Here’s Why Multiple Sclerosis Is Actually Lyme disease

Why multiple sclerosis is lyme disease

One of the biggest medical scandal’s of the last 100 years is the fact that since 1911 the medical establishment has known that Multiple Sclerosis is caused by a bacterium, and that Big Pharma have covered this up in order to profit from so called “MS patients”.

Medical research shows that the living Borrelia bacteria were found in the brains of people who had been diagnosed with MS.

Theeventchronicle.com reports: Time and time again. By at least a dozen medical researchers. In at least ten countries. Since 1911 – the past one hundred years. Several older but also recent autopsy findings linked to in this article found that all deceased MS patients’ brains harbored living Lyme spirochetes. Even when tests, notorious for their large percentage of false negatives were used on living MS patients, staggeringly many tested positive for active Lyme borreliosis.

Then why isn’t this common knowledge? Surely, those thousands of MS experts and MS researchers can’t be all wrong?

Let’s examine the reality on the ground.

1. Multiple Sclerosis Societies.

Every Western country has at least one MS Society. Each of those tax-exempt societies typically receives tens of millions of dollars in funding from various sources, year after year. The people running those societies usually award themselves CEO-level salaries and run them as one would run a highly commercial corporation. Advertising is used to solicit funds but if you don’t read ads then you’ll bump into them, one day, begging you for money on the street. For all those billions that have been pumped over the decades in those hundreds of MS societies worldwide, not a single one has ever done anything really useful for MS patients. The worst that could possibly happen for the bosses of those setups is that the cause of MS would become known. A known cause would either mean the development of either a cure or at least better symptom relievers, and that would rapidly result in the obsoleteness of their money making machine – the chicken that lays the golden eggs if you will. Such MS societies are working in concert with MS “researchers” employed by Big Pharma.

2. Big Pharma.

Multinational pharmaceutical corporations are the only ones doing MS research nowadays, mainly using donations to MS societies. Those multinationals decide which researchers get the cash. Researchers wanting to test the postulation of bacterial etiology of MS are shunned as if they were crackpots. Big Pharma makes billions a year on MS symptom relievers and they trickle millions down to their footsoldiers, the “MS experts”. A cure would be a severe financial blow. Even more so, because there is strong evidence that many other neurological illnesses are caused by germs as well. Because due to the phenomenon of immune privilege there is an inadequate immune response in the brain and spinal cord, making these organs the ideal place for certain slow-dividing spirochetal bacteria to entrench, multiply and cause lesions. The entire concept of antibiotic-resistant, hard-to-test-for chronic CNS infections leading to a plethora of neurological syndromes has to be suppressed and what can’t be suppressed will be craftily discredited. Better to give every expression of a neurological infection its own name such as “MS”, “Alzheimers”, “Parkinsons,” “ALS” and “Fibromyalgia”. And fund armies of ignorant “experts” to obfuscate the issue, whilst boycotting, firing, censoring, smearing and suing those few real experts that refuse to stay in line. Big Pharma is in business to make money, and money is made when people are ill, not when they’re healthy. Anyone standing in their way is relegated to the sidelines. Patents are being bought and shelved so that cures will never see the light of day.

3. Patient advocacy groups.

MS patient groups are, without exception, populated with clueless individuals for the simple reason that those who did their homework and read the relevant research have been ostracized by the group. They always were and they always will, because that’s how group dynamics works. As soon as you insist on voicing an opinion outside of the mainstream, no matter how well argued – you’ll be an outcast, a pariah. They don’t want rogue activists, “lone nutters”, giving them a bad name. Also the advocacy groups are raking in the dough and are run by folks whose main concern is that membership dues are paid in time. No MS, no advocacy group. Of course if there ever will emerge a lobby group insisting on more microbiological research pertaining Multiple sclerosis, they’ll be branded “lunatic fringe” and their efforts will be in vain.

