PROOF!  A New Designer “AIDS”

PROOF! A New Designer “AIDS”

http://www.maxresistance.com/proof-new-designer-aids/


PROOF!  A New Designer “AIDS”

We at Max Resistance we’re shocked by this personal story of Karen Lambert, we are so pleased she contacted us to put her story forward and support her on this important journey.

Karen has fought this battle bravely with the main stream media refusing to acknowledge or report on this. Which leaves it up to us in the Alternate Media to spread her plight.


 

“Could I be you?” Karen Lambert’s Struggle with HIV-Negative AIDS

 

I have Chronic Fatigue Immune Dysfunction Syndrome (CFS/CFIDS/ME) and HIV-NEGATIVE AIDS, idiopathic CD lymphocytopenia. With these two clinical diagnoses, I believe that makes me living proof that the AIDS-like CFS/ME is transmissible, something that the medical establishment seems unable to admit or to acknowledge. I also believe it makes me living proof that CFS and HIV-NEGATIVE AIDS are basically the same mysterious immune disorder.

Three years ago, after a heterosexual sexual encounter, I became seriously ill with what looks like the natural disease progression of AIDS. After an “acute infection” and a “period of asymptomatic
health”, I have fallen extremely ill to an unrelenting, progressively-worsening AIDS-like demise. I can pinpoint exactly when I was infected with my “chronic viral syndrome of unknown etiology”
and because the “acute infection” stage was so distinguishable, I can also pinpoint exactly when my undiagnosed pathogen left my body and infected yet another host.

Whatever I am currently dealing with, it strongly resembles classic textbook HIV/AIDS disease. But, to add to my inquiry, I also clinically satisfy the CDC’s criteria for the diagnosis of Chronic Fatigue Syndrome.

by Karen Lambert

www.cfsstraighttalk.blogspot.com

Continue reading Karens story here

Karen_lambart+vials

 

Allied NATO Government is hiding millions of infectious NON HIV AIDS cases

under the “Chronic Fatigue Syndrome (CFS)” ICD-code.

  •  Dr. Lorraine Day on Cptn. Joyce Riley’s military show THE POWER HOUR (09/12): “…HIV-Negative AIDS cases falsely reported and treated as CFS cases may be one of the biggest cover-ups…”
  • In 1992 (i.e., after Gulf War 1) “…Newsweek made an even more shocking announcement: …CFS patients who had the same immune system deficiencies as the NON-HIV AIDS cases…”
  • Dr. Judy Mikovits stated on In Short Order (11/12) about CFS & Myalgic Encephalopathy (ME): “…consider this as NON HIV AIDS.”
  • Chapter 33 of Hillary Johnson’s acclaimed book “Osler’s Web: Inside the Labyrinth of CFS” is entitled “HIV-Negative AIDS.”
  • Neenyah Ostrom’s book “America’s Biggest Cover-up: 50 More Things…CFS & Its Link To AIDS” cites: “Some CFS Patients May Be Non-HIV AIDS Cases.”

 


Who is Karen Lambert?

 

Karen_lambert_photo

I have a Master’s degree. I am a director at my firm. I used to be a triathlete. I have never used IV drugs. I have never traveled abroad. I can count my sexual partners on two hands. Statistically speaking, I know that my undiagnosed infectious and communicable disease is not rare…so, you tell me, if they are not in the miscellaneous CFS/ME category, where are all these other immuno-suppressed people?

Anyone with CFIDS, who does not consider the possibility that CFS/ME will eventually progress to a NON-HIV AIDS diagnosis, is very well trumping their own ability to diagnosis the root cause of their illness.

Why isn’t CFS/ME a reportable disease overseen by our public health department? Why are CFS
and ME (i.e., the same exact disorder) suspiciously categorized as two separate illnesses on a
worldwide level (i.e., by ICD codes)? Doesn’t anyone else but me, very clearly see, the
catastrophic cover-up going on here?

