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Ebola: Case X, the mysterious person behind the disease spreading to Africa and the US

In Uncategorized on November 6, 2014 at 8:53 AM

Ebola: Case X, the mysterious person behind the disease spreading to Africa and the US

11/05/14
0833

The US Government, Tulane University, Department of Defense, the CDC and a host of others inside a vast consortium are responsible for the past and recent Ebola outbreaks in Africa and now in the United States of America.

In Africa, exhausted from a Civil War that ravaged most of Africa in the 1990s, natives must now fight another war of sorts, a biological war, imposed by the US Government and our military.

With the recent acknowledgement that the US owns and has patented the exact strand of Ebola that is now infecting a great number of people in Sierra Leone, the US and surrounding countries, the dots begin to connect revealing an unpleasant odor of evil and deciet.

All researched signs point to either a containment outbreak, a purposeful deliberate spread or simply the disease was genetically too strong to restrain from spreading, perhaps going airborne. 

The route of infection, the vector is still  unknown but it has been suggested that fruit bats have spread the disease. My research has revealed fruit bats do not migrate, neither do rats or monkeys. 

The most likely vector I can pinpoint beyond a doubt belongs to a group of scientists at Kenema labs in Sierra Leone and that Vector is human. The chosen vehicle is Case X!!!

This vector aboard a biological warfare experimenting machine from our US Government and Military is very dangerous and all indicators show this spread was either by accident or willful intent, either way it’s purposeful, the intent questionable.

While researching, I came to a place that was uncomfortable at best. In today’s political environment where conservative bloggers are frowned upon and great efforts are spent on shutting them up, I stumbled upon a statement that may make you scratch your head and me check my steps…..and my six.

Here are the facts that if disputed by naysayers could be labeled irresponsible and their efforts to dispel it lazy and uninformed in light of such glowing facts. 

Here is what we do know.

In 2007 and again in 2014, in Sierra Leone something very bad happened. 

Many people were killed and many died because of a deadly strain of Ebola created by our own US Government.

A deadly virus escaped either purposefully or by accident, by mistruths or by a failed experiment. 

Thousands were being studied and researched by several entities inside a consortium aforementioned. 

Those being treated and subsequent patients being treated became very sick and many of them died. 

Doctors and Nurses that had been treating the sick for up to 20 to 30 years were suddenly dying unexpectedly. Many became  sick and most died in a short period of time. Untouched many years prior to this time span.

Doctors without Borders pulled out of the area citing they were losing too many healthcare workers in a short time period.

Local Africans patients began reporting they were being killed by Western Scientists in Kenema Hospital and its supporting biological Kenema labs. They said they were being lied to and injected with unknown substances for unknown reasons.

The local government, via the MOH, Ministry of Health, reacted and shut the doors of Kenema Labs.

Tulane University was ordered to stop all research and experiments during this outbreak. (link below)

The Sierra Leone government asked the  United Nations to intervene charging ethical and human rights violations by the US on it’s local citizens.

Identical and coincidental outbreaks occurred in the same area and by the same strand of EBOLA in great numbers. A result of continued research?

My research has revealed the same strand owned and patented by the US Department of Health, the DOD, our Government and the CDC is the same one that infected employees, Doctors and Nurses working at or around the Kenema Hospital and biological warfare lab in Sierra Leone and is the current topic of discussion.

Those surviving Doctors and nurses from this same region have now transported this same US government Ebola strand to the United States and it began with Case X.

The US President has recently gone on record saying that further “research” and “experiments” in this same region be halted. In other words, confirming that the alleged experimental activity is being performed regardless of current US law against using and experimenting with bio weapons in the field, and stating it must stop…..now!

A few short years ago, as if our memory wanes we had another almost identical “outbreak” using the same old tired methods. It’s almost as if we keep trying we will eventually harm greater numbers as if that is a goal of our US Government.

How it all started: 

The first trial known was performed upon unfortunate guinea pigs in Africa, a virus released from our own arsenal of US Bio-weapons. To prove this point, let’s go back a few years and see that the happenings of today is directly relevant to 2007 and Case X.

The NIH, (National Institute of Heath) states from the link provided below.

In 2007, inside the “Death Triangle” consisting of Liberia, Uganda and Sierra Leone, the hub of an Ebola outbreak, a “new” strand of Ebola was identified and emerged from the Kenema Lab.One of the biggest outbreaks in recent times.

