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Buddhist Times News – China’s dams in Tibet may pose threat to India’s water supply

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Buddhist Times News – China’s dams in Tibet may pose threat to India’s water supply

Col Vinayak Bhat for India Today. Read the original article here.

[REPRESENTATIVE IMAGE] File photo of Three Gorges Dam in China’s Hubei, world’s biggest hydropower project (Photo Credits: AP)
Over a period of 10 years, China has managed to construct three dams on the Brahmaputra river in parts of Tibet close to the Indian border. It plans to construct at least eight more such dams.

China’s rapid pace of dam constructions that includes at least eight new ones on the Brahmaputra River in Tibet has sparked concerns about the Chinese attempting to tame India’s water supply. The proposed dams on the Yarlung Tsangpo river in Tibet are close to the Indian border in Arunachal Pradesh.

In this region, the Chinese have managed to construct three dams within a distance of 24 km on the Brahmaputra River over a period of 10 years. This construction of dams at an unprecedented pace and scale has taken place in Tibet’s Sangri Lokha. Construction of a similar ‘triplet dam’ has been observed on the Nyang river near the town of Nyingchi in Tibet’s Nyingchi county.

Lokha, also known as Shanan lies in the northeast of Bhutan and south of Lhasa while Nyingchi is further east, both bordering Arunachal Pradesh.

Satellite image of Sangri Lokha (Photo Credits: India Today)

In order to find out the aim of these massive construction projects, India Today OSINT team investigated them using Google Earth images.

The ability to control India’s water supply in the hands of the Chinese has always been a legitimate concern. China can use this to cause flash flooding or to divert water that could dry up rivers across India.

Zangmo Dam

A comparative analysis of satellite images of the Zangmo dam shows how its width has increased fourfold from 100 m in 2012 when the construction began to 400 m as seen on August 4, 2020, while the water levels have risen almost 150 m.

Thus, the reservoir which spans across almost 10 km can hold more than 600 mn cubic meters of water, an indication that a massive amount of water is under Chinese control in Tibet.

Satellite image of Zangmo dam on Brahmaputra in Sangri Lokha (Photo Credits: India Today)

However, government sources say these dam constructions are being monitored closely. “It is something that has always been discussed between the two governments closely,” a government official tracking developments in this regard asserted. While claiming that the threat of China using these dams to cause flash flooding or block water to Indian territory is not visible, sources said, “For flash flooding, water has to be accumulated but there has not been anything abnormal that has been noticed.”

Amid the India-China military standoff in eastern Ladakh, Chinese activities including dam constructions along the Indian border are under the scanner once again.

New dams proposed on the Brahmaputra

China has proposed to build at least eight more dams on the Brahmaputra River in Tibet. These dams are to be built within the next 10 years at Bayu, Jiexi, Langta, Dakpa, Nang, Demo, Namcha and Metok towns that do not have more than a hundred households each. This has sparked speculation that the aim of these dams is only to build reservoirs and export electric energy from Tibet to mainland China.

Satellite image of new dams proposed by China in Tibet (Photo Credits: India Today)

Need for shared data on dam construction, water flow

Satellite images very clearly indicate that China is not building a large number of dams on the Brahmaputra River for the benefit of the people of Tibet. The area is scantly populated and electricity demands in the region could be met with a single hydroelectricity project like the Zangmo dam.

The Chinese could also aim to use these dam reservoirs such as the Dagu dam to divert Brahmaputra’s water to dry areas in Xinjiang or Central China. Evidence for such diversions is yet to come to light. However, reports have cited locals talking about it in recent years.

The third and perhaps the most worrying explanation for China storing water at eleven dams on the Brahmaputra River could be to control the water flowing into India.

Experts feel China’s dam construction is a key concern and the Chinese dispensation must be more transparent over the issue. Director of the Kubernein Initiative, Ambika Vishwanath tracks water diplomacy and security across the globe. She feels it is not just the quantity but also the quality of water that should be a matter of concern in the long run.

“There needs to be a closer study on not just the quantity of water flow but also the quality which can be extremely detrimental in the long run. It can have an impact on people’s lives in downstream regions. There are very little information and an understanding of the region. The entire Himalayas is a black hole of data,” Ambika says. She further added, “Scientists, researchers need more access to the areas and require more data to understand short and long term impact to aid in better policymaking.”

Ambika also says that one way of ensuring more transparency is joint initiatives, such as data sharing or construction of dams within joint management of river basins, but that does not seem likely anytime soon. “If there are joint constructions, responsibilities are also shared to safeguard installations on either side,” she points out.

Satellite image of Chinese dams on the Brahmaputra (Photo Credits: India Today)

Use of water supply as a weapon against India?

Blocking India’s water supply even for a few days can lead to rivers drying up across the country.

On the other hand, many feel low lying areas in India will be completely inundated if China suddenly releases all this stored up water, as seen in the case of the Three Gorges dam in Hubei province. A purposeful release of water from all the dams on the Brahmaputra can wreak havoc in India, many feel.

As per Indo-Sino bilateral agreements, China is expected to share data with India during the monsoon in order for the latter to keep track of water levels and prepare for floods.