Why are we not reading about NON-HIV AIDS cases (and/or the AIDS-like nature of CFIDS)
on the front pages of every newspaper in the world? And if CFS/ME is NON-HIV AIDS, then,
depending on who you believe, there are anywhere between 500,000 – 14,000,000 Americans out

there with a transmissible illness. If that is what it truly is, our new form of AIDS dwarfs the
‘original’ AIDS epidemic —> TENFOLD.

I am not afraid to say that I have AIDS without HIV –> idiopathic CD lymphocytopenia. I am equally as unafraid of saying the most obvious thing about CFS/ME: IT SURE DOES LOOK
LIKE AIDS TO ME.

If it takes courage to think and to say the things that I do, I hope that there will be a miraculous
outbreak of bravery from coast-to-coast. I stopped fighting for myself a long, long time ago. I
fight for humanity.

I demand a CFS/HIV revolution. Vive La Revolución .

CFSgate = AIDSgate

The medical establishment will have you believe that Chronic Fatigue Syndrome/Myalgic
Encephalomyelitis (CFS/ME) is some sort of mysterious illness, but it’s no mystery to me;
CFS/ME leads to NON-HIV AIDS, idiopathic CD lympocytopena (ICL), a clinical diagnosis I
possess.

How can the AIDS establishment continue with a stale “it’s caused by HIV” theory when there
are ICL cases cited in medical journals dating back to 1992? While millions of ailing
immunodeficient CFS/ME patients get belittled and neglected, perfectly healthy HIV+ people are
allocated billions of dollars in taxpayer money. How can it make sense to anyone?

In the U.S. last year, the NIH spent $3.1 Billion of our tax money drugging perfectly healthy HIV+ people. Sick, ailing immunodeficienct (some of us dying)

CFIDS patients received $6 Million. How can it make sense to you?
source:
report.nih.gov/categorical_spending.aspx
It’s so easy to see that the medical establishment simply has these paradigms (CFIDS, HIV) inverted. AIDS patients are simply more CFIDS patients, who also happen to harbor a seemingly harmless virus, HIV. AIDS patients are just the tip of the CFIDS iceberg, and it’s already well-documented that HIV is not the cause.

How else do you explain why there is no CFS/ME pandemic in the HIV+ population? CFS/ME
does not discriminate. The answer is that there is; any otherwise perfectly healthy HIV+ person that is:

  • 1) symptomatic,
  • 2) better on ARV’s, and/or 3) severely immunosuppressed (AIDS)……is a CFIDS patient.

Putting causal pathogens aside, simply rename CFIDS, ME, and AIDS all to be “low natural killer cell disease” and only diagnosis patients with “low NK cells” with it. Everyone would clearly see that:
CFIDS + ME + AIDS = low NK cell disease = one catastrophic pandemic * * not caused by HIV

Allied government sold-out global public health for sake of profit–> industry, oil, and Orwellian greed. If I weren’t only 25% alive, I often wonder if I should  ‘Occupy’ the White House.

Now that the mystery has been solved, could we please stop wasting time and re-allocate all HIV

funding into CFIDS/ME/AIDS research?

More on this topic:

 

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35 Comments

  1. Avatar
    Angela March 31, 2016

    I had a similar problem. I am well now. Go to this website and see if this is what you’re going through: Dr.Lam.com.
    Then call Bryan Bradford in Texas (which is local for me). He helped me personally get back to normal with vitamins and herbs. I know it sounds crazy, but I was desperate and it worked. He will need your blood work report. It is $50 for a thirty minute meeting, which he normally spends an hour with you for the same price. Don’t let people call you crazy and put you on muscle relaxers and antidepressants. Get help.

    • Avatar
      Vicky November 21, 2016

      What city in Texas?