Coincidentally, this “new” strand of Ebola is  known as the EBOLA-B, Bundibugyo. You may recall this strand complete with it’s genre of “ancestor” genes from the Ebola Zaire, Lassa and Marburg virus was created and patented by our US Government, oh lets say around this same time in 2007.

With the commercial, patent and inventive rights to EBOLA-B applied for and secured. The virus was shared with thousands in the name of science. This adds a peculiar element to the equation. 

The timing to apply for a patent, create and invent a virulent Ebola disease at the exact same time the disease starts spreading wildly of this same disease in 2007 is suspect. 

The responsibility and fault for the spread of this awful disease lies with the United States Government and it’s associates.

Researchers and scientist at the following link describe the 2007 event and the reasons for it:

http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3294552/#!po=0.847458
 
We also know this:

Coincidentally in 2007, Tulane University received a grant from NIH to develop tests for bioterror agents such as Ebola.

From the National Institute of Health, NIH site above: And I quote,

Abstract

“The first known Ebola hemorrhagic fever (EHF) outbreak caused by Bundibugyo Ebola virus (the strand owned by our US Government) occurred in Bundibugyo District, Uganda, in 2007. 

“Fifty-six cases of EHF were laboratory confirmed. Although signs and symptoms were largely nonspecific and similar to those of EHF outbreaks caused by Zaire and Sudan Ebola viruses, proportion of deaths among those infected was lower (≈40%).”

” The Bundibugyo District is located in western Uganda, which borders the Democratic Republic of Congo. After reports of a mysterious illness in Bundibugyo District, the presence of a NOVEL, fifth EBOV virus species, Bundibugyo ebolavirus (BEBOV), was identified in diagnostic samples submitted to the Centers for Disease Control and Prevention (CDC), Atlanta, Georgia, USA, in November 2007″

“Anecdotal reports suggested that human illness consistent with a viral hemorrhagic fever arose in Bundibugyo District as early as August 2007. After EHF (Ebola Hemmorhagic Fever) was confirmed, isolation wards were established at 2 medical facilities in the district. (Kenema biowarfare lab already existed) Diagnostic samples from hospitalized patients with acute illness and community residents who had febrile illnesses and multiple additional signs, symptoms, or epidemiologic exposures suggestive of EHF, were routinely collected for EBOV testing”

This is where it gets very interesting. This tiny detail would have escaped me had I not have read between the lines and sought answers.

Enter Case X! What is case X? It is the human vector we have talked about previously. This person, male? Female? Young or old? I do not know. But it was human. 

Case X, the one person that is solely being held responsible for this multi country pandemic to include the one in the United States. This person was rumored to have been a “holy man”, a healer in the community that became infected by taking care of these natives. This  person was determined to be the vector responsible for spreading the deadly US created virus to the people of this region of Africa and eventually into the US.

Case X was discovered by researchers and healthcare workers by a questionnaire reportedly filled out by patients entering Kenema labs for treatment as the reason for this outbreak. We know very little about Case X , other than that he or she is being blamed as the source or vector of this “new” Ebola strand and that he/she may have been a healer, perhaps an elder taking care of his/her people. One question still remains. The origin of the disease is still in question. Case X as he is being labeled by scientists is being blamed without one huge question being answered. How did he get it?

My guess is he was probably the first to be “vaccinated” during an experiment, released back into the community to tend to others within his village or town that also had been unknowingly “vaccinated” with the Ebola virus, further advancing their research.

When this virus spread beyond those intended and his scope of reach underestimated, the virus became uncontrollable and out of hand.

When hundreds, in a very short time started flowing into their “research” centers or care sites, researchers began to ask,”where did you get this sickness, many fingers pointed to CASE X! Case X was now carrying a huge burden and was being blamed for the death of many because after all he was taking care of them, right? After all, Case X was easily identifiable! Maybe a little scripted?

According to this memo on an NIH site, 

“As part of the standardized surveillance case-report form, patients were also asked whether they had had contact with a sick person during the 3 weeks before development of illness. A large portion of the laboratory-confirmed case-patients in this outbreak reported direct contact with a specific person, (case X), who died of a severe hemorrhagic febrile illness consistent with EHF (no diagnostic specimens were collected from this person) in November 2007. Using the date of last contact for those reporting contact with case X or reporting contact with another laboratory-confirmed case-patient to the date of symptom onset. (Case X may I remind you was rumored to be taking care of those sick, but the conclusion was Case X gave the virus to everyone.) 

