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What’s the Link Between Glaucoma and Dry Eyes? – Healthline

June 26th, 2022 2:09 am

Glaucoma is a vision condition that results from damage to your optic nerve, often due to elevated pressure in the eye. Its one of the most common causes of vision loss in adults and can lead to blindness without treatment.

Eye drops and other treatments can cause dry eyes in many people with glaucoma. People who have glaucoma might already be at heightened risk for developing dry eyes because the conditions share some risk factors.

Dry eyes can be chronic and uncomfortable, interfering with daily life. Its possible to treat both glaucoma and dry eyes with a combination approach. Well overview the link between these conditions, symptoms, and available treatment options.

Its common for dry eye and glaucoma to occur together. Dry eye is a type of ocular surface disease (OSD), which also includes blepharitis (eyelid inflammation).

2020 research states the global prevalence of OSD in people with glaucoma is around 40 to 59 percent, substantially higher than the general population.

There are a few reasons for this, including:

Dry eye and glaucoma can be difficult to treat. Although dry eye is often more painful and irritating for the patient, glaucoma is a more serious condition as it can lead to blindness. Because of this, eye doctors will focus on treating glaucoma first, even if that makes relief of dry eyes more difficult.

However, your doctor will do their best to ensure both dry eye and glaucoma are treated for the best quality of life outcome.

Glaucoma is the name for a group of conditions that cause damage to the nerves in your eyes. Glaucoma results in vision loss and can lead to blindness without treatment. It can occur in one or both eyes.

Medical researchers have long thought that glaucoma only occurred when the pressure built up inside the eyes. Newer research indicates that glaucoma can develop even when the pressure inside the eyes is normal.

Glaucoma doesnt always cause symptoms early on, so people are often unaware they have it in the early stages. This is especially true if you have a type of glaucoma called open-angle glaucoma. About 90 percent of people with glaucoma have this type, and its the second leading cause of legal blindness in the U.S.

When symptoms of any type of glaucoma develop, they may include:

While its possible to slow or stop the progression of glaucoma, any vision loss caused by glaucoma is irreversible. Detecting glaucoma early and getting treatment quickly can prevent blindness. Its important to see an eye doctor as soon as possible if you have any glaucoma symptoms.

Glaucoma can be screened for and detected by a routine eye exam with your ophthalmologist. The American Academy of Ophthalmology (AAO) advises adults have a comprehensive medical eye examination at age 40 if they havent had one yet.

Dry eye is a common eye condition. It happens when your eyes cant make enough tears, or when the tears your eyes make dont keep your eyes moist enough. When your eyes arent well moisturized, they can become uncomfortable and inflamed.

In some cases, dry eye is temporary. For example, you might get a flare of dry eye from being outside on a very windy day, or from a long shift of computer work. In other cases, dry eye can be a chronic condition.

Dry eye can be very irritating and can make it difficult to complete everyday tasks. Especially when chronic, dry eye can have far-reaching impacts on your quality of life.

Symptoms of dry eye can include:

Some people with dry eyes may experience discharge from their eyes or eyelids. Discharge can also be a sign of eye infection.

Some cases of night vision can be treated with over-the-counter eye drops. However, prescription-strength treatment and lifestyle changes can help many people.

Youll likely need a combination of treatments to help both dry eye and glaucoma. You might go through several treatment options until you find the combination that is most helpful for your eyes.

According to NIH and AAO, treatment approaches include:

Your doctor might also recommend lifestyle changes, such as:

Factors that are unrelated to glaucoma can also cause dry eye. Sometimes these factors can occur alongside glaucoma and can make treating it more challenging.

Dry eye and glaucoma commonly occur together. They share risk factors such as age and having diabetes, and some glaucoma treatments can cause dry eye.

Treating both conditions together can be challenging. While dry eye may be more painful and difficult to deal with in the short term, glaucoma is more dangerous to your vision in the long term. This means glaucoma treatment will be prioritized.

However, doctors will always attempt to treat both conditions. In most cases, youll receive a combination of treatment approaches that can help preserve your vision and restore your eye comfort.

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Lisa Durden’s upcoming documentary "Blind Divas" follows Krystle Allen and Naquela Wright-Prevoe, two Black women entrepreneurs, determined…

June 26th, 2022 2:09 am

Lisa Durden, an award-winning director/producer and media personality leads the production of Blind Divas, a documentary following Krystle Allen and Naquela Wright-Prevoe, two blind, Black women entrepreneurs, determined to challenge the stigmas and stereotypes about the blindness community. This is not just a story about two determined women who are everyday champions in the blindness community, its also a story of triumph.

Durden, Allen and Wright-Prevoe joined WBGO Journal host and News Director Doug Doyle to talk about the project and what ahead.

Durden says this film will pull back the curtain of curiosity about the abilities of women with vision loss, as we document their national Finding Miss Blind Diva Tour; Hosted by Eyes Like Mine Inc. and the Greater Vision Foundation, The Miss Blind Diva Empowerment Pageant is honoring marvelous moms with disabilities. Join them for an afternoon of empowerment, entertainment, giveaways, and more.

Here are some of the upcoming events :June 25, 2022 - Community Baby Shower, Newark, NJ July 5-10, 2022 - National Federation of the Blind National Convention,New Orleans, Louisiana, LA

For her focus on this compelling story, Lisa Durden, was the WINNER of the national short documentary pitch competition, sponsored by African American Women in Cinema Film Festival (AAWIC), in collaboration with the distributor, Lightbeam TV; A streaming platform featuring stories that shine a light on inspiring people and organizations making the world a better, more hopeful place.

Lisa Durden earned her Masters In Fine Arts Degree, in Social Documentary Film, from New Yorks School Of Visual Arts. Ms. Durden took the leap and launched Lisa Durden Unlimited Productions, a Multi-Media Company, specializing in developing content for linear television, film, digital and live audiences, with a focus on telling compelling stories about underserved communities, featuring big, entertaining, characters.

Some of Ms. Durdens award-winning projects include: Director/Producer, short documentaryGirls Matter, which WON Best Animation at the Tokyo International Short Film Festival 21;Assistant Director of the VerizonCommercial,Conversations With Mom; Producer of award-winning PBS 2019 Online FestivalShortFilm,Paris Blues in Harlem; Senior Producer of ImageNations star studded Revolution Awards; Co-Producer of the provocative, award-winning, feature filmTITLE VII; Conceived & ProducedPBSMaya Angelou Films successful Live Twitter Chat, which garnered 8 Million Impressions; The former Broadcast Manager with the Black Public Media,AfroPoP Series; Associate Producer of PBS documentary, Soul Food Junkies; and Associate Producer of Peabody award-winning, Prime-Time Emmy and NAACP Image awards nominated, Sundance Channels, docu-series, Brick City 1.

You can SEE the entire interview here.

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Trump election lies may fit legal concept of willful blindness – Chicago Tribune

June 26th, 2022 2:09 am

Monday night, two neighbors and I enjoyed each others company and conversation around a backyard fire to celebrate the summer solstice.

Politics came up. One neighbor said she didnt think Joe Biden legitimately won the 2020 presidential election. The other said he didnt think too many people were paying much attention to the House select committees historic hearings about the Jan. 6, 2021 riot at the U.S. Capitol.

I did not argue with my neighbors or try to persuade them to change their minds. I asked what they thought of Rep. Adam Kinzinger and Vice President Mike Pence, Republicans who refused to go along with President Donald Trumps plot to overturn results of a free and fair election.

RINOs, the one neighbor said, meaning Republicans In Name Only. Many share her view that loyalty to the GOP matters more than oaths sworn to uphold the U.S. Constitution.

The House committee is building its case to the American people. Through witness testimony, documents, emails, text messages, video and other evidence, the committee is showing how Trump tried to stay in office despite losing the popular vote to Biden by about 7 million votes.

Trumps lust for the power drove him to convince millions of his followers that the 2020 election was fraudulent. Former New York City Mayor Rudy Giuliani, Fox News hosts and other influential people publicly went along with the scheme. The committee has heard from former U.S. Attorney General Bill Barr and others, who testified they repeatedly told Trump his ploy was illegal.

If fraud had occurred, Trumps proper recourse was to plead his case in court. His supporters filed more than 60 lawsuits in state and federal courts, but no one could present any evidence of fraud, only lies and hearsay. Judges, including some appointed by Trump, dismissed the cases.

Trumps unwillingness to accept the reality of his loss may involve a concept known as willful blindness, legal analysts have written. Trump himself might have believed there was fraud, but testimony shows he refused to listen to anyone who told him the evidence said Bidens win was legitimate.

To this day, many Republican voters and elected officials refuse to publicly admit Biden won the presidency. Many believe fictional stories about mules harvesting illegal votes cast by purported dead people or immigrants. Theyve been told to believe electronic voting equipment was somehow manipulated to favor Biden.

The false narratives collectively known as Trumps big lie cast doubt on the integrity of our voting systems and democracy.

Not only is Trump willfully blind, the hearings show that millions of fellow Americans deliberately refuse to acknowledge mounting evidence that violence at the Capitol that day was no accident. Rather, it was the culmination of an illegal ploy to halt the certification of Electoral College results.

Insurrectionists loyal to President Donald Trump breach the Capitol in Washington, D.C. Jan. 6, 2021. (AP Photo/John Minchillo/AP)

Trump embraced the plan to violently overturn the outcome, but Pence refused to go along with the scheme. There was no legal basis to a cockamamie theory that the vice president could reject the will of voters by legitimizing slates of phony electors in several swing states that Trump lost.

The plan was to kick Electoral College slates back to certain states where Republicans held legislative majorities. The scheme never made it that far. Our institutions held, but barely. You may recall 121 House Republicans and six GOP senators voted to reject results from Arizona.