  2. Avatar
    Edith Gibbs March 09, 2016

    I was a very healthy person despite a severe reaction to a smallpox inoculation when I was eighteen years old and had recurring sore throat infections which caused me to have a tonsilectomy. I came to the U.S. in 1973 and was required to get a Hepatitis B shot to work in the ER. Following this shot my health deteriorated with symptoms of chronic fatigue. I was diagnosed with Fibromylagia since then. I am now 73 years old and have had fatigue and muscular pain almost every day of my life since then.I think I got an infection from that shot. Prior to the shot I was full of life and was able to ha e a full time job,go to college part time and I enjoyed vacations etc. Following this shot I was Jane to do any more than my job. I was Jane to join in family fun and I dragged down many of my family and friends.
    From my own research I believe I was infected with the “AIDS” virus. This was given to me when the New York vaccine was contaminated. It had a very bad effect on my life. I would like to assist anyone I can with similar problems.

    So merely E.G.

    • Avatar
      Melissa August 21, 2016

      It sounds like the batch from which your shot was stored became contaminated with fungi aka a fungal antigen. Humans do not tolerate fungi of any kind very well. Fungal antigens cause immunosuppression and reactivate latent herpes viruses like EBV. I’m dealing with the same non AIDS like illness except my fungal contamination was from contracting Lyme disease (aka Borrelia burgendorferi, which is bacteria-like organism that causes Lyme disease). This particular organism is a spirochete, which has a outer protein coat/layer that houses yet another organism called OspA – a Pam3cys fungal antigen.

  3. Avatar
    shirley stevenson January 09, 2016

    P.S I am fifty-two ! lol

  4. Avatar
    shirley stevenson January 09, 2016

    Well…My whole family has auto immune . My sister died from Lupas my Older brother has Chrones my older sister has Lupas my younger brother has Rheumatoid arthritis my younger sister suffers but seems to be ok . And I .. I have chrones and fibromyalgia, and who knows what else.. I have been sick since I was five years old and the last 10 years have been unbelievable . I have been in the hospital every year at least once and sometimes up to ten . I have had at least one hospitalization a year for at least 4 – 7 weeks long and the answer is always chrones flareup ! If that is so then why call it a flare if it never stops . I can write several books on how sick I have been and I for one do not believe what they are telling me . I am very sick and no medications are working and I really call them poisions ! I have no hope and my doctors think I am crazy !

  5. Avatar
    Deb May 27, 2015

    i strongly suggest you get tested for Lyme and coinfections thru igenex.com. It is well known in the Lyme community that CFS, fibro, lupus, MS, all auto immune diseases are caused by Lyme and Coinfections but that standard testing is so bad that most are labeled with “symptoms of unknown origin” diseases. Lyme, a spirichetal organism is the smarted cousin of syphilis. It hides in tissue and white matter, muscles, joints, brain, organs and central nervous system, and inside of red blood cells so it looks like the body is attacking itself. It is growing at 10 times the rate of AIDS. It transfers inutero and thru breastmilk like AIDs and it is sexually transmitted. It kills if untreated. Hundreds of thousands of people are going g undiagnosed, misdiagnosed, untreated every year because CDC won’t treat it. Contact me if you would like more info.

    • Avatar
      Dee January 31, 2016

      I would like to know what test could i have done to see if i have it

  6. Avatar
    alissa May 17, 2015

    Can you relate this to Morgellons & possible chemtrails exposure?

  7. Avatar
    Charla Shamhart May 02, 2015

    It is possible to reduce the viral load in the body by reducing L-arginine foods and boosting L-lysine. Anti-viral herbs and nutrition has helped many dealing with viruses. Dr. Tent from Detroit speaks about this in a video on auto-immune disorders, which he claims are all viruses.

  8. Avatar
    lemonfoundation March 08, 2015

    JOIN US ON FACEBOOK:

    HIV NEGATIVE AIDS?

    facebook/HIV-Negative-AIDS

  9. Avatar
    Jill McLaughlin February 26, 2015

    ME and CFS are not the same. ME is a neurological illness, not a fatigue syndrome. They are in different chapters of the ICD for good reason, not due to conspiracy. ME was recognized long before AIDS existed. CFS is such a broad diagnosis that some patients may have these abnormalities but do not just hitch it on to other illnesses. Stop misrepresenting other illnesses.
    One person is not proof of anything.

