It was snowing in Stanthorpe just south of Brisbane a couple of hours after my last post.
The funny thing was that Al Gore was on Australian TV the night before talking up Global Warming.
My problem with Global Warming is that we should forget Carbon Dioxide for a minute and think about all the toxins we are choking on, Benzene, Sulphur Dioxide, Diesel particulates etc.
I just want some fresh air.
I should have also said in my last post “my friend ‘chose’ to abort because she was bullied to while she was worried about what the many drugs given may have done to her fetus”.
This piece of science was also printed in Nature a week and a half ago where French scientists digging around in Gorilla droppings in Africa decided to add two and two together and create the illusion that eating Gorillas is the reason for HIV spreading into humans.
“ONE more reason not to eat our close living relatives. Of the three strains of HIV known to infect humans, we know that two - the one causing the global AIDS epidemic and another that has infected a small number of people in Cameroon - came from a chimpanzee virus called SIV. The source of the third strain, which infects people in western central Africa, was a mystery. Now we know it came from gorillas.
Martine Peeters and colleagues at the University of Montpelier in France have discovered the virus in the droppings of gorillas living in remote forests in Cameroon (Nature, vol 444, p 164). The infected gorillas lived up to 400 kilometres apart, so the researchers think it must be a normal or endemic virus in the animals, as SIV is in chimps.”
Gorillas missing link in HIV mysteryhttp://www.newscientist.com/article/mg1922...iv-mystery.html
Now someone pointed out to me that this might stop the munching of Gorillas and I hope they are right.
But we’ve seen what panic over Bird Flu has done to millions of chickens so I’m not sure and knowing cows are rampant with Bovine Leukemia Virus doesn’t stop us getting hungry and ordering a burger.
This is the problem with this mode of retroviral thinking.
Are they really infectious or are we just picking up the normal retroviruses that were always in the genome of these animals and only have noticed now because we have some fancy new testing gear?
This is the same retrovirus SIV but here it’s turning up in Baboon placentas, go figure?
“Electron microscopic studies have revealed the presence of endogenous retroviral (ERV) particles in normal primate placental tissues. These particles have ultrastructural similarities to type C retroviral particles and are mainly associated with the trophoblast. In normal human placental tissues, they have antigenic similarity with exogenous retroviruses, such as the human immunodeficiency virus (HIV), and may have a role to play in the regulation of cellular gene expression, syncytiotrophoblast formation or pregnancy-related immunosuppression.”
“The results of this study confirm the specific expression of retroviral cross-reactive antigens in normal baboon placental tissues and suggest placental cellular proteins may have antigenic similarity with those recognized by anti-HIV/SIV antibodies. The role of these retroviral-related proteins expressed at the maternal-fetal interface remain unclear.”
Characterization of antigens expressed in normal baboon trophoblast and cross-reactive with HIV/SIV antibodies.http://www.ncbi.nlm.nih.gov/entrez/query.f...1&dopt=Abstract
And then if you look in the related studies beside that Pubmed study you find this one.
“We previously reported that monoclonal antibodies directed against HIV-1 envelope and gag proteins react with normal human villous trophoblast. The nature and/or potential function of these particles/proteins has not yet been fully defined. We previously reported that monoclonal antibodies directed against HIV-1 envelope and gag proteins react with normal human villous trophoblast. In this study, we report that extravillous trophoblast (EVT) from second- and third-trimester tissue are also cross-reactive with anti-HIV-1 gp120/160 and p17/18 antibodies.”
Expression of endogenous HIV-1 crossreactive antigens within normal human extravillous trophoblast cells.http://www.ncbi.nlm.nih.gov/entrez/query.f...st_uids=7473433
So I may be wrong about the gp24 Transmembrane Unit in the HERV-W retrovirus cross-reacting with the P24 antigen of the HIV test but here we have in black and white other ‘HIV’ antigens in women’s placentas.
This is one of our most common retroviruses and this is the question I keep asking that puts the whole HIV paradigm into a spin.
How on earth do we know ‘HIV’ was ever transmitted and wasn’t one of our own retroviruses all the time?
This stuff is quite new and Robert Gallo who discovered ‘HIV’ didn’t have the best equipment to answer that question.
I think he eagerly jumped the gun.
Ideas and belief systems can change as rapidly as fashion.
I’m not sure about the Big Bang Theory after reading ‘The Cosmic Ecosystem’ by Alan Johnson, he just pointed out that red shift could due to light traveling a long way and not the stars moving away from us.