Americans who ignore the truth of Jan. 6 use mental gymnastics to create an alternate reality. They deny evidence. They deflect by talking about gas prices or other concerns. They try to discredit those presenting evidence by calling the effort to seek accountability a partisan witch hunt.

The select committees important task is to show Americans that the threat to democracy is ongoing. Last week, a Republican-led county commission in New Mexico relented and voted to certify election results after initially refusing to do so. The states supreme court ordered the panel to certify results that the commission initially rejected due to unfounded conspiracy theories, Reuters reported.

Our institutions held in late 2020 and early 2021 because enough people of integrity were in positions to refuse to go along with illegal schemes to overturn election results. Now there are fewer people of integrity left in gatekeeper positions. Some left amid threats and intimidation.

Rep. Adam Kinzinger, R-Ill., listens Tuesday as the House select committee investigating the Jan. 6 attack on the U.S. Capitol continues to reveal its findings of a year-long investigation. (AP Photo/Jacquelyn Martin/AP)

Twice-weekly

News updates from the south suburbs delivered every Monday and Wednesday

Kinzinger on Sunday shared a letter he received at his home in Channahon. The writer threatened to execute the congressman, his wife and their 5-month-old child because of the Republicans efforts to uphold democracy.

The Darkness is spreading courtesy of cowardly leaders fearful of truth, Kinzinger wrote on Twitter. The threats Ive gotten dont scare me. They make me more determined.

Many are concerned insurrectionists will try again in 2024 to overturn election results if they disagree with the outcome. Evidence of the ongoing plot to destroy our democracy ought to strengthen the resolve of every American to vote and exercise their rights.

The battle for American democracy reminds me of The Skin of Our Teeth, a 1942 play by Thornton Wilder. We have always faced existential threats, and have barely survived many of them. Fascism, nuclear war and economic collapse, to name a few.

Somehow weve pulled through, sometimes by razor-thin margins. Whatever the future holds, I expect it will be close. A few votes here and there could make a world of difference.

Ted Slowik is a columnist for the Daily Southtown.

tslowik@tribpub.com

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Sightsavers relaunches its thematic strategy The Sun Nigeria – Daily Sun

June 26th, 2022 2:09 am

From Charity Nwakaudu, Abuja

In its global fight against poverty and avoidable blindness, an international organization, Sightsavers, has relaunced its thematic strategy to ensure that it reaches out to those affected and support their overall health system.

Speaking in Abuja, NIgeria, Country Director Sightsavers , Dr Sunday Ishiyaku stated that as part of strategies towards achieving its goals, the organization has developed capacities by making investments in growth and learning to ensure that there are adequate resources to tackling a wide range of complex diseases more innovatively and strategically premised on system strengthening to drive sustainability.

Ishiyaku noted that the strategy was conceived as a five- year framework with four major change theme such as Health, Education, Social inclusion, Community participation and development as well as eye health programmed.

He said that as an organization, it was working hard to prevent unavoidable blindness whilst also ensuring that those with disabilities participate equally in the Society.

We are a global organization working in more than 30 countries in African and Asian continents to prevent avoidable blindness whilst ensuring that those with disabilities participate equally in the society.

Sightsavers started out as an international service delivery- oriented charity and this was the case until 2009 when it transited into an international development organization requiring that it looked at tackling a wide range of complex diseases.

In the years covering the strategy (2009-2019), Sightsavers was committed to implementing its ambitious strategy that includes four major themes i.e eye health, education, social inclusion and community development and participation.

The Country Director explained that in the renewed global efforts to leave no one behind, Sightsavers also initiated the Sustainable Development Goals ( Agenda 2023), with the specific inclusion of an Neglected Tropical Diseases, NTD, target in SDG3.

Launching the Sightsavers thematic strategy virtually, Vice President, Board of Trustees, Sightsavers, Professor Uche Amazigo pointed out that its essence was to achieve the vision of a world where no one is blind from avoidable causes and where people with disabilities could participate equally in the society.

She that research has shown that there were almost 2 billion people suffering from blindness or partial impairment and Nigeria was with the highest number in this group hence the need for this alliance, adding that we should imagine a Nigeria with positive change in education, champions of Child Rights.

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Trachoma elimination: millions more to benefit from donated azithromycin – World Health Organization

June 26th, 2022 2:09 am

The World Health Organization (WHO) today welcomed the announcement by Pfizer Inc. that it will extend its donation of the antibiotic Zithromax (azithromycin) for trachoma elimination until 2030, building on the companys 23-year commitment to fight the worlds leading infectious cause of blindness.

Caused by repeated bacterial infection of the eyes, trachoma blinds the poorest people in the world. WHO recommends a four-part strategy to eliminate trachoma as a public health problem. This strategy takes the acronym SAFE, representing: surgery for advanced disease, antibiotics to clear infection, and facial cleanliness and environmental improvement (particularly increased access to water and sanitation) to reduce transmission. Pfizers Zithromax donation is a critical part of SAFE, and is managed by the International Trachoma Initiative at the Task Force for Global Health, Decatur (GA), USA, an organization in official relations with WHO.

Continuing the donation programme will bring relief to millions of people around the world who are affected by this preventable neglected tropical disease, said Dr Ren Minghui, WHOs Assistant Director-General for Universal Health Coverage/Communicable and Noncommunicable Diseases. WHO is very grateful for Pfizers ongoing commitment to helping prevent trachomatous blindness.

Caroline Roan, Senior Vice-President Global Health & Patient Impact, Pfizer Inc., commented, Trachoma is a debilitating disease that should no longer wreak havoc on peoples lives and livelihoods. We are proud to support our longstanding trachoma partners working tirelessly towards elimination and improving lives worldwide.

Between 2002 and 2021, due to a combination of SAFE strategy implementation, improved living conditions and better data, the estimated number of people living in trachoma-endemic areas worldwide fell 91% from 1517 million to 136 million. But over the past 2 years, the coronavirus disease (COVID-19) pandemic has limited the activity of programmes against neglected tropical diseases in many countries. Community-based work, such as antibiotic mass drug administration for trachoma, has been particularly adversely affected.

In the road map for neglected tropical diseases 20212030, endorsed by the World Health Assembly in November 2020, trachoma is targeted for global elimination as a public health problem by 2030. To date, 13 countries (Cambodia, China, the Islamic Republic of Iran, the Lao Peoples Democratic Republic, the Gambia, Ghana, Mexico, Morocco, Myanmar, Nepal, Oman, Saudi Arabia and Togo) have been validated as having achieved this milestone.

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Dangers of super gonorrhoea from infertility to blindness as global warning issued – Daily Star

June 26th, 2022 2:09 am

A new strain of super gonorrhoea has been reported after an Austrian man had unprotected sex with a Cambodian sex worker.

What makes this strain so worrying is that it is resistant to most antibiotics commonly used to treat the infection, scientists have warned.

Adding to this risk, experts have cited that if multidrug-resistant strains of gonorrhoea keep spreading, many cases of the STD might become untreatable.

This was highlighted in a study published recently in the medical journal Eurosurveillance, part of the European Centre for Disease Prevention and Control.

The disease is caused by the bacterium called Neisseria gonorrhoeae.

The infection is spread by unprotected vaginal, oral and anal sex.

Lead author of the report, Dr Sonja Pleininger of the Austrian Agency for Health and Food Safety, said such a strain poses a major global public health threat.

If such strains manage to establish a sustained transmission, many gonorrhoea cases might become untreatable, she added.

The unidentified Austrian man in his 50s complained of unusual symptoms five days after his sexual encounter.

His symptoms reported included pain while peeing and a discharge coming out of his penis.

The man was initially treated with azithromycin and ceftriaxone.

Two weeks later, his symptoms resolved, but a penile swab showed he still had gonorrhoea.

Tests showed his "super" bug was still immune to treatment.

Typical symptoms of gonorrhoea include a thick green or yellow discharge from the vagina or penis, pain when peeing and, in women, bleeding between periods, warns the NHS.

The national health body added: But around one in 10 infected men and almost half of infected women do not experience any symptoms.

The bacteria that cause gonorrhoea are mainly found in discharge from the penis and in vaginal fluid.

In women, it can lead to pelvic inflammatory disease, which could cause problems with fertility and future pregnancy.

It may also increase the risk of ectopic pregnancy, a medical emergency.

Gonorrhoea can also increase the risk of transmitting or acquiring HIV.

According to Dr Teodara Wi, World Health Organisations (WHO) medical officer specialising in STIs, other serious risks of super gonorrhoea include:

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The Week That Was: All of Lawfare in One Post – Lawfare – Lawfare

June 26th, 2022 2:09 am

Jen Patja Howell shared an episode of the Lawfare Podcast in which Benjamin Wittes Wittes sat down on Twitter Spaces with Roger Parloff, Quinta Jurecic, and Molly Reynolds to discuss day four of the Jan. 6 committee hearings:

She alsoshared an episode of the Lawfare Podcast in which Wittes talked with Jurecic, Parloff, and Katie Benner of the New York Times about day five of the Jan. 6 select committee hearings:

Pollard shared a livestream of day four of the Jan. 6 select committee hearings. He also shared a livestream of day five of the Jan. 6 select committee hearings.

Elena Kagan shared an episode of Lawfare No Bull which features audio from the fourth public hearing held by the Jan. 6 select committee:

Bob Bauer argued that presidents seeking reelection can pose unique challenges to democratic elections in situations in which their desire to win can lead to disastrous results.

Daniel Richman discussed the role that the doctrine of willful blindness might have in proving Trumps criminal liability if a case were brought against the former president for his role in the Jan. 6 Capitol attack.

