Africa

Thousands calls for the president to leave now even though he has withdrawn his re-election bid.

Kishan Kumarsingh, lead negotiator for Trinidad and Tobago on climate change. Credit: Jewel Fraser/IPS

By Jewel Fraser
PORT OF SPAIN, Mar 15 2019 (IPS)

Trinidad and Tobago unveiled its monitoring, reporting and verification system in mid-March with a flourish, with government authorities underscoring the launch of the Monitoring, Reporting, Verification as a milestone in that country’s efforts to reduce its emissions in line with its commitments under the 2016 Paris agreement.

And even while acknowledging the Intergovernmental Panel on Climate Change’s report that current efforts such as these globally are unlikely to protect the world from warming more than 1.5 degrees above pre-industrial levels, Trinidad and Tobago’s lead negotiator at climate negotiations since 1998, Kishan Kumarsingh, remains upbeat. He told IPS the Paris agreement is the foundation for a world a transition thanks to the exercise of “political will” and national sovereignty.

“It all goes back to the function of political will,” he said. “Because the efficacy of international law is invariably a function of political will because it is underpinned by national sovereignty.” He said it was governments that would create an enabling environment for a carbon free world since it was these same governments, not private citizens, that negotiate climate agreements.

But Dr. Leon Sealey-Huggins, a senior teaching fellow in Global Sustainable Development at the University of Warwick and a self-proclaimed scholar activist, is of the view that that is where the problem lies for the Caribbean in its efforts to secure its future against climate change. “Whether or not it’s even possible through the United Nations framework to achieve the kind of change needed for the Caribbean is questionable,” Sealey-Huggins told IPS. “The global structures of decision-making such as the UN are born out of a legacy of imperialism and globalism,” he said, with its unequal power structures and wealth distribution that have contributed to the current difficulties the Caribbean faces with climate change and its inability to successfully defend itself against it.

As a consequence, Sealey-Huggins said, the solutions promoted at climate change negotiations tended to focus on funding for“more technical approaches” like MRV systems that do not allow for the kinds of “social, political and economic reorganisation” that could shift the climate agenda towards more meaningful transformation and innovative solutions.

Trinidad and Tobago’s new MRV system will focus on emissions from industry, transportation and power generation, enabling identification of the source and quantity of emissions, and helping with efforts to reduce emissions in these three sectors by 15 percent by 2030, a press release from that country’s Ministry of Planning and Development said..

But such solutions “limit other options in terms of what is funded”, limiting research on other potential solutions, said Sealey-Huggins, in spite of the evidence that the global trajectory on carbon emissions reductions is insufficient to achieve the Paris goals.

Nevertheless, Kumarsingh maintains there are signs of real progress, particularly since Copenhagen. He points to the launch of the Green Climate Fund which was agreed upon at Copenhagen, and the establishment of the Warsaw International Mechanism for dealing with the sticky question of loss and damage.

“The Green Climate Fund is one manifestation of advancement for provision of finances and support…to developing countries,” he said. “It is not a cut and dried issue that the interests of developing countries are locked out of negotiations, because they are negotiations by nature and even among the developed countries, among the developing countries there are varying interests.”

He said the issue of loss and damage has proved to be “challenging”. Besides this, however, “there is widespread acceptance that beyond adaptation there is the issue of permanent loss, permanent damage that needs to be addressed.”

But how these issues would be addressed remains to be determined since monetary compensation alone might not be sufficient to compensate for the loss. “Would a monetary compensation for the loss of an island be adequate for the people themselves?…. these ideas are now being ventilated and discussed. But the cut and dried issue of compensation just won’t happen because of the historical nature of the negotiations themselves,” Kumarsingh told IPS.

He stressed that countries sit at the negotiating table with the intention uppermost in mind of protecting their own country’s interest, not that of another. And while developed countries had accepted they have a responsibility towards SIDS in terms of technology transfer and financing, he acknowledged that their delivery of such help could be increased.

“Of course more could be done to advance the multilateral cooperation to protect the planet as a whole from climate change because climate change is everybody’s business, particularly given the urgency and the accelerating rate of climate change we have seen in recent years,” Kumarsingh added.

Grenada’s former Ambassador to the UN Dessima Williams, who was chair of the Association of Small Island States from 2009 to 2012, told IPS that the effects of climate events on the region’s economic development was a cause for great concern and needed greater action. “The issue of risk has to be broadened from beyond climate events” to factor in the increasing financial burdens these events are placing on countries that are already strapped with development debt, she said. Williams said the question of climate financing must be placed firmly on the climate agenda “in a meaningful way to impact debt reduction and share the burden in an equitable way.”