“I runno?”…..as Scooby Doo would say.
In 3 decades psych drugs went from Barbiturates to Tricyclics to SSRI’s.
Al Gore talks up Global Warming, in the ‘70’s an Ice Age was coming, I switch on the TV and see shows on Global Dimming….aaaagh, I’m confused, I just know I’ve got a doonah and blanket on my bed in mid November in here in Queensland, Australia when there would normally be only a sheet, mosquito net and sweating at night.
This global warming is pretty cool at the moment until the end of the week and I’ll be panting.
500 years ago witches and demons were blamed for most of our problems and it was also Theology Faculties in the Universities of the time that rubber-stamped ‘The Malleus Maleficarum’ for approval as a legal document to convict these ‘witches’ with.
It should be used as an example of how mad our scientists can become, it’s really ridiculous, a very long piece of woffle and caused a lot of suffering.
If we go back to the early ‘80’s and think about our belief systems they weren’t really fun.
I was a teenager in England expecting a 4minute warning and a nuclear war with Russia and I never expected to be writing this.
Many of my friends also didn’t expect to and I have a list of about six who ‘partied’ too much and died from Narcotics and another four who died rather violently from Alcohol abuse, who needs HIV/AIDS?
Gays had come out in force and with that coming out began a party with probably too much indulgence and all the dangers that go with it.
I’ve never written about sex when talking about HIV/AIDS, I’ve mentioned preservatives in sexual lubricants because they can be poisonous and get absorbed at higher doses when used internally.
There’s a difference between skin and the rectal lining.
Amyl Nitrate is toxic and it’s a sex aid.
But back in the ‘80’s it was a big party, now we have ‘Ice’ to keep the party going even longer.
There was a fundamentalist Christian government in power in America as there is now.
‘HIV’ fitted into their “told you so, too much sex is bad” way of thinking.
I’m brutally scientific about it and say “Yes, sex with drugs and dodgy lubricants can get too toxic”.
We are in my opinion highly evolved apes that are stressed out, often quite unhappy and could do with a lot of loving.
No sex becomes pathological at times.
And the reality is that everyone is potentially Bi.
Just messing with your heads, big smiles.
‘HIV’ just left my paradigm once I had discovered AZT and it’s effects.
So let’s mention HERV-K and ask could ‘HIV’ be just another strain of HERV that is barely different to HERV-K.
Here is an example that shows HERV-K RNA sequences in the blood of HIV-1 patients at a rate of 95%.
“Approximately 8% of the human genome sequence is composed by human endogenous retroviruses (HERVs), most of which are defective. HERV-K(HML-2) is the youngest and most active family and has maintained some proviruses with intact open reading frames (ORFs) that code for viral proteins that may assemble into viral particles. Many HERV-K(HML-2) sequences are polymorphic in humans (present in some individuals but not in others) and probably many others may be unfixed (not inserted permanently in a specific chromosomal location of the human genome). In the present study HIV-1 and HCV-1-positive plasma samples were screened for the presence of HERV-K(HML-2) RNA in an RT-PCR using HERV-K pol specific primers. HERV-K(HML-2) viral RNA sequences were found almost universally in HIV-1(+) plasma samples (95.33%) but were rarely detected in HCV-1 patients (5.2%) or control subjects (7.69%). Other HERV-K(HML-2) viral segments of the RNA genome including gag, prt, and both env regions, surface (su), and transmembrane were amplified from HERV-K pol-positive plasma of HIV-1 patients. Type 1 and type 2 HERV-K(HML- 2) viral RNA genomes were found to coexist in the same plasma of HIV-1 patients. These results suggest the HERV-K(HML-2) viral particles are induced in HIV-1-infected individuals.
Detection of HERV-K(HML-2) viral RNA in plasma of HIV type 1-infected individuals.http://www.ncbi.nlm.nih.gov/entrez/query.f...t_uids=17067267
We could then also blame HERV-K for AIDS and Cancer but why would HERV-K also turn up in skin, thyroid gland, placenta, and tissues of reproductive organs?
“Most active members of HERV families were found in mRNA prepared from skin, thyroid gland, placenta, and tissues of reproductive organs. In contrast, only few active HERVs were detectable in muscle cells. Human tissues that lack HERV transcription could not be found, confirming that human endogenous retroviruses are permanent components of the human transcriptome.”
