The AIDS-like Disease Seldom Mentioned

Flickr-HIV-NIAIDKaren Lambert, Guest
Waking Times

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.

Increasingly, I have become concerned that my systemic diagnosis is caught up in the treacherous politics of CFS/ME and AIDS. Most people with CFS/ME do not like to talk about the many symptoms and immune abnormalities that they share with AIDS patients. I also suspect that most ailing patients would rather be told that they have the very mysterious CFS than to be told that they have AIDS.

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 immunosuppressed people?

Anyone with Chronic Fatigue Syndrome, 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 ME and CFS (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 CFS) 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 want honest answers for myself, for everyone who is suffering from this hideous illness, and especially for those who remain uninfected by my undiagnosed infectious and communicable disease.

As worrisome as my health is to me, I am extremely troubled by the strong likelihood that more people are being infected every minute that Non-HIV AIDS cases (like mine) are allowed to go undetected – especially if it turns out that AIDS and CFIDS/ME are basically the same disorder.

You can label my AIDS-like illness whatever you wish. I would even allow you to call it infectious-CFS, even though it is utterly beyond my realm of comprehension as to how the medical establishment can generically name an entire disease paradigm based on just one (of my numerous) symptom(s).

Regardless of how politics may try to dissuade or delude you, all you need to know is that my idiopathic immune dysfunction is infectious! It is contagious! And it is spreading, unleashed, in the world’s population!

I am not afraid to say that I have AIDS without HIV — idiopathic CD lymphocytopenia — my second official clinical diagnosis. I am equally as unafraid of saying the most obvious thing about CFS/ME: it sure does look like AIDS to me.

We talk openly about preparing for an impending Avian Flu pandemic. Why not talk about the HIV-NEGATIVE AIDS epidemic that already exists (and is spreading) amongst us?

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.

To learn more about non-HIV AIDS, and to see the *new* face of AIDS, please visit: CFS Straight Talk

Could I be you?

About the Author

Karen Lambert has a Master’s degree. She was a director at her firm. She used to be a triathlete. She has never used IV drugs, nor traveled abroad. She can count her sexual partners on two hands. CFS Straight Talk

This article is offered under Creative Commons license. It’s okay to republish it anywhere as long as attribution bio is included and all links remain intact.

~~ Help Waking Times to raise the vibration by sharing this article with the buttons below…

  • Anonymous

    It never occurred to me that it could be similar to HIV/Aids. I suffered from CFS/ME for almost 40 years. I did not now how I could be so ill and any doctor I visited only became angry with me. After about 20 years I finally realized what was the matter with me. Life had been very difficult as I had to cope like everyone else. It still has not left me but is just chronic instead which means I sometimes feel ill but learned how to cope with the symptoms which are not so extreme any more as in the first 6 years or so. Maria

  • Great sharing. There i also “CHEMICAL AIDS” which those who have had toxic/chemical exposures have related to Multiple Chemical Sensitivity. Which mean 3 or more body organs are sensitiveo certain toxin/chemicals. I have occupational asthma from a job injury and horrific exposure that burned off mucous membrane in body. IN recent years we know more about probiotics . Personally it seems the good bacteria can’t quite fight the bad on the low level exposures in this current world even though I use perfume free products, etc.There seems to be a probiotic for many different areas of body and I use one with many kinds. I’ve asked (I AMS NOT A SCIENTIST0 if after injury if one shouldn’t aost bathe the injured area with the probiotic for that part. Since mine is nmore respiratory, salivarius probiotic is uded and I hold it in my mouth and let it disolve forst, etc. I’m very sensitive to formalehyde and continued exposure when I tried to work in themodern office enviroment after injury was blood work of abnormal white cells. Leukeopenia plus elevated red cells/ One is to be an oxygen patient from beginning f injury I didn;t get this until 19 years ago seems its a learning process for the medical profession too. HHS doesn’t recognize toxins/chemicals harm and has even pushed ozone emitters on us. For me they are deadly inflmmation, bleeding infections etc. So use liw-quid. HHS SEEMS TO BE IN CONTROl OF THE POLLUTERS OF THIS WORLD> Getting may health plans to pay for tests the medical profession accepts seem to have been withdrawn from coverage. 25 years ago, I was able to get the needed ones done. Little has been added to treatments either. AIDS is “AcQURIRED IMMUNE DEFICIENCY and doesn’t have to be acquired from Aids virus nor even from intimate contact.
    AS for fatigue; my doctors told me my lungs aged 50 years when exposed and occ asthma is also called Reactve aorway dysfunction Syndrome. THEY DON”Y WORK AS THEY SHOULD> I was injured 1/10/89 before those cam home from the first Gulf war after toxic /chemical exposures. One of my Doctors back then wrote a paper re the damage done to mucous membrane ascausing a lot of problems. For me, the only cantagian is those germs/viruses one catchese more easily and until treated can be.