After Pasighat in Arunachal Pradesh, the Brahmaputra River expands to almost 10 km in width. Its width varies from 8 to 10 km in Assam. Bridges in these states are surprisingly smaller than the width of the river. During monsoon every year, the bridges get flooded with their abutments almost always underwater.

Careful monitoring of these dams will provide a 15-day early warning since this is the time it takes for river water to travel from Tibet’s Lokha county to Pasighat in Arunachal Pradesh.

Zangmo, Gyatsa, and Dagu

There are three dams on the main Brahmaputra River built in unusually close proximity to each other. These dams are located within a very short distance of 24 km. With only the single village of Gyatsa and its population of barely 150 households, having three dams is unprecedented.

While the Zangmo dam has been commissioned, the Gyatsa dam is complete and awaiting commissioning. The third and largest of the trio, the Dagu dam has been under construction since 2017.

Satellite image of Dagu dam on Brahmaputra (Photo Credits: India Today)

Dagu surprisingly has two inlets and two outlets for water to pass through the mountain despite it being a run of the river hydroelectricity dam. Such dams have electricity generators underground, in an area below the dam, and do not require additional tunnels for water flow.

This has led to doubts supported by rumors that Brahmaputra’s water may be diverted to the dry Xinjiang deserts through underground tunnels using the Dagu dam. Once all three are complete, the triplet dams will be able to collect almost a billion cubic meters of water in their reservoirs.

Pagsum, Langsai and Nyang

The three dams in Nyingchi county are being constructed on a tributary called Nyang that feeds Brahmaputra River. The dams at Pagsum, Langsai, and Nyang are much smaller in size but hold enough water to add to the Brahmaputra River flow.

Land barrier dam

Around October and November of 2018, rumor had it that China had clamped down on the Brahmaputra river and water flow had almost come to a halt. Reports of water being unusually muddy at the time had also come to light.
Satellite images revealed much later that a large landslide from the southeastern face of Sodong Ri Mountain had blocked the Brahmaputra almost completely.

International obligations dictate that China must seek permission from downstream countries before constructing any dam upstream on the Brahmaputra river. Despite its bilateral agreements with India, China still does not share any data in this regard.

Although New Delhi is paying a hefty sum of Rs 80 lakhs to Beijing for this data each year, the response India gets from the Chinese every time is the same- water in the Brahmaputra river washed the measuring instruments away.

“The people in Lebanon can count on the European Union” – Charles Michel

Aerial View of City Buildings
Photo by Nate Hovee

“The people in Lebanon can count on the European Union” – press release following President Charles Michel’s visit to Beirut

Charles Michel, President of the European Council, travelled to Beirut on 8 August 2020 to convey EU solidarity with the people in Lebanon after the devastating explosions on 4 August.

The President visited the Port of Beirut to witness the scale of the disaster. He called for an independent enquiry to shed light on the causes of this catastrophe and offered European expertise. During his visit, President Michel met with representatives of the Lebanese Red Cross and paid his respect to the rescue teams, including Europeans, working around the clock and showing tremendous courage.

I’m touched by the bravery of the Lebanese people who have been hit by this tragedy in an already difficult context. The EU is a long-standing friend and partner. We are in full solidarity with Lebanon more than ever in these difficult times.
Charles Michel

President Michel repeated the EU readiness to continue the provision of urgent assistance to help the people in Lebanon. The EU has already activated its emergency mechanisms. It has mobilised EUR 33 million for emergency needs and more than 250 rescuers from European Member States are on the ground. Tons of emergency supplies have been made available and more will follow. Together with the President of the European Commission, President Michel urged all EU Member States to intensify their support to Lebanon both for the immediate needs and for the longer-term reconstruction. It is key that assistance reaches those who need it.

During his visit, the President of the European Council met with President Michel Aoun, Speaker of the Parliament Nabih Berri and President of the Council of Ministers Hassan Diab. The unity and stability of Lebanon are all the more crucial today, both internally, and also for the whole region. President Michel also underlined the importance of structural reforms in line with the government’s reform plan and Lebanon’s international commitments and as called by the Lebanese people. An agreement with the International Monetary Fund is urgently needed. He therefore called for concrete steps to reform the financial system and to adopt anti-corruption measures.

Local political forces should seize the opportunity and unite around a national effort to respond to the immediate needs but also more long term challenges the country is facing. It’s of critical importance for Lebanon to implement the fundamental structural reforms. The Lebanese can count on the European Union in this effort – but internal unity is key.
Charles Michel

Lifting of travel restrictions: Council reviews the list of third countries

Lifting of travel restrictions: Council reviews the list of third countries

Following a review under the recommendation on the gradual lifting of the temporary restrictions on non-essential travel into the EU, the Council updated the list of countries for which travel restrictions should be lifted. As stipulated in the Council recommendation, this list will continue to be reviewed regularly and, as the case may be, updated.

Based on the criteria and conditions set out in the recommendation, as from 8 August member states should gradually lift the travel restrictions at the external borders for residents of the following third countries:

  • Australia
  • Canada
  • Georgia
  • Japan
  • New Zealand
  • Rwanda
  • South Korea
  • Thailand
  • Tunisia
  • Uruguay
  • China, subject to confirmation of reciprocity

Residents of Andorra, Monaco, San Marino and the Vatican should be considered as EU residents for the purpose of this recommendation.