David Priess shared an episode of Chatter in which Shane Harris sat down with Tim Naftali to discuss the legacy of Watergate in light of the Jan. 6 Capitol attack:

Howell shared an episode of the Lawfare Podcast from the November 2020 archives in which Evelyn Douek and Jurecic sat down with Alex Stamos to discuss the state of election security and the difficulty of countering false election claims:

Robert Chesney and Steve Vladeck shared an episode of the National Security Law Podcast in which they discussed the latest Jan. 6 conspiracy indictment, the Navarro contempt of Congress charge, the lawsuits challenging the Texas and Florida social media content-moderation laws, and more:

Stewart Baker shared an episode of the Cyberlaw Podcast in which he sat down with Amy Gajda to discuss her book, Seek and Hide: The Tangled History of the Right to Privacy:

Baker shared another episode of the Cyberlaw Podcast in which he sat down with Matthew Heiman, Scott Shapiro, and Nick Weaver to discuss the bipartisan effort to transform the Committee on Foreign Investment in the United States, cryptocurrency firms on the verge of collapse, TikTok, and more:

Herb Lin discussed the functional trade-offs in baked-in cybersecurity in product management.

Susan Landau argued that the EU proposal on combating child sexual abuse material online could present national security problems and relies on technology that does not exist yet.

Steve Bunnell reviewed James E. Bakers The Centaurs Dilemma: National Security Law for the Coming AI Revolution (Brookings Institution, 2020).

Howell shared an episode of the Lawfare Podcast in which Wittes sat down with Asfandyar Mir and Daniel Byman to discuss the current position of al-Qaeda in the world:

Howell also shared an episode of Rational Security in which Alan Rozenshtein, Jurecic, and Scott R. Anderson sat down to discuss the extradition of Julian Assange, Chinese access to TikTok customer data, and Googles potentially sentient LaMDA artificial intelligence program:

Jordan Schneider shared an episode of ChinaTalk in which he sat down with Weijian Shan to discuss Shans personal story of exile during the Cultural Revolution and his view on Chinas economic transformation:

Anoush Baghdassarian analyzed recent cases from the International Court of Justice that Armenia and Azerbaijan each brought against one other for alleged violations of the International Convention on the Elimination of All Forms of Racial Discrimination.

Max Johnston and Bryce Klehm shared the final episode of Allies, which they discuss the uncertain long-term legal status of Mahnaz, a former member of the Afghan militarys Female Tactical Platoon, and other Afghans who are on parole after coming to the U.S. during the U.S.s withdrawal from Afghanistan:

Matthew Tokson discussed what a recent ruling from the First Circuit means for Fourth Amendment cases concerning the use of telephone pole cameras for surveillance purposes.

Kyleanne Hunter discussed the potential impacts that overturning Roe v. Wade would have on women in uniform.

And Hyemin Han and Katherine Pompilio shared an application for the fall 2022 Lawfare internship.

And that was the week that was.

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How The SMH Got That Rebel Wilson Story So Wrong – Junkee

June 26th, 2022 2:09 am

How the illusion of a post-queer society let actor Rebel Wilson down.

Its been nearly two weeks since we heard the Sydney Morning Herald had a hand in making the actor Rebel Wilson reveal she was dating another woman.But as the news cycle swiftly barrels on, there are questions that continue to linger.

Namely, how could reporter Andrew Hornery and editor Bevan Shields who are both gay not understand that threatening to reveal a celebritys first same-sex relationship is an inherently harmful idea? How could they have been so blind?

Thats the theme that kept sticking out to me: sustained, wilful blindness. Blindness to the fact that we continue to inhabit a culture where queer people are marginalised, regardless of how many legal gains may have been made.

As both Hornery and Shields pushed out their articles over the weekend, at first furiously agreeing with each other before conceding that some harm may have been done, there was a common through-line: Both went out of their way to use non-gendered language. Rebel was simply in a new relationship; Ramona Agruma was her new partner, they were simply trying to break the news of this celebrity romance.

Both men seemed desperate to ignore the elephant in the room Rebel Wilson, an actress who most people know as straight, was in a same-sex relationship. And Hornerys email, regardless of what he intended, threatened to out her.

I couldnt help but be reminded of the problem of colour-blindness; the people who insist they dont see race, a narrative captured in the platitude, theres only one race, the human race. Its this same spirit that permeated the Sydney Morning Heralds recent festival of cluelessness, but this time, it wasnt colour blindness, but its LGBTIQ analogue: queer blindfolding.

In the way that colour-blindness perpetuates racism by denying the existence of white privilege, queer blindfolding is the process of perpetuating homophobia by not acknowledging it exists. The concept was coined by US researchers Richard Shin and Lance Smith, who define it as well-intentioned heterosexual identifying individuals that results in the disappearing of queer identities. And while straight people probably thinks that theyre doing a good thing by ignoring a persons sexuality were all just people, are we not? the narrative comes with pernicious consequences.

Namely, adopting the ideology of queer blindfolding can result in minimising or even denying the marginalisation that is experienced by those who identify as queer. And in my opinion, it is this wilfully blind way of looking at the world that has contributed to the Sydney Morning Heraldunknowingly threatening Wilson with an ultimatum.

Both Andrew Hornery and Bevan Shields used language that indicated that they were fans of this school of thought. Consider the following turns of phrase: [We] asked Wilson if she wished to comment about her new partner, wrote Bevan Shields in his initial supportive response to Andrew Hornerys first article. We would have asked the same questions had Wilsons new partner been a man.

Similarly, in Hornerys (now deleted) initial article, he was at a loss as to why a woman who previously used to brag about her handsome ex-boyfriend wouldnt do the same with her same girlfriend. Of course, who anyone dates is their business, but Wilson happily fed such prurient interest when she had a hunky boyfriend on her arm, he adds.

Here, both Shields and Hornery are taking the bizarre stance that when youre a woman, having a girlfriend is equally as socially acceptable as having a boyfriend.

And that, in a nutshell, is clear blindfolding: wilfully ignoring the heterosexism that we swim in every day.

While Shin and Smith point out that heterosexual attitudes toward LGBTIQ folks are generally improving, were not exactly in some post-gay utopia. Heterosexuality is obviously the dominant sexual orientation in our culture. Take, for example, the fact that most love stories in our culture involve cis-gendered men and cis-gendered women; the fact that we assume people are straight by default; and that a fear of abuse still means that many queer people hide their sexuality at work.

Or the teacher who was sacked because of their sexuality in 2021, or the constant targeting of trans peopleduring the lead-up to the federal election. Or the current horrendous discourse around trans participation in elite swimming. Just the simple fact that straight people dont need to come out tells you that straight people and queer people are obviously not on a level playing field.

And yet, we get Hornery coming out with the astonishing take that thanks to decades of battling for equality sexual orientation is no longer something to be hidden, even in Hollywood, adding that same-sex marriage is legal in many parts of the world, as though Wilson, by not publicly coming out to the entire world right away, is being overly dramatic or creating a problem that isnt there.

They are. Both reporter Andrew Hornery and editor Bevan Shields identify as gay men. But while Shin and Smith say that its heterosexual identifying people who are prone to queer blindfolding, queer folks arent immune to taking on the same.

In particular, studies have found its not uncommon for gay men who are white, cis-gendered, and affluent to use queer blindfolding as a narrative strategy. Those who inhabit other marginalised identities, though queer women of colour, for example tend to consider their queerness within the context of a matrix of domination. As such, people like Shields and Hornery may not realise that queerness in other bodies unlike theirs has different implications.

Thats where the importance ofintersectionality comes in a concept that describes the way that systems of inequality based on gender, race, ethnicity, sexual orientation, gender identity, disability, class and other forms of discrimination intersect to create unique dynamics and effects. While Rebel is white, she deals with the added marginalisation of being a woman plus, shes dealt with fatphobia in the past.

The reason that Hornery and Shields went so wrong with Rebel Wilson is simple: they assumed that homophobia was an artefact of the past. In doing so, they ended up causing harm to a person who, like everyone, has a right to come out on her own terms.

Weve heard little from Rebel Wilson herself about the situation, but she wrote on Twitter that it was a very hard situation and she was trying to handle it with grace. But she never should have had to deal with this in the first place, with grace or otherwise.

Perhaps the current trend of epistemic deference has something to do with this: the idea that people who inhabit the same marginalised identities have each others back. But like white supremacy, which no longer needs white people for it to function, weve seen that homophobia, too it no longer requires straight folks to thrive.

Reena Gupta is Junkees culture writer. Follow her on Twitter.

Photo Credit: Future Publishing, Getty Images

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Fifty years of Title IX: What is it, what does it cover and do we still need it? – The Athletic

June 26th, 2022 2:09 am

On June 23, 1972, President Richard Nixon signed the Education Amendments of 1972 into law. Title IX of those amendments, which spanned sections 1681-1688, covered key protections for students in education programs: discrimination based on sex or blindness.

Fifty years later, that protection has become popularly known as Title IX: No person in the United States shall, on the basis of sex, be excluded from participation in, be denied the benefits of, or be subjected to discrimination under any education program or activity receiving Federal financial assistance.

Its a law that youve certainly heard referenced most often when talking about womens college sports but how did it come to be? What does it actually cover? And what does its future look like? Heres what you need to know about Title IX.

Title IX was a follow-up to the Civil Rights Act of 1964, which was enacted to end discrimination based on race, color, religion, sex or national origin in regard to employment and public accommodation. But when it came to the college classroom, significant gaps remained.

Eight years after that landmark 1964 Act, the Title IX portion of the 1972 amendments sought to expand those protections by focusing on educational funding.

Today, I am signing into law the Education Amendments of 1972, President Nixon said. This legislation includes comprehensive higher education provisions, authority for a new effort to revitalize our educational research effort and authority to provide financial assistance to school districts to meet special problems incident to desegregation.