Did you catch that? The “human vector”, the most important piece of this puzzle, the person being solely held to be the biggest cause of this new outbreak and we don’t know their name, their address, didn’t draw blood, titers, nor did we even test him/her for Ebola, nothing, nada, that we are aware of. 

The CDC and all those investigating said  “no diagnostic specimens were collected from this person.” Nothing! This smells of a cover up. Case X remains a mystery. My guess and to date I have not been able to locate any more info on this person but seems to me that this person was perhaps “infected” with this new strand of Ebola and sent out into the community.  (That last statement is unsupported by evidence and is only a hunch) A new scenario: Big unknown. A mystery continues. A brand new virus, created by our government, and Case X “gets” it, and no one took the extra step to find out where he got it? I believe we know the reason Case X was not tested or his identity known. He was the initial human vector, the specimen selected to test the virility of our new biological warfare toy on his/her community.

More of what we know:

Dr. Cyril Broderick, A Liberian scientist and a former professor of Plant Pathology at the University of Liberia’s College of Agriculture and Forestry wrote to the Daily Observer, Monrovias largest newspaper and said regarding the 2014 Ebola B outbreak, reflecting on that original trial in 2007.

“The US Department of Defense (DoD) is funding Ebola trials on humans, trials which started just weeks before the Ebola outbreak in Guinea and Sierra Leone. The reports continue and state that the DoD gave a contract worth $140 million dollars to Tekmira, a Canadian pharmaceutical company, to conduct Ebola research. This research work involved injecting and infusing healthy humans with the deadly Ebola virus. Hence, the DoD is listed as a collaborator in a “First in Human” Ebola clinical trial (NCT02041715, which started in January 2014 shortly before an Ebola epidemic was declared in West Africa in March.”

Case X was only the beginning. I am afraid many more have carried the deed unknowingly to it’s intended destination. 

We are seeing an all too powerful government run away with it’s power  and unfortunately we have enough sheep willing to dismiss these facts as unbelievable and conspiratorial. this alone seemingly enough to drop the discussion.

The facts presented were collected from government and University websites and direct quotes supplied from those on the ground in that time period.

Suspension of belief is your decision, me, I continue to ask questions, seek answers and refuse to take blanket statements at face value from our government. I fortunately do not live in a bubble where I trust everyone. 

This next paragraph is directly from the CDC and I’ll close with their statement.  Please look at this supporting link below and observe who one of the contributing writers is, J.S. Towner, the inventor of Ebola-B virus and owner of the patent for the virus.
http://wwwnc.cdc.gov/eid/article/16/12/10-0627_article

The CDC states:
“It is apparent that novel emerging infections continue to occur. The outbreak of EHF described in this report involved a previously unidentified EBOV species, with a proportion of deaths of 40%. BEBOV represents the fourth EBOV species–associated disease in humans, and the third species to cause large human outbreaks of EHF. Although proportion of deaths was lower than that documented in previous EHF outbreaks, BEBOV is a severe human pathogen with epidemic potential. These findings demonstrate the need for increased surveillance and diagnostic capabilities, as well as the capacity to respond quickly to emerging human infections……………

Additional information and links:

The Lassa Fever Program in Sierra Leone at Kenema Labs, the site and current feeder of Ebola patients.

Today, the work of the Lassa Fever Program has expanded to include treatment, containment, prevention and research. The current team consists of medical staff led by Dr. Donald S. Grant, the Chief Physician at the Lassa ward, and supervised by Nurse Mballu Fonnie. 

The day to day activities of the Lassa Fever Program are being lead by Program Coordinator Simbirie Jalloh. In addition, the Program has an Outreach team that is responsible for case investigation, surveillance and sensitization campaigns. They work closely with the Ecology team who are tasked with rodent trapping and extracting samples from the multimammate rat, Mastomys natalensis.

