? In order to remain on solid, factual ground, let me directly give you a few pieces of information, since indirectly the CDC quite frequently visits my Internet site. The fact is, nevertheless, that we have epidemiologically, morphologically and biologically many similarities to a kind of fungus or fungus-like protozoan infection. Quite similar to what arises in California and southern U.S. states with fungi, such as Coccidioides immitis and Microsporum canis.
Even with the Coccidioides immitis fungus, scientists have found new mutations of it never known before. Usually known as a fungus, where its hyphae always roll themselves together into spherical shapes (cocci). According to old scientific studies, this fungus cannot create long thin hyphae in the host body, but under certain stress conditions, they found out in the latest results that these and other fungi really can. Why does the CDC not do any research in the direction of such fungi at least?
Dr. Mark Eberhard: These sort of fungal infections are well known to me, but we do not as yet have evidence connecting these and other types of infections to Morgellons disease.
Marc Neumann: Allright, but it is more than evident that it must be a kind of fungus, perhaps a mutated form, causing Morgellons. In addition, epidemiologically, is the spreading caused either due to global warming, or is it because of a massive forced usage of fungi and other pathogens used as biological insecticides embedded in hollow fibers, which have been used for approximately 30 years now to fight fire-ants and all kinds of crop pests in the U.S.? Even ticks and mosquitos are now fought with such biological insecticides in forest and meadow areas. What happens with the pathogens that these pests carry, if they get eaten up by such fungi which spread uncontrolled later? In addition every new technology, as these fibers with embedded pathogens, can be used also by the military or any other evil fringe groups to spread diseases, right?
Dr. Mark Eberhard: No comment...
Marc Neumann: Furthermore, it cannot be as the CDC states, that this Morgellons illness is not contagious. How can all concerned have been infected then. What kind of research has the CDC actually done? Besides, if one ignores the delusional theory now, the question must be, why so many mammals have been infected, and why even a worldwide spread could occur! Myself and others have investigated that over many years, but the CDC did not!
Dr. Mark Eberhard: (praising the work of the CDC, bla bla, bla...)
Marc Neumann: Anyway, do you have any idea at all, what harm the CDC has caused with this unprofessional statement? It means gross negligence or deliberate bodily injury directly caused by the CDC. I think, there will be many more complaints and lawsuits to follow! All family members, who have a weaker immune system, from the child up to the parents and grandparents can be infected, and also neighbors and pets, can be affected by it! Mainly these fungal spores are actually spread by direct body contact. If you are too weak, you will lose!
Dr. Mark Eberhard: Well, according to Kaiser Permanente and other researchers, it doesn`t seem to be contagious!
Marc Neumann: What? Sincerely, I cannot understand this careless attitude of the CDC which drives many humans into financial and physical ruin! Even if I can understand, to some extent, this stance for political and economical reasons, that the CDC may never admit that there are these and other contagious diseases present at this time in the U.S. at all (excluding now bed bugs in New York and Lyme disease epidemics in 49 U.S. states). Just because no more tourists would visit the U.S. or goods from the U.S. would be rejected by other countries, as it happened already with beef that was contaminated with BSE (Bovine Spongiform Encephalitis, or Mad Cow Disease). Korea and other countries nevertheless sent back such supplies, did they not? Are U.S. citizens at least informed at all about the fact that BSE is still present in the U.S.?
Dr. Mark Eberhard: Hmm, I would not like to say anything about such claims, but yes indeed, the CDC has to be careful about such statements anyway.
Marc Neumann: Well, the truth was always too precious, so it must remain hidden behind a lie, even ignoring human lives, right?
Dr. Mark Eberhard: No comment...
Marc Neumann: To finish this call, if I would send you from this living organic liquid (protoplasm), which is actually embedded in inorganic hollow fibers first (polymer-carriers), the extracted DNA by simple means, would the CDC do any DNA sequence then to find more out? Do you have any interest at all in it, since the CDC allegedly still could not find anything that causes this disease?
