More problems with protease inhibitors specifically & ARVs in general
“Premature senescence?” You mean “accelerated aging?”
This will be a short post, but we haven’t seen much about the protease inhibitors recently because they are rarely used, so it seems significant when they make the news. It seems that the problems with these drugs are not limited to the lipodystrophy and liver damage that were so prevalent in the 1990s—they also cause rapid aging.
We’ve discussed accelerated aging in “HIV” positivity before, questioning whether it was due to the drug or to the disease.
Lopinavir is of course a protease inhibitor. So they cause arthritis now? Quick quote, the article itself is pretty basic:
Debate regarding the premature aging of knee joints in acquired immune deficiency syndrome (AIDS) patients has remained contentious, with conjectures pointing towards its correlation with distinct antiviral regimes. Protease inhibitors (PIs) stand as a prominent class of antiviral agents frequently utilized in AIDS management and have been significantly linked to premature senescence.
I’m not even going to go into the details of this report, because it’s just more of the same propaganda, and you can click the link to read it. What I really want to talk about is the fact that EVERY SINGLE ONE of these “anti-HIV” drugs have horrific toxicities, which the mainstream is forced to admit exist because they are severe enough to inspire a 26,000+ plaintiff class action lawsuit against Gilead Sciences for their having hidden the toxicities of Truvada until its patent expired.
What I really want to talk about is the fact that these drugs are lauded as being “miraculous” and “life saving” and not toxic at all, when a look at the actual medical literature indicates that not only are these drugs indeed toxic—again, see the Truvada disaster and oh, all of AZT— but they don’t even work for 10-40% of those that take them.
What I really want to talk about is the fact that globally, 10-20% of “HIV” positive individuals are unaware of their status, so they certainly are not on treatment (they can’t be on it for PrEP either, because PrEP patients are continually tested); of the 80-90% that do know, only about 70% are on treatment, yet there is no massive 1980s style AIDS epidemic. I wonder why that might be.
What I really want to talk about is the fact that we are being sold a total illusion. The only thing propping up the long since falsified HIV AIDS story is this total lie that the drugs are nothing short of miraculous, with zero toxicities. However, even a cursory look at the literature proves this to be a lie. If about one third of the estimated 37 million “HIV” positive people worldwide are not even on treatment, why are the ERs the world over not overflowing with pneumocystis and the like? What happened to proto-AIDS? Clearly, the drugs are not working in the way we are told. They may be “working” in some fashion, but not in any “antiviral” fashion.
Let me know in the comments what other craziness about the “anti-HIV” drugs you’ve heard. Also, as a teaser for Thursday’s live stream, I’ve discovered something very interesting indeed about the integrase inhibitors that, along with the oldest class of “anti-HIV” drugs, form the backbone of current ARV and PrEP formulations, which we will discuss because it may well turn out to be very important.
"AIDS patients suffer... due to lopinavir-induced Zmpste24 inhibition"
This is the kind of AIDS language that keeps people in the matrix. It's the same language used in the 'HIV and Hard Belly' ads I see on FB all the time. Instead of just saying, '...suffer because of lopinavir' or 'hard belly because of ARVs', they have to make sure you know it's an 'HIV and AIDS'. No, it's not an 'HIV and AIDS' thing, it's a pharmaceutical thing that would equally damage 'negative' people taking these drugs.