The criteria to determine the third countries for which the current travel restriction should be lifted cover in particular the epidemiological situation and containment measures, including physical distancing, as well as economic and social considerations. They are applied cumulatively.

Regarding the epidemiological situation, third countries listed should meet the following criteria, in particular:

  • number of new COVID-19 cases over the last 14 days and per 100 000 inhabitants close to or below the EU average (as it stood on 15 June 2020)
  • stable or decreasing trend of new cases over this period in comparison to the previous 14 days
  • overall response to COVID-19 taking into account available information, including on aspects such as testing, surveillance, contact tracing, containment, treatment and reporting, as well as the reliability of the information and, if needed, the total average score for International Health Regulations (IHR). Information provided by EU delegations on these aspects should also be taken into account.

Reciprocity should also be taken into account regularly and on a case-by-case basis.

For countries where travel restrictions continue to apply, the following categories of people should be exempted from the restrictions:

  • EU citizens and their family members
  • long-term EU residents and their family members
  • travellers with an essential function or need, as listed in the Recommendation.

Schengen associated countries (Iceland, Lichtenstein, Norway, Switzerland) also take part in this recommendation.

Table of Contents

Next steps

The Council recommendation is not a legally binding instrument. The authorities of the member states remain responsible for implementing the content of the recommendation. They may, in full transparency, lift only progressively travel restrictions towards countries listed.

A Member State should not decide to lift the travel restrictions for non-listed third countries before this has been decided in a coordinated manner.

This list of third countries should continue to be reviewed regularly and may be further updated by the Council, as the case may be, after close consultations with the Commission and the relevant EU agencies and services following an overall assessment based on the criteria above.

Travel restrictions may be totally or partially lifted or reintroduced for a specific third country already listed according to changes in some of the conditions and, as a consequence, in the assessment of the epidemiological situation. If the situation in a listed third country worsens quickly, rapid decision-making should be applied.

Background

On 16 March 2020, the Commission adopted a communication recommending a temporary restriction of all non-essential travel from third countries into the EU for one month. EU heads of state or government agreed to implement this restriction on 17 March. The travel restriction was extended for a further month respectively on 8 April 2020 and 8 May 2020.

On 11 June the Commission adopted a communication recommending the further extension of the restriction until 30 June 2020 and setting out an approach for a gradual lifting of the restriction on non-essential travel into the EU as of 1 July 2020.

On 30 June the Council adopted a recommendation on the gradual lifting of the temporary restrictions on non-essential travel into the EU, including an initial list of countries for which member states should start lifting the travel restrictions at the external borders. This list was updated on 16 July and 30 July.

Spanish human rights attorney writes to Von der Leyen on planned violations of fundamental health rights

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Luis de Miguel Ortega, SCABELUM
Luis de Miguel Ortega, SCABELUM

A Spanish consumers association Atty Luis de Miguel Ortega, with a coalition of other associations, has written the President of the European Commission requesting urgent response and adjustment to the law in different health issues related to the current situation of pandemic, saying that:

This institutional behavior, together with the evident collusion with philanthropic-looking pharmaceutical research, production and distribution entities, not only affects the freedom of the market but also the essential rights of citizens and consumers who are left out of the slightest decision.

At the end of the letter (which can be found below the article) request Von der Leyen the following.

1) Have associations by persons in the procedure of the Proposal for a REGULATION OF THE EUROPEAN PARLIAMENT AND OF THE COUNCIL relative to the performance of clinical trials and the supply of medicines for human use that contain genetically modified organisms or are composed of these organisms, intended to treat or prevent coronavirus disease.

2) These associations are considered an interested party and their legitimacy and direct interest are recognized.

3) The file or, where appropriate, all the information related to said modification that is legitimately accessible to interested persons is transferred to us.

4) It is considered announced that if this claim is not answered within the deadline, a claim will be filed with the Court of Justice of the EU, as established in the provisions that regulate access to said jurisdiction. However, the European Commission requires acknowledgment of receipt stating the corresponding deadlines and resources.

HERE YOU MAY FAIND THE FULL LETTER

To: European Commission – President Mrs. Ursula Von der Leyen – Vice President Ms. Věra Jourová Values ​​and Transparency – Commissioner Mrs. Stella Kyriakides Health and Food Safety European Commission / Secretary General B – 1049 Brussels / BELGIUM

Mr. Luis de Miguel Ortega, as Attorney and in the name and representation of the associations indicated above [Association SCABELUM of Consumers], appears in a timely manner and respectfully SAYS:

FIRST:

That the associations mentioned in this writing, watch over the interests of consumers, especially their health rights and are concerned about the consequences that any reduction in guarantees for human health and the environment may have for the citizens they represent.

Proposing the release and use of genetically modified organisms without guaranteeing the safety of the environment and citizens, seems a crazy idea when not directly terrifying in a context of biological risk that may not only not obtain the adequate response, but may also further aggravate the situation.

The precautionary principle is established to avoid unnecessary risks and has been a doctrinal constant over the years, and in this sense it should be remembered that the seriousness of a situation, by itself, cannot be a reason for a reduction in guarantees and caution as proposed by the Commission.

