Four Palestinian journalists were injured by Israeli army fire in the occupied West Bank town of Kafr Dan, the Red Crescent Society said today.
The society said two journalists were treated on the spot by its medics while two others were transferred to hospital.
Jaraah Khalaf, one of the injured journalists, said he and other reporters were covering an Israeli siege on a house in Kafr Dan, in the Jenin Governorate, when they came under direct Israeli fire.
“We were all wearing vests that clearly had press identification labels in English (PRESS), and our vehicles carried the same insignia,” he said.
Israeli occupation forces raided the town early today and besieged a house, calling on its occupants to surrender via loudspeakers, according to witnesses.
The house was later demolished by Israeli military bulldozers, while a child and another Palestinian were injured during the raid, according to the Ministry of Health.
US microchip giant Intel faces what’s been characterized as the most difficult moment in its 56-year history, hiring banksters to advise the company on whether to trim, slash or sell off its manufacturing business. That’s bad news for Washington, which greenlit $280 billion in funding in 2022 toward boosting domestic semiconductor manufacturing.
Intel’s stock has had a rough year-to-date, plummeting nearly 60% since January and falling off a cliff in early August as investors led by billionaire Warren Buffett began a massive selloff which led leading tech stocks to shed nearly $3 trillion in value amid a perfect storm of recession fears, concerns over rising AI-related capital expenditure, and inflation.
The shock stock drop shed more light on the difficult situation at Intel, with a flurry of reports beginning late last week citing informed sources revealing that the company is in the “most difficult period in its 56-year history,” looking for strategic advice from the likes of Morgan Stanley and Goldman Sachs, and considering selling off its chip manufacturing capacity.
The news carries grave significance for Washington, with Axiospointing out in a report last Friday that Intel isn’t just one of America’s oldest US chipmakers, but “a key national security asset,” signaling the US’s ability (or as it happens, inability) to compete with Taiwan, South Korea, China and other chip-making power players in an increasingly demanding world market for microchips.
All eyes are now on Intel’s mid-September board of directors meeting, at which company CEO Pat Gelsinger is expected to present the company’s recovery plan, from cost cuts achieved by shedding “unnecessary businesses,” possibly including US-based programmable chip manufacturing, and even the potential sale of its foundry business to a foreign buyer like TSMC.
Intel currently has more than two dozen fab and post-fab sites, most of them in Oregon, Arizona, California, New Mexico, Colorado and Ohio, but also Ireland and Israel. The potential slash in investment threatens to jeopardize the company’s ambitious expansion plans, both domestically and in Germany and Poland, with capital expenditures expected to drop by $10 billion, to $21.5 billion, in 2025. Among the casualties is a reported move to freeze construction of a $32.8 billion factory complex in Magdeburg, Germany.
Intel’s troubles are also bad news for the Biden administration specifically, which pumped $8.5 billion into the company’s coffers in March from the 2022 $280 billion CHIPS & Science Act, which includes $39 billion in subsidies for US chip manufacturing, $13 billion for semiconductor research and workforce training, and major tax incentives. Intel also enjoys up to $11 billion in Chips Act loans for modernization and new production.
The current administration has made subsidies to microchip manufacturing a key plank of its economic agenda. In addition to a broad array of civilian uses, from computers to vehicles, companies like Intel produce chips for use in military and space applications.
The company’s multi-year $100 billion+ US expansion plans fell to the wayside after its stagnant second-quarter earnings ($12.8 billion), sparking massive layoffs of over 15% of its workforce in August. The same month, veteran exec Lip-Bu Tan resigned from Intel’s board, reportedly over differences about the future of the company, and its failure to listen to proposals to make Intel’s contract manufacturing more customer-centric.
“Simply put, we must align our cost structure with our new operating model and fundamentally change the way we operate,” Intel chief Pat Gelsinger wrote in a memo in early August while announcing the cuts and firings.
A pioneer in microchip manufacturing and the developer of the Intel 4004 – the world’s first commercial microprocessor, in the 1970s, Intel produced the most popular chip of the 80s – the Intel 8088, which ended up powering the IBM PC. Fast forward to the 1990s, and Intel’s engineers developed the revolutionary 32 bit Pentium x86 processors – which were heavily improved upon by former Soviet supercomputer designer Vladimir Pentkovski. In the late 2008, Intel introduced the Intel Core lineup of multicore processers, assuring it superiority over competitors for over a decade before being surpassed by AMD in 2022. A few short years on, Intel has dropped out of the top ten largest global microchip manufacturers entirely by market capitalization.