However, whether Caribbean SIDS do get their concerns over financing on the agenda “could very well be an issue of negotiating capacity and negotiating skills to actually get what [we] want,” Kumarsingh concluded.

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The post Scholar Questions ‘Techie’ Approach to Dealing with Climate Change appeared first on Inter Press Service.

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By Fabiana Frayssinet
RÍO DE JANEIRO, Mar 15 2019 (IPS)

“More than 50 countries in the world have discriminatory laws against people affected by Hansen’s disease. There is also a lot of discrimination in the public administration…and in society,” Alice Cruz, U.N. Special Rapporteur on the elimination of discrimination against persons affected by leprosy and their family members, said in this interview with IPS (in Spanish, with English subtitles).

The Portuguese-born expert is one of the special participants in the First Latin American and Caribbean Assembly of Organisations of People Affected by Hansen’s Disease – another name for leprosy – taking place in Rio de Janeiro, Brazil on Mar. 12-14.

 

 

Among the many examples of violations of the rights of those affected by the disease, Cruz cited the case of children who are expelled from school.

“People lose their jobs, there is discrimination in the community, they aren’t allowed to enter places of worship, etc, and there is discrimination in the family too,” added the Special Rapporteur in the Office of the United Nations High Commissioner for Human Rights.

Cruz pointed out that in 2010, the United Nations adopted “a human rights instrument to guarantee the rights of people affected by Hansen’s disease.”

According to this document, entitled “Draft principles and guidelines for the elimination of discrimination against persons affected by leprosy and their family members”, “States should enforce this instrument which covers all areas of affected persons and protects them from the violations mentioned,” she stressed.

This is the first time that a meeting has been held in Latin America dedicated to people affected by a disease that the World Health Organisation defines as infectious and chronic, caused by the bacillus Mycobacterium leprae and which mainly damages the skin, peripheral nerves, the mucosa of the upper respiratory tract, and the eyes.

Brazil, the host country, accounts for 95 percent of all cases in the Americas, with between 25,000 and 30,000 new diagnoses per year.

The regional meeting is an initiative of the Brazilian Movement for the Reintegration of People Affected by Hanseniasis and the Colombian Federation of Organisations of People Affected by Hanseniasis, with support from Brazil’s Health Ministry and the independent Nippon Foundation.

The region’s findings, together with the ones that emerged from similar assemblies in Asia and Africa, will be incorporated into the proposals for the World Congress on Leprosy, to be held in the Philippines in September.

 

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The post VIDEO: “People Affected by Leprosy Suffer Severe Discrimination” appeared first on Inter Press Service.

A farmer in Woliyta area of Ethiopia experiences higher yields of taro since adopting disease-resistant and drought tolerant seed varieties. Credit: Ed McKenna/IPS

By Esther Ngumbi
ILLINOIS, United States, Mar 15 2019 (IPS)

The latest UN Food and Agriculture Organization’s annual Africa Regional Overview of Food Security and Nutrition Report highlighted drought as one of the key factors contributing to the continuing rise in the number of hungry people in sub-Saharan Africa. And in South Africa, the Government’s Crop Estimates Committee announced that the country would harvest 20 percent less maize in 2019 because of drought conditions. 

Drought, a period of inadequate rain or no rainfall, is the main cause of crop yield loss in Africa, ultimately causing food insecurity and famines. In early 2018, over 15 million people from countries ranging across the continent — including Somalia, Ethiopia, South Africa and Kenya — were affected by drought.

Drought isn’t uncommon in Africa. It happens somewhere on the continent every year. But weather patterns are becoming more unpredictable, as well as more severe. For example, the droughts of 2014, 2015, 2016, and 2017 made headlines across the continent and total cost the region an estimated at USD$ 372 billion.

Smallholder farmers are most affected by drought because many don’t have irrigation technology and rely on rainfall for their crops. With the unpredictability of rainfall patterns smallholder farmers are no longer able to plan their planting seasons.

To ultimately become drought resilient, Africa's smallholder farmers must grow drought tolerant crops. Growing drought tolerant crops has many benefits including increasing on farm crop yields

To deal with this, various stakeholders — from national governments to non-governmental organizations — have used different approaches, like food aid and funds, safety net systems ( like water storage) to help cover citizens during droughts and the implementation of irrigation schemes. But to ultimately become drought resilient, Africa’s smallholder farmers must grow drought tolerant crops. Growing drought tolerant crops has many benefits including increasing on farm crop yields.