    • Avatar
      lemonfoundation March 08, 2015

      Myalgic Encephalomyelitis (ME) existed long before Gulf War Syndrome/Illness (GWS/I, which started to present after Gulf War 1, circa 1992).

      “Dr. Melvin Ramsay formally coined the name “ME” in 1956…” that would be the decade we started using commercial nuclear power and vaccination programs commenced.

      check inforwars search health hiv negative aids it is scs me gws or aids.

    • Avatar
      Cassie June 15, 2015

      In my oppinion the NHS GP’s and Consultants need to be educated and informed! I have Neurological problems which after recent stroke like illness I now believe is Lyme Neuroboreliosis, spine and brain problems, joints, body temp control problem, Vitiligo in fact a list as long as your arm and exactly as many diagnosed with MS! I am told I don’t have MS and I didn’t have a stroke but they don’t know what is wrong with me (I am now about 40% recovered) other than my lesions are consistent with migraine and I have swollen vascular vein on my central cord! I can only describe that I completely “BROKE” brain and body three years ago and all I get is “it’s Migraine and possible CFS”. I am not going to push any longer as I believe all the medication almost killed me and that is all I get! Constant misdiagnosing for myself and now what hurts more is my daughter, she has been dropped from A levels due to the constant migraines, cant walk for long due to joint pain like arthritis and can’t eat as so often feels sick – she now has no friends, school, job or life as we have no money and all she is getting is “tension headaches and possible CFS” IT JUST ISN’T GOOD ENOUGH! She managed to get 15 GCSE’s but now her brain doesn’t work and if she tries – migraine kicks in big time! 🙁
      Unfortunately the NHS now seem to call it ALL “CFS” regardless of the severity of symptoms and I believe it’s because they just don’t have a clue!!!!

  10. Avatar
    James Ettles February 26, 2015

    I can pinpoint my first period of illness back in the very early 80’s. I went to bed a very active child (and I mean very active) and then woke on the start of the summer holidays (I was about 12), spent that summer in bed, with no energy. Only found out off my mum recently that they were so worried and fought with doctors for help. I did recover, but not to the same levels as before and not long after I fell seriously ill with Chicken Pox, spent most of a couple of weeks asleep. Recovered enough to spend the next 15 years with a close to normal life, but still at 50% of previous ability activity wise.

    Now I am not unqualified, I left High School with good exam results, even though I missed nearly a whole year of schooling, went on to gain qualifications as a photographer and a motor technician (that was a 3 year course passed in 1), then a self taught computer builder and technician.

    All that said, I fell ill again in the late 90’s, which slowly started sapping what energy I had left. This was towards the end of the motor tech course. My condition has slowly deteriated to the point that I struggle to do normal daily tasks.

    I do not know the cause and although I am diagnosed with ME, I believe there is more to it than that. On top of that, since the birth of our 4th child my wife has started to develop the same sort of symptoms and so has our child. Coincidence I don’t think so!

  11. Avatar
    Donna February 25, 2015

    I have slow-onset ME. I trace it back to a bad reaction to a tetanus vaccine I had when I was a teen. I was not sexually active for years after my first symptoms began, nor have I had any blood transfusions. I have two children who are healthy, and do not appear to have ME.

    Immune dysfunction is a not a primary symptom of my ME – post-exertional malaise, myalgia, focus and short-term memory issues are. (I have all the symptoms needed for diagnosis of SEID under the new IOM criteria, or ME via CCC – the diagnosis I was given, since I live in the US, is chronic fatigue syndrome).

    Due to the shenanigans around defining and diagnosing ME as CFS in the US, it would not surprise me if there are other diseases hiding within that diagnosis.