4. MS “experts”.

Those “experts” get away with calling themselves thus, because Big Pharma gives them their seal of approval in the form of research grants and medical media exposure. However they are only experts in doing exactly what Big Pharma wants them to do: Obscuring the cause of Multiple Sclerosis! In return, the “experts” get regular cash injections for their “promising research” and other goodies such as all-in holidays to exotic destinations. There never will be a cure for MS until the scandal breaks and new antibiotics are developed that work better than the few currently available antibiotics that cross the blood-brain barrier. As it stands, it has been more than twenty years ago since any new antibiotic was developed. As soon as it was found that Minocycline helped with MS, its manufacturer, Lederle, tripled its price.

After long consideration I came to the conclusion that at least a crucial part of this debâcle was due to a real conspiracy – mainly a conspiracy of silence of those few MS researchers bright enough to realize that the cause for MS has been known for at least a hundred years. As is always the case with medical cover-ups, it continues to exist due to a mix of ignorance, indifference, cowardice and corruption.  The saying goes: “Do not attribute to malice that what can be adequately blamed on ignorance”. All the “experts” really are interested in is being “experts”, not curing Multiple sclerosis.  However it still is a conspiracy. It is completely normal for conspiracies to succeed because the lion share of the people who could point it out don’t care, are too lazy to get educated or feel too intimidated to stick out their necks. Microbiologist Tom Grier calls them cowards. The fact that most conspiracies are silently facilitated by an army of “useful idiots” with a stake in it being kept under the rug does not make it any less a conspiracy.

  • TR3B

    Money makes the world go round, the world go round …

  • Mollie_Norris

    Psychiatric Lyme:
    What Every Mental Health Specialist
    Should Know About Lyme and
    Tick Borne Illness

  • Mollie_Norris

    The coverup behind the institutional corruption and greed; Lyme Disease is a Nazionist biowarfare agent:

    ​The Creation of Lyme Disease on Plum Island: The Logic of Claims​

    ​February 10, 2016 in Science & Research by Chris, Editor-in-Chief of Public Health Alert
    http://www.publichealthalert.org/the-creation-of-lyme-disease-on-plum-island-the-logic-of-claims.html

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  • Fingal Carson

    Maybe parasites, but lyme disease is a sheeple farce. Almost no one gets it, and if you do, you KNOW you got it. You’d take antibiotics and get over it in a few days.

    • Emmett Grogan

      Um, sorry, but you dont seem to know the facts. Fact is LOTS of people get it, press just doesnt mention it and many docs will tell you it doesnt exist. However, I lived at ground zero when this was discovered there. Lots of people had it there, and one even died not long ago. Im married to an immunologist who explained to me what it was, what caused it etc. The science all holds together. Ive known quite a few folks in my life who had it and my husband, who worked for the state has certainly seen any number of cases.

      • Fingal Carson

        many docs will tell you it doesnt exist

        LOL! God you’re an idiot. It’s the opposite. Doctors tell everyone it exists to keep pushing unnecessary antibiotics (oftentimes for years). Get your shit straight.

        • kali amanita

          again, NO. name calling doesn’t make you right…..you are pushing bad information, please stop.

          • Fingal Carson

            Truth = bad information, to you. Talking about Orwellian. LOL!!

        • Lymie

          You are incorrect. Lyme is very underdiagnosed and improperly treated most of the time. Most docs are not educated on proper diagnosis and treatment. Big pharma loves Lyme to be misdiagnosed. Then it becomes chronic. Instead of the simple 30 day cheap doxy, you are now on several meds for life. Insurance companies don’t want to acknowledge Lyme because it is very costly to test and treat properly.

          • Fingal Carson

            How much does Big Pharma pay you to play devil’s advocate? Must be nice.

    • Emmett Grogan

      P.S. – And no, you don’t atibiotics and get over it in a few days. They must be taken as soon as exposure happens but it doesn’t always work, I’ve personally known folks that it didnt work for.

    • kungfool

      Some people get over it, some people do not. Sometimes the symptoms are suppressed by the antibiotics and when they are stopped, the symptoms come back, but the doctor denies that they are caused by Lyme because the book says that the antibiotics are supposed to cure it. These are not Lyme-literate doctors. Many more people are misdiagnosed because the Western Blot test often returns a false negative. That’s well documented, but most doctors are unaware of it.