Before Nixon signed the 1972 amendments, the college sports landscape was dominated by men. The NCAA was founded in 1906 to govern college football before gradually growing as a discussion group and rules committee for a plethora of sports.

By 1972, 200,000 athletes were competing in college sports. Just 30,000 of them were women.

Athletic scholarships were virtually nonexistent for women and no national championships were held for womens teams. According to the History Channel, just 2 percent of college athletic budgets went toward women athletes.

Off the field, women were discriminated against in the classroom as well. Many universities barred women from attending while many others offered male-only classes, which ranged from criminal justice to wood shop.

NCAA data from 2016 shows the gender disparity in college athletes has shrunk dramatically in the 50 years since Title IXs inception. Of the 486,859 athletes who participated in college sports, 211,886 were women. Additionally, women received 45 percent of the total athletic scholarship dollars at DI schools in 2016.

The law has also done far more than increase the size of the scholarship slice. The historic 1980 Alexander v. Yale case was the first to use Title IX in charges of sexual harassment against an educational institution. Title IX has also been credited with helping increase the number of women who pursue higher education.

And from 2010 to 2016, the Obama administration expanded the protection of Title IX to protect transgender students from gender discrimination.

However, Title IX advocates argue there is still significant progress to be made. While the participation gap has narrowed, data shows the opportunity gap remains. Despite Title IXs intention for women to receive opportunities proportionate to the schools enrollment, a report from the Womens Sports Foundation found that 86 percent of colleges are offering a disproportionate number of athletic opportunities to men compared to their enrollment. They argue that this resulted in 60,000 missed opportunities for women athletes.

We should absolutely celebrate the fact that girls participation in high school sports is nearly 12 times higher than it was when Title IX was passed, but we cannot rest on it, WSF founder Billie Jean King said. The mere existence of Title IX does not ensure equal opportunities unless it is enforced for everyone, particularly among girls and women of color, those with disabilities and the LGBTQ+ community where the gap is consistently the widest.

While the answer may be clear that Title IX was effective for most of its initial intentions, many have debated in recent years if our structure of collegiate athletics has outgrown the now-50-year-old law. Some have proposed that the future of college sports may need a revamped Title IX to scale with the ever-changing landscape of the industry.

One such change has been the recent opportunity for college athletes to profit off their name, image and likeness (NIL). Some have argued that NIL legislation and Title IX protections are on a collision course that the 1972 law never could have imagined.

The stakes are high; the potential for making money is huge. Here is the issue: As soon as a university, its employees, or its booster clubs play any role in helping athletes earn money or make deals, the school is necessarily providing a benefit to them, attorneys Arthur Bryant and Cary Joshi wrote for Sportico. And Title IX requires that male and female athletes be treated equally. If the university arranges or offers deals for men and not women, or vice versa, it has trouble under the law.

However, while changes like NIL will continue to shift the college sports world every few years, the now-50-year-old law has proven to provide much-needed protections for who will be impacted by those changes. Regardless of what the next 50 years bring, no one can deny that Title IX has left an undeniable imprint on the college sports landscape, for the betterment of millions of women athletes.

(Top photo: Andrew Wevers / USA TODAY Sports)

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Why Brad Pitt quit smoking and drinking altogether during the pandemic – BusinessGhana

June 26th, 2022 2:09 am

It's Brad Pitts world and were all just living in it!

The superstar actor and producer, 58, recently opened up about life, art and everything in between in a new interview with GQ, during which he explained how hes been pretty much hiding out in his Los Angeles home for much of the pandemic and how hes used that time to quit smoking and drinking altogether.

While chewing a nicotine mint, Pitt explained that he quit smoking cigarettes during the pandemic after realizing he didn't have it in him to simply "cut back."

I dont have that ability to do just one or two a day, he explained. Its not in my makeup. Im all in. And Im going to drive into the ground. Ive lost my privileges.

The actor went on to explain that after his ex, Angelina Jolie, filed for divorce in 2016, he got sober and spent a year and a half attending Alcoholics Anonymous though, given his star status, has had to make adjustments for the sake of maintaining his privacy.

I had a really cool mens group here that was really private and selective, so it was safe, he said. Because Id seen things of other people who had been recorded while they were spilling their guts, and thats just atrocious to me.

Pitt shares six kids with Jolie: Maddox, 20; Pax, 18; Zahara, 17; Shiloh, 16; and twins Vivienne, and Knox, 13. Jolie had adopted Maddox and Zahara before her relationship with Pitt (he later adopted them both as well).

Still, while he cherishes old memories of smoking a cigarette in the morning, with the coffee just delicious," he also knows his body cant handle it the same way others can, like, say, the British painter David Hockney. Hes still chaining, the hard-core English way. It looks great, Pitt says of Hockney. I dont think I have that. Im just at that age when nothing good comes from it.

The actor also spoke candidly about his struggle to remember new people and to recognize their faces, which has been a hindrance his entire adult life especially at parties.

Pitt believes he may suffer from prosopagnosia, an inability to recognize peoples faces (otherwise known as face blindness). Though he wants to remember the people he meets and hes ashamed he cant above all, he fears the condition has led people to assume hes remote or aloof or self-absorbed.

Nobody believes me! he said.

As for finding solace, the actor says he always finds it in art and music. "Im one of those creatures that speaks through art. I just want to always make. If Im not making, Im dying in some way."

Music fills me with so much joy," he continued. "I think joys been a newer discovery, later in life. I was always moving with the currents, drifting in a way, and onto the next. I think I spent years with a low-grade depression, and its not until coming to terms with that, trying to embrace all sides of self the beauty and the ugly that Ive been able to catch those moments of joy.

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Watch your eye – The New Indian Express

June 26th, 2022 2:09 am

Express News Service

HYDERABAD: The recent spell of rain has brought respite after months of scorching heat. But these rains bring about a rise in humidity, meaning, higher chances of eye infection.Our eyes are one of the most sensitive yet ignored parts of our body. And unfortunately, the rainy season can make us susceptible to eye infections. Explaining why, Dr Deepthi, consultant ophthalmologist and retina specialist at Care Hospitals, HITEC City, says, The moisture content in the air creates a favourable condition for bacteria, viruses and other germs to grow and multiply, especially in your eyes.

The doctor names conjunctivitis as one of the most common eye infections during the monsoon. Some of the common symptoms of conjunctivitis include redness of the eye, swelling, yellow sticky discharge from the eyes, and itching, associated with pain. Fortunately, it is an easily treatable eye problem. Proper eye care should become a priority during monsoons to help protect from infections like conjunctivitis, dry eyes and corneal ulcers which can lead to blindness. Commonly known as pink eye, the infection can be easily spread from one person to another by touch, she informs.

Other common eye infections during the monsoon include keratitis and trachoma. This infection of the cornea caused by injury to the eyes, due to routine of contact lenses. If left unattended, the infection can even lead to blindness, the Dr Deepthi warns.

Trachoma is a bacterial infection responsible for blindness in almost 1.9 million people across the globe! This irreversible blindness can be caused through direct touch or towels and flies that have come in contact with the eyes or nose of an infected person. So it calls for more care than one might think, the doctor shares.

Dr Aparna Saripalli, general physician, Ankura Hospital, Boduppal, says, Kids should avoid touching or rubbing the eyes. Infections spread faster commonly touched items.

Keep infectionsat bay:

Dr Swapna, ophthalmologist, Care Hospitals, Nampally

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Olivia Brouwer’s art is for everyone to see and touch – Hamilton Spectator

June 26th, 2022 2:09 am

A Hamilton artist wants you to forget about the no touching rule. The Scales That Fall From Our Eyes at Centre [3] goes against the formalities of an art gallery and invites visitors to experience it through touch and sound.

Olivia Brouwer, 27, is a partially blind artist aiming to bring accessible art to the visually impaired community. With abstract visuals and Braille language exhibits, Brouwer addresses her disability with tactile paintings and challenges the idea that art does not need to be touched in order to be felt.

I am partially blind in one eye and so I wanted to discuss that in my work and become more confident in myself by doing that, said Brouwer.

The exhibit brings a series of conversations with Brouwers friends Tim Peters, Eric Bourgeois and Jesse Hannigan about the meaning of blindness and colour blindness in their lives while raising awareness of the inclusivity and accessibility needed for the visually impaired.

I interviewed each of them individually, questioning how they would describe their perception of the world through the lens of their experience of blindness in a positive light, but also allowing them to express challenges associated with their form of blindness, said Brouwer.

Each conversation is translated into Braille and painted on a tactile canvas with acrylic paint. Visitors can also listen to the interviews with headphones activated by touching a conduit paint on the wall.

This is the first time Im showing work that is tactile. It will be interesting to see how people respond to it just as we come out of the pandemic. People can grab some gloves available to touch the pieces if theyre not comfortable, said Brouwer.

Inspired and influenced by Christianity, The Scales That Fall From Our Eyes visuals portray Brouwers interpretation of the Biblical story of Saul. He was a Jewish leader who persecuted Christians, and became blind for three days because of that. When he realized what he was doing wrong, the blindness spell fell like scales from his eyes.

According to Brouwer, the story of Saul represents the change that takes place when prejudiced barriers are removed, contributing to justice and inclusivity for minorities.

I like this kind of metaphor for realizing whats wrong in the world and releasing those scales and bringing clarity to what we need to change. Justice needs to happen, accessibility needs to be implemented not just to art galleries, she said.

Even though she brought her Christian faith to the exhibits title and concept, there was a moment of hesitancy throughout the creation process due to fear of negative feedback.