“For example, some members of the HERV-K family encode retroviral enzymes with specific activities, such as protease, reverse transcriptase (RT), integrase, and nonstructural proteins with functional similarities to human immunodeficiency virus (HIV) and human T-cell lymphotropic virus (HTLV) Rev and Rex proteins. Recently, a novel accessory gene, np9, that is located within the HERV-K env reading frame was found to be expressed in various human tumor tissues and transformed cell lines”
Comprehensive Analysis of Human Endogenous Retrovirus Transcriptional Activity in Human Tissues with a Retrovirus-Specific Microarray 2005http://www.pubmedcentral.nih.gov/articlere...gi?artid=538696
When we medicate with protease inhibitors are we trying to stop HIV or HERV-K?
AZT and other anti-retrovirals are meant to stop Reverse Transcriptase, again are we trying to stop HIV or HERV-K?
And what do these drugs do to our skin, thyroid glands, placentas, and tissues of reproductive organs?
Reverse transcriptase activity from human embryonal carcinoma cells NTera2D1.http://www.ncbi.nlm.nih.gov/entrez/query.f...st_uids=1698616
When we did the Human Genome Project I’m sure many in the genetic field with their penchant for a bit of genome purity and Eugenics thought the ‘crime’ genes and ‘gay’ genes would turn up and we could tidy up the genome and make society safe from the ‘undesirables’.
It’s not really like that though, sure there’s the possibility that some folk have the ‘testosterone’ gene and are a bit angrier than the other apes.
But a lot of crime is learnt, neglected and abused kids have realized if they are naughty they will get more attention, this is why you often see rich children grow into psychopaths.
They were in fact neglected and money didn’t stop that neglect.
The Human Genome Project opened a can of worms though and that was the fact that 40% of our genome is made of retrotransposons and 8% of that is our retroviruses.
So now there is a scramble to work out what this ‘Junk DNA’ does and how we can cash in on the new discovery?
I’m hoping it sends us in the right direction and I’m trying to steer a change in the course of history just by writing this.
And why not?
My ideas on the subject are like this.
If HERV-K turns up in AIDS, Cancer and all the autoimmune diseases then why?
“These data suggest that different HERV-K proviruses are transcribed in human teratocarcinoma cell lines.”
Phenotypic heterogeneity of human endogenous retrovirus particles produced by teratocarcinoma cell lines.http://www.ncbi.nlm.nih.gov/entrez/query.f...t_uids=11172100
“Compared with controls, HERV-W and HERV-K expression was increased in brain tissue from patients with multiple sclerosis or human immunodeficiency virus infection or AIDS”
Monocyte activation and differentiation augment human endogenous retrovirus expression: implications for inflammatory brain diseases.http://www.ncbi.nlm.nih.gov/entrez/query.f...4&dopt=Abstract
Why are HERV-W, HERV-K and HIV all turning up in inflammatory brain diseases?
HERV-W is also called Syncytin and they found it was involved in attaching the fetus to the placenta.
“Syncytin is a membrane protein derived from the envelope gene of an endogenous retrovirus of the HERV-W family. The gene appears to be almost exclusively expressed in placenta; the protein was found in particular in syncytiotrophoblast. After transfection into various cell types it has proven to be a very fusogenic protein, inducing the formation of syncytia. Therefore, the question rises as to whether syncytin is responsible for the fusion process of villous cytotrophoblast into syncytiotrophoblast in vivo. If so, how is this fusion process regulated if syncytin is found all over the syncytiotrophoblast?”
Syncytin: the major regulator of trophoblast fusion? http://www.ncbi.nlm.nih.gov/entrez/query.f...t_uids=15333590
So our HERV’s also can’t be deadly if they turn up skin, thyroid glands, placentas, and tissues of reproductive organs.
Something else is going on, this is not an infection and I think Pasteur’s disciples have a bit to answer for here.
There’s more to ‘infection’ than just a bug that jumps on you and starts replicating.
You need to be prone to going down, this is why some get flu for a day and others can die.
So I believe if HERV’s are in normal tissue they are probably involved in cell division, mainly because they turn up in our Cancer cells too, I could be wrong, I don’t have a lab to check.
“These data suggest that HERV-W elements are actively expressed in human tissues and cancer cells. These active HERV-W elements deserve further investigation as potential causative agents of various human diseases including cancers.”