    I do not, however, think that ME itself is primarily an immune deficiency disease. Instead, I think it is more likely to be an autoimmune disorder, which produces immune deficiency symptoms in some patients. (Or, perhaps those with CFIDS have a different disease than those with ME).

    Is ME communicable? There have been outbreaks. If it were communicable, though, all of our spouses would have it, wouldn’t they? This is why I feel it’s likely there is more than one disease under this umbrella.

    • Avatar
      lemonfoundation March 08, 2015

      By present-day definition, there are 29 separate and distinct “diseases” under the AIDS “syndrome” umbrella. Only every 29th AIDS patient is unlike. There have to be 29 types of “CFS,” only one type being “ME.”

      Contagion aside (i.e., infectious or not), all CFS cases were “acquired.”

      11+ years’ of perfectly-cited research (books, documentaries, interviews w/ scientists, CSPAN & PrimeTime News clip, medical journal citations, etc) —> seach cfsstaighttalk.blogspot

  12. Avatar
    linda smith February 17, 2015

    have you had your cortisol level checked? Either by saliva test or the lab drawing a baseline, given a dose of cositrophin 250 mg iv and blood drawn 30, 60, 90, and 120 min. Afterwards. Will also need testerone level checked. A lot of these symptoms sound like adrenal insufficiency either primary by low cortisol or secondary low testerone… This is Addison’s Disease. I am not a doctor, but an RN with hashimotis and Addison’s disease .. Air hunger, salt cravings, brain fog, painful joints, constipation, dizziness especially when standing, difficulty walking a straight line. Total exhaustion and difficulty comprehending. Dry skin, hand peeling, ridges on finger nails and brown spots especially scars. It took me 9 yrs of existing before I was finally diagnoised. I may be way off base but if this information can help one person it is worth posting. God bless all of you with these autoimmune illnesses

  13. Avatar
    Sapna February 09, 2015

    I have been very sick for 6 years and was getting better until a car accident last year. Now I’m back at square one.
    I was “diagnosed” with CFS ME and Fibromyalgia.

    I can barely get out if bed and when I do can get only a couple if simple taste done a day.
    I read the article but am very confused by it because if my cognitive condition

  14. Avatar
    sandy February 08, 2015

    Is MMS contraindicated if one has hemolytic anemia and severe gastritis?

  15. Avatar
    Marie December 30, 2014

    I would suggest that anyone with CFS/ME get tested and look closely in to chronic lyme disease and tick borne illness. 300k American’s a year are being infected and the CDC is hiding it. It is the cause of most CFS, neurological problems, depression and fibro.

    • Avatar
      Marti Scheppke January 16, 2015

      I have been struggling as an ER Nurse for 14 years to figure out why I cannot get a difinitive diagnosis, 1 CDC positive Lyme disease test, of course the CDC requires 2 to be “POSITIVE!” My CD 57 ( Killer T) was 31 initially, I know my mother has it and my daughter also tested positive for lyme but only once with an even lower CD 57 13!!!! No doctors understand and I cannot talk about it to other nurses or doctors without them passing judgement that I might be NUTS!!! I wish I could help you in your fight. I work 40 hours a week if not more. I pop more supplements than you can imagine, I eat no gluten, no sugar, no nothing but nothing works. I take adderall at times to keep me from falling asleep when I drive, Yet very little improvement! We need an answer!!! I want to fight!!

      Sincerely one pissed off Mother, Nurse, daughter, CFS/ME/Lyme Disease/Non HIV AIDS Human Being!!!!

      • Avatar
        Donna February 25, 2015

        This is the lab to use to get a good Lyme test that’s less likely to throw a false negative:
        http://www.igenex.com/Website/
        (this is what I’ve been hearing from Lyme advocate people).

        The definitive symptom of ME/SEID which distinguishes it from Lyme and other diseases is post-exertional malaise. Lyme does not cause post-exertional malaise.