It was a bit confusing for me, so I stepped away from it for a while. I have a hard time bringing it into my art because I didnt want it to be evangelical, Brouwer said. I think the story of Saul will come into my work in the future. Theres a lot of stories in the Bible that talk about blindness and healing, but I think its more about how everybody sees what needs to change, what accessibility there is.

In March 2020, Brouwer was selected to participate in a three month long Emerging Artist Residency at Centre [3] which has extended until this year because of the pandemic. During the residency, Brouwer started a CONTACT kit which introduces Braille decoding to sighted viewers with the goal of bringing awareness to visually impaired folks.

The kit contains a tactile painting, an embossed booklet, interactive Braille pieces to read and decode, and a Braille translation of the English text describing the instructions and meaning of the project. The idea of the kit kind of kick started the work that Im doing now. How can we give voices to these minority groups? With the pandemic, blind people are very limited to touching things.

Brouwer, a Bachelor of Fine Arts at the University of Toronto and Sheridan College grew up in a creative family filled with illustrators and woodworkers who gave her space and incentive to follow a career in the arts. However, the artist struggled to understand who she was as an artist and accept her disability.

In high school, I was always self-conscious about it. In university, I was trying to figure out what I wanted to say and who I was as an artist. I think being partially blind is part of who I am. Its important for me to put that into my artwork, especially because art is mostly visual, said Brouwer.

The Scales That Fall From Our Eyes will run until July 2 at Centre [3], a not-for-profit, charitable artist-run centre on 173 James St N.

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Monkeypox may not mutate as fast as coronaviruses, but that doesn’t mean it can’t adapt to its new hosts – The Conversation

June 26th, 2022 2:09 am

The recent outbreak of monkeypox virus has called into question the capabilities of these kinds large DNA viruses to evolve, adapt and change their biology.

Compared with small RNA viruses such as coronavirus, monkeypox virus and other large DNA viruses are thought to evolve slowly. Yet theres clear evidence that this really isnt a hindrance to these viruses. In fact, they can adapt to new environments like us.

Although most infections remain mild, monkeypox can be a serious life-threatening disease, resulting in sepsis, encephalitis (brain inflammation) and blindness. The most common symptoms are rash and skin lesions, alongside flu-like symptoms and swollen lymph nodes.

Cumulative monkeypox cases in current outbreak

Monkeypox virus naturally infects wild rodents, such as squirrels and rats, in west and central Africa but it can jump species into humans and other animals. However, once it has jumped to humans, it cannot keep transmission going and eventually outbreaks die out. This is probably because monkeypox has not adapted itself to its new environment of humans, as spillback into wild rodents from infected humans is unlikely.

Monkeypox is closely related to the viruses that caused smallpox (variola viruses) and the virus that we use to vaccinate and eradicate smallpox (vaccinia virus). This group of viruses, referred to as poxviruses, are a kind of large DNA virus, meaning that their genome is composed of a chemical known as DNA, like our genome. (Coronavirus and related viruses use a cousin molecule called RNA.)

Other DNA viruses are the large DNA viruses adenoviruses and herpesviruses, but also small ones like papillomaviruses and parvoviruses. The viral genomes composed of either DNA or RNA essentially are the instructions to make new viruses, infect us and cause disease. Changes to the instructions can change virus biology.

As we have seen with SARS-CoV-2 and its variants, viruses can change how they behave with regards to spreading, disease severity and vaccine sensitivity. This is because of changes accumulating in the virus genome. Virus replication generates diversity in its genome, which can be acted on by evolutionary forces such as natural selection, to increase in frequency and maybe even out-compete older versions.

Evolutionary changes can occur when the virus encounters a new environment that it is not fully adapted to. Although all viruses can evolve rapidly due to their vast population sizes and rapid generation times, RNA viruses are thought to be masters of evolution because they have high mutation rates due to their small size, and many often lack error-correcting ability meaning more mutations occur every time they replicate.

Poxviruses have some characteristics that make them more generalist, including stable infectious particles, giving them more chances to infect. They use very common molecules on your cells to gain entry and infect, unlike SARS-CoV-2 which needs the specific ACE2 protein to gain entry to our cells.

Large DNA viruses such as monkeypox also contain lots of genes that target and manipulate different parts of the immune system.

However, theres clear evidence that improvements can be made, because, in humans, monkeypox transmission is relatively inefficient, with long incubation periods.

In general, large DNA viruses such as monkeypox are no different from other viruses, and their mutability is the basis for our ability to track and trace monkeypox outbreaks. They make mistakes and errors accumulate, which can be used as fuel for evolution and biological changes. Theres even evidence from the recent monkeypox outbreak that the host cell is directly mutating the virus genome.

Studies focusing on related poxviruses like the vaccinia virus have even uncovered new tricks they can use, which include rapidly amplifying the number of genes they use to attack our immune system. They could even borrow some of our own genes to help them infect us.

We cant predict the trajectory that monkeypox evolution will take, so we must take the threat of this virus adapting to its new hosts (humans) seriously. And we need to use all the public health tools at our disposal to halt the current outbreak in all countries including those where it is endemic.

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Monkeypox may not mutate as fast as coronaviruses, but that doesn't mean it can't adapt to its new hosts - The Conversation

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Former American Express Foundation President Takes Helm of Signature Theatre – The Chronicle of Philanthropy

June 26th, 2022 2:09 am

Signature Theatre

Timothy McClimon, interim executive director for the past six months, will continue in the role permanently.

Before joining the Off-Broadway nonprofit theater, he was president of the American Express Foundation and senior vice president of corporate social responsibility at the American Express Company from 2006 until 2021.

Jason Menzo has been promoted from president and chief operating officer to CEO of the $181 million foundation. He succeeds Ben Yerxa, who has led the foundation since 2017 and will now become CEO of Opus Genetics.

In addition, Russell Kelley has been promoted to managing director of the Retinal Degeneration Fund, the foundations venture arm. Most recently he was the funds senior vice president of investments and alliances.

Gary Ginstling, executive director of the National Symphony Orchestra, will start as its executive director on November 1. He will then become president and CEO of the New York performing-arts group on June 30, 2023.

Ginstling will replace Deborah Borda, who will remain with the orchestra as executive adviser to the president and Board of Directors, beginning next summer.

Tom Cotter, director of emergency response and preparedness at Project HOPE, has been appointed executive director of Healthcare Ready.

Marisa Rohn will be the next president of the Sisters of Charity Foundation of Canton. Most recently she was vice president of advancement, human resources, and partnerships at Stark State College and executive director of the Stark State College Foundation.

Renee Archawski is now managing director of development at Caring for Friends. Most recently she was managing director of development and interim executive director of Teach for America Metro Atlanta, and a development coach for the education organizations national team.

Selena Deckelmann will become chief product and technology officer at the Wikimedia Foundation on August 1. She is currently senior vice president at Mozilla, where she oversees its Firefox web browser.

Paul Dien, head of strategic partnerships for Good and Upworthy, has joined the Grammy Museum as vice president of advancement and partnerships.

Anupa Fabian, evaluation manager at Catholic Charities Brooklyn and Queens, is joining the Mother Cabrini Health Foundation as its first chief evaluation and learning officer. She succeeds Daniel Frascella, who was promoted from managing director for programs and grants to chief programs and grants officer.

Anedra Kerr, a senior consulting associate at the Morten Group, will now serve as vice president of development at the Jeremiah Program.

Otis Kollie has joined the Global Fund for Children as a program specialist for Africa and Asia. Previously he was assistant project coordinator at Lifewater Liberia.

Judy Nagai has joined the University of Hawaii Foundation as senior executive director of campaign planning. She most recently worked at the University of the Pacific as associate vice president for development.

Brian Siegel, senior vice president of global arts and culture at Bank of America, has been promoted to global arts and heritage executive.

Oren Etzioni, founding CEO of the Allen Institute for AI, will step down on September 30 after leading the artificial-intelligence group for nine years. He will become technical director of the AI2 Incubator.

Send an email to people@philanthropy.com.

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Junk Science Week: Net-Zero Edition John Constable & Debra Lieberman: The energy of nations and the creation of wealth – Financial Post

June 26th, 2022 2:09 am

Breadcrumb Trail Links

Faltering or falling energy consumption, particularly electricity, is not an indication of a healthy economy

Since 2007, something historically unprecedented has been happening in most Western economies energy consumption is in a nosedive.

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U.K. energy use has fallen by 30 per cent to quantities not seen since the 1950s, while the rest of Europe has regressed 30 years to 1990s levels. The U.S. is following suit. Whereas total energy consumption had been flatlining, it then fell 13 per cent by 2020, approaching levels not seen since the mid-1990s. A subsequent post-covid increase gives one hope but may not reverse the trend.. This downward spiral also holds for electricity usage, the very index of a modern society, with the U.K. dropping over the past decade to levels last seen in the 1970s. The Canadian case is less dramatic but still concerning: both total energy and electricity consumption have flatlined over this period, and since 2018 have begun to decline.

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Faltering or falling energy consumption, particularly electricity, is not an indication of a healthy economy. You might think otherwise its evidence of increased efficiency, right? For some individual consumers, in the short run, potentially, yes. For society as a whole, in the longer run, emphatically not. As a rule, gains in efficiency will increase demand for the now cheaper goods or services, or save energy for another purpose, so total consumption rises. Savings from LEDs, for example, will first be translated into more lighting. (Who knew a lit driveway looked so pretty?) And when that demand becomes satisfied it will be spent on vacations, better health care, and education, and further out in the economic system on roads or defence. Like cash, energy is never left on the table, and given its availability, there is no limit to possible improvements in human well-being. Put simply, efficiency fuels welfare-enhancing consumption.