Drought tolerant crops — like maize, cowpeas and rice — have been bred through conventional plant breeding techniques or biotechnology and continue to grow and produce even when rains fail. They’ve been around since the 20th century, but the last two decades have seen an increase in drought tolerance research that targets staple crops like maize, rice and wheat.

There are some challenges involved, however. Breeding crops for drought tolerance takes time. On average, bringing new drought tolerant crops to market can take an about five years. Testing the seeds to accurately characterize the traits involved can take many years and requires several locations. Another challenge is that significant investment is needed to breed drought tolerant crops and make them available to farmers.

Nonetheless, the uptake of  these crops has been promising. Though the scale with which they are adopted by farmers varies by country, about 40 million smallholder farmers across sub-Saharan Africa benefit are using more than 200 drought tolerant maize varieties, benefits that include increases in crop yields.

But, there are still several hurdles to overcome.

For example, unlike traditional seeds, drought tolerant seeds have to be bought every year. Though drought tolerant crops produce seeds, they lose some of their drought protection capacities so farmers are encouraged to buy new seeds, not save them from the previous harvest. Many farmers are afraid of being locked in this cycle of financial obligation.

Secondly, just like any other new technology, there are several determinants to whether it’s successfully adopted by farmers. For the case of drought tolerant crops, research shows that early adopters to drought tolerant maize are more educated and have better access to agricultural extension personnel.

Nevertheless, research has demonstrated that the pros of adoption, and costs involved, outweigh the cons. And the good news is that drought tolerant crops are available across Africa. For the past decade, institutions like the International Maize and Wheat Improvement Centre, Kenya’s Agricultural Research Institute and private foundations like the Bill and Melinda Gates Foundation have invested in breeding and strengthening the adoption of drought tolerant crop varieties across the continent.

Importantly, there are benefits of planting drought tolerant crops including producing larger crop yields. According to research, planting climate resilient maize varieties in most environments leads to 25% more crop yield. This is because these crops are still able to grow in periods when the rains fail. In Zimbabwe, for example, farmers earned USD$240 more per hectare when they planted drought-tolerant maize varieties because of larger yields.

Of course, even though there are benefits to planting drought resistant varieties, they aren’t a silver bullet. There are other steps farmers must take to make the most out of planting these tolerant varieties. For example, they must still look after the health of soils and practice mulching — covering soil between plants with a layer of material to keep the soil moist — to keep moisture in during periods of drought.

But they are still a smart strategy and investment for Africa’s smallholder farmers. They offer a buffer to drought, both now and in the future, bringing greater yields, improved incomes and increased food security.

 

Esther Ngumbi is Distinguished Post Doctoral Researcher, Entomology Department at the University of Illinois at Urbana Champaign, Illinois. She was the 2015 Clinton Global University (CGI U) Mentor for Agriculture and 2015 New Voices Fellow at the Aspen Institute.

 

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A selection of the week's best photos from across the continent and beyond.

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Family photo of part of the 111 participants in the First Latin American and Caribbean Assembly of Organisations of People Affected by Hansen's Disease, on the steps of the Morisco Palace, the headquarters of the Oswaldo Cruz Foundation, which hosted the three-day meeting in Rio de Janeiro, Brazil. Credit: Mario Osava/IPS

By Mario Osava
RIO DE JANEIRO, Mar 14 2019 (IPS)

With the decision to found a regional coalition to promote rights and greater participation in national and international forums and decisions, the First Latin American and Caribbean Assembly of Organisations of People Affected by Hansen’s disease, popularly known – and stigmatised – as leprosy, came to an end.

The final session of the meeting, on Mar. 14, approved 40 of the 58 proposals presented by the 111 participants in three days of debates at the headquarters of the Oswaldo Cruz Foundation, a renowned scientific, medical and epidemiological research centre in Rio de Janeiro, Brazil.

José Picanço, 46, separated from his family and taken as a newborn to an orphanage because his parents were diagnosed with the disease in 1972, is one of those affected whose right to reparations remains unfulfilled. His three siblings are in the same situation.

When the family was reunited eight years later, the father turned his back on the children. The mother took them in, but died shortly afterwards. “I only lived with her, a saint, for five months,” Picanço recalled, barely managing to hold in his tears while giving testimony at the meeting.