Tulane University has a long-standing partnership with the Lassa Fever Program at the KGH. When it was established in 2004, Tulane was contracted as the principle implementing partner of the Mano River Unione Lassa Fever Network program (MRU-LFN), a diverse group of organizations working together to develop national and regional prevention and control strategies for Lassa Fever, as well as focusing on building the capacity of the laboratory at the hospital. Since then, the work conducted by Tulane and its partners at KGH has grown to include new lines of research and public health surveillance.

http://vhfc.org/consortium/partners/kgh

http://www.washingtonsblog.com/2014/10/ebola-2.html

http://m.thiscantbehappening.net/node/2525

http://m.thiscantbehappening.net/print/2525?page=2

http://www.smirkingchimp.com/thread/dave-lindorff/59216/expert-traces-outbreak-to-us-bio-weapons-lab-why-s-this-ebola-pandemic-in-west-africa-so-virulent-and

http://www.globalresearch.ca/a-liberian-scientist-claims-the-u-s-is-responsible-for-the-ebola-outbreak-in-west-africa/5408459

http://www.who.int/csr/don/2012_09_14/en/

http://en.m.wikipedia.org/wiki/Bundibugyo_virus

https://bradleycountynews.wordpress.com/2014/10/05/ebola-the-reasons-behind-an-american-outbreak-may-surprise-you/

Tulane disputes they were shut down by MOH at height of ebloa outbreak despite MOH statements saying they did so.
http://tulane.edu/news/newwave/081414_ebola_virus_outbreak_facts.cfm

MOH stating they shut down Tulane research:
http://www.google.com/url?q=https://www.facebook.com/permalink.php%3Fstory_fbid%3D322983307878518%26id%3D281064805403702&sa=U&ei=GWdXVMO7OMmfgwTvvITIDQ&ved=0CB0QFjAH&usg=AFQjCNHj4kN8X2SLlSnvo6VAKec-6SRbSA

Tulane scientist collaborates with USArmy, USAMRIID.
“She collaborates with the U.S. Army to develop therapies for arenaviruses and filoviruses, as well as conducting field studies in the Democratic Republic”
http://tulane.edu/som/lassa-fever/kathleen-rubins.cfm

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3 million Ebola vaccines have been produced by Crucell, stockpiled since 2003

In Uncategorized on October 20, 2014 at 8:42 AM

3 million Ebola vaccines have been produced by Crucell, stockpiled since 2003

10/26/2014
0832 am

The United States has had a vaccine for Ebola for nearly 11 years. The 3 million vaccines mass produced are a result of funding for Project Bioshield. 

The Ebola vaccines have been approved,tested in humans and ready to go but are being stockpiled in some military vault out of the publics reach.

CRUCELL labs has had the contract for many years to develop the vaccines. They delivered on their pact with the US Government to develop a vaccine. The vaccine is available.

The information below, nearly all of it, was pulled from the websites of CRUCELL and other governmental agencies.

To see this information so readily available and not reported simply amazes me. Then yet again, I am of the opinion that many things are left unsaid by our MSM, mainstream media,for a purpose.

Take a look at this information provided to you by CRUCELL the producer of the Ebola vaccines. This information is directly from the links provided. I have provided some text in parentheses.

In 2005, “Crucell is (has) developing an Ebola vaccine in collaboration with the Vaccine Research Center (VRC) of the NIH National Institute of Allergy and Infectious Diseases (NIAID). It has been shown to completely protect monkeys against the virus with a single dose of the vaccine.
Under the terms of the agreement with VRC, Crucell has an option for exclusive worldwide commercialization rights to the Ebola vaccine.”

“Crucell’s Ebola vaccine entered Phase I clinical trials in Q3 2006.  Two groups of 16 volunteers were enrolled and vaccinated. ”

“The study showed safety and immunogenicity at the doses evaluated.”

“In October 2008, Crucell secured a NIAID/NIH award to advance the development of Ebola and Marburg vaccines, with the ultimate aim of developing a multivalent filovirus vaccine.”

“The award provides funding of up to $30 million, with additional options, worth a further $40 million.”

“Development rationale:
To date, numerous attempts to PROTECT against Ebola infection using a variety of strategies have failed.”

“However, in 2003 a National Institutes of Health (NIH) study published in Nature demonstrated that a SINGLE DOSE of a recombinant vaccine provided solid protection against an otherwise deadly infection in animal models. Based on these results, we DECIDED TO DEVELOP an Ebola vaccine using the same approach.(For humans)”

“Furthermore, the Ebola virus is on the US government’s Category “A” list of bioterror agents.” 