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Energy demand is falling because of environmental policies, including subsidies to modern renewables such as wind and solar. As distasteful as this might sound, it is nonetheless true. So far, both the U.S. and Canada are relatively minor players, the U.S. having spent a mere US$125 billion between 2008-2018, and while Canadian national totals are lower, the province of Ontario alone is reported to have spent about US$30 billion in the period 2006 to 2014. But the EU, where the biggest energy collapse is observed, has spent a staggering US$800 billion since 2008, a total that has been increasing at $US70 billion a year. And the U.K., a country of 65 million people, is shelling out well over US$10 billion every year.

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The intention of these subsidies was to reduce costs, but the gamble has not paid off nor will it so long as Mother Nature and her laws of physics are at the table. Wind and solar remain stubbornly expensive for consumers in spite of a blizzard of misinformation and propaganda claiming otherwise.

How did we get here? The answer lies in our intuitive understanding of energy itself. The human mind contains programs enabling us to reason about survival-dependent concepts mating, food, co-operation. The physics of energy is not such a concept. Without science we lack the lens to focus effectively on energy, leaving us more or less energy-blind. Energy is a strange concept in the strict scientific sense it isnt a substance, such as coal or oil, but instead an abstract property of all substances, namely the capacity to cause change in the world, to do work.

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Moreover, energy varies in quality, not just quantity. To support complex society a fuel must be of high quality, that is, structured so that it has the potential to do a lot of work. In thermodynamics, this is referred to as a fuels degree of disorder or entropy. Greater disorder equals greater entropy equals less work. But our energy-blindness, the inability to easily grasp thermodynamic principles, means that we must rely on physics to see and what it reveals is that fossil fuels and uranium are highly ordered and rich in their potential to do work, making them cheap, while wind and solar are the reverse.

In fact, to render wind and solar functional requires much additional work and resources, both often supplied by fossils. Transforming renewables into useable grid electricity relies on turbines and photovoltaic panels, themselves complex and expensive states of matter, to say nothing of the management costs of buffering the electricity system against their variability.

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The sunshine and wind might be free, but their extraction, conversion, and delivery to market are not. If you are concerned about carbon dioxide emissions, as we are, then it is critical to acknowledge our energy-blindness and follow the physics: fossil fuels are the necessary bridge to a nuclear-based, low-carbon future. The optics of wind and solar are superficially attractive but their promise of a green, low-carbon nirvana is empty. But dont blame us, blame Mother Nature.

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At stake are the creation and maintenance of wealth. The availability of high-quality energy created the tools and technologies that make human lives healthier, longer, and more fulfilling. Mortality rates, particularly for children, are extraordinarily low by historical standards. Many people in the world today, not just the richest, have temperature control in their homes, low levels of pathogens in their food supplies, transport essentially at will, phones, and access to vast information-storage systems. These highly improbable states exist only by virtue of the work done by energy-dense fuels such as fossils and nuclear.

By spending heavily on wind and solar, world leaders are degrading the quality and productivity of national energy supplies, causing rising costs and falling consumption. The causal linkage is on display across the West. This will damage not just the ability to create new wealth, but also to maintain a complex, pleasant and secure environment in which to live and raise our families, and this damage is already happening.

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Before you dismiss us as Chicken Littles screaming that the sky is falling (though we are and it is), we grant that the world currently looks far from dystopian. Countries where energy consumption is plummeting dont feel much pain yet. And there is a good reason for that. One country is increasing its energy use, propping up Western consumption with exports and giving us a false sense of well-being. That country is, of course, China.

Since the West began its energy starvation diet, Chinese energy consumption has increased by over 50 per cent and its electricity consumption has increased by 200 per cent, overtaking the U.S. by a large margin. China, unlike the EU, U.K. and U.S., is still 90 per cent reliant on fossil fuels and nuclear. Whats more, only some of the immense wealth these fuels are generating is being exported. What is China doing with the rest? Time will tell.

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But right now, as a matter of urgency, we must reverse the decline in Western energy quality and consumption by ending impoverishing renewable subsidies and clearing the path for fossil fuels and nuclear. Toying with low-density, thermodynamically incompetent renewables is an indulgence we cannot afford. With the Chinese economy on an energetically sound footing and those in the West not, the world has turned upside down. The economic consequences of this reversal are serious, the security implications terrifying. Our energy blindness is both costly and dangerous.

JohnConstable is energy director of the Global Warming Policy Foundation in London and author of its forthcomingstudyEuropesGreen Experiment: A costly failure in unilateral climate policy.Debra Lieberman is a professor of psychology at the University of Miami and author ofObjection: Disgust, Morality, and the Law(OUP, 2018).

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Ancient Art and Genetics Reveal Origin of World’s Most Expensive Spice – The Wire Science

June 26th, 2022 2:08 am

A spoon of saffron derived from the flower of Crocus sativus. Photo: Salonik Saffron/Wikimedia Commons, CC BY-SA 4.0

Saffron, the worlds most expensive spice, is extracted from the flowers of the saffron crocus, Crocus sativus. It has been grown for thousands of years in the Mediterranean region. But when and where was saffron first domesticated by our ancestors? In a review in Frontiers in Plant Science, researchers conclude that lines of evidence from ancient art and genetics converge on the same region.

Both ancient artworks and genetics point to Bronze Age Greece, in approximately 1700 BC or earlier, as the origin of saffrons domestication, said Ludwig Mann, one of the leading authors and a PhD student at Technische Universitt Dresden, Germany.

The genus Crocus, with approximately 250 species, ranges from South and Central Europe and North Africa to Western China. Unlike domesticated saffron, these species reproduce sexually in the wild. The first known use by humans of wild crocuses was as pigment for cave paintings, approximately 50,000 years ago in todays Iraq. Ancient texts from Sumer, Assyria and Babylonia also describe the use of wild crocuses in medicine and dye.

Asexually propagated by humans

In contrast, domesticated saffron doesnt grow in the wild, and can only be propagated asexually with human help, by dividing its underground corms stem-like storage organs. The process was first described by the Greek philosopher Theophrastus in the fourth to third century BC.

Today, domesticated saffron is grown around the globe, for use in cooking and perfumes and as a yellow dye. Between 15,000 and 16,000 flowers, requiring between 370 and 470 person-hours to collect, yield a single kilo, worth between $1,300 and $10,000.

Finding out where and when saffron was first domesticated isnt straightforward: the species is difficult to study genetically, because it has three copies of every chromosome instead of the usual two, and a large genome containing a high percentage of difficult-to-sequence repetitive DNA, said leading author Seyyedeh-Sanam Kazemi-Shahandashti, a PhD student at the Institute of Bio- and Geosciences of the Forschungszentrum Jlich, Germany.

As there are no ancient crocus remains preserved from ancient times, we here revisit ancient artworks that depict saffron-like plants. We expected that these could point us to specific regions.

Two independent lines of evidence

The authors argue that artworks from the Minoan civilization of ancient Greece are likely the oldest to depict domesticated saffron. For example, the dense patches of crocus flowers on the fresco The Saffron Gatherers from the island of Santorini (approximately 1600 BC) suggest cultivation. Another fresco on the same island, The Adorants, shows flowers with long, dark-red stigmas which overtop dark violet petals, typical of domesticated saffron.

Flowers with these traits are also depicted on ceramics and cloth from Bronze Age Greece, and symbolically rendered in the ideogram for saffron in the ancient Linear B script. In Egypt, tombs from the 15th and 14th centuries BC depict how ambassadors from Crete brought tribute in the form of textiles dyed with saffron.

An origin in Bronze Age Greece agrees with results from genetic studies from 2019, which showed that C. cartwrightianus, which only occurs in mainland Greece and Crete, is saffrons closest wild relative.

The authors believe that the modern saffron crocus with its three genomes arose naturally from the wild, either exclusively from C. cartwrightianus or from hybrids between C. cartwrightianus and another crocus species. The saffron crocus would then have been retained by the Bronze Age Greeks because of its superior qualities as a spice.

The authors will continue to trace saffrons properties, said final author Tony Heitkam, leader of the plant genomics group at Technische Universitt Dresden: Around the globe today, all saffron crocuses are effectively clones dating back to saffrons emergence in ancient Greece. Nevertheless, despite sharing the same genome, saffron can have different properties depending on the region. We have started to investigate the molecular causes, in particular so-called epigenetic differences, for this regional variation.

This article was first published on the Frontiers news blog.

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Myriad Genetics Teams Up with Epic to Make Genetic Testing Accessible to More Patients with Electronic Health Record (EHR) Integration – GlobeNewswire

June 26th, 2022 2:07 am

SALT LAKE CITY, June 23, 2022 (GLOBE NEWSWIRE) -- Myriad Genetics, Inc., (NASDAQ: MYGN), a leader in genetic testing and precision medicine, today announced a partnership with Epic, the industry leading healthcare software company, to integrate Myriads full line of genetic tests with Epics expansive network of 600,000 physicians and more than 250 million patients.

The integration creates a seamless, end-to-end workflow solution for healthcare providers to order Myriad tests and review results directly within their everyday Epic platform without additional steps or manual ordering processes. Epic enables a secure exchange of information between healthcare institutions that care for patients.

With the ability to review pertinent health information, order tests, and receive results natively in Epic, providers will have the critical genetic insights and related information they need to drive better health outcomes and improve the patient experience. Patients will also be able to easily access their Myriad test results and other health information directly within their EHR portal.

Simplifying the process of genetic testing by making it more accessible and interoperable with electronic health records is a key component of our mission to advance health and well-being for all, said Paul J. Diaz, president and CEO, Myriad Genetics. Our collaboration with Epic reflects our strategy to partner with other healthcare industry leaders so we can advance precision medicine together. Increasing access to genetic insights and integrating our tests into Epics vast network of healthcare systems represents a significant step forward to better serve patients and healthcare providers.