Analyses by the New York Fed and the Center for Strategic and International Studies confirm that US semiconductor companies are losing tens of billions of dollars per year in sales. In an 18-month period immediately following strict sanctions against US chip exports to China, US companies lost an average of $770 million in market capitalization, with $130 billion in lost market cap industry wide.
In company-specific examples, Micron has lost half of its revenues as a result of China export restrictions. In 2024 alone, Qualcomm will forego $10 billion in lost sales of 7-nanometer chips which are now manufactured by SMIC, a Chinese semiconductor firm.
The United States now faces strong challenges from companies in allied countries, who are resisting calls to further decouple from China’s semiconductor market, the world’s largest.
Commerce Department Implements New Export Controls on Advanced Computing and Semiconductor Manufacturing Items to the People’s Republic of China (PRC) https://www.bis.doc.gov/index.php/doc…
US calls for Netherlands, Germany, South Korea, Japan to tighten chip curbs on China, drawing resistance from allies https://www.scmp.com/tech/tech-war/ar…
Facebook CEO, Mark Zuckerberg, finally addressed the censorship the social media giant engaged in through an open letter to House Representative Jim Jordan this week, outlining the pressure he received from the Biden White House and the media to remove COVID-19 and Hunter Biden laptop posts. Many are questioning why he is coming clean and apologizing now.
Japanese citizens were shocked on the morning of August 28 as their largest national broadcaster, NHK, decided to air a special feature on the COVID-19 vaccine relief system. This program highlighted real-life experiences of individuals who have suffered severe side effects, prompting an overwhelming public response with over 2000 messages received.
In a surprising turn of events, NHK’s popular Morning Show, Asaichi, has taken a bold step. Once dismissive of doubts about vaccine safety, the show recently focused on the challenges and realities faced by those affected by mRNA experimental vaccine side effects. This change in stance marks a pivotal U-Turn in the ongoing national conversation about the experimental mRNA’s safety and transparency.
The program’s new focus was echoed in the unexpected surge of viewer engagement. “We have received more than 2000 messages from viewers today. Thank you very much,” the host announced, signaling widespread public interest and concern.
One chilling account came from a viewer who detailed their struggle after the third vaccine dose: “My headaches became severe. Although they have lessened since the beginning, the symptoms have persisted for more than two years. It has been two and a half years of vaccine aftereffects.” Frustration with the bureaucratic hurdles in seeking relief was evident: “It’s difficult to go collect documents because of my leg pain, so I urgently wish the process to be simplified as soon as possible.”
Another viewer recounted a deeply personal tragedy: “Right after vaccination, my mother developed a serious illness and passed away.” Their story was not just about personal loss, but also about the social repercussions of questioning vaccine side effects. “During the period when I was collecting application documents after my mother’s illness and passing, I’ve been met repeatedly with heartless comments just for questioning the connection with the vaccine.”
The show also featured Misu from Ibaraki Prefecture, a former healthcare worker in her 40s, who shared her ongoing battle. Since receiving her third dose, she has struggled with “pain and numbness in the vaccinated arm, fatigue, and other symptoms.” Misu’s plea was simple yet profound: “I hope the government and media report this properly. Voices are being raised to spread awareness about the suffering caused by side effects.”
This feature on NHK’s Asaichi has not only brought attention to individual struggles but has also highlighted a broader societal issue: the difficulty in openly discussing vaccine side effects without backlash. It presents a call to action for society to foster an environment where sharing such experiences does not invite judgment but rather understanding and empathy.
🚨🚨🚨
Japanese citizens were left stunned when NHK, Japan's largest national broadcaster, on 28th Aug aired an hour long comprehensive report on the harms of the COVID-19 mRNA vaccine.
The program received messages from over 2,000 viewers, revealing that the extent of the… pic.twitter.com/9vlH6LrYhm
Two days following the national broadcast, Japan’s Health Minister, Keizō Takemi, made an unexpected statement: “Regarding whether health damage from the COVID-19 vaccine constitutes drug-induced injury, our response at this point is that we would like to refrain from commenting.”
It looks like they are no longer saying that it is 100% safe and effective!