Expression of the human endogenous retrovirus HERV-W family in various human tissues and cancer cells http://vir.sgmjournals.org/cgi/content/full/85/5/1203
The other possibility is they come out with cell breakdown.
You look at Cancer and Autoimmune diseases and there’s a common denominator.
Cancer cells release Metalloproteinase, an enzyme our cells use to dissolve collagen and also make new arteries, a bit like ripping up tarmac and putting new stuff down.
When you get Arthritis, Multiple Sclerosis, Psoriasis, Lupus and other Autoimmune diseases our white blood cells rush to areas of our body which our inflammatory cytokines or T-cells have tagged to be a battle zone.
They are the exactly the same disease but in different organs, my opinion.
Then the white blood cells release Nitric Oxide to burn the zone that has been tagged.
They are trying to dissolve something that shouldn’t be there, be it viral, bacterial, chemical or just a bit of pollen.
The enzyme Metalloproteinase also turns up in the data of Autoimmune diseases and of course our collagen is getting cooked.
Collagen is the stuff that holds us together.
Nerds should know of Linus Pauling, the double Nobel winner who’s chemistry Watson and Crick used to work out the DNA helix.
The story I describe is helical.
Most people still won’t know that in the early ‘90’s before Linus died he came up with a simple regimen of Lysine and Vitamin C to cure Heart Disease, which he saw as a Collagen deficiency problem.http://www.paulingtherapy.com
The rascally Dr. Rath, his co-inventor of the idea, uses it to inhibit Metalloproteinase for keeping Cancer cells in check.
Natural Eradication of Cancerhttp://www4.dr-rath-foundation.org/NHC/can...r_solutions.htm
Metalloproteinase inhibitors in drug forms are used for Cancer and there has been a lot of interest and a gold rush to make new ones in recent years.
Lysine and some lemon juice are cheaper.
Before 2001 my skin was fine, now I can watch in real time live action my immune system go into overdrive if it doesn’t like something and release these enzymes that can dissolve my skin so I use Linus Pauling’s therapy, it doesn’t hurt and I think it works.
Bouncers have asked me for ID twice this year and a bus driver asked if I wanted an adult fare, I didn’t know whether to be insulted or if that could be a complement? (I don’t look that young)
I’ll be 42 soon, of course all my chemical exposure and stress of discovering this could stuff me up in the years ahead but I think I’m on the road to healing.
These were the symptoms after working like a maniac with Phenol and Amine glues for 3 to 4 years, I found out only this year that the Solder Flux I used for the 4 years after escaping the glues also creates Phenol when heated.
They were rapid weight loss, night sweats, severe insomnia, lymph swelling, nausea, shakes and headaches.
This later led to my white blood cells rushing to my skin where thousands of pores filled with pus, my skin fell off, I had lesions, fevers, chills and was later told I could have gone into a coma.
It was really a massive allergy attack because Prednilisone didn’t work but another Cortisone did later and I was at least stabilized in less that a week.
The hospital staff wanted to give me a bed for 3 days, this doesn’t happen here in Queensland unless you’re really sick, I just went home and put on the cream with a big thank you.
It was diagnosed Pustular Psoriasis but photos I had of myself at the time showed I had googly eyes as in possible Grave’s disease, an autoimmune hyperthyroid drama, the doctors didn’t notice, nether did I until later.
So I can’t help but ask questions like “what are all these HERV’s doing in my skin?”.
“METHODS: HERV expression was analysed at the mRNA level after degenerated reverse transcription-polymerase chain reaction (RT-PCR) of retroviral pol sequences followed by sequencing. Screening for a specific variant was performed by RT-PCR on lesional and nonlesional psoriatic skin and compared with normal and atopic dermatitis skin. RESULTS: We report the expression of three HERV families in psoriatic lesions, namely HERV-W, K and E.”
A new endogenous retroviral sequence is expressed in skin of patients with psoriasishttp://skinrashes.researchtoday.net/archive/2/7/468.htm
I found out from this website that Copper deficiency can cause hyperthyroid and because Brazil nuts have a fair bit of Copper they went into my diet.
“Thyroid and immune system health are crucially dependent upon copper. As far as I can see now, copper deficiency is the most important factor in the development of hyperthyroidism. Virtually all hypers in the hyperthyroidism group have found that copper supplementation reduced their symptoms, usually within hours or a few days at most.”
Copper and Hyperthyroidismhttp://www.ithyroid.com/copper.htm
So I munch 4 or 5 Brazil nuts in my muesli each day to patch up damage, eat cashews in stirfrys, etc.
