This is the deal with “Lyme disease”- There are three sides to every story

The CRYME is the disease.  The DISEASE is the cryme.  This is the deal-

  • Spirochetes are Relapsing Fever organisms.  That means that they are capable of antigenic variation, which is the term used to describe their ability to change their outer surface proteins (Osps).  It’s like taking off one coat and putting on another.  They have different forms, too, like cysts, granules, L-form…etc.  It has been known for over 100 years that you cannot kill spirochetes (with even arsenic, they just go into cysts when they feel threatened) and that they are permanent brain and lymph node infections.  Antibodies do no good because as soon as they are made by the host they just “change their coat”.  Antigenic variation is also the reason why a vaccine for spirochetes is impossible.
  • . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
  • These shed blebs are endotoxins and they are what cause illness.  These triacylated lipoproteins are TLR 2/1 agonist which means that they are fungal-like and they shut down the typical chain reaction of immunity.  For example OspA is pam3cys.  You can literally buy pam3cys and use it to induce sepsis for experiments.  When you have spirochetes in your body constantly shedding these endotoxic blebs you end up with chronic sepsis or post sepsis syndrome (PSS), eventually losing the ability to recognize other pathogens as well.  This is called endotoxin tolerance or immune tolerance or cross tolerance.  Common latent viruses that everyone has (like EBV, CMV, or Herpes etc.) reactivate when given the chance and they cause a whole plethora of syndromes and diseases on their own.  What this boils down to is a B cell AIDS like disease with characteristics very similar to leukemia or lymphoma.  (Click HERE for a post about “Lyme disease is like CANCER and AIDS”)
  • . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
  • Antibiotics or herbs or rife machines or diet or anything you could think of that LLMDs make available to patients will not reverse this damage to B cells.  It has been said definitively that patients fail treatment due to pathologic changes BEFORE any treatments take place.  So, if you’re bitten by an infected tick you have a 50/50 chance of eventually becoming disabled no matter what.  ILADS nor anyone else seem to recognize what this disease actually is.
  • . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
  • If the LYMErix vaccine caused the disease and was only OspA that tells us that this disease is not about spirochetes, but about the Osps and that is because the Osps are endotoxins as mentioned above.  It took me a while to understand that, but it eventually did click and then I finally could understand why so many of us continue to get worse no matter how much money we spend or how many different “treatments” we put ourselves through.  It’s not about biofilm, either.  Killing spirochetes or any other pathogen in the host will not fix the damaged B cells.
  • . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
  • The worst part about betrayal from ILADS of withholding the truth about what this disease is actually is- THEY KNOW.  They know that the disease is not treatable with antibiotics or about persistence/biofilms because Kathleen Dickson, the LYMErix whistleblower and former analytic chemist from Pfizer, told them as she was a part of the organization years ago.  Kathleen is the main author of their Klempner rebuttal.  Yeah.  Ouch.

 

“The truth will set you free, but first it will piss you off.”

 

It’s not denial from the CDC preventing our access to proper diagnosis and subsequent treatment.  It’s worse.  

  • Before this went down the disease was called “Lyme borreliosis”.  The name “Lyme disease” is a misnomer as it only describes a very narrow minority of patients who have an odd hypersensitivity/allergy response to spirochetes.  The rest of us, the sickest patients, are left to be slowly tortured to death.  The 85% excluded from the opportunity of early diagnosis and subsequent treatment (a million people a year) have been slandered and libeled and called crazy for the past few decades.
  •  . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
  • Allen Steere, Alan Barbour, and Barbara Johnson along with members of the ALDF colluded to spin the disease to fit their vaccine model.
  •  . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
  • Allen Steere traveled to Europe in 1992 to illegally change the testing.  Implementing the two-tier method he raised the bar on the cut-off for the ELISA to rule out all the chronic neuro outcomes who get immunosuppression in the first step.  Then, he used high-passage strains that had dropped the OspA/B plasmid so that these primary immunodominant antigens would be omitted from western blots.  This is scientific FRAUD.
  • . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
  • Then in 1994 Barbara Johnson set up the famous “Consensus Conference” in Dearborn, Michigan.  She invited labs from all over the country to participate but ignored their recommendations even though it was found that their method for testing was only 15% accurate.  The two-tier method that we are still stuck with today is designed to only pick up the cases of “Lyme disease” that are the HLA-linked hypersensitivity response (lots of antibodies, this is what “CDC positive” is) and these patients mount a strong enough immune response to prohibit them from getting sick like the other 85% of us, their only symptom really is an arthritic knee (except for 1.2% of cases who are unlucky enough to get both according to Brian Fallon).
  •  . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
  • Since, both the testing and the very case definition of “Lyme disease” is a straight up FRAUD CRYME.  All because they wanted to sell an endotoxin (OspA is pam3cys) and call it a vaccine
  • . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
  • Inevitably when it became apparent that this fake vaccine was making people very sick the slander had already began against their victims.  In 1999 ActionLyme, founded by Kathleen Dickson, started getting phone calls from recipients who were telling her that they had “Lyme again”.  She thought “How could this be?  There are not whole spirochetes in LYMErix?”.  The campaign began to get the adverse events reported.  This led to lawsuits being filed against the manufacturer, SmithKline, and an FDA hearing was called to assess the claims.
  • . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
  • It ended with the FDA giving SmithKline an ultimatum- either they voluntarily take LYMErix off the market of they would.  This was because Karen Forschener of the LDF gave them a patent owned by Brigitte Huber of Tufts University that said OspA was an endotoxin.  It was not due to low sales or “anti-vaxxers”.
  • . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
  • Richard Blumenthal was the Attorney General in Connecticut at the time that he filed an anti-trust suit against the IDSA over the testing.  Nothing ever came of this, obviously.  In 2003 he advised Kathleen to file a complaint with the Department of Justice (DOJ) about this cryme.  Numerous attempts have been made in the meantime to get this prosecuted.  It has been 13 years and here we still are, waiting for them to do their job.