MOSCOW – The number of civilians wounded in the Ukrainian shelling of the Russian city of Belgorod and the Belgorod Region has risen to 46, Governor Vyacheslav Gladkov said.
On Friday evening, the governor said air defenses worked over Belgorod and the surrounding region, several air targets were shot down near the city. Later, he reported that the shelling had been carried out from the Vampire multiple launch rocket systems (MLRS), five people were killed, 37 were wounded.
“We have again lost civilians as a result of shelling of the city of Belgorod by the Armed Forces of Ukraine. Five civilians were killed… 46 civilians were wounded. There are currently 37 people in hospitals, seven of them are children. One child is in serious condition,” Gladkov said in a video published on Telegram.
Video appearing to be from the attack posted on social media show civilian vehicles being hit and no military targets in the area.
Nothing to see here, just the Ukrainians rocketing a random intersection in Belgorod to kill and terrorize civilians.
If the Russians did this we'd have a week of international condemnation, sob-story news articles and deranged posts on this website.
MOSCOW – The Russian Foreign Ministry called on international organizations on Saturday to condemn the recent shelling of the city of Belgorod and its suburbs by Ukraine, which killed five civilians and injured 46 others.
“We once again urge all responsible governments and relevant international institutions to resolutely condemn this brutal act of terrorism and publicly distance themselves from the Kiev regime and its Western patrons, who commit such crimes,” the statement read.
“Silence in response to the unbridled barbarism of the Ukrainian nationalists and their puppeteers from ‘civilized democracies’ would be tantamount to complicity in their bloody deeds,” the ministry warned.
The Friday shelling was planned in advance and constitutes an act of intimidation of the civilian population, the ministry said. Ukrainian troops fired cluster munitions using Czech-made Vampire multiple launch rocket systems, in what it said was another attempt by the regime in Kiev to “kill as many Russians as possible.”
Novavax is offering parents up to $3,000 to enroll their children in the vaccine maker’s Phase 2/3 COVID-19 vaccine trial for infants and children ages 6 months to 11 years. The offer also includes a stuffed animal for each child.
The “Hummingbird” trial is testing two primary shots and a booster shot of Novavax’s adjuvanted recombinant spike protein nanoparticle vaccine in children. The study, which began in 2022, is enrolling 3,600 children.
The study, which began in the U.S., is expected to run through 2025 and will be conducted in the U.S. and other countries.
The children will receive three injections and visit the clinic eight times. Parents will participate in three phone calls and keep an e-diary of the vaccine’s effects on their child. Some children will receive two additional injections, for a total of five shots.
The study website promises, “You will be compensated for your time and travel regardless of your immigration status. Transportation to the study site may also be provided, as available. No health insurance is required to participate.”
Recruitment materials from Be Well Clinical Studies, which is running one of the U.S. trials, state that compensation can be more than $3,000 over two years.
A 2023 video explaining the study also promises incentives for the children, including “a Covid stuffed animal.”
In the video, a pastor from Louisiana who has four children enrolled in the study said incentives like the stuffed animal made the kids even “more excited than the parents” to participate.
The video features Dr. Jibran Atwi who is running a Hummingbird trial in Lafayette, Louisiana. He encouraged people to participate in the study, because COVID-19 severely affected kids, particularly through lockdowns and lost schooling.
Atwi also said that COVID-19 can be “very disruptive” because if a child has to stay home from school, parents may not be able to go work and the child may have to be isolated from their grandparents.
“Prevention,” he said, “is the best medicine.” He added that there had been an “impressive response” from parents who wanted to participate.
Most of that funding came from Genzyme — a Sanofi subsidiary — and from Sanofi, which shares the co-exclusive licensing agreement with Novavax to commercialize its COVID-19 vaccine.
In 2022, Atwi received over $1 million, largely from AstraZeneca and Genzyme.
Last week, the U.S. Food and Drug Administration (FDA) granted emergency use authorization to Pfizer and Moderna’s 2024-2025 mRNA COVID-19 shots, but Novavax’s 2024-2025 formula has not yet been authorized.
The FDA has authorized previous versions of the Novavax vaccine, but only for children ages 12 and up.