As part of its transformation and growth plan, Myriad is focusing on new customer-centric, tech-enabled tools to make the genetic testing process easier for patients and clinicians. With the recent launch of Myriads Precise Oncology Solutions, providers can now place a single order for multiple Myriad tests and receive timely results through a unified online portal. Now, through the partnership with Epic, Myriad is expanding efforts to help physicians and health systems gain access to genetic testing faster and conveniently within the platform they use every day.

Genetic testing and precision medicine save lives, said Alan Hutchison, vice president of Population Health at Epic. Through this relationship, were bringing genetic insights to the point of care at scale, giving providers and patients the information they need to make more timely, informed decisions.

Myriads integration with Epic is expected to go live later this year.

About Myriad Genetics Myriad Genetics is a leading genetic testing and precision medicine company dedicated to advancing health and well-being for all. Myriad develops and commercializes genetic tests that help assess the risk of developing disease or disease progression and guide treatment decisions across medical specialties where genetic insights can significantly improve patient care and lower healthcare costs. Fast Company named Myriad among the Worlds Most Innovative Companies for 2022. For more information, visit http://www.myriad.com.

Myriad, the Myriad logo, BRACAnalysis, BRACAnalysis CDx, Colaris, Colaris AP, MyRisk, Myriad MyRisk, MyRisk Hereditary Cancer, MyChoice CDx, Prequel, Prequel with Amplify, Amplify, Foresight, Precise, FirstGene, Health.Illuminated., RiskScore, Prolaris, GeneSight, and EndoPredict are trademarks or registered trademarks of Myriad Genetics, Inc. 2022 Myriad Genetics, Inc. All rights reserved.

Safe Harbor StatementThis press release contains forward-looking statements within the meaning of the Private Securities Litigation Reform Act of 1995, including statements relating to the integration of the companys genetic tests with Epics network of physicians and patients and the expected timing of the integration; the companys growth plan to scale customer-centric, tech-enabled commercial capabilities with 600+ EHR integrations this year; the anticipated benefits of the integration, including that the integration will create an end-to-end workflow solution for healthcare providers to order Myriad tests and review results directly with their everyday Epic workflows, provide providers with critical genetic insights and related information they need to drive better health outcomes and improve the patient experience, and allow patients to easily access their Myriad test results directly from their EHR portal; and the companys strategic imperatives under the caption About Myriad Genetics. These forward-looking statements are managements present expectations of future events and are subject to a number of risks and uncertainties that could cause actual results to differ materially and adversely from those described in the forward-looking statements. These risks include, but are not limited to: uncertainties associated with COVID-19, including its possible effects on the companys operations and the demand for its products and services and the companys ability to efficiently and flexibly manage its business; the risk that sales and profit margins of the companys existing molecular diagnostic tests may decline or that the company may not be able to operate its business on a profitable basis; risks related to the companys ability to generate sufficient revenue from its existing product portfolio or in launching and commercializing new tests; risks related to changes in governmental or private insurers coverage and reimbursement levels for the companys tests or the companys ability to obtain reimbursement for its new tests at comparable levels to its existing tests; risks related to increased competition and the development of new competing tests and services; the risk that the company may be unable to develop or achieve commercial success for additional molecular diagnostic tests in a timely manner, or at all; the risk that the company may not successfully develop new markets for its molecular diagnostic tests, including the companys ability to successfully generate revenue outside the United States; the risk that licenses to the technology underlying the companys molecular diagnostic tests and any future tests are terminated or cannot be maintained on satisfactory terms; risks related to delays or other problems with operating and constructing the companys laboratory testing facilities; risks related to public concern over genetic testing in general or the companys tests in particular; risks related to regulatory requirements or enforcement in the United States and foreign countries and changes in the structure of the healthcare system or healthcare payment systems; risks related to the companys ability to obtain new corporate collaborations or licenses and acquire or develop new technologies or businesses on satisfactory terms, if at all; risks related to the companys ability to successfully integrate and derive benefits from any technologies or businesses that it licenses, acquires or develops; risks related to the companys projections about the potential market opportunity for the companys current and future products; the risk that the company or its licensors may be unable to protect or that third parties will infringe the proprietary technologies underlying the companys tests; the risk of patent-infringement claims or challenges to the validity of the companys patents; risks related to changes in intellectual property laws covering the companys molecular diagnostic tests, or patents or enforcement, in the United States and foreign countries; risks related to security breaches, loss of data and other disruptions, including from cyberattacks; risks of new, changing and competitive technologies and regulations in the United States and internationally; the risk that the company may be unable to comply with financial operating covenants under the companys credit or lending agreements; risks related to the material weakness related to general information technology controls, including the impact thereof and the companys remediation plan, and its ability to achieve and maintain effective disclosure controls and procedures and internal control over financial reporting; risks related to current and future lawsuits, including product or professional liability claims; and other factors discussed under the heading Risk Factors contained in Item 1A of the companys Annual Report on Form 10-K filed with the Securities and Exchange Commission on February 25, 2022, as well as any updates to those risk factors filed from time to time in the companys Quarterly Reports on Form 10-Q or Current Reports on Form 8-K. The reported number of physicians and patients in Epics network were provided by Epic.

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Myriad Genetics Teams Up with Epic to Make Genetic Testing Accessible to More Patients with Electronic Health Record (EHR) Integration - GlobeNewswire

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Obesity and genetics: Expert shares insights – Hindustan Times

June 26th, 2022 2:07 am

Obesity is a health condition which involves accumulation of a large amount of fat. Unlike what we think, Obesity is not just a cosmetic condition. It, in fact, involves and increases the risk of a lot of other disorders such as heart disease, diabetes, high blood pressure and even certain types of cancers. Obesity is caused by a range of factors it usually involves eating a lot of calories and not burning enough of them which causes the fat to accumulate. Genetics is also one of the causes of obesity. Speaking to HT Lifestyle, Yash Vardhan Swami, Nutritionist, Health and Fitness Expert said, To gain weight we need to eat more calories than we burn (over time) and to lose weight, we need to eat lesser calories. To control this equation, we can eat more or fewer calories, or we can burn more or fewer calories. We can also do a bit of both.

Yash Vardhan Swami further added that this formula applies to everyone irrespective of the genetic makeup that they are a part of. Can our genes make it harder to lose weight? Certain gene variants can make it easier for us to gain weight by making it easier for us to eat more calories than what we burn over time which would lead to weight gain by increasing drive to eat (hunger and cravings) or reducing drive to move/burn calories (in simple terms, making us lazier).

ALSO READ: Health tips for adolescents: 5 problems due to obesity, ways to lose weight

The nutritionist further referred to the presence of the FTO Gene also known as the obesity gene, FTO gene is Fat Mass and Obesity Associated Gene which raises the risk of obesity. Referring to the part played by the FTO gene, the expert added, If you have one copy of gene (one parent), there would be a difference of 1.5kgs only (on an average). If you have two copies of the gene (both parents), there would be a difference of 3kgs only (on an average). So, if we are up to 3kgs up, we can blame our genetics. If it's more, genetics are not to be blamed. The expert recommended regular exercise which can reduce and slash the effect of the FTO gene and can prevent obesity.

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Obesity and genetics: Expert shares insights - Hindustan Times

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Where science meets fiction: the dark history of eugenics – The Guardian

June 26th, 2022 2:07 am

Its a quirk of history that the foundations of modern biology and as a consequence, some of the worst atrocities of the 20th century should rely so heavily on peas. Cast your mind back to school biology, and Gregor Mendel, whose 200th birthday we mark next month. Though Mendel is invariably described as a friar, his formidable legacy is not in Augustinian theology, but in the mainstream science of genetics.

In the middle of the 19th century, Mendel (whose real name was Johann Gregor was his Augustinian appellation) bred more than 28,000 pea plants, crossing tall with short, wrinkly seeds with smooth, and purple flowers with white. What he found in that forest of pea plants was that these traits segregated in the offspring, and did not blend, but re-emerged in predictable ratios. What Mendel had discovered were the rules of inheritance. Characteristics were inherited in discrete units what we now call genes and the way these units flowed through pedigrees followed neat mathematical patterns.

These rules are taught in every secondary school as a core part of how we understand fundamental biology genes, DNA and evolution. We also teach this history, for it is a good story. Mendels work, published in 1866, was being done at the same time as Darwin was carving out his greatest idea. But this genius Moravian friar was ignored until both men were dead, only to be rediscovered at the beginning of the new century, which resolved Darwinian evolution with Mendelian genetics, midwifing the modern era of biology.

But theres a lesser-known story that shaped the course of the 20th century in a different way. The origins of genetics are inextricably wedded to eugenics. Since Plato suggested the pairing of high-quality parents, and Plutarch described Spartan infanticide, the principles of population control have been in place, probably in all cultures. But in the time of Victorian industrialisation, with an ever-expanding working class, and in the wake of Darwinian evolution, Darwins half-cousin, Francis Galton, added a scientific and statistical sheen to the deliberate sculpting of society, and he named it eugenics. It was a political ideology that co-opted the very new and immature science of evolution, and came to be one of the defining and most deadly ideas of the 20th century.

The UK came within a whisker of having involuntary sterilisation of undesirables as legislation, something that Churchill robustly campaigned for in his years in the Asquith government, but which the MP Josiah Wedgwood successfully resisted. In the US though, eugenics policies were enacted from 1907 and over most of the next century in 31 states, an estimated 80,000 people were sterilised by the state in the name of purification.

American eugenics was faithfully married to Mendels laws though Mendel himself had nothing to do with these policies. Led by Charles Davenport a biologist and Galton devotee the Eugenics Record Office in Cold Spring Harbor, New York, set out in 1910 to promote a racist, ableist ideology, and to harvest the pedigrees of Americans. With this data, Davenport figured, they could establish the inheritance of traits both desirable and defective, and thus purify the American people. Thus they could fight the imagined threat of great replacement theory facing white America: undesirable people, with their unruly fecundity, will spread inferior genes, and the ruling classes will be erased.