Dr. Mark Eberhard: What, DNA? No (inaudible), I must unfortunately break the discussion off now, sorry.
Marc Neumann: Now, well, thanks anyway for your time and the informative discussion and bye, bye.
------------Check also references and Video-Trailer below----------------
---- VIDEO-TRAILER-DOKUMENTATION PART 1 - MORGELLONS IN GERMANY ----
This latest Youtube video (part 1) shown in German is a new documentary trailer made with my collaboration. There will be more video parts which will be subtitled in the future in English. Even if you do not understand anything now, just watch the first few minutes and the darkfield microscopy pictures shown at the beginning.
It shows according to my research, hollow filaments or hyphae (sometimes with a kind of hook) with an embedded biomass (protoplasm), with integrated particles and/or DNA cell cores. This biomass is growing out of the fibers in slow motion (over hours) creating new hyphae or blebs/bubbles.
It is exactly that these new created forms with a typical biology of fungal organisms, which have left the hollow carrier fibers, have to be investigated more by DNA tests to find out the pathogen which is causing the Morgellons disease. Many researchers looked only on the surface of the fibers instead of looking inside of them to come further! Therefore, I would call some researcher just dilettantes, or even corrupt because they won`t find out more maybe on purpose, as it might not be in their best interests!
July 28, 2012
M-R-O Statement on Borreliose-Center-Augsburg, Germany (BCA)
Many patients have written to me that they were not satisfied at all with blood tests and treatments performed by BCA. By patients, I mean Germans and foreigners who even moved to Augsburg, Germany, from other countries for Lyme treatment. Their concensus is that BCA diagnoses mostly chlamydia but rarely finds Lyme disease, even in cases where there has been other evidence of Lyme. Treatment at BCA resulted in no substantial improvement or healing for the most of these patients, only further disappointment. I have never received any treatment from BCA, though I contacted them initially (2008) regarding research on Morgellons illness.
I expected reasonable cooperation from them, but, unfortunately, my experiences with their team of physicians were unsatisfactory and comprised of unfulfilled promises and inadequate laboratory equipment (e.g. a 30 dollar microscope for kids). After many information requests yielding poor response, I can only conclude that BCA is doing no substantive research (clinicians and scientific research? no way!) and has no notion of Morgellons or how to treat it! The fact is that I would like to have nothing further to do with the BCA Lyme disease clinic, nor with most physicians of the ILADS group, most (though not all!) of whom require enormous sums of money for treating Lyme patients, abusing the situation of desperate patients who been ignored from regular physicians.
My personal opinion is that BCA jumped from the Lyme to the Morgellons bandwagon, for the purpose of attracting also more Morgellons sufferers now with empty promises! Furthermore, BCA's basic claim that Lyme disease is curable (also in the final stage?) is more than despicable to myself and many other patients and German Lyme associations and foundations. Every other laboratory and physician in your own country can do the same job just as well. You don't need to come to Germany for treatment, just because you may think that German medicine is superior! Medicine for Lyme and Morgellons in Germany, the USA, and many other countries is mostly the same standard-crap! Actually, it is really funny (both strange and amusing) that American Lyme patients come to Europe for treatment, and Europeans go to the USA for the same. What travel madness that is, and all based on mistaken presumptions and hope! So, it is up to you, individually, to choose whether you use BCA or not.
July 22, 2012
Global Challenges in Diagnosing and Managing Lyme Disease - Lyme Disease Association, Inc.
The 2 hour July 17, 2012 hearing, Global Challenges in Diagnosing and Managing Lyme Disease - Closing Knowledge Gaps, was held on July 17, 2012 in Washington, DC. The significance of the hearing is that it is the first time Congress has looked at the global implications of Lyme disease and chronic Lyme disease, and focused on the science and putting patients first. Witnesses gave testimony about how policies and actions by government agencies such as CDC and NIH and of the Infectious Diseases Society of America (IDSA) have prevented research on chronic Lyme disease from moving forward and have hindered patient diagnosis and treatment. Solid science was presented for the record showing persistence in animal studies and cutting edge testing for Lyme was examined. Read more on lymediseaseassociation.org
May 17, 2012
Morgellons sufferer died from pancreatic cancer...