High payments place children ‘at risk of coercion’
Other pharmaceutical companies that have paid research subjects large sums of money have come under scrutiny. In the United Kingdom (U.K.), Moderna was criticized for initially offering children’s families 1,505 pounds ($1,984 dollars) to participate in its NextCOVE clinical trial, which is testing Moderna’s mRNA vaccine in children ages 12 and up.
The Children’s Covid Vaccine Advisory Council submitted a complaint to the U.K.’s Prescription Medicines Code of Practice Authority (PMCPA) — an industry trade group that regulates ethical practices — raising concerns about “inappropriate financial inducement” offered to children and their parents to participate in the trial.
The council cited concerns raised by the research ethics committee (REC) that approved the clinical study. Regarding the 1,500-pound payment they wrote:
“This amount seems much higher than what would be considered a reasonable reimbursement and therefore would contravene clinical trial regulations. The Medicines for Human Use (Clinical Trials) Regulations (2004) explicitly prohibit the giving of incentives or financial inducements to children… or their parents.”
The REC said the amount, “placed the children at risk of coercion,” and the organization required that Moderna reduce the offer before recruitment could begin. Moderna reduced the amount to 185 pounds ($244 dollars).
Yet, according to the complaint, at least one pediatrician continued to offer the high enrollment compensation.
The PMCPA sanctioned Moderna, and the case report on the issue is currently pending.
If the PMCPA determines a pharmaceutical company has breached the industry code, it can require the company to pay administrative charges or issue a corrective statement. Or, it may request a compulsory audit of the company.
In the U.S., Be Well is also advertising that it will pay parents $2,400 for enrolling their infants and toddlers, ages 5-23 months, in Moderna’s Rhyme Trial for an mRNA RSV and a human metapneumovirus (hMPV) vaccine.
According to the clinicaltrials.gov website, Be Well withdrew from the Moderna RSV study, but the website is still advertising to recruit participants.
Be Well is run by founder and director Dr. Mark Carlson, a geriatrician, who has taken nearly $3 million in research funding from Big Pharma, mostly from Moderna, since 2021.
Moderna did not respond to The Defender’s inquiry about compensation offered to children’s families to participate in these studies.
The attorney from the Department of Justice who defended the Food & Drug Administration in court admitted on undercover camera that the agency’s actions were an abuse of authority by the government during its public campaign against ivermectin to treat COVID-19.
A trio of doctors recently won a major legal victory in a multi-year lawsuit sparked by the FDA’s viral 2021 public health guidance advising against the use of ivermectin for treating COVID-19. The most notable offending tweet stated, “You are not a horse. You are a not a cow. Seriously, y’all. Stop it.”
Department of Justice trial lawyer, Isaac Belfer, defended the FDA in this suit brought by Drs. Mary Talley Bowden, Robert L. Apter, and Paul E. Marik. On undercover camera, Belfer admits to a Project Veritas journalist that his client’s legal loss was deserved because the agency overstepped its statutory authority when it publicly tweeted medical advice.
Belfer told our journalist, “So, what the agency has done… [is] unquestionably beyond its authority. Making a recommendation of what drugs to take or not to take, that’s the practice of medicine. And FDA can’t practice medicine.”
The FDA’s public relations campaign also failed to inform the public that the award-winning antiparasitic medicine had a decades-long track record of successful medical usage in humans.
During the COVID-19 pandemic, the doctors prescribed ivermectin to tens of thousands of patients and found the drug to be a cheap and effective treatment.
The doctors told Project Veritas that they suspect that the suppression campaign against ivermectin was motivated by the government’s interest in fast-tracking the experimental COVID-19 vaccination. This speedy vaccine roll-out could only be accomplished through the FDA’s emergency use authorization [EUA], and only if no other alternative medications existed to treat COVID-19.
The FDA’s tweets caused a deadly chain reaction. The agency’s pronouncements were swiftly enforced by national medical associations and regulatory agencies, pharmacists refused to fill prescriptions, insurance refused to pay for it, and doctors who prescribed it faced career ruin.
Drs Apter and Bowden told Project Veritas that suppression of ivermectin led to a prolonged pandemic, and potentially millions in excess COVID deaths.
Apter: “It’s not unreasonable to think that there have been a million unnecessary deaths from COVID in the United States because of the public health agency suppression of effective early treatment with repurposed inexpensive medications.”
Bowden: “If more people had access to early treatment in the form of ivermectin, monoclonal antibodies, hydroxychloroquine… we could have nipped the pandemic in the bud.”