It is also proposed in a confusing way, without explaining the true object of such modification, which is none other than experimentation with vaccines resulting from genetic engineering, as an experiment for use in the population, without guaranteeing safety -without causing harm-, efficacy – achieving a concrete and measurable objective- and efficiency -at a reasonable cost-.

Throughout the health crisis, there has been a lack of data transparency and an obsession to conduct experiments on human beings, avoid possible responses and treatments, and insist on a vaccine for which there is no prior experience or guarantee.

Real and effective treatments such as artemisia, hydroxychloroquine, chlorine dioxide or vitamin C in high doses, have been banned, reviled, censored and even persecuted, pretending that the objective of the institutions and states was not life, the health and safety of its citizens, but a strange business that we fail to understand.

This institutional behavior, together with the evident collusion with philanthropic-looking pharmaceutical research, production and distribution entities, not only affects the freedom of the market but also the essential rights of citizens and consumers who are left out of the slightest decision.

SECOND:

That this part has studied in detail the Proposal for a REGULATION OF THE EUROPEAN PARLIAMENT AND OF THE COUNCIL relating to the performance of clinical trials and the supply of medicinal products for human use that contain genetically modified organisms or are composed of these organisms, intended to treat or prevent coronavirus disease (Text with EEA relevance).

That said modification affects the following Directives that we have studied:

Directive 2009/41 / CE, relative to the contained use of genetically modified microorganisms.

Directive 2001/18 / CE, on the deliberate release into the environment of genetically modified organisms.

Directive 2001/20 / CE, on clinical trials (Directive 2001/18 / CE and Directive 2009/41 / CE).

Directive 2001/83 / EC (Article 83 of Regulation (EC) No. 726/2004).

REGULATION (EU) No 536/2014 OF THE EUROPEAN PARLIAMENT AND OF THE COUNCIL of April 16, 2014 on clinical trials of medicinal products for human use, and by which Directive 2001/20 / EC is repealed (Text relevant to the purposes of the EEA )

THIRD:

What we have studied in detail:

“ Coordinated EU action to fight the COVID-19 pandemic and its consequences. European Parliament resolution of 17 April 2020 on coordinated action by the Union to combat the COVID – 19 pandemic and its consequences (2020/2616 (RSP)). “

” COMMUNICATION FROM THE COMMISSION TO THE EUROPEAN PARLIAMENT, TO THE EUROPEAN COUNCIL, THE COUNCIL, THE ECONOMIC AND SOCIAL COMMITTEE AND TO THE COMMITTEE OF THE REGIONS The time for Europe to repair the damage and prepare the future for the next generation {SWD (2020) 98 final}”

” European Parliament resolution on the European Union’s public health strategy after COVID-19 (2020/2691 (RSP))”

FIFTH:

Having regard to the TFEU, the Commission’s Internal Regulations [C (2000) 3614], the CODE OF GOOD ADMINISTRATIVE CONDUCT FOR THE STAFF OF THE EUROPEAN COMMISSION IN THEIR RELATIONS WITH THE PUBLIC, the Statute of the Court of Justice of the European Union ( 1-5-2019) and the Rules of Procedure of the Court of Justice (1-1-2020), we understand that there are reasons to appear before that commission.

SIXTH:

That the Proposal for a REGULATION OF THE EUROPEAN PARLIAMENT AND OF THE COUNCIL regarding the performance of clinical trials and the supply of medicinal products for human use that contain genetically modified organisms or are composed of these organisms, intended to treat or prevent coronavirus disease, affects:

1) DIRECTIVE 2011/83 / EU OF THE EUROPEAN PARLIAMENT AND OF THE COUNCIL of October 25, 2011 on consumer rights, amending Council Directive 93/13 / EEC and Directive 1999/44 / EC of the European Parliament and of the Council and Directive 85/577 / EEC of the Council and Directive 97/7 / EC of the European Parliament and of the Council (Text with EEA relevance) are repealed.

2) DIRECTIVE 2004/35 / CE OF THE EUROPEAN PARLIAMENT AND OF THE COUNCIL of April 21, 2004 on environmental liability in relation to the prevention and repair of environmental damage.

3) The TFEU, in its articles:

Article 11 (ex Article 6 TEC) The requirements of environmental protection must be integrated into the definition and implementation of Union policies and actions, in particular with a view to promoting sustainable development.

Article 12 (ex Article 153 (2) TEC) When defining and implementing other Union policies and actions, consumer protection requirements shall be taken into account.

Article 15 (ex Article 255 TEC) 1. In order to promote good governance and to guarantee the participation of civil society, the institutions, bodies and agencies of the Union shall act with the greatest possible respect for the principle of openness.

3. Every citizen of the Union, as well as every natural or legal person who resides or has its registered office in a Member State, shall have the right to access the documents of the institutions, bodies and agencies of the Union, whatever their support. , in accordance with the principles and conditions to be established in accordance with this section.

Article 101 (former Article 81 TEC) 1. All agreements between companies, decisions of associations of companies and concerted practices that may affect trade between Member States and that have as their object or purpose shall be prohibited. The effect of preventing, restricting or distorting the game of competition within the internal market.