Pedigrees were a major part of the US eugenics movement, and Davenport had feverishly latched on to Mendelian inheritance to explain all manner of human foibles: alcoholism, criminality, feeblemindedness (and, weirdly, a tendency to seafaring). Heredity, he wrote in 1910, stands as the one great hope of the human race; its saviour from imbecility, poverty, disease, immorality, and like all of the enthusiastic eugenicists, he attributed the inheritance of these complex traits to genes nature over nurture. It is from Davenport that we have the first genetic studies of Huntingtons disease, which strictly obeys a Mendelian inheritance, and of eye colour, which, despite what we still teach in schools, does not.

One particular tale from this era stands out. The psychologist Henry Goddard had been studying a girl with the pseudonym Deborah Kallikak in his New Jersey clinic since she was eight. He described her as a high-grade feeble-minded person, the moron, the delinquent, the kind of girl or woman that fills our reformatories. In order to trace the origin of her troubles, Goddard produced a detailed pedigree of the Kallikaks. He identified as the founder of this bloodline Martin Kallikak, who stopped off en route home from the war of independence to his genteel Quaker wife to impregnate a feeble-minded but attractive barmaid, with whom he had no further contact.

In Goddards influential 1912 book, The Kallikak Family: A Study in the Heredity of Feeble-Mindedness, he traced a perfect pattern of Mendelian inheritance for traits good and bad. The legitimate family was eminently successful, whereas his bastard progeny produced a clan of criminals and disabled defectives, eventually concluding with Deborah. With this, Goddard concluded that the feeble-mindedness of the Kallikaks was encoded in a gene, a single unit of defective inheritance passed down from generation to generation, just like in Mendels peas.

A contemporary geneticist will frown at this, for multiple reasons. The first is the terminology feeble-minded, which was a vague, pseudopsychiatric bucket diagnosis that we presume included a wide range of todays clinical conditions. We might also reject his Mendelian conclusion on the grounds that complex psychiatric disorders rarely have a single genetic root, and are always profoundly influenced by the environment. The presence of a particular gene will not determine the outcome of a trait, though it may well contribute to the probability of it.

This is a modern understanding of the extreme complexity of the human genome, probably the richest dataset in the known universe. But a meticulous contemporary analysis is not even required in the case of the Kallikaks, because the barmaid never existed.

Martin Kallikaks legitimate family was indeed packed with celebrated achievers men of medicine, the law and the clergy. But Goddard had invented the illegitimate branch, by misidentifying an unrelated man called John Wolverton as Kallikaks bastard son, and dreaming up his barmaid mother. There were people with disabilities among Wolvertons descendants, but the photos in Goddards book show some of the children with facial characteristics that are associated with foetal alcohol syndrome, a condition that is entirely determined not by genetic inheritance, but by exposure to high levels of alcohol in utero. Despite the family tree being completely false, this case study remained in psychology textbooks until the 1950s as a model of human inheritance, and a justification for enforced sterilisation. The Kallikaks had become the founding myth of American eugenics.

The German eugenics movement had also begun at the beginning of the 20th century, and grown steadily through the years of the Weimar Republic. By the time of the rise of the Third Reich, principles such as Lebensunwertes Leben life unworthy of life were a core part of the national eugenics ideology for purifying the Nordic stock of German people. One of the first pieces of legislation to be passed after Hitler seized power in 1933 was the Law for the Prevention of Genetically Diseased Offspring, which required sterilisation of people with schizophrenia, deafness, blindness, epilepsy, Huntingtons disease, and other conditions that were deemed clearly genetic. As with the Americans tenacious but fallacious grip on heredity, most of these conditions are not straightforwardly Mendelian, and in one case where it is Huntingtons the disease takes effect after reproductive age. Sterilisation had no effect on its inheritance.

The development of the Nazis eugenics programmes was supported intellectually and financially by the American eugenicists, erroneously obsessed as they were with finding single Mendelian genes for complex traits, and plotting them on pedigrees. In 1935, a short propaganda film called Das Erbe (The Inheritance) was released in Germany. In it, a young scientist observes a couple of stag beetles rutting. Confused, she consults her professor, who sits her down to explain the Darwinian struggles for life and shows her a film of a cat hunting a bird, cocks sparring. Suddenly she gets it, and exclaims, to roars of laughter: Animals pursue their own racial policies!

The muddled propaganda is clear: nature purges the weak, and so must we.

The film then shows a pedigree of a hunting dog, just the type that you might get from the Kennel Club today. And then, up comes an animation of the family tree of the Kallikaks, on one side Erbgesunde Frau and on the other, Erbkranke Frau genetically healthy and hereditarily defective women. On the diseased side, the positions of all of the miscreants and deviants pulse to show the flow of undesirable people through the generations, as the voiceover explains. Das Erbe was a film to promote public acceptance of the Nazi eugenics laws, and what follows the entirely fictional Kallikak family tree is its asserted legacy: shock images of seriously disabled people in sanatoriums, followed by healthy marching Nazis, and a message from Hitler: He who is physically and mentally not healthy and worthy, may not perpetuate his suffering in the body of his child. Approximately 400,000 people were sterilised under this policy. A scientific lie had become a pillar of genocide in just 20 years.

Science has and will always be politicised. People turn to the authority of science to justify their ideologies. Today, we see the same pattern, but with new genetics. After the supermarket shootings in Buffalo in May, there was heated discussion in genetics communities, as the murderer had cited specific academic work in his deranged manifesto, legitimate papers on the genetics of intelligence and the genetic basis of Jewish ancestry, coupled with the persistent pseudoscience of the great replacement.

Science strives to be apolitical, to rise above the grubby worlds of politics and the psychological biases that we are encumbered with. But all new scientific discoveries exist within the culture into which they are born, and are always susceptible to abuse. This does not mean we should shrug and accept that our scientific endeavours are imperfect and can be bastardised with nefarious purpose, nor does it mean we should censor academic research.

But we should know our own history. We teach a version of genetics that is easily simplified to the point of being wrong. The laws in biology have a somewhat tricksy tendency to be beset by qualifications, complexities and caveats. Biology is inherently messy, and evolution preserves what works, not what is simple. In the simplicity of Mendels peas is a science which is easily co-opted, and marshalled into a racist, fascist ideology, as it was in the US, in Nazi Germany and in dozens of other countries. To know our history is to inoculate ourselves against it being repeated.

This article was amended on 20 June 2022. The mass shooting in Buffalo, US, in May 2022 was at a supermarket, not a school as an earlier version said.

Control: The Dark History and Troubling Present of Eugenics by Adam Rutherford is published by Weidenfeld & Nicolson (12.99). To support the Guardian and Observer order your copy at guardianbookshop.com. Delivery charges may apply

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Researchers discover genetic variants that increase Alzheimer’s risk – WCVB Boston

June 26th, 2022 2:07 am

Researchers at Boston University on Thursday announced a breakthrough discovery about a gene associated with the risk of Alzheimer's disease.This risk is tied to the APOE4 gene, which destroys brain cells if a person carries the gene. It puts them at higher risk for developing the disease, although inheriting the gene doesn't necessarily mean one will develop the disease, according to the NIH. The APOE3 gene is the most common and isn't known to affect Alzheimer's risk.Although the link between the gene and the disease is well established, the mechanism responsible for the underlying risk in brain cells has been unclear in research until the recent discovery, according to researchers from the BU School of Medicine.Alzheimer's is a progressive neurodegenerative disorder and is the most common cause of dementia. It affects more than 5.8 million individuals in the United States.In the recent finding, two important aspects of the gene were discovered the human genetic background associated with the gene is unique to APOE 4 patients and the genetic defects are unique to human cells.Our study demonstrated what the APOE4 gene does and which brain cells get affected the most in humans by comparing human and mouse models. These are important findings as we can find therapeutics if we understand how and where this risk gene is destroying our brain," said assistant professor in the BU School of Medicine Julia TCW.Researchers used three models to investigate the effects of the gene on brain cells, human-induced pluripotent stem cells, post-mortem human brains and experimental models.It is also known that the gene carries a risk for Parkinson's disease and rare genetic diseases.

Researchers at Boston University on Thursday announced a breakthrough discovery about a gene associated with the risk of Alzheimer's disease.

This risk is tied to the APOE4 gene, which destroys brain cells if a person carries the gene. It puts them at higher risk for developing the disease, although inheriting the gene doesn't necessarily mean one will develop the disease, according to the NIH. The APOE3 gene is the most common and isn't known to affect Alzheimer's risk.

Although the link between the gene and the disease is well established, the mechanism responsible for the underlying risk in brain cells has been unclear in research until the recent discovery, according to researchers from the BU School of Medicine.

Alzheimer's is a progressive neurodegenerative disorder and is the most common cause of dementia. It affects more than 5.8 million individuals in the United States.

In the recent finding, two important aspects of the gene were discovered the human genetic background associated with the gene is unique to APOE 4 patients and the genetic defects are unique to human cells.

Our study demonstrated what the APOE4 gene does and which brain cells get affected the most in humans by comparing human and mouse models. These are important findings as we can find therapeutics if we understand how and where this risk gene is destroying our brain," said assistant professor in the BU School of Medicine Julia TCW.

Researchers used three models to investigate the effects of the gene on brain cells, human-induced pluripotent stem cells, post-mortem human brains and experimental models.

It is also known that the gene carries a risk for Parkinson's disease and rare genetic diseases.

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Researchers discover genetic variants that increase Alzheimer's risk - WCVB Boston

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