“In 2003 the US government announced that, once available, an Ebola vaccine may be STOCKPILED as part of its preparation for bio-terror attacks under Project Bioshield.”

“The Bioshield Act was enacted in July 2004, with a total appropriation of US$ 5.6 billion across all programs.”

“Development status:
In 2002, we entered into a Collaborative Research and Development Agreement (CRADA) with the VRC of the NIH to develop jointly, test and manufacture an adenovirus-based Ebola vaccine. ”

“Under the terms of the agreement, we have an option for exclusive worldwide commercialization rights to the Ebola vaccine resulting from this collaboration.” 

“In August 2002, the CRADA was extended to cover vaccines against Marburg and Lassa infections. (Ebola-Z, Marburg and Lassa hemmorhagic fevers are the viruses responsible for destroying West Africa and now the US.)”

“In experiments conducted in 2004 by the VRC together with the U.S. Army Medical Research Institute of Infectious Diseases (USAMRIID), our vaccine candidate confirmed single-dose protection of monkeys against Ebola. Our results are distinct from the earlier trials in that our vaccine is based on PER.C6® cells, making it SUITABLE for large-scale manufacturing.”

“In 2005, we extended the CRADA with the VRC (Vaccine Research Center) of the NIH to develop and produce vaccines against Ebola, Marburg and Lassa infections.”

“Crucell was also granted an exclusive license to patents owned by the NIH to develop and commercialize vaccines against Ebola. ”

“Furthermore, Crucell signed a contract of up to €21.4 million (27 million US dollars)  with the NIH to produce Ebola vaccines. (In 2005, need I remind you)”

“Crucell’s Ebola vaccine entered Phase I studies in Q3 2006.” 

“For this randomized, double-blind, placebo-controlled study, two groups of 16 healthy volunteers were enrolled and vaccinated. The study showed safety SHOWED SAFETYand IMMUNOGENICITY at the doses evaluated.”

“Based on these results, a second Phase I study is anticipated (was done). This will use alternative multivalent adenovirus vectors that are able to bypass pre-existing immunity against the more commonly used adenovirus serotype 5 (Ad5).”

Look for your self at the link below! It’s evidently no big secret, just underreported!

http://www.crucell.com/R_AND_D_CLINICAL_DEVELOPMENT_EB.HTM

http://www.crucell.com/PAGE/DOWNLOADS/FACTSHEET_DEVELOPING_EBOLA___MA.PDF

Here is another offering of information about the development and production of an Ebola vaccine.

Crucell Lands EUR21M NIH (National Institute of Health) Contract To Produce Ebola Virus Vaccine (2005)

According to Cormac Sheridan, BioWorld International Correspondent: “Crucell NV gained what Chief Financial Officer Leonard Kruimer described as a larger-than-expected contract from the Vaccine Research Center at the National Institute of Allergy and Infectious Diseases, part of the National Institutes of Health.”

“The contract is for manufacturing 10 clinical-grade batches of Ebola virus vaccine for use in Phase I and Phase II studies. The full value of the contract, which is set for about two and a half years, stands at €21.4 million (US$27.9 million)” (This amount backs up previous links)

“The vaccine is being developed (in 2005) under a Cooperative Research and Development Agreement between Crucell and the NIH, which also includes provisions for the development of vaccines against two other viruses that cause hemorrhagic infection, Marburg and Lassa.”

“The program is due to move into the clinic in the fourth quarter. Depending on the outcome of the initial studies, the NIH, of Bethesda, Md., might decide not to proceed with all 10 trials, Kruimer said.”

“Then you do not get all the revenues from this contract, but you have a product,” he said. The vaccine, which Crucell, of Leiden, the Netherlands, will produce using its PER.C6 human cell culture system, will not be eligible for full FDA approval but will be available under U.S. biopreparedness plans for administration to key personnel, including the military, government officials and health care workers, IN THE EVENT OF AN OUTBREAK!

“The government has indicated that they would be able to buy 3 million doses,” Kruimer said. “You’re talking about a market of $100 million, and that’s what we’re going for.”