As a result of the lawsuit, the FDA was forced to delete its social media posts warning against the use of ivermectin for treating COVID-19. Though the FDA removed its public statements, the agency did not change its policy or directives. Because major state and national medical governing authorities look to the FDA as an authoritative source on the appropriate use of drugs, pharmacies still refuse to prescribe ivermectin, and doctors face professional repercussions for prescribing it.
Dr. Talley Bowden was forced to resign her privileges from Houston Methodist Hospital; Apter was referred to the Washington Medical Commission and Arizona Medical Board for disciplinary proceedings; and Marik was forced to resign from his positions at Eastern Virginia Medical School.
Apter: “Because of my prescription of ivermectin for COVID I am still facing persecution by the medical licensing boards in spite of the fact that they have not been able to show a single adverse event in my care.”
Bowden: “I have a medical board coming after me because I tried to help a patient get ivermectin. We all had professional repercussions because of our use of ivermectin.”
Though the doctors continue to face professional consequences for their advocacy of ivermectin use for COVID-19, Belfer admits that the doctors dealt a significant blow to the government with their court victory. He told Project Veritas that the agency will think twice before issuing any misguided health advice in the future.
“I think going forward they’ll [FDA] probably be a bit more careful. They [the doctors] got an opinion that was good for them. That kind of limited FDA’s authority. It’s not okay to… actually tell people, ‘You should not take this drug.’”
Dr. Bowden says the fight against government overreach was worth it, because now doctors are vindicated in their years-long quest to protect the health of their patients.
Bowden: “One thing this case did is set a precedent. I think it permanently tarnished the reputation of the FDA. I think the public will takes the FDA little less seriously now, and it keeps them from making the same bold, reckless move in the future when it comes to telling patients what they can and cannot do. Like Isaac [Belfer] said, and we have all said, the FDA is not your doctor. The FDA has no business telling patients what they can take. And we proved in the court of law that they cannot do that.”
Most Europeans know the United States provoked the conflict in Ukraine, profits from banning Russian oil and gas, and remain uneasy about the mysterious destruction of the Nordstream pipelines. The American government promoted a mindless NATO expansion strategy that caused a disastrous war and weakened NATO nations, who were pressured to donate billions of dollars and much of their military equipment to Ukraine, even though it isn’t a member of the NATO alliance.
Eastern European states were excited to join NATO and the European Union economic block, called the EU, but were soon pressured to boost military spending to buy American weaponry, accept foreign migrants, host foreign troops, and donate money and arms to a lost cause in Ukraine. Profitable trade and tourism with Russia sharply declined while energy costs soared, causing economic decline.
The people of some European nations have already decided that joining NATO and the EU was a bad idea. Hungarian Prime Minister Viktor Orban openly states his dislike of EU mandates to allow mass immigration and continued trade sanctions on Russia. EU leaders denounce Orban and threaten sanctions because they can abuse Hungary since it is landlocked and surrounded by Ukraine and EU members.
But if Russian troops reach Ukraine’s western border, Hungary may defect. Conquered Ukraine would become a close Russian ally and allow access to energy pipelines to import cheap Russian oil and gas, and permit rail and road access to Russia and all of Asia. There are several neighboring nations who may also defect from the American empire. This explains why NATO is considering sending forces to secure western Ukraine to keep its vassal states captive.
“Kyiv Will Face Retaliation”; EU nation Slovakia has issued an open threat to Ukraine amid war with Russia. Slovakia said it would take retaliatory measures against Ukraine if Kyiv continues to stop Russian oil transiting via the Druzhba pipeline.; “Times of India”; July 25, 2024; • ‘Kyiv Will Face Retaliation…’: NATO…
“MEPs call to strip Hungary’s EU voting rights amid Orbán’s ‘peace missions’”; Steb Starcevic; Politico; July 16, 2024; https://www.politico.eu/article/lette…
Richard Thomas Medhurst (1992) is an independent journalist, political commentator, and analyst from the United Kingdom with a focus on international affairs, US politics, and the Middle East.
Medhurst is known for his coverage of the Julian Assange extradition case in London, as one of the only journalists to report on the trial of the WikiLeaks founder from inside the court.
He has also covered the Iran nuclear deal talks on the ground in Vienna. Medhurst was born in Damascus, Syria.
