AIDS and the Doctors of Death- In other words, these doctors are also the cause of M.E patients not receiving treatment.
Reknown Dr. Anthony Fauci, HIV/AIDS is his baby. He used to keep a roster of patients who were the HIV Negative AIDS patients which are the M.E. or the CDC Construct- “CFS” patients.
Dr Anthony Fauci does not want anyone to know that you do not have to have HIV to have AIDS which a % of M.E or the CDC construct “CFS” patients have.
Dr. Robert Gallo, worked in the same lab as M.E scientist Dr Elaine Defreitas at the Wistar Institute in the 80’s and early 90’s. Dr Elaine Defreitas helped Dr Gallo map out the HTLV virus and Dr Gallo was helping Dr Elaine Defreitas with “CFS” Retroviral research. When Dr Elaine Defreitas was about to make the breakthrough, she was in a car accident where she had to take a early retirement because of her injuries. How convienient was that!
It is also known that Dr Gallo fired Dr Frank Ruscetti because he did not want anyone else to get credit for the HTLV virus discovery.
Dr. Gallo happens to friends with Dr. Fauci- how convienient is that too. It is because of Dr. Fauci, that M.E or CDC “construct” “CFS” has been behind in research over 20 years and also actually does not have any research because M.E/CFS research funding is $5 Million dollar a year thanks to Dr Anthony Fauci who directs all of the research money at NIH, and notice, most of it goes to AIDS.
I do believe NIH has their own Mafia Don!
Gambino Crime Family Boss John Gotti, was called “The Teflon Don”, he was called “The Teflon Don” because they could not get a case stick. But in the end, the Teflon wore out, and John Gotti went to prison! Its only a matter of time that the “Teflon” will wear out at the NIH!
Monthly Archives: August 2014
Man-Made AIDS & The Scientific Cover-Up
9 Things You Wish You Could Tell Someone After They Commit Suicide
I would tell them….. Please don’t go……
1. I wish I could’ve talked to you about how serious your problems were getting. I’m someone who doesn’t let many people into my life, because I know what it feels like to have a part of yourself walk away with someone, even acquaintances. When you open up to someone, they become a part of your story. I wish you would have let me have a bigger role in your story.
2. I wish I could tell you that know what it’s like to wake up and feel like nothing around you is worth going through another day, or that life is completely meaningless. I know that when you’re in that state of mind, it’s hard to really hear the kind words of another person. Maybe if we could have just sat there in silence together, just thinking and waiting for the moment of insight when we…
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Karina Hansen: Prisoner of Denmark
Karina Hansen: Diagnosed Severe ME in 2008 was forcibly removed from her home, February of 2013, taken to the Hammel Neurocenter in Denmark under the orders of Professor Per Fink for mandatory treatment as a psychiatric patient.
Despite the efforts of Karina’s family, friends, The International ME community, and legal team, Karina still remains a psychiatric patient at the Hammel Neuro Center via the orders of Psychiatrists Nils Balle Christensen and Professor Per Fink.
Nils Balle Christensen and Professor Per Fink do not recognize the medical diagnosis of Myalgic Encephalomyalitis as medical diagnosis but as a “Functional Somatic Disorder.”
Justice For Karina: http://justiceforkarina.webs.com
Hammel Neurocenter: http://www.hospitalsenhedmidt.dk/
Many of you will already be aware of the case of Karina Hansen. However, for those of you who are unfamiliar with her situation, this is a short re-cap of the facts as far as we know:
Karina, now aged 25, is a citizen of Denmark, a member state of the European Union. She was diagnosed in 2008 with a severe case of the illness Myalgic Encephalomyelitis/Chronic Fatigue Syndrome (ME/CFS). Her family cared for her at home until February 2013 when state intervention caused her to be forcibly removed to the Hammel Neurocenter for mandatory treatment as a de facto psychiatric patient. Despite the efforts of her family, friends and the international ME/CFS patient community to secure her release and return home, she has remained there ever since. The British charity Invest in ME has offered advice and assistance to the Danish authorities but has, so far, been ignored.
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In the last…
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Global Health: Time to Pay Attention to Chronic Diseases
NIH Director’s Blog: Time To Pay Attention To Chronic Diseases by Dr. Francis Collins
If you do a search through Dr Collins Blog, you will not find anything on M.E., Myalgic Encephalomyelitis or even the “Construct” “Chronic Fatigue Syndrome/CFS
Caption: Projected deaths (in millions) by cause in low-income countries. Note increase in non-communicable diseases (orange).
Credit: Adapted from Beaglehole R, Bonita R. Lancet. 2008 Dec 6;372(9654):1988-96.
Greetings from China. I’m here in Shanghai with other biomedical research leaders for two major meetings. The first one, which is the topic of my blog today, is on global health. So, you might expect there to be a lot of talk about malaria, influenza, MERS-CoV, Ebola virus, sleeping sickness, dengue fever, tuberculosis, HIV/AIDS, and other infectious diseases. And those are most certainly topics of intense interest to NIH and our colleagues around the world. But this particular meeting is about a different kind of global health threat that’s becoming a rapidly growing problem: chronic diseases.
While infectious diseases remain a significant problem in the developing world, cancer, heart disease, obesity, diabetes, and other non-communicable diseases are now among the fastest growing causes…
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One More Update
One More Update from Brooke.
Her doctor was able to get hospice care reinstated for her for 60 days.
Today, we live in a time where, being sick is not acceptable, and people who have misunderstood chronic illnesses, there aren’t many medical practitioners who are cut out to care for them. Not only not cut out to care for them, they have no compassion and pass the patients off as depressed.
Today, it seems as if you don’t have something like cancer or AIDS, your illness doesn’t qualify, as in Brooke’s case, her hospice care was discontinued because she wasn’t “considered to be dying.” That’s just so awful.
People with chronic illness who are basically living a “living death”, there are no words because I can’t even think of the words because I’m one of those people. I know I myself will probably die alone, no hospice, no support, nothing. And I know there is nothing I can do about it. I have come to accept it because unfortunately that’s the way it is.
I ask everyone to pray for peace and comfort for Brooke during this time.
Dear Friends,
Recently there have been a lot of questions in the community about what has happened to me and where I am with things. I am now very near the end of life, and writing posts has become next to impossible, but I wanted to try to get one more out. This post will be written in many parts, and may seem rough around the edges, but it is the best that I can do at this point. I know you will understand.
First, regarding care. My initial reevaluation for hospice care was denied – in part due to misinformation coming from the whole CFS mixup. After this, my doctor agreed to treat me himself, without the aid of nurses since he couldn’t find a way to get any into the home. Things began going downhill so fast, however, that he recently talked the hospice team into readmitting me…
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