After many years of struggling with Morgellons disease, Joe Mistretta passed away on May 13, in Niagara, NY.
I will miss him and many other Morgellons sufferers with cancer, who are not among us anymore...
April 02, 2012
Mayday Lyme Disease Protest on May 12th in Washington DC
This year in Lafayette Park in Washington DC at the Whitehouse Lyme Patients and family members from all over the world will come together to demonstrate how Lyme has affected their lives.
Last year Lyme patients gathered in front of the White House in Washington DC to protest the wrong guidelines that the IDSA (Infectious Disease Society Of America) states for treating Lyme Disease.
My IDSA information from April 2010
IDSA, released a report that is the official guideline for doctors worldwide for Lyme disease treatment. It is shockingly ignorant, and devastating for Lyme patients. It basically says, "Lyme disease is all a delusion." This is very bad news also for Morgellons patients. This has sent shockwaves through the lives of Lyme patients.
Here is the report:
Here are official responses and reactions from Lyme advocacy organizations:
And the mocking and very disrespectful (to patients) article from Forbes, the leading business magazine that is read by all of Wall Street and Big Pharma:
Or read more here about...
January 26, 2012
Finally the delusional Morgellons CDC Fake Study was published...
Based on Kaiser Permanente zero value research. What a coincidence that Bayer and GlaxoSmithKline paid out 258 million in fines for defrauding the US Medical system in order to provide discounted prices to Kaiser Permanente.
Randy Wymore`s answer to this fake study
My answer to all that corrupt medical mafia bogus is very simple...
"time is on my side....yes it is!"
In the meantime, occupy CDC!!
November 06, 2011
Morgellons - Old Medical Cases Centuries Ago
September 08, 2011
Benefit of intravenous antibiotic therapy for neurologic Lyme disease
Lyme patient left alone by the German health care system - Last Hope is Stem Cell Therapy
Doctor who has changed his tune towards Lyme Disease!
June 10, 2011
New helpful Treatment for Lyme and Morgellons
Particulary for open non-healing wounds the Hyperbaric Chamber treatment is very effective
and it might be possible to obtain a home-unit from MEDICARE if you are housebound or disabled.
Ask for a prescription from you physician first and then MEDICARE...
More information on Supplemental Home Oxygen Therapy and Services
June 11, 2011
THE AUSTRALIAN HEALTH REPORT INTERVIEW WITH MORGELLONS SUFFERERS
An Article from Lyme Disease Association of Australia
Court grants Lyme disease autopsy after dead
May 19, 2011
MAYO CLINIC REPORT IS JUST A BOGUS AND AGAINST SUFFERERS DIGNITY!
Sara A. Hylwa, B.S. and colleagues from the Mayo Medical School and Mayo Clinic in Rochester, Minn. conducted a
retrospective review of Delusional Infestation cases seen at the Mayo Clinic between 2001 and 2007.
The latest statement from Mayo Clinic about Morgellons disease, implicating this old study, is just a dumb hoax
from small-brain debunkers! Why now, did they pull out this old study from 2001-2007, 3 years later, in 2011?
What comes next, "GONE WITH THE WIND" gets another Oscar?? Is Dr. Sara A. Hylwa even a real person?
A job well done, from those who want to discredit Morgellons disease. Who is behind of all? BAYER AG?
Almost all Morgellons sufferers do suffer from Lyme disease and an unknown fungus-like pathogen.
This is a fact and cannot be ignored by anyone! There are no delusional conceptions, but ineffective blood tests...