  • Jay

    Plus one with this horrible AIDS-like garbage. First acute symptoms appeared around 6 mths ago. All the doctors can see in my bloodwork is recent infection with Influenza A and B. I also am pretty sure I have EBV as I had mono at 11.

  • Bob

    Author doesn’t make clear whether she had unprotected sex. If she is posting to alert others of risks, it would be better if she wrote exactly what she did and didn’t do.
    Sorry about your health condition, but stating your sexual practices in more detail is more relevant than stating you have a masters degree.

  • Rachel

    It’s true that it doesn’t matter what you call it. There are all kinds of weird diseases going around that never used to exist but have been created both intentionally (like lyme, morgellons) and also a menagerie of various infections that are mutated and become chronic from the electromagnetic environment we are all living in.

    I agree with Laura–treat it like it’s lyme disease (lyme is very widespread and complicated) and tackle the beast from every direction: protection from EMF’s, heavy metal chelation, high antioxidant intake, parasite cleanses, strict diet, etc. Most doctors are ignorant because these diseases are new and they are taught money-makin’ lies, so find a “lyme literate” doctor that leans toward a natural aproach or learn about what they know and treat yourself like whatever it is is curable (it could be!). My personal choice (if I could afford it finacially) would be someone who has been trained at the Klinghardt Academy. I have morgellons and don’t know what it is, just that it’s horrible and makes sores on my skin with fibry stuff that comes out and other “things” but I have improved my condition by following certain lyme disease guidelines. Lyme treatment will treat anything to some degree because it gets to the core of the problems that cause disease like metal toxicity.

    Keep hopeful and don’t let the doctors bring you down! Remember they are just ordinary people who went to school and memorized crap they didn’t even have time to think about and determine if it was true. Most doctors don’t really know what is going on with these new diseases. They are just “practicing,” right? Be strong! You CAN improve your condition.

  • Have you consider you have gluten intolerance. That is the symptom of such an auto immune. I have such myself and I had a spell today. Doc said what is from.

    I would watch your diet if so. Most people that have it don’t know it and if they do they still eat gluten foods which says it is gluten free but is not so they don’t improve. Sometimes you find out too late and get CFS anyhow because you did not know to change the diet and you develop auto immune issues.

  • I’m puzzled as to why you mentioned in the article that you have a Master’s degree and you are a director of a firm. So what? Is that supposed to preclude a person from getting a sexually transmitted disease? You also mentioned that you can count the number of sexual encounters on two hands. So. It only takes one sexual encounter to acquire the disease. No promiscuous sex, no disease. It is difficult for most people to get concerned about government using taxpayer money to study sexually communicable diseases, when we consider it wrong to have sex outside of marriage. And you admit you infected another “host”?

    • practicus

      She’s providing evidence that she’s not an irresponsible person as it takes considerable focus and determination to achieve her status. Stop nitpicking. The woman is sick and it’s probably due to a man made weaponized pathogen. People need to wake the fuck up. The skies are being sprayed every day all around the globe with God only knows what and it probably includes weaponized pathogens. We are at war with a psychopathic elite who control this planet. At least those of us who are awake are.

  • Laura

    Have you been tested for Lyme Disease? Have you consulted with a Lyme Specialist Doctor? I had CFS and fibromyalgia, was bedridden for 1 1/2 years. Was sick for 8 years, eventually got a positive diagnosis for Lyme after 3 bloodtests had tested negative for Lyme. There are only 3 labs in the USA that are reliable for testing for Lyme – Igenex, Clongen and Stony Brook. When I read a book called Out of the Woods by Katina I. Makris everything fell into place. Once I knew what it was I started treatment, all natural and am now about 90% better and still taking homeopathic remedies and improving all the time.

    • Anders

      Homeopathic medicines does not cure any diseases. Probably you have imagined that you were sick. Homeopathy is fake.

      • practicus

        YOU are a fake.
        Or rather a troll.

  • windy

    Anal intercourse is a filthy, disease producing practice, similar to bathing in raw sewage.

  • dimitri ledkovsky

    How about a statement or advice about “casual sex”?

  • poser


  • Bill Burke

    Eat fish. Not farmed salmon or shrimp, deep ocean fish. Sardines of a good source qualify. Eat no foods that the poisons are in. You don’t know the world of men, the poisoning is deliberate.

  • Miles Smith

    An Australian medical study were strongly of the view that true CFS was the end result of having had glandular fever, making it a virus based illness.

Thank you for sharing. Follow us for the latest updates.

Send this to friend