Brazil nuts also have a lot of Selenium so I don’t know if it was the Copper or Selenium that helped?
I did get better though and symptoms that went were immediate cessation of rashes coming out near my lower neck, night sweats were no more, I now don’t have asthma.
My skin was and still is a bit damaged and doesn’t like the modern world.
This is about Selenium and DNA damage.
“In human tissues, it has been estimated that each cell sustains approximately 10 000 potentially mutagenic (if not repaired) lesions per day due to endogenous DNA damage. Almost no studies have addressed the potential for selenium compounds to induce DNA repair, a potential mechanism for their cancer-preventive actions. We show that selenium in the form of selenomethionine induces a DNA repair response in normal human fibroblasts in vitro, and protects cells from DNA damage.”
Selenomethionine induction of DNA repair response in human fibroblasts.http://www.ncbi.nlm.nih.gov/entrez/query.f...4&dopt=Abstract
The googly eyes got my brain ticking over about the possibility I had Hyperthyroid Autoimmune dramas, I use past tense because I the symptoms were gone by the time I thought about it.
All the other symptoms were similar to Grave’s Hyperthyroid Disease, they are also very similar to Lupus, an Autoimmune liver disease some alcoholics and drug addicts can get.
Remember I believe all the Autoimmune diseases have the same cause but they just occur in different organs, my skin went because it was saturated with Phenol.
And Autoimmune disease and Allergies coincide, my opinion.
So Selenium is also vital for Thyroid function.
“Several minerals and trace elements are essential for normal thyroid hormone metabolism, e.g., iodine, iron, selenium, and zinc. Coexisting deficiencies of these elements can impair thyroid function. Iron deficiency impairs thyroid hormone synthesis by reducing activity of heme-dependent thyroid peroxidase. Iron-deficiency anemia blunts and iron supplementation improves the efficacy of iodine supplementation. Combined selenium and iodine deficiency leads to myxedematous cretinism. The normal thyroid gland retains high selenium concentrations even under conditions of inadequate selenium supply and expresses many of the known selenocysteine-containing proteins. Among these selenoproteins are the glutathione peroxidase, deiodinase, and thioredoxine reductase families of enzymes. Adequate selenium nutrition supports efficient thyroid hormone synthesis and metabolism and protects the thyroid gland from damage by excessive iodide exposure. In regions of combined severe iodine and selenium deficiency, normalization of iodine supply is mandatory before initiation of selenium supplementation in order to prevent hypothyroidism. Selenium deficiency and disturbed thyroid hormone economy may develop under conditions of special dietary regimens such as long-term total parenteral nutrition, phenylketonuria diet, cystic fibrosis, or may be the result of imbalanced nutrition in children, elderly people, or sick patients.”
The impact of iron and selenium deficiencies on iodine and thyroid metabolism: biochemistry and relevance to public health.http://www.ncbi.nlm.nih.gov/entrez/query.f...9&dopt=Abstract
AIDS IN AFRICA AND IODIZED SALT
To start with there’s TB and Malaria that can kill you in six months or less, then there are all the infections associated with dirty water, no sewage, no refrigerators and old and moldy food.
Add in starvation with pollution and that’s enough trouble.
The responsible pregnant African mums are also lining up at the HIV testing centers where the test could very likely pick up those evil retroviruses going rampant in their placentas.
Well I have another take on AIDS in Africa and that’s the introduction of Iodized salt.
I don’t know if anyone has noticed this, there’s one lone nutritionist in India called Ashok Jaisinghani that I found on the net one day, at a first look he looks crazy but he may be quite right.
“Ever since iodized salt has been introduced for consumption in food in India, the cases of AIDS have increased by leaps and bounds in our country. Excessive intake of IODINE is one of the main causes of AIDS in human beings. Iodized salt has caused AIDS in millions of susceptible people in India, and elsewhere, leading to their early deaths.”
Iodized Salt Causes AIDS (hang it’s fascist promoters)http://wonder-cures.com/art2.htm
I’m chuckling at the “hang it’s fascist promoters”.
I’ll quote this again.
“Adequate selenium nutrition supports efficient thyroid hormone synthesis and metabolism and protects the thyroid gland from damage by excessive iodide exposure.”
It’s not that Iodine is bad, we do need it to stop Goiter and Cretinism but if we are selling Iodized salt to people who don’t eat much and have low Selenium in the diet we’re causing a new disease.