Article 102 (former Article 82 TEC) It shall be incompatible with the internal market and, insofar as it may affect trade between Member States, the abusive exploitation, by one or more companies, of a dominant position in the internal market or a substantial part of it.

Article 107 (former Article 87 TEC) 1. Unless the Treaties provide otherwise, the aid granted by the States or through State funds shall be incompatible with the internal market, insofar as they affect trade between Member States. in any way, that distort or threaten to distort competition, favoring certain companies or productions.

Article 191 (ex Article 174 TEC) 1. Union policy in the field of the environment shall contribute to achieving the following objectives: – the conservation, protection and improvement of the quality of the environment.

– the protection of people’s health,

– the prudent and rational use of natural resources, – the promotion of measures at international level to deal with regional or global environmental problems. and in particular to fight against climate change.

2. Union policy in the field of the environment shall aim to achieve a high level of protection, bearing in mind the diversity of situations existing in the different regions of the Union. It will be based on the principles of precaution and preventive action, on the principle of correcting attacks on the environment, preferably at the source itself, and on the principle that the polluter pays. In this context, the harmonization measures necessary to meet environmental protection requirements will include, where appropriate, a safeguard clause authorizing Member States to adopt, for non-economic environmental reasons, provisional measures subject to a Union control procedure.

3. In drawing up its policy in the area of ​​the environment, the Union shall take into account:

– the scientific and technical data available,

– environmental conditions in the various regions.

– the benefits and burdens that may result from action or lack of action,

– the economic and social development of the Union as a whole and the balanced development of its regions.

4. Within the framework of their respective competences, the Union and the Member States shall cooperate with third countries and competent international organizations. The modalities of the Union’s cooperation may be the subject of agreements between the latter and interested third parties. The preceding paragraph shall be understood without prejudice to the competence of the member states to negotiate in international institutions and to conclude international agreements.

4) It also affects the rights included in the Charter of Fundamental Rights of the EU (2000 / C 364/01)

CHAPTER I on dignity, arts 1, 2 and 3

CHAPTER III on equality, arts. 24, 25 and 26

CHAPTER IV on solidarity, arts. 35, 37 and 38

CHAPTER V on citizenship, arts. 41 and 42

SEVENTH:

The Court of Justice of the European Union shall control the legality of legislative acts, of acts of the Council, of the Commission and of the European Central Bank that are not recommendations or opinions, and of acts of the European Parliament and of the European Council intended to produce legal effects against third parties. It will also control the legality of the acts of the organs or agencies of the Union intended to produce legal effects against third parties.

Any natural or legal person may file an appeal, under the conditions set forth in the first and second paragraphs, against the acts of which it is the recipient or that affect it directly and individually and against the regulatory acts that affect it directly and that do not include measures of execution.

The appeals provided for in this article must be filed within a period of two months from, depending on the case, of the publication of the act, of its notification to the appellant or, in the absence thereof, from the day the appellant had knowledge of the same.

In the event that, in violation of the Treaties, the European Parliament, the European Council, the Council, the Commission or the European Central Bank abstain from acting, the Member States and the other institutions of the Union may appeal to the Court of Justice of the European Union in order to declare such violation. This article shall apply, under the same conditions, to the organs and agencies of the Union that refrain from making a pronouncement.

Any natural or legal person may appeal a complaint to the Court, under the conditions indicated in the preceding paragraphs, because one of the institutions, or one of the organs or agencies of the Union, has not directed an act other than a recommendation or an opinion.

Based on all the above, the signatory associations request:

1) Have associations by persons in the procedure of the Proposal for a REGULATION OF THE EUROPEAN PARLIAMENT AND OF THE COUNCIL relative to the performance of clinical trials and the supply of medicines for human use that contain genetically modified organisms or are composed of these organisms, intended to treat or prevent coronavirus disease.

2) These associations are considered an interested party and their legitimacy and direct interest are recognized.

3) The file or, where appropriate, all the information related to said modification that is legitimately accessible to interested persons is transferred to us.

4) It is considered announced that if this claim is not answered within the deadline, a claim will be filed with the Court of Justice of the EU, as established in the provisions that regulate access to said jurisdiction. However, the European Commission requires acknowledgment of receipt stating the corresponding deadlines and resources.

In Burgos on July 25, 2020

Original publication can be found at: https://www.scabelum.com/post/letter-to-president-of-european-commision

Dalai Lama reinvigorates call for world peace

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Buddhist Times News – His Holiness the Dalai Lama reinvigorates call for world peace on 75th Anniversary of the Atomic Bombings of Hiroshima and Nagasaki

His Holiness the Dalai Lama reinvigorates call for world peace on 75th Anniversary of the Atomic Bombings of Hiroshima and Nagasaki

By Bureau Reporter His Holiness the Dalai Lama and fellow Nobel Laureates paying their respects at Hiroshima Memorial Park in Hiroshima, Japan on November 14, 2010. Photo by Taikan Usui

In his statement on the occasion of the 75th anniversary of the atomic bombings of Hiroshima and Nagasaki, Tibetan spiritual leader and peace icon, His Holiness the Dalai Lama urged governments, organizations and individuals to “rededicate themselves to making the achievement of peace the centrepiece of our lives”.