      • Sha Black

        Fuck it I have ms

        • kungfool

          You might want to be checked for Lyme by a Lyme literate doctor. These are few and far between. I don’t know if you have Lyme but I do know that MS is the disease without any cause. No one knows what causes it and the MS societies and pharmaceuticals are not interested in finding out..

    • kungfool

      And by the way, my wife contracted it in the early 90’s, long before anyone knew how to diagnose it. So she was infected for 15 years before we finally figured out the cause. All that time we were told she has MS. She can’t tolerate the antibiotics either.

      • Fingal Carson

        You really believe a person can live with LYMES for 15 fucking years? LOL, my GOD you people have been duped…

        • kungfool

          So you don’t believe in test results?

        • kali amanita

          your ignorance is showing, you’re making an ass out of yourself..but i bet you get that a lot. please stop!

          • Fingal Carson

            WHAA!! I can’t handle the truth. Here’s a mirror:

            your ignorance is showing, you’re making an ass out of yourself..but i bet you get that a lot. please stop!

        • canardtahiti

          my daughter contracted lyme at age 15, it became chronic and she died of it last year at the age of 46 after of life in hell. YOU ARE AN a-hole.

          • Fingal Carson

            Paid big pharma shill.

          • canardtahiti

            not at all, my daughter was allergic to antibiotics and to ALL pharma meds…on what planet do you live, Fingal? Despite that, we helped her through a difficult life with only natural substances, whereas Big Pharma wanted only to give her anti-depressants.

    • Desmond Kahn

      That is an ignorant statement by someone who has been badly misinformed. So badly misinformed that there is no point in discussing things with him.

      • Fingal Carson

        You might (think you) have lyme’s disease for decades, but you’ve had and will have the libtard/Marxist/Zion disease for a lifetime.

    • https://twitter.com/KenSlackBledsoe Slackaveli

      shut the fuck up, nazi

    • kali amanita

      that is incorrect. please do not spread false information, too dangerous.

    • Mary Gounsolin

      said the idiot who knows nothing about it

      • Watcher

        This ‘idiot’ knows everything about it. The CDC employs people who watch sites like this. They also comment on Lyme articles on the internet. They’re paid to do this in an effort to discredit information posted by those who know the truth about Lyme and other vector-borne illnesses. By arguing with us, they create uncertainty in people who don’t know much about Lyme and aren’t sure what to believe. The CDC’s home page is full of them.