His father is English and mother is Syrian. Both his parents served in United Nations Peacekeeping and Observer missions and were among the UN Peacekeepers awarded the Nobel Peace Prize in 1988. Owing to his parents’ professional mobility, he has lived in Syria, Pakistan, Switzerland, and Austria.
He speaks four languages fluently: English, Arabic, French, and German. As an independent journalist, Medhurst regularly hosts live broadcasts and video reports on his YouTube channel.
Previous guests include the Foreign Minister of Venezuela, the Dep Foreign Minister of Iran; the Palestinian, Russian and Cuban ambassadors to the United Nations in Vienna; the former British Ambassador to Syria; and various UN officials, journalists, and more.
Medhurst’s reports and analysis on Yemen, Ukraine, Syria, Niger, Lebanon, Iran, the Israeli occupation in Palestine and its genocide in Gaza have gone viral countless times, racking up millions of views.
Richard Medhurst has a combined following of roughly one million people online, and appears regularly on international news outlets including Al Jazeera, WikiLeaks, Black Agenda Report, Al Mayadeen, The Times, LBC, and others.
Award-winning South African political cartoonist and talk show host Jeremy “Jerm” Nell interviews world-class academic Denis Rancourt (h-index 41 & i10 index of 91) on his latest paper showing an estimated 31 million dead from the Covid “vaccines” and the government’s Covid policies. We have a summary of the interview and full transcript at https://artofliberty.substack.com/p/dr-denis-rancourt-31-million-dead
… What is known about 9/11 is that there are many incredible facts that continue to be ignored by the government and the mainstream media. Here are fourteen.
An outline of what was to become the 9/11 Commission Report was produced before the investigation began. The outline was kept secret from the Commission’s staff and appears to have determined the outcome of the investigation.
The 9/11 Commission claimed sixty-three (63) times in its Report that it could find “no evidence” related to important aspects of the crimes.
One person, Shayna Steiger, issued 12 visas to the alleged hijackers in Saudi Arabia. Steiger issued some of the visas without interviewing the applicants and fought with another employee at the embassy who tried to prevent her lax approach.
This site is provided as a research and reference tool. Although we make every reasonable effort to ensure that the information and data provided at this site are useful, accurate, and current, we cannot guarantee that the information and data provided here will be error-free. By using this site, you assume all responsibility for and risk arising from your use of and reliance upon the contents of this site.
This site and the information available through it do not, and are not intended to constitute legal advice. Should you require legal advice, you should consult your own attorney.
Nothing within this site or linked to by this site constitutes investment advice or medical advice.
Materials accessible from or added to this site by third parties, such as comments posted, are strictly the responsibility of the third party who added such materials or made them accessible and we neither endorse nor undertake to control, monitor, edit or assume responsibility for any such third-party material.
The posting of stories, commentaries, reports, documents and links (embedded or otherwise) on this site does not in any way, shape or form, implied or otherwise, necessarily express or suggest endorsement or support of any of such posted material or parts therein.
The word “alleged” is deemed to occur before the word “fraud.” Since the rule of law still applies. To peasants, at least.
Fair Use
This site contains copyrighted material the use of which has not always been specifically authorized by the copyright owner. We are making such material available in our efforts to advance understanding of environmental, political, human rights, economic, democracy, scientific, and social justice issues, etc. We believe this constitutes a ‘fair use’ of any such copyrighted material as provided for in section 107 of the US Copyright Law. In accordance with Title 17 U.S.C. Section 107, the material on this site is distributed without profit to those who have expressed a prior interest in receiving the included information for research and educational purposes. For more info go to: http://www.law.cornell.edu/uscode/17/107.shtml. If you wish to use copyrighted material from this site for purposes of your own that go beyond ‘fair use’, you must obtain permission from the copyright owner.
DMCA Contact
This is information for anyone that wishes to challenge our “fair use” of copyrighted material.
If you are a legal copyright holder or a designated agent for such and you believe that content residing on or accessible through our website infringes a copyright and falls outside the boundaries of “Fair Use”, please send a notice of infringement by contacting atheonews@gmail.com.
We will respond and take necessary action immediately.
If notice is given of an alleged copyright violation we will act expeditiously to remove or disable access to the material(s) in question.
All 3rd party material posted on this website is copyright the respective owners / authors. Aletho News makes no claim of copyright on such material.
Aletho News 