Japan on Thursday remembered the victims of the bombings on Hiroshima and Nagasaki, the world’s first atomic bomb attack.

“Despite many great developments that also took place, the 20th century was an era of violence in which some 200 million people were killed, including the horrific use of nuclear weapons,” His Holiness said. “Now, in our increasingly interdependent world, we have a chance to make this a more peaceful century.”

Reiterating his call for global peace and demilitarisation, His Holiness said: “When conflicts arise they should be settled through dialogue, not the use of force. We need to eliminate the threat of nuclear weapons, with the ultimate aim of a demilitarized world. War means killing. Violence leads to counter violence. We need to put an end to combat and the production of weapons and construct a more peaceful world.”

“We human beings have created many of the problems in today’s world. As long as we have strong negative emotions and we view our fellow beings in terms of ‘us’ and ‘them’, there will be a tendency to try to destroy them. We must recognise the oneness of humanity, and understand that we will not achieve peace merely through prayer; we need to take action.”

Turkmen Court Sentences Brothers Eldor and Sanjarbek Saburov to Two Years in Prison

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Left to right: Siblings, Brothers Eldor and Sanjarbek Saburov
Left to right: Siblings, Brothers Eldor and Sanjarbek Saburov

On August 6, 2020, a Turkmen court sentenced Brothers Eldor and Sanjarbek Saburov to two years in prison for their conscientious objection to military service. The siblings are 21 and 25 years old, respectively. The court refused the brothers’ request to appeal. This is the second time both were convicted for their neutrality.

In 2016, Brother Sanjarbek Saburov respectfully refused to be drafted into the army. Subsequently, he was convicted and sentenced to two years of probation.

The following year, Sanjarbek’s younger brother, Eldor, also refused to participate in military service. He was sentenced to two years of correctional labor with 20 percent of his wages garnished by the State.

According to Turkmen law, conscientious objectors can be criminally charged a second time if they continue to refuse military service. In April 2020, the military recruiting office again summoned the brothers to enlist. Both brothers refused to be drafted. They were criminally prosecuted, which resulted in their imprisonment.

Beyond the emotional toll, imprisonment will cause acute hardship for the brothers’ parents. Their father suffers from chronic back pain, which impairs his ability to work. His sons support the family by growing cotton. Now that they have been imprisoned, their parents will no longer have the financial support they need. Instead, the parents will now have to care for their sons’ needs in prison.

Turkmenistan does not offer alternative civilian service. Consequently, young brothers who refuse military service on the grounds of conscientious objection face one to four years in prison. Including the Saburov brothers, there are ten young Witnesses in prison in Turkmenistan for their neutrality.

We know Jehovah will bless our young brothers in Turkmenistan for their courageous stand. May each of them recall Jehovah’s promise to King Asa: “You, be strong and do not become discouraged, for your activity will be rewarded.”

Global cooperation is our only choice against COVID-19, says WHO chief

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Global cooperation is our only choice against COVID-19, says WHO chief

Global cooperation – Tedros Adhanom Ghebreyesus, Director-General of the World Health Organization (WHO) was addressing the Aspen Security Forum, which brings together top-level present and former government officials from the United States.

The Americas remain the current epicentre of the COVID-19 pandemic.

“For all our differences, we are one human race sharing the same planet and our security is interdependent – no country will be safe, until we’re all safe”, he told the virtual meeting.

“I urge all leaders to choose the path of cooperation and act now to end this pandemic! It’s not just the smart choice, it’s the right choice and it’s the only choice we have.”

Invest in preparedness

Tedros said the pandemic has “stress tested” the global political, economic, cultural and social infrastructure, pushing national health systems everywhere, to their limits.

“The world spends billions every year preparing for potential terrorist attacks but we’ve learned lessons the hard way that unless we invest in pandemic preparedness and the climate crisis, we leave ourselves open to enormous harm”, he said.

As no country can fight the virus alone, Tedros said “our best way forward is to stick with science, solutions and solidarity, and together we can overcome this pandemic.”

Against “vaccine nationalism”

During a question-and-answer session moderated by US network TV news host, Lester Holt, the WHO chief was asked about ensuring fair distribution of a COVID-19 vaccine when one is developed.

Tedros warned against “vaccine nationalism” in a globalized world.

In April, WHO and partners launched the ACT Accelerator to speed up development of vaccines and medicines against the disease, and to ensure that they will be available to people everywhere.

“But to make it happen, especially fair distribution, there should be a global consensus to make a vaccine, any product, a global public product. And this is a political choice, a political commitment, and we want political leaders to decide on this,” he said.

“What we’re saying is sharing vaccines, or sharing other tools, actually helps the world to recover together, and the economic recovery can be faster and the damage from COVID-19 could be less.”

New humanitarian air service boosts COVID-19 response in the Pacific

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New humanitarian air service boosts COVID-19 response in the Pacific

The supplies were transported on behalf of the Pacific Islands Forum, the region’s premier political and economic policy organization.

With commercial air services greatly reduced due to airport closures, and other measures to prevent further spread of the disease, the 18-member bloc has established a platform to facilitate the timely and rapid movement of medical and humanitarian assistance, known as the Pacific Humanitarian Pathway on COVID-19.