So here are a couple of studies that shows what can happen, one from China and one from Africa.
“The average annual incidence of hyperthyroidism after iodine supplementation was 36.87 per 100,000, a three-time increase as compared with that before iodine supplementation. The incidence of hyperthyroidism began to show a significant rise in 1996. The year with highest annual incidence was 1997, remaining at high level after supplying iodized salt. Since then the annual relative risk for hyperthyroidism had been increasing. CONCLUSION: The number of patients with thyroid diseases showed a significant increase after mass iodine supplement.”
Study on the effects of increased iodized salt intake on the incidence of thyroid diseaseshttp://www.ncbi.nlm.nih.gov/entrez/query.f...4&dopt=Abstract
“Biochemical signs of hyperthyroidism, or even overt and possibly lethal clinical hyperthyroidism were reported in 2 severely iodine-deficient African countries (Zimbabwe and Democratic Republic of Congo, RDC) soon after the introduction of iodized salt.”
Risks of iodine-induced hyperthyroidism after correction of iodine deficiency by iodized salt.http://www.ncbi.nlm.nih.gov/entrez/query.f...6&dopt=Abstract
Hyperthyroid Autoimmune Diseases have a quite a high probability of cross-reaction with the HIV antibody test and the HERV’s will go up and the viral load test will pick that up.
I’d better show some studies again to prove this, Sjogren's syndrome and Grave’s disease are different forms of Hyperthyroid Autoimmune Disease.
“The first set of experiments performed on four patients with Sjogren's syndrome (SjS) and four patients with systemic lupus erythematosus (SLE) revealed a significant anti-gp120 antibody reactivity in autoimmune patients when compared to healthy HIV-negative controls.”
“A significant anti-p24 reactivity was observed in 18 of 29 sera from SjS patients and in 13 of 25 sera from SLE patients”
Epitope specificity of anti-HIV antibodies in human and murine autoimmune diseases.http://www.ncbi.nlm.nih.gov/entrez/query.f...4&dopt=Abstract
“RESULTS: Sera from five of 15 patients with Sjogren's syndrome (33%) reacted against p24 group specific antigen (gag) of human immunodeficiency virus (HIV). Labial salivary gland biopsy specimens from seven of the 15 patients with Sjogren's syndrome (47%) contained an epithelial cytoplasmic protein reactive with a monoclonal antibody to p24 of HIV.”
Retrovirus in salivary glands from patients with Sjogren's syndrome.http://www.ncbi.nlm.nih.gov/entrez/query.f...3&dopt=Abstract
“We previously reported that 30% of SS patients and 36% of systemic lupus erythematosus (SLE) patients have serum antibodies to the p24 gag protein of HIV-1.”
“The p24 gag protein shares a proline-rich epitope with the Sm nucleoprotein to which many SLE patients have antibodies.”
Are endogenous retroviruses involved in human autoimmune disease?http://www.ncbi.nlm.nih.gov/entrez/query.f...8&dopt=Abstract
“On Southern blotting of DNA extracted from thyroid glands of five patients with Graves' disease, two probes (720 bp and 942 bp) for gag human immunodeficiency virus type 1 (HIV-1) gave a positive hybridisation signal in all samples tested.”
Retrovirus-like sequences in Graves' disease: implications for human autoimmunity.http://www.ncbi.nlm.nih.gov/entrez/query.f...9&dopt=Abstract
Or there can be Grave’s disease in AIDS patients.
Sequential Occurrence of Thyroid Autoantibodies and Graves’ Disease after Immune Restoration in Severely Immunocompromised Human Immunodeficiency Virus-1-Infected Patientshttp://jcem.endojournals.org/cgi/content/full/85/11/4254
So here’s a list of hyperthyroid symptoms.
“Symptoms of hyperthyroidism, regardless of the cause, reflect the speeding up of body functions: increased heart rate and blood pressure, abnormal heart rhythms (arrhythmias), excessive sweating, hand tremors (shakiness), nervousness and anxiety, difficulty sleeping (insomnia), weight loss despite increased appetite, increased activity level despite fatigue and weakness, and frequent bowel movements, occasionally with diarrhea.”
And these are a list of HIV/AIDS symptoms.
“However, fever, rashes, swollen lymph nodes, fatigue, and a variety of less common symptoms may develop within a few weeks of HIV infection and last a few weeks.”