        PEM is a worsening of symptoms anywhere from a few hours to a few days after exertion. It’s also characterized by delayed recovery from exertion. It can be diagnosed by running an exercise to exhaustion test on a stationary bike for two days in a row – but this is quite dangerous for people who have ME, and will absolutely result in PEM. A person may be ill for months afterward (or even longer).

        If you do not have PEM, you don’t have ME.

      • Avatar
        lemonfoundation March 08, 2015

        Resistance, revolt, and revolution are history’s only proven solutions. “How To Survive a Plague” is an excellent award-winning documentary on what needs to get done.

        11+ years’ of perfectly-cited research (books, documentaries, interviews w/ scientists, CSPAN & PrimeTime News clip, medical journal citations, etc) —> search: cfsstaighttalk.blogspot

    • Avatar
      Donna February 25, 2015

      The new SEID diagnostic criteria place the most prominent attention on the symptom which is virtually unique to ME, and is not found in fibromyalgia or Lyme disease: Post-exertional malaise.

      There is no evidence that most people diagnosed with CFS/ME have Lyme disease. On the contrary, most people with that diagnosis have PEM; and thus they absolutely do have ME.

      However, ME can be triggered by anything which assaults the immune system in susceptible people – from a viral infection to a vaccination, and more. It’s perfectly reasonable that a brush with Lyme disease could trigger ME.
      Perhaps this is actually what some people with ‘chronic Lyme’ actually have.

      • Avatar
        Pam March 24, 2015

        Post exertional malaise is indeed a symptom of lyme disease.

    • Avatar
      lemonfoundation March 08, 2015

      “Let’s talk retroviruses, Non-HIV/AIDS, ME/CFS, Lyme, Fibromyalgia, politics, and more.”

      60-minutes w/ Dr. Judy Mikovits –>

      “Plague: An Interview With Judy Mikovits”

  16. Avatar
    Erwin Alber November 08, 2014

    The HIV test is a fraud – it even says so on the package insert – which means there is no such thing as “HIV-positive” or “HIV-negative”. The HIV-virus doesn’t exist – it has never been isolated.

    All manner of diseases and disorders including CF are put in circulation with vaccinations. AVOID!

    • Avatar
      Francine November 25, 2014

      Yes Erwin I believe this is the truth, these diseases are mostly man made, by big pharma, isn’t Aids a from of cancer, and Aids can be controlled with medication, it would not be a stretch, to treat cancer with Aides drugs. I wonder if they know already. Change the name of the disease, change the name of the drugs, wow this is really the shell game on steroids. Big pharma is laughing all the way to the bank.

    • Avatar
      Donna February 25, 2015

      Of course it’s been isolated. Christ, spend 3 seconds using Google before you buy into some ridiculous anti-science conspiracy theory.
      They not only isolated it, they photographed it and mapped its genome. You can buy a freaking plushy modeled after the thing.

  17. Avatar
    Evan September 18, 2014

    Along with mms there is an Ayurvedic practice called shivambu which has brought back People with AIDS and cancer all sorts of fatal diseases. Been doing it awhile myself and my psoriasis and skin are getting way better . If u can get past the gag reflex do it it’s well worth it the pharaohs did it as well as the ancient Buddhists and Hindus of ancient India. One of the first books of man 5000 years ago was on shivambu and if it didn’t work they wouldn’t have made carvings in clay or stone , check it out and good luck.

  18. Avatar
    Royce Hamer August 01, 2014

    You should read up on MMS we have been clearing up Aids/Hiv in 21 days with no side effects and may I mention Malaria in 4 hrs. for .005 cents per victim. To view the malaria test you tube the words “malaria,MMS, Ugands, Redcross” The proof it works is the fact that FDA claims to have placed a ban on it due to corruption. CACL Canadian Anti Corruption League.

    • Avatar
      DEAMNO March 01, 2015

      MMS NEVER WORKED FOR ME TORE MY GUT UP 7 YEARS AGO TOOK SEVERAL YEARS TO RECOVER I GOT HEP C

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