Protecting people, supporting health systems

“The humanitarian air service flights are a welcome demonstration that the Pacific Humanitarian Pathway on COVID-19 is doing what leaders intended – protecting citizens and supporting health systems”, said Dame Meg Taylor, Pacific Islands Forum Secretary General.

The Pacific region is comprised of more than 20 countries and territories scattered across an area that represents roughly 15 per cent of the  earth’s surface.

Therefore, air and sea transport “is nothing short of a lifeline”, according to Jo Pilgrim, Director of WFP’s Pacific Multi-Country Office, which is located in Fiji.

Impact of COVID-19

Although border closures have helped curb the COVID-19 threat, she said impacts have been significant, particularly as the region relies on tourism revenue.

“It’s also affected international supply chains, especially for air cargo, and this makes it very difficult for Pacific governments and international aid organizations to import goods, especially medical equipment like the personal protective equipment that you need to protect our health workers”, Ms. Pilgrim told UN News.

“Even shipping routes across the Pacific, which are major avenues for the importation of food and fuel, for example, have been affected. Even though they are still running, the services are reduced, and the costs are increasing.”

WFP support to nations

Unlike other WFP operations, the Pacific Office does not work on food aid distribution or food assistance. Instead, it supports governments with emergency preparedness in a region that is highly susceptible to cyclones and other extreme weather events.

During the pandemic, staff have been assisting national authorities in three areas: establishing COVID-19 call centres and tele-health initiatives, conducting remote surveys on food security at the household level, and in logistics.

“A good example for logistics is that with the shut-down of the aviation sector affecting the ability of governments and aid organizations to import goods, we have established the Pacific humanitarian air service which will deliver cargo to those countries where there are no viable commercial options available for the importation of freight by air”, said Ms. Pilgrim.

Filling the gap

The Pacific humanitarian air service will transport medical items, medicines, and equipment on behalf of UN agencies such as UNICEF and the World Health Organization (WHO), as well as the International Federation of the Red Cross.

Flights will also deliver supplies on behalf of countries, coordinated through the Pacific Islands Forum Secretariat and the Pacific Humanitarian Pathway for COVID-19.

“Normally, humanitarian air services only move cargo on behalf of humanitarian organizations”, Ms. Pilgrim explained. “But in this particular case in the Pacific, because of the unprecedented circumstances we find ourselves in, where no one can get anything on a plane, we’re also moving medical cargo for the governments.”

Ms. Pilgrim expressed hope that commercial flights will be back in the air soon.

“We don’t want to do anything that would contradict this or that would disincentivize the aviation sector commercially”, she said, “so all the flights that we will operate will be limited as much as possible to those sectors without commercial options.”

The Pacific humanitarian air service is currently funded by Australia and the United States, and the hope is that other donors will step up.

“WFP is a voluntary-funded organization and we rely completely on donations from governments and the private sector, so we can keep flying for as long as we’ve got funds coming in,” said Ms. Pilgrim. “And hopefully we will have enough support from the donor community to allow us to fill the gap in the aviation sector until it’s restored and our services are no longer required.”

Spain: EIB provides €20 million in financing to Sanifit

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Spain: Biotech innovation - the EIB provides €20 million in financing to Sanifit to develop treatments for vascular calcification

Spain: Biotech innovation – the EIB provides €20 million in financing to Sanifit to develop treatments for vascular calcification

  • The EU bank will support Palma-based Sanifit in its work to develop cutting-edge solutions in biomedical research.
  • The venture debt operation is supported by the Investment Plan for Europe.

The European Investment Bank (EIB) is set to support the development of new treatments for progressive vascular calcification, an area of significant unmet medical need where there are currently no approved treatments. To this end, the EU bank will provide a €20 million loan to Spanish biopharmaceutical company Sanifit, which is developing novel treatments in two disease indications linked to calcification.

The EIB is advancing funds for this research, development and innovation (RDI) project by way of a venture debt operation with Investment Plan for Europe support, a financing instrument used by the EU bank to assist leading companies in innovative sectors. Since it was launched by the EIB under the Juncker Plan in 2016, this initiative has granted over €2 billion in financing for projects in areas such as robotics, artificial intelligence and biomedicine.

The EIB will provide Sanifit with long-term finance to drive the development of treatments for progressive vascular calcification disorders. The Company, founded as a spin-off out of the University of the Balearic Islands, has developed SNF472, a selective and potent inhibitor of hydroxyapatite (HAP) crystallisation, the final common pathway that leads to vascular calcification.

SNF472 is currently being investigated in a Phase 3 study for the treatment of calciphylaxis, a devastating rare disease where small blood vessels in skin and fat tissue are blocked due to severe calcification, leading to the death of approximately 55% of patients within the first year of diagnosis. A Phase 3 trial in a second indication, peripheral arterial disease, a major driver of morbidity and death in end-stage kidney disease patients, will launch in 2021.

EIB Vice-President Emma Navarro, responsible for the Bank’s operations in Spain, highlighted the “positive impact of this operation on strengthening the competitiveness of the European biomedical industry, a sector requiring large-scale investment and tailored financing solutions. We are delighted to help a leading Spanish company to develop new medical treatments for vascular calcification that will have clear benefits for human health and wellbeing. This agreement underscores the EIB’s commitment to supporting European innovation, which is now more vital than ever to promoting economic recovery and job creation.