“Humiliated as the children of lepers, suffering bullying and sexual harassment, many of the other children who were with me at the orphanage fell into drug abuse and alcoholism. It was a holocaust,” he said. “I hit my brother on the head, not knowing he was my own brother.”

“Of the 15,000 to 20,000 children separated from their families, more than 80 percent suffer from depression,” said Picanço in an interview with IPS, detailing some of the damage caused by the old rule of segregating the people then called “lepers”.

Mandatory isolation was widespread around the world, during different historical periods, and continues in some countries, even though it is known that the disease is curable and that patients cease to be contagious shortly after starting treatment.

Officially, Brazil abolished this practice in 1976, although it actually lasted 10 more years. Its direct victims were compensated starting in 2007, but their children were not. The activists gathered in Rio de Janeiro called for working for policies of reparations for children separated from their families.

Their complaints and proposals will be taken to the World Congress of associations of people affected by leprosy in Manila in September, which will also receive contributions from Africa and Asia, approved at recent similar regional assemblies.

“The goal is to form a large network of activists, to strengthen the movement” for the eradication of the disease and for care and reparations for those affected, said Kiyomi Takahashi of the independent Nippon Foundation, which is driving this international process of debate and cooperation.

The meeting in Rio de Janeiro fostered “a high-level dialogue, the result of Morhan and Felehansen’s long history of activities,” the Japanese expert told IPS, referring to the Movement for the Reintegration of People Affected by Hanseniasis (Morhan) in Brazil, and the National Federation of Entities Affected by Leprosy or Hansen’s Disease (Felehansen) in Colombia, the two organisers of the regional meeting.

Brazilian activists José Picanço (front) and Evelyne Leandro testified about how Hansen’s disease affected them during a Latin American and Caribbean meeting in Rio de Janeiro. Picanço was separated from his parents when they were diagnosed with leprosy when he was born in 1972 and was only reunited with them eight years later, shortly before his mother died. Leandro wrote a book about the difficulties of being diagnosed with the disease in Germany, where she lives. Credit: Mario Osava/IPS

“Morhan is my safe haven, to preach that separated children should be heard and have opportunities,” said Picanço, who explained that he joined the movement in 1992. Today he gives talks on the direct and indirect effects of the stigma still surrounding the disease, that is suffered by those affected and their families.

A blessing

The disease “was a blessing for me,” Isaias Dussan Weck, 50, the vice-president of the Colombian association Felehansen, told IPS without hesitation.

The diagnosis in 2006 destroyed him, he said. He lost the desire to work or to go out, he let his business of supplying cleaning products to companies go bankrupt, he even contemplated suicide. He ignored the stains on his body that did not prevent him from working and traveling, until they spread to his face, and he noticed that parts of his body were going numb.

He received treatment and was cured, left with only slight numbness in one arm and pains in his left leg.

But everything went badly for him until he was invited to meetings with other people affected by leprosy. “I began to understand, when I heard their testimonies and tears, why a young black girl with severe disabilities said that leprosy was a blessing to her,” Dussan said.

Activism for the benefit of those affected, against the stigma and the damage caused by the disease, in the association of the department of Huila, in southwestern Colombia, allowed him “to gain new meaning for life and to understand and practice love for my neighbour.”

“Helping and seeing a patient’s life improve is a wonderful emotion, and you help other people want to live,” he concluded. That new passion led him to Felehansen, where he took on leadership roles in the federation.

Irma Romero, 42, president of the Nuevo Amanecer Foundation in Barranquilla, on Colombia’s northern coast, had a similar experience. Her lengthy odyssey to a specialist’s diagnosis five years ago reveals the medical system’s shortcomings when it comes to detecting and treating the disease, also known as hanseniasis, which is still viewed by many as “a divine punishment.”

Romero stopped working in the textile industry due to disability and depression. “I couldn’t even walk,” she recalled. “I even denied God,” she told IPS.

Colombian activist Irma Romero, a native of the city of Barranquilla, sitting on the bus that transported the participants of the First Latin American and Caribbean Assembly of Organisations of People Affected by Hansen’s Disease, held Mar. 12-14 in Rio de Janeiro, Brazil. Credit: Mario Osava/IPS

Treatment using medicinal herbs, self-medication, rejection by relatives, attempts to separate her from her two children and abandonment by her husband all formed part of her suffering, which did not end with her treatment and cure.

The only permanent physical effects are numbness in her hands and feet, and sciatic nerve pain. But the discrimination continued.