My “hiv experience” started in 2015 when I was detained in southern Spain at the Alhaurin prison, known as Finca Morega. Shortly after my arrival, I voluntarily provided blood samples for standard tests, including an HIV test. After a considerable period without any communication, I assumed everything was fine. (Infection was discovered in 2015 but dates back to around 2011.) Approximately five months later, I sought medical attention for a fungal infection between my toes (athlete's foot), a common issue due to communal showers with inadequate drainage. Upon visiting the doctor, he did not need to examine my feet and promptly provided me with a treatment tube. Just as I was about to leave, he asked me to stay and looked intently at his computer screen. He inquired if I was aware of a “infecion”. Confused, and with limited Spanish at the time, I asked what he meant, he was talking about an “infección magik gonson”, I still shrugged my shoulders and he started to crumple up an A4 and throw it into an imaginary basket, I thought for a moment that the old doctor with his reading glasses had lost his mind, irritated he taps on his keyboard and turns the screen towards me, a picture of Magic Johnson, then it dawned on me, I had the magic Johnson virus, I was hiv positive. The news was devastating, and in a state of shock, I was placed in a suicide cell for two weeks to "calmly" reflect on my diagnosis, without any psychological support or information. Despite the existence of an international protocol stating that individuals diagnosed with HIV should receive anti-retroviral treatment as soon as possible, it took nearly 18 months before I was prescribed this treatment. This delay was only rectified after my family informed the Dutch embassy surrounding the fact that the prison medical service denied me my medication and thereby violating the WHO protocol.
The doctors at the local public Virgen hospital also deemed it unnecessary to provide me with medication during those 18 months, resulting in a total delay of almost 2 years. After my release from detention in Spain, I began receiving my medication from the Costa del Sol hospital and resumed my life. However, I was left questioning the actions of the doctors at both the prison and the Virgen hospital, wondering why they had been so negligent regarding my health. A seed was planted I wanted to find out why these doctors were so frivolous about my so called “deadly infection”, it was like “What do they know what I don’t know?” So I went on a quest, a quest that someone who is HIV negative would never make in their life, and after many hundreds, perhaps thousands of hours, I came across a well-hidden but very different story than what has been echoing in the media for 50 years.
WHO protocol from WHO. Int.
Following my release, I was incredibly hungry for information and I began to investigate the topic online. In the meantime I was posing challenging questions to my healthcare providers. There was a question I always asked, “If the doctors who treated me in the initial phase did not find it necessary to treat me with blood values that matched those once I was in liberty, why do I have to take those drugs now and it was not necessary back then?” Despite my inquiries, none of the physicians I consulted could answer my questions, instead, many remained silent or expressed understanding. I have reached out to HIV organizations and virologists, never receiving responses. Engaging with support groups and exploring alternative platforms has proven more enlightening than discussions with my healthcare providers, who seem entrenched in the prevailing narrative. I have extensively researched various reports, even got a subscription of various scientific sites like the one of the Stanford university and watched numerous interviews and documentaries, leading me to conclude that the official HIV narrative, echoing in the media for nearly five decades, is fundamentally wacky, full of lies and controversial.
In the initial months post-detention, I regularly visited the hospital for blood tests and consultations with HIV specialists. Each visit I had to hear the same violin music, “please sir, it is very important you take your medication”, and despite my undetectable viral load, which supposedly negated the risk of transmission, every time they told me I had to use a condom. It’s like they’re telling everyone the same drummed-in tune there,
But due to my inconsistent medication adherence, a detectable “viral load” ( I put viral load in quotes because I have reached a stage where I no longer believe that they count a virus) eventually emerged, prompting inquiries about my compliance. Although I occasionally forgot my medication while traveling, my intuition/gut feeling suggested that my health was not at risk, despite the dire narrative surrounding HIV.
A pivotal moment occurred while renovating a villa in Marbella, where I met a general practitioner from England. During our conversation in which we talked about my remarkable recovery from necrotizing fasciitis which happened on the Dominican Republic, she suggested I possessed an exceptionally strong immune system, and this led automatically that I revealed that I was HIV positive and the casual approach of doctors towards my treatment. First thing she said was “ Because they know” She revealed that many physicians are aware that HIV is not the dire disease it was portrait. She further explained that HIV transmission is more challenging than previously understood, and many patients remain healthy with stable viral loads despite irregular medication or even without medication. Her revelation and all the controversial pieces and the stories of other HIV-infected people who, in some cases, have not taken medication for decades (and are healthy) made me decide never to take ARV medication again, this has been almost 8 years now and I am as healthy as a fish