March 10, 2011
Morgellons in the bowels
February 24, 2011
Roundup Or Roundup-Ready Crops And An Unknown Pathogen
May Be Causing Animal Miscarriages and Infertility
October 24, 2010
American Medical Association Release "Morgellons is systemic"
Small Bowel Capsule Findings Suggest that Morgellon's Disease has an Organic Basis and is Not Psychosomatic in Origin!
Daniel Chao, MD, David Cave, MD, PhD University of Massachusetts Medical Center, Worcester, MA.
Purpose: Background: Morgellon's disease is a poorly described, severe ulcerative skin condition that histologically is consistent with dermatitis artefacta. It has therefore been dismissed as a psychosomatic disorder, much as was the case with ulcerative colitis in the period from 1930 to 1960. We present the first case of a patient with Morgellon's syndrome who had additional findings suggesting that it is a systemic disease.
Case report: A 65 year old white female presents to us with an unexplained iron deficiency anemia. She had a history of systemic lupus and a 2 year history of severe skin ulcerations. The ulcers contained fragments of black material. She had been seen by multiple specialists who told her that the lesions were self-inflicted and that she should get psychiatric care. Physical exam was of note for numerous papules with erythematous, ulcerated centers measuring 2 to 12 mm located on the trunk, back, upper and lower limbs and outer ear canal.
The ulcers were notable for sharply angulated corners and clearly demarcated edges. She had extensive scarring on her arms and legs. Her labs were notable for a hemoglobin of 9.1 g/dL with MCV 83.3, serum albumin 3.4, and ESR 32. ANA was negative. She had recently completed a course of intravenous iron. A video capsule was performed. This showed denuded villous patches in the jejunem, which were unusual for their sharply angulated appearance, similar to her skin lesions. Small bowel biopsies were normal. Skin biopsy showed hemorrhage and non-specific inflammation. Histology of the black debris from her ulcers suggested vegetable matter. Repeat capsule examination 6 months later showed spontaneous resolution of the denuded patches. Occlusion treatment on one limb led to some improvement.
Discussion: This patient demonstrated cutaneous ulceration consistent with Morgellon's syndrome, but she had co-existing evidence for systemic disease with iron deficiency, low albumin and small bowel villous changes consistent with a mild enteritis. This is the first time that evidence for systemic disease has been demonstrated in association with what has previously been considered a disorder limited to the skin. Further investigations are warranted in a larger patient population.
ADDED: Latest news from an Australian Morgellons sufferer
New, deadly and so far incurable Murine leukemia retrovirus found in immunocompromised individuals and now also in Morgellons sufferers. They don`t know much about MLV-XMRV and contamination processes except that it can be given by blood transfusion and animals. This was initially a virus found only on mice but it has mutated and adapted to humans. Therefore I must repeat it again: you need to test not only bacterial infections but also fungal and viral infections followed with appropriate treatments. This virus is triggered by stress hormones as cortisol and female hormones.
August 15, 2010
German Morgellons sufferer committed suicide!
I am deeply saddened and speechless about this very sad story, which took place in my region of Germany. I was in contact with Monika on a few occasions, but she was already so exhausted by the fight against her condition. I feel so sorry that I could not help her more!
After a nightmare of many psychatric hospitalizations and ingnorance of all doctors she planned her death and arranged her private affairs months in advance, before jumping to her death from the balloon one week ago. In her last letter, she wanted to help other sufferers with her death, to force authorities and doctors to be more aware about the Morgellons disease and the immense suffering it causes!
She wrote that she hoped her death would not be in vain, not senseless at all! Please pray for her. How many poor people must still die, until the media, politicians and the medical profession wake up? What a shame for humanity!
August 03, 2010
Morgellons Interviews with Worldwide Sufferers
July 14, 2010
May 10, 2010
FIRST GERMAN LYME CLINIC THAT ADMITTS MORGELLONS TO MAKE MONEY!!