“My life changed when I joined the association of affected people” four years ago, she said. “There I found people who had things in common with me, and a newfound love of my neighbour that I did not feel before,” said the activist, who became president of the Foundation the following year and reconciled with God.

Her foundation currently has 60 members. In Barranquilla she estimates that there are “about 200 affected people, but many more are hidden.”

The foundation is one of the 10 associations that make up Felehansen, eight of which call the disease hanseniasis or Hansen’s disease, one of which uses the term leprosy, and another of which refers to disabled people and is made up of patients who received a very late diagnosis.

The World Health Organisation (WHO) defines leprosy – the term it uses – as an infectious and chronic disease “transmitted by air through droplets from the nose and mouth, during close and frequent contacts with untreated cases.” It also specifies that leprosy is “one of the least infectious diseases.”

WHO reports that in 2017 there were 211,009 new cases worldwide, according to official data from 159 countries. That amounts to 0.3 cases per 10,000 inhabitants, which means it classifies as having been “eliminated,” according to WHO criteria.

Change of name: another recommendation

Proposing hanseniasis as the official name for the disease is one of the proposals that came out of the Latin American meeting, headed by Brazil, which has already adopted it, even prohibiting the mention of leprosy in the health system since 1995.

They are different concepts, because leprosy and leper have very negative connotations of “dirt, plague, impurities and divine punishment,” strengthened by numerous mentions with that moral burden in the Bible, argued Faustino Pinto, one of Morhan’s national coordinators.

But the activists from Colombia are not convinced. “People only know leprosy, they don’t know it’s Hanseniasis. To explain the issue to the population, you have to mention leprosy,” argued Romero.

“It will be necessary to educate the new generations about the concept of Hansen,” the Norwegian doctor Gerhard Hansen who discovered the bacillus that causes the disease, because adults are not likely to forget the stigma, said Dussan. “It’s harder to unlearn than to learn,” he added.

Another proposal of the Latin American Assembly is to extend the current Committee for Assistance to Brazilian Immigrants Affected by Hanseniasis to all Latin Americans and people from the Caribbean, in addition to extending it to other regions.

The reference point in this is Evelyne Leandro, a 37-year-old Brazilian who has lived in Germany for nine years and had a lot of difficulties getting diagnosed with the disease in a country where it is very rare and where very few doctors are familiar with it.

She was helped by her mother’s suspicion, awakened in Brazil by an outreach campaign on the disease, and by the Institutes of Tropical Medicine in Germany.

Her case and those of other immigrants in Europe are recounted in her book “The Living Death: the struggle with a long forgotten disease”.

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The post People Affected by Leprosy in Latin America Unite for Their Rights and Their Voice appeared first on Inter Press Service.

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By Kenton X. Chance
KINGSTOWN, Mar 14 2019 (IPS)

From an influx of sargassum in near-shore waters, to fish venturing further out to sea to find cooler, more oxygenated water, fishers in St. Vincent and the Grenadines are battling the vagaries of climate change. The country is doing what it can to respond.

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The post Helping St. Vincent’s Fishers Maintain an Essential Industry in a Changing Climate appeared first on Inter Press Service.

A cigarette vendor in Manila sells a pack of 20 sticks for less than a dollar. Credit: Kara Santos/IPS

By Wendell Balderas and Mary Assunta
BANGKOK, Thailand, Mar 14 2019 (IPS)

International Women’s Day on 8 March recognized and celebrated the progress women are making globally. The day also acknowledged the risks, exploitation and suffering many continue to endure.

The Southeast Asia Tobacco Control Alliance (SEATCA) puts the spotlight on the tobacco industry’s marketing tactics targeting women and girls especially in Asia to market its deadly products.

While smoking prevalence among females remains relatively low in Asia, smoking rates among adolescent girls in the Philippines, Malaysia, and Thailand however are higher than the rate among adult women respectively (9.1% vs 5.8%; 2.4% vs 1.4%; 5.2% vs 1.7%). Despite governments’ efforts to protect public health, tobacco use remains at epidemic proportions.

This is no coincidence. The tobacco industry needs “replacement” customers to maintain and increase its profits, and women and girls are an important market segment which represent the largest product-marketing opportunity the tobacco industry exploits.

Internal tobacco industry documents reveal that the tobacco industry has been notoriously targeting women and girls through their ads and novel products that promote social desirability, independence, sophistication, glamor, romance, and fun.