Fever, rashes and swollen lymph nodes can be just autoimmune symptoms because the immune system is in overdrive.
I even called it an ‘autoimmune flu’ and people just turn up to a clinic when they have symptoms and hence take a HIV test.
“These symptoms include swollen lymph nodes, weight loss, fatigue, recurring fever or diarrhea, anemia, and thrush (a fungal infection of the mouth).”
Anemia can be copper deficiency and copper deficiency lowers white blood cells and encourages bacterial infection because bacteria live off excess iron in the gut, a lack of copper can cause diarrhea.
“HIV can also directly infect the brain, causing memory loss, weakness, difficulty walking, and difficulty in thinking and concentrating (dementia).”
The problem with these symptoms is they are the same as MS and you can get encephalitis just from Herpes.
“In some people, HIV is probably directly responsible for AIDS wasting, which is a significant loss of weight with or without an obvious cause.”
These are hyperthyroid symptoms.
“Kaposi's sarcoma, a cancer that appears as painless, red to purple, raised patches on the skin, affects many people with AIDS, especially homosexual men.”
Kaposi’s seems to occur in Nitrate users and coincides with Herpes infections that can then degrade collagen and allow cancers to happen.
“Cancers of the immune system (lymphomas, typically non-Hodgkin's lymphoma) may develop, sometimes first appearing in the brain, where they can cause confusion, personality changes, and memory loss. Women are prone to developing cancer of the cervix. Homosexual men are prone to developing cancer of the rectum.”
AZT and other AIDS drugs, Sexual Lubricants and the Wart Virus can cause these cancers.
Human immunodeficiency virus (HIV) infection http://www.merck.com/mmhe/sec17/ch199/ch19...h199-ch199a-952
“Night sweats occur very frequently in people living with HIV.”
Night Sweats...Facts and Solutionshttp://aids.about.com/od/otherconditions/a/nightsweats.htm
Night sweats are another Hyperthyroid symptom.
So do we really know what causes AIDS or not?
And do we know what sort of retrovirus HIV really is?
On top of that there is the possibility of Selenium deficiency exacerbating other real viral infections.
“In April, the scientists reported discovering that inadequate intake of selenium boosts damage caused by influenza viruses.
"We believe our latest findings are both important and potentially disturbing because they suggest nutritional deficiencies can promote epidemics in a way not appreciated before," Beck said. "Here we looked at flu virus because it hospitalizes more than 100,000 people each year in the United States alone. But what we found conceivably could be true for any RNA virus -- cold virus, AIDS virus and Ebola virus."
She and Nelson worked with colleagues at the U.S. Department of Agriculture and the Nestle Research Center in Switzerland. They fed groups of mice either selenium-deficient or normal diets. Later, they exposed both groups to a mild strain of human influenza virus known as Influenza A Bangkok. Rodents consuming too little selenium developed significantly more harmful lung inflammation, which also lasted considerably longer, than animals that developed the flu but whose diets were normal. The difference between the mice's illnesses was the difference between mild pneumonia and severe pneumonia, which can be life-threatening, they said.”
Selenium Deficiency Causes Flu Virus To Mutatehttp://www.sciencedaily.com/releases/2001/...10608081506.htm
This is all helical, I’ve been circling and circling outside the square every else’s heads reside in.
I’ve watched ‘HIV’ tagged people in despair tell me their woes via my email box, I became sick as well (in fact the HIV positives emailing me are often not sick) and I had become ill while trying to study microbiology part-time at university.
So I wondered what was happening to me while the new studies appeared in my Google search.
By censoring so called ‘AIDS dissidents’ we sent ourselves paddling up the wrong creek.
The retro-virologist Peter Duesberg should have had his right of reply in Nature, the debate he could have started may have prevented all of this muddle.
As for me this became quite a burden when I realized I could type in ‘AIDS Methylation’ and come up a few times on the front page.http://www.google.com.au/search?hl=en&q=ai...nG=Search&meta=
I’m the one suggesting ‘The AIDS Retrovirus Expression Is Regulated by Methylation’ and The Free Information Society banned me for talking about it and they give me the message “You have been banned from this forum.”
This Physorg.com link comes up, so you folk are cool.
I so want everyone else to pick up on this and talk about it.
I don’t get paid for this and thinking about it by myself is a bit tiring, I mostly want some good sleep and to sing some songs and forget about how I got here.
So if you can help me out then just show your friends this link and pass it on because it is important.
And thanks again to Physorg.