“Additional human and animal studies would be required for full approval. A single dose of the recombinant vaccine, which is based on Crucell’s replication-deficient adenovirus vector expressing Ebola viral antigens, bestowed protection on macaque monkeys challenged with a lethal dose of Ebola virus in studies conducted last year by the Vaccine Research Center and the U.S. Army Medical Research Institute of Infectious Disease, located in Frederick, Md.”

“We are the only company in the world, which has developed a vaccine which keeps animals alive and disease-free after vaccination,” Kruimer said.

“Administrations in other countries also have expressed interest in the Ebola program, he said. IMPORTANT TO NOTE-“We will make sure it works in the United States and then we’ll take it from there.” (This was said in 2005)
http://www.bioworld.com/content/crucell-lands-eur21m-nih-contract-produce-ebola-virus-vaccine-0
Published: BioWorld Today, April 20, 2005

After years of research dating back to 2002, and making 3 million doses of the vaccine for the bio-terror program of the US Military, another Stage 1 trial is underway today, in 2014?  I don’t get it. Why are we initiating 2 trials 10 years apart to duplicate a product we already have and have stockpiled somewhere and could have easily produced enough in 10 years to offer us protection?
http://www.niaid.nih.gov/topics/ebolamarburg/research/pages/default.aspx

Fast forward to 2014-2015

Johnson and Johnson, who acquired CRUCELL recently says that the Ebola vaccine was tested on 8,300 patients and even added rabies vaccine tests. (Was this perhaps what locals were referring to when they said “they were giving them the virus?” Where did these 8300 come form and how are they now? And why are today doing vaccine research on 16 patients and why are we duplicating this process? )

The Ebola Vaccination trials going on as we speak for Ebola Zaire to develop a monovalent vaccine is underway with a trivalent Ebola, Marburg and Lassa vaccine on the horizon. Folks, we have already done this! We are doing it again? Why? Money?

We have a mono and a trivalent vaccine and had CRUCELL produce 3 million doses under Project Bioshield? Perhaps I’m missing something. Why are we going through 2 separate trials if our first one was wildly successful?

It would make sense to me that if we could mass produce 3 million Ebola vaccines bouncing around FDA approval via a fast track method couldn’t we also mass produce another batch of vaccines or produce more ZMAPP that has been shown to work at a fairly high efficacy?

Where are those 3 million vaccines being stored? At some US Military Bio lab? Perhaps in Fort Dietrich?

Russia recently asked for the vaccines successfully created in CRUCELLs initial vaccine production effort.

To date the Obama administration has refused Russia access to these vaccines. Russia is referring to the wildly successful 3 million vaccines produced under the guises of “Project Bioshield” and our 50.6 billion dollars.

http://www.whatdoesitmean.com/index1810.htm

The Project BioShield Act authorizes expedited procurement, streamlined personnel appointments, expedited peer review, biomedical countermeasures procurement, emergency use of medical countermeasures, and other biodefense activities.
http://www.astho.org/Programs/Preparedness/Public-Health-Emergency-Law/Emergency-Use-Authorization-Toolkit/Project-BioShield-Act-Fact-Sheet/

Project Bioshield, passed by the 108th US Congress, allocated 50 billion to fight potential bio terrorism. Bioshields funding was also to go forward to stockpile protective equipment, increased surveillance, detection of biological weapons and  to prepare State and Civilian hospital in the event the Ebola were to spread to American soil. I think we missed that target by a wide margin.

From my observations and recent experiences for some reason that 50 billion did not trickle down to US  hospitals badly in need of that stimulus money to protect nurses and healthcare workers.

I believe Congressional oversight  and other regulatory committees should be held accountable for this and other blunders regarding our nations response to this most recent US outbreak of Ebola.

This confirms our Bio Warfare efforts to not only produce a virulent and dangerous disease but to hold the treatment from a suffering public. 

Why have we said that the vaccines will not be ready till 2015? 

Why have 3 million vaccine shots hoarded in some military vault somewhere while thousands are dying and suffering? 

We had the funding, ie Project Bioshield and its 5.6 billion dollar infusion. Was this money wisely spent?

5.6 billion dollars could produce a whole lot of vaccines. At 3 million per hundred million we could have produced more than we needed for our entire populace and alot of Africa.

Obviously, this was not a priority.

http://en.m.wikipedia.org/wiki/Project_Bioshield_Act

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