Women and girls, especially in low and middle-income countries (LMICs), are smoking in greater numbers than ever before. The tobacco industry has been introducing new products framed as “innovation” by refreshing brand marketing devices and imagery to appeal to women and young girls.

Through these product “innovation”, transnational tobacco companies (TTCs) introduce cigarette brands with new characteristics as flavored capsules and flavored filters and packaged and labelled with glitzy promotion.

These so-called innovations are gimmicks on specific product designs including filters, capsules, flavors, shape, color and perceived product’s strength or mildness.

Credit: Bigstock

Some of the tobacco industry’s deceptive tactics which blur the truth about the hazards of tobacco and instead promote smoking in developing countries among women and girls include the following:

• • In Indonesia, Malaysia and Singapore, some cigarettes brands are in “Lipstick” packs. Female-targeted elegant slims or super slim cigarettes are also packaged in slimmer packs and influences beliefs about smoking and weight control – an important predictor of smoking behavior among women.

 

• • In Malaysia, Cambodia and Vietnam “Less smoke smell (LSS)” technology has been used to promote cigarettes designed to reduce secondhand smoke odor.

 

• • Kiddie packs (10 to 12 sticks) are also available in Indonesia and the Philippines.

 

• • Flavor capsules in cigarettes are becoming increasingly popular and increase attractiveness of smoking. Some cigarettes sold in Cambodia, Indonesia, Malaysia, Philippines, Singapore and Vietnam have capsule filters that can be crushed to release additional menthol or other flavoring.

 

• Colors play an important role to enhance cigarette packaging and labeling to represent flavors and strength within brand families. The brand image is created by attention-grabbing designs and appealing colors to indicate flavors (such as strawberry, orange and apple) and communicate the false impression of lower tar or mild cigarette. Gold and silver convey ‘low-tar’, green for menthol and blue for ‘light’ or icy/cool.

To divert public attention away from the harm and damage caused by the industry, the TTCs have been conducting public relations stunts about employment and gender equity.

Philip Morris International boasted an ‘Equal-Salary certification’ it received, conveniently timed for International Women’s Day. TTCs routinely receive an obscure ‘top employer’ awards while simultaneously fighting smoke-free policies.

According to the US Centers for Disease Control and Prevention (CDC), “a woman’s risk of dying from smoking has more than tripled and is now equal to men’s risk”. This means that women are also at higher risk for heart attacks, strokes, lung cancer, emphysema, and other serious chronic illnesses such as diabetes.

A sudden concern for smoking is the new public rhetoric of the tobacco industry to justify a new range of so-called “less harmful” products such as heated tobacco products, while simultaneously selling regular cigarettes which form the bulk of their profits.

The current sixty-third session of the Commission on the Status of Women (CSW) at the United Nations Headquarters in New York, (11 – 22 March) is expected address women empowerment and their vital roles as agents of development in making progress across all Sustainable Development Goals (SDGs) and targets.

It is timely to discuss the tobacco epidemic among women especially in the LMICs and the concerted effort governments must make to curb this scourge.

Preventing an epidemic of tobacco-related diseases among women in the LMICs is one of the greatest public health opportunities for governments of our time. The global health treaty, WHO Framework Convention on Tobacco Control (FCTC) has been explicitly identified as a means to achieve the SDG health goal.

Steps governments should take to prevent this epidemic include banning tobacco advertising and promotions such as pack displays and applying plain packaging which requires cigarette packs to be sold in a standardized size, shape, and drab brown color, free of any logos or images.

In September 2019, Thailand’s legislation on standardized packaging of tobacco will take effect and Singapore will follow soon. Standardized packaging removes the attractiveness of tobacco products and reduces the ability of tobacco packaging to mislead consumers about its harmful effects.

Other equally important actions in the FCTC include increasing tobacco taxes and making public and work places 100% smoke-free.

*SEATCA is a multi-sectoral non-governmental alliance promoting health and saving lives by assisting ASEAN countries to accelerate and effectively implement the evidence-based tobacco control measures contained in the WHO FCTC. Acknowledged by governments, academic institutions, and civil society for its advancement of tobacco control movements in Southeast Asia, the WHO bestowed on SEATCA the World No Tobacco Day Award in 2004 and the WHO Director-General’s Special Recognition Award in 2014.

The post Tobacco Industry Targets Women in Asia appeared first on Inter Press Service.

Excerpt:

Wendell Balderas is Media & Communications Manager & Mary Assunta is Senior Policy Advisor, Southeast Asia Tobacco Control Alliance (SEATCA)*

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