    • Kay Rowe

      Fingal, Your statement about many people getting over Lyme is true for a lot of people. But in many people, such as myself, I am allergic to Doxycycline, the first choice of treatment for Lyme Disease. I also have had Rheumatoid Arthritis for 28 years. It is an autoimmune disease that compromises the immune system, so those were “double whammies” for me. Lyme was positive in my blood for five years 2005-2010, and for twelve years, I felt like I had the flu everyday, until in June 2016, a lab technician in my RA doctor’s office took my hands and said a prayer for me. I could tell that she is a person who is really close to God, and knows the Bible inside and out. Three days later, I woke up and as soon as I opened my eyes, I realized that I did not feel like I flu. But Lyme Disease affected my nervous system. Sometimes, when I am getting ready to go somewhere, I get so nervous, that I feel like I am having a panic attack. I have to allow myself extra time, so that I can sit in my recliner for a while, take deep breaths, pray, and talk myself down- just so I will be safe to drive. From Aug. 2016-Aug. 2017, I suffered with a lung problem. I have never smoked, so when I started spitting up sputum everyday, only once daily, I took a sample to my PCP doctor. He did a regular lung x-ray, and it showed small nodules in my lungs. Thereinafter, it was found that I had two bacteria in my lungs. I had to take antibiotics for almost a year, and go off of my Enbrel SureClick injections for my RA, as the Enbrel kills your immune system, so your synovial fluid will not attack your joints. Then, I had to go on Prednisone for that year, and go off of Enbrel, as the antibiotics and Enbrel would be working against each other. The Prednisone, which you may know, causes patients to gain weight. I could write a book, but there are thousands of people out there with Lyme Disease who are not getting the proper treatment. I was referred to an infectious disease doctor because of the Lyme. She talked to me for three hours, and wanted to give me IV antibiotics. Whenever a patient is being treated for Lyme Disease, the doctor has to report it to the Centers for Disease Control. I was so excited, after seven years of suffering, that someone was finally going to help me. But, alas, the doctor called and said that the CDC would not let her treat me with IV antibiotics. Come to find out, there was a doctor in North Carolina who was giving IV treatments to patients with Lyme Disease. It was a big deal, went through the courts, etc., and he ended up losing his Medical Degree. Even the Medical College of Virginia, a research hospital will not see people with Lyme Disease, as it mimics so many other diseases. It is called “The Great Imitator”. Last year, I was diagnosed with Raynauds. It is not really a disease within itself, it is a symptom, that people who have compromised immune systems will sometimes get. It is a condition that causes you fingers to be numb, tingly, peel, and th fingertips, and so slippery,, it is hard to work with paperwork. They are just slick feeling on the bottom, and sometimes they look like I have been swimming in water. Oh, and they are cold all the time. There is a lot more to tell about my difficult struggle with this horrible disease. I know some people think I am just looking for a “pity party”, but that is the farthest thing from mind, that is just a small part that I have dealt with since I was age 55. Now, I am 67, soon to be 68, and it has been devastating to my life. I just pray when I go to the hospital next week for my third CT scan, that the nodules will still be small. I am chronically fatigued, have anxiety and depression, which then leave to isolation. It has been a very difficult road to tow. I don’t know if you are familiar with Avril Lavigne. She is a young singer, who became very sick. They did an interview with her on ABC, which you can see if you search her. In the interview, she said she just felt like she could do nothing. She would stay in bed all day. The doctors took seven months to figure out that she had Lyme. Anyway, I watched that video, and it made me so sad, as I could totally could relate to what she was saying. Also, Crosby Stills, of Croby, Stills, Nash and Young- he died from Lyme disease, as did Johnny Cash’s sister. When I was in the “throws of Lyme”, I would go to bed at night, and pray to God, not to let me wake up the next day. Then, when the next day came along, I would cry for like 2 hours, with my dog coming over and putting his head on my legs. I would put my arms around his neck, and just cry. I had him for 14 years through that journey. He was a beautiful gold and white border collie, with a blonde nose and green eyes. I miss him so much, even though it has been 4 years since he passed away. My family had a lot of dogs over my lifetime, and they all lived a long time. All of them at Purina Dog Food. Sometimes, if we were using paper plates, we would let them lick the plate- and you would have thought we were giving them a steak. Each dog had their own personalities, but my border collie was my own dog, and she was so smart. She would know the days that I felt worse than others, and she would not ask to go out as much. Sometimes, I would feel so badly, that I would open the back door, the door to the garage, and the door exiting the garage to the six foot privacy wall and the large backyard. He was then able to come and go as he pleased. But ever so often, he would come in to check-up on me. I don’t have any worst enemies, but if I did, I would not wish Lyme upon any of them. Sorry, I got so carried away. Take care- Kay

  • Kane

    Its not one of the biggest cat all bits just one of hundreds of normal business operations principles and practices they train their staff with The biggest scandal is that ” they” are all frauds and money hungry thieving lying parasites evolved from the torture chambers run by the sadists under the inquisition ,witch hunts and other community goodies activities which have conditioned the world into living under the reign of terror imposed by them and marketed as good deeds done daily for mankind’s salvation .

    • Kane

      Its not one of the biggest scandals ,——sorry for my auto corrections ” remedies ” ,especially since its actually turned off on my device ,but somehow manages to just make it’s presence felt regardless .

  • https://www.facebook.com/beefree Chaffee

    if want to get over MS and or Lyme check out spooky2 I had lyme 40 years and nuked it out of my brain body… almost died… lyme disease is deadly most people do not know what it really is… lyme is a gmo biowarfare delivery system to take out US enemy’s the problem was that there was an accident..now everyone is infected…fastest growing std in the world right now

  • Desmond Kahn

    This is written with a rather ridiculous tone. Can you please cite peer-reviewed papers that document Borrelia in the brains of MS patients? You have not done so. In fact, you have provided no evidence to back up your claim. Cough it up, Sean.