 

“It has to be prosecuted in order to vindicate and validate all of the suffering out there.  All the misery, all the rejection, being declined social security disability, social ostracization, and all of the misery of having to live like you’re a ghost in society.  Nobody sees you, nobody cares about you, you’re just not there.  The only way we can bring these people back into the world is to have it prosecuted.  Thats what our agenda is.”   -Kathleen Dickson, LYMErix Whistleblower/Chemist- Quote from the free documentary “Lyme Cryme” on YouTube

 

What has been going on the past 2 decades since?  A lot of nothing.  A lot of wasted research monies thrown in the garbage because it is all still based on this made up version of the disease.  A lot of fake non-profits (like the LDA) have been started where the presidents make a cozy $90,000 a year salary while forfeiting telling patients the truth about the disease that is literally burying them alive.  A lot of wasted money spent by patients on treatments that will do them no good, bought from an organization (ILADS) that knows it will do them no good.  This is the ultimate betrayal.  This is the shameful affair that Willy Burgdorfer spoke of.

The only ones that want this to get better are us.  No one else cares about us.  Why would they?  Leaving things the way they are is good business for them.  People are homeless and killing themselves, babies are being born congenitally infected every single day.  The horror and suffering is increasing at an alarming rate and we are getting raped for our last pennies from every side.  The false dichotomy between ILADS and the CDC that we have to choose from is as relentless as the disease itself, infecting not only our brains but our livelihoods and entire future.  All of us victims share a collective story, the victims who get the diseases that no one cares about.  Let’s start telling our collective story and stop being encouraged to focus on personal narrative that gets us nowhere.

The truth is more powerful than their lies.  The truth is like that little candle in a room full of darkness, even though it is small it is enough to show us our surroundings.  Once their lies are shown by the light there is no going back.  All of us are in the same room, suffering because of the same crime, but we react to the light in a different way.  Some people have been in the dark so long that the light hurts their eyes so they keep them closed.   Other people see the light and could care less, they just want out of the room and they don’t care that anyone else stays trapped by their silence.  Others even try to blow the candle out so that it stays dark because they don’t want anyone to see the truth.  Then there are those of who make it our mission to keep the candle burning, and try to make it brighter by using it to light more candles because we want everyone to have light in their lives again.  We make it our mission to make sure that no one is left in the dark, cold and alone.   Probably my favorite thing that Kathleen has ever said is “Love means do”.  So I do what I can, because another thing that she has said is “this is a soul thing”, I believe that wholeheartedly.

“So if you get bit by an infected tick you have a 50/50 chance of ending up.. completely screwed.  So we need to start thinking differently about activism.  Activism isn’t about commiserating with other sufferers online- it’s about the bigger picture of who else in the world is suffering.  We’ve got two million people a year, a million of them becoming  disabled eventually, so we’re talking about the million who are going to become disabled next year, and the year after that, and the year after that.  Activism is not about talking in circles about who is suffering the worst.  It’s about helping these other people down the line.  Because you keep talking in circles, an nobody hears a thing you say.”    – Beaux Reliosis, Real Activist and Co-Founder of TruthCures

Prosecution is the only thing capable of mounting profound enough change to make a positive difference in the life of every single person out there suffering right now and in the years to come.  We are currently looking for bloggers and true activists to help us accomplish this monumental task.  We can do this.  There are better treatments (Rituximab was shown to work and it fits the disease mechanism model), people could get disability, not become homeless, friends and family would stop abandoning us, people wouldn’t feel like they need to commit suicide as their only treatment option.  The data TruthCures has vindicates and validates every single person out there.  You, the person reading this, DESERVE RESPECT AND TRUTH.  We can prove that you are as sick as you feel to the entire world and make sure that no one else has to suffer as we have.

Let’s do this.  Let’s fight.

Visit TruthCures.org

Find us on Facebook at https://www.facebook.com/truthcureslyme/

Join our activist group on Facebook at https://www.facebook.com/groups/OccupyUSDOJ/?ref=bookmarks 

 

Leave a Reply

Fill in your details below or click an icon to log in:

WordPress.com Logo

You are commenting using your WordPress.com account. Log Out /  Change )

Google photo

You are commenting using your Google account. Log Out /  Change )

Twitter picture

You are commenting using your Twitter account. Log Out /  Change )

Facebook photo

You are commenting using your Facebook account. Log Out /  Change )

Connecting to %s