After a lot of work and evidence from me to convince German physicians that Morgellons disease is real, I finally succeeded. The Lyme clinic (BCA) in my own hometown now states officially the existence of this disease called Morgellons. Latest information: I did split from them now due to many complains from worldwide patients!!
The clinic attests to Morgellons disease for their patients, but mainly to make more money without accurate serology or treatments. Myself and even most German Lyme association or foundations gives them no more credit at all!
April 28, 2010
Deathly Airborne Fungus In The USA!!
Scientists are slowly waking up now. Read the article, and see who gets harmed by this fungus. Humans, animals, and insects all get infected, all with symptoms similar to those of a Morgellons fungal infection. The facts are the same as those I wrote under "Epidemiology" about Morgellons spreading. But this deathly fungus is not Morgellons, let's be clear!!
April 17, 2010
Bayer admits GMO out of control (helpless losers!!)
April 02, 2010
"MYIASIS", "FILLAN" AND "THE MORGELLONS"
Despite that many are believing in Chemtrails as cause of Morgellons, read this "British Medical Journal" article below from 1946 send to me from a sufferer a few weeks ago. You can believe that it`s a fly, worm, fungus or what ever you want, but don`t tell me that all comes from Chemtrails and they want to kill us with parasites coming down from the sky!! There are many other reasons as possible cause but not Chemtrails or UFO`S!! And yes, also flies can carry fungal spores, viruses and all sort of bacteria.
March 18, 2010
Chemtrails are real but Morgellons disease is not caused by Chemtrails!
Most of the facts speak against that theory!! If Morgellons disease came from Chemtrails, we would see a larger number of infected mammals. Logically, one drop of any virus or similar substance dropped into any water treatment plant would more efficiently deliver disease than visible striking or spraying actions!!
Chemtrails (light-reflecting polymers) are sprayed mostly over the carbon dioxide (CO2)-producing major cities and serve only to stop global climate warming. This is done by covering cities with an artificial, cloud-like shield to reflects UV light and perhaps to absorb CO2, thereby reducing the average global temperature.
September 15, 2009
I am one of the many RNs with this dread disease. Early on, I had an MRI Scan done (head) that revealed lesions in the white matter of the brain. These could never be explained. I have always felt this was a significant finding in Morgellons Disease especially when I learned of others with this same finding. Presently, I am working with some qualified doctors ( neurologist, radiologist, etc.) to review as many of our MRI scans as possible to see if there are any commonalities or other issues within them.
If anyone has had a MRI Scan of the brain (head) since or even prior to contracting Morgellons and would be interested in taking part, please send me an email at email@example.com If this works out, there should not even be a cost since most medical facilities will send scans, reports, etc. to another medical provider at no charge to the patient. I sure hope this continues to be true.
will be getting back in touch with everyone sometime after Labor Day. I
don’t want to miss anyone that wants to be included..
Say prays and keep the power of God with us.
Please pass this request on to others who might be interested.
May 28, 2009
Kaiser Permanente is visiting my site quite often. If they really want to help sufferers, why they don`t even try to contact me? They, among others, can just visit me anonymously to see what I have found out or not. So, they do really have no clue about and they get even payed therefore visiting my site!! Is that their kind of investigations on Morgellons disease?
Kaiser Permanente did get last year 330.000 Dollar from CDC to investigate on Morgellons disease. For what? And this year?? And how much money actually did they have received from Monsanto or Bayer AG, to be quiet, how much?? We really want to know it!!
Maybe we should ask the CEO of Kaisers? http://xnet.kp.org/newscenter/aboutkp/bios/national/halvorson.html
Also the CDC (center of no disease control) comes sometimes on my site. They should rather give to me that money and they will get more regarding doing research. Do you really think that anyone of them has the will or spirit to contact me, just to help all U.S. sufferers and finishing this nightmare soon? I know you have already lost your money, home, work, partners, friends and health and nobody cares about you anymore, and many are living already in their cars, due to the lost of their homes and jobs.
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