Dr Joan Perelló, Chief Executive Officer of Sanifit, commented: “The support of the EIB represents a significant endorsement of our technology and its potential to help patients suffering from debilitating conditions related to progressive vascular calcification. This is an extremely exciting time for Sanifit as we progress SNF472 through the clinic, and this further investment will be invaluable as we gather the late stage data required for approval, and to deliver treatment options to patients in need.”

Sanifit is a clinical-stage biopharmaceutical company focused on treatments for vascular calcification disorders. The company is a spin-off from the University of the Balearic Islands and has offices in Spain and the U.S. The company’s lead asset, SNF472, has successfully completed a Phase 2 proof of concept study in calciphylaxis and showed a significant reduction in progression of coronary calcification in a Phase 2b study among hemodialysis patients.  A Phase 3 pivotal study in calciphylaxis is currently underway and a Phase 3 trial in Peripheral Arterial Disease in End-Stage Kidney Disease patients will launch in 2021. Sanifit has raised approximately $130M, including a 2019 Series D round of $61.8M (€55.2M) in mid-2019. For more information please visit www.sanifit.com

EU support for Italian biotech’s red blood cell technology to treat rare diseases

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EU support for Italian biotech’s red blood cell technology to treat rare diseases
    • EIB awards €30 million loan to EryDel for development of novel RBC treatment of rare diseases.
    • EryDel’s treatment platform under development for use in treating rare childhood diseases such as Ataxia Telangiectasia (AT).
    • Financing supported under the European Fund for Strategic Investments, the main component of the European Commission’s Investment Plan for Europe.

The European Investment Bank (EIB) and Italian biotech company EryDel SpA have signed a contract to provide a loan of €30 million to EryDel. This late-stage biotech company aims to develop and commercialise therapies based on its proprietary RBC technology for the treatment of rare diseases. The EU bank’s loan is backed by a guarantee from the European Fund for Strategic Investments (EFSI), the main pillar of the Investment Plan for Europe under which the EIB and the European Commission are working together as strategic partners, with the EIB’s financing operations boosting the competitiveness of the European economy.

EryDel’s proprietary platform technology is an easy-to-use, fast and automatic bedside procedure for encapsulating small and large molecules including therapeutic enzymes in patients’ own red blood cells. The cells are immediately re-infused into patients, providing prolonged half-life in circulation, reduced immunogenicity, better tolerability and predictable vascular distribution. EryDel’s most advanced product is being developed to treat AT, a rare neurodegenerative childhood disease that causes severe disability. EryDel’s platform RBC technology will be applied to treat other rare diseases as well. The financing will support ongoing R&D by the company and its network of partners, which encompasses research institutes, clinical centres and patient associations.

EIB Vice-President Dario Scannapieco commented: “The fact that EryDel is developing therapies for very rare diseases is all the more reason for us to be proud to support this initiative. With the backing of the EFSI, the EIB is happy to finance EryDel’s development of their autologous RBC encapsulation therapy to treat very serious childhood diseases. As the bank of the European Union, we have to ensure that new innovative EU-based companies continue to have access to finance, so that they can bring their technologies to market to help improve people’s lives.”

European Commissioner for the Economy, Paolo Gentiloni, said: “The Investment Plan for Europe has a very strong track record in identifying and supporting innovative technology companies. With the financing of the Italian company EryDel and its pioneering RBC technology, we will help push the boundaries of what is possible in the treatment of rare diseases to the benefit of patients in Europe and across the world.”

EryDel CEO Luca Benatti said: “We’re delighted to receive this financing from the EIB, which supports our vision of becoming a fully integrated company that can bring innovative therapies to patients. The EIB clearly recognises the unmet medical need for effective therapies for rare diseases and the potential to help patients in Europe and around the world, and supports our belief that in the future there will be effective therapies developed by EryDel for a wide range of rare diseases. The funds will be used for planned expenditures for research and development and capital expenditure activities. Now that we have completed enrolment for our Phase 3 clinical trial ATTeST, the largest clinical study ever conducted in Ataxia Telangiectasia, the support and collaboration we are receiving from the EIB is significant.”

EryDel CCO Ronan Gannon said: “We’re honoured to have the EIB as a partner who shares our market view and technology vision and trusts EryDel to play a leading role in the global rare disease market. It also demonstrates that Europe plays an important role in leading-edge innovations.”

EryDel SpA is a global, late-stage biotech company aiming to use its proprietary red blood cell (RBC) technology to develop and commercialise therapies for the treatment of rare diseases. Its most advanced product EryDex is under late-stage development for the treatment of Ataxia Telangiectasia, a rare autosomal recessive disorder for which no therapy is currently available. A completed Phase II trial in AT patients demonstrated statistically significant efficacy of EryDex on both the primary and secondary endpoints. An international multi-centre Phase III pivotal study, ATTeST, is currently being conducted. EryDel has a pipeline of pre-clinical programmes that are working with its proprietary RBC delivery technology in treating other rare diseases, which includes the use of enzyme replacement therapies.