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Gay Men Wanted to Donate Blood in Orlando. They’re Still Not Allowed To.

Mother Jones

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By the early afternoon on June 12, hours after a gunman slaughtered 49 people at a gay nightclub in Orlando, hundreds of sympathizers had lined up to donate blood to the 53 young men and women who had survived the shooting. There were many gay men who would have liked to help but couldn’t. Last December, the Food and Drug Administration lifted its lifetime ban on blood donations by men who have sex with men (often referred to as MSM). Gay men could now give blood, the agency announced—but only if they’ve been celibate for a year beforehand. For gay men in America, it is still easier to purchase an assault rifle than to donate blood.

The lifetime ban was implemented during the early 1980s to help stem the spread of AIDS, which doctors had no way to diagnose or treat at the time. Three decades later, HIV/AIDS is a chronic condition, and advances in diagnostics have made it possible to detect infection within as few as nine days of exposure. But medical progress and political progress are asymmetrical. Despite years of criticism from the American Association of Blood Banks, the New York City Council, and the American Medical Association (AMA), the prohibition remained in place. “The lifetime ban on blood donation for men who have sex with men is discriminatory and not based on sound science,” the AMA declared in 2013.

So the FDA finally relented, somewhat, by reducing the lifetime ban to a yearlong moratorium on donations after the last male-to-male sexual encounter. “The 12-month deferral window is supported by the best available scientific evidence,” Dr. Peter Marks, head of the FDA branch that crafted the recommendation, said in a statement announcing the new policy.

Dan Bruner, the senior director of policy at Washington, DC’s premier HIV clinic, Whitman-Walker Health, was disappointed. “The updated policy is still discriminatory and not rooted in the reality of HIV testing today,” he wrote in response. “The deferral period should be no longer than 30 days.”

In the aftermath of Orlando, as a flurry of politicians, mourners, and activists have renewed their call for the FDA to rethink its 12-month policy, old arguments about public health and identity politics have re-emerged. Once again, health authorities, doctors, and LGBTQ advocates are looking at the same studies and clinical data and coming away with opposing conclusions on what constitutes the “best” scientific evidence.

There’s an emotional history here. By the time the FDA released the first reliable HIV test in 1985, more than 14,000 surgery patients and hemophiliacs were known to have been infected by blood transfusions—a veritable death sentence. Thousands of the fatal donations came from closeted gay men. Even with a test available, infected blood still snuck into the blood supply, because there is a window during which the virus is undetectable in the bloodstream of an infected person. The most common HIV test looks for antibodies against the virus rather than the virus itself. Just as there’s a lag between the intrusion of a burglar and the arrival of police, there’s a lag between pathogen and antibody. In the 1980s, the lag period was around a month. Today, every unit of blood collected in America must pass a nucleic acid test, which can detect HIV nine days after a person is infected.

Bruner, who is gay, is frustrated by the disparity between the FDA’s new policy and modern HIV diagnostics. “I’m married and have been in a monogamous relationship for 33 years,” he says. “If the Red Cross had a blood drive and I wanted to give, I could hold off on sex for a month. I could understand that. But the one-year ban is illusory progress. It says, ‘You can’t donate if you have a sex life.'” Bruner compares the current situation to the exclusion of homosexuals from the military for the sake of troop cohesion. “Don’t Ask, Don’t Tell,” a policy enacted in 1994 under President Bill Clinton and eliminated in 2011, allowed homosexuals to serve only if they remained in the closet, putting gay sex at odds with civic duty. “Donating blood is something normal people do,” Bruner says. “The FDA’s policy treats MSM as if they’re not normal, as if they have an infection even when they don’t.”

Indeed, the FDA does not consider MSM normal when it comes to HIV. “A history of male-to-male sexual contact was associated with a 62-fold increased risk for being HIV positive,” Marks tells me. He adds that MSM comprise 2 percent of the population but account for two-thirds of new HIV infections. “If everyone was 100 percent truthful and never cheated, the current nucleic acid test would be able to take care of things,” he explains. “Say you and your partner always use condoms. That also has a failure rate. With anal receptive intercourse it’s 1 to 2 percent.” That adds up fast when your agency is responsible for the safety of millions of Americans.

The FDA relies on data to craft policy, and because American researchers have not thoroughly studied a shorter deferral period for MSM, the agency instead looked to Australia, whose HIV epidemiology and blood screening systems are similar to those in the United States, according to Marks. In 2000, Australia replaced its own indefinite ban on MSM blood donations with a 12-month deferral for sexually active gay men. Australian researchers then studied millions of blood donors from the mid-1990s to the mid-2000s and found no statistically significant increase in the number of HIV-positive donors under the new policy, much less transfusion-borne infections.

Health officials in Italy tried something different: They eliminated MSM deferrals entirely in 2001 and began assessing each donor’s risk with an extensive questionnaire. In 2013, Italian researchers concluded that this individual risk assessment was just as effective at screening out HIV-positive donors (regardless of sexuality) as their nation’s mandatory MSM deferral had been.

Preempting questions about these findings on C-SPAN, Marks said that heterosexuals account for a much larger proportion of new HIV infections in Italy than in the United States. He claimed that getting rid of deferrals and relying only on HIV testing would quadruple the rate of infection through the blood supply. In a subsequent interview, he also said it “wasn’t too big a leap” to make policy based on a six-year-old study of another country’s policy. “We want data we can hang our hat on,” he said.

Public health, of course, is not clinical medicine in aggregate. Doctors treat individuals and can see the result of a prescription in days, but public health officials deal in million-person trends and decade-long studies. It’s therefore not surprising that the FDA’s blood-donation policy lags a decade behind modern diagnostics. “For every letter we got saying we should advance the policy, we got one saying that we shouldn’t change the policy,” Marks says. Imagine the response had the FDA tried to end its MSM ban six years ago, when Australian researchers first published their study. In 2010, a majority of Americans opposed same-sex marriage, including President Barack Obama (publicly, at least). Today, we are more sympathetic to LGBTQ people, but the association of AIDS with gay men endures, in part because the latter still account for a staggering proportion of the US HIV-positive population—more than 40 percent as of 2011.

Dr. Gerald Friedland, an AIDS expert at Yale New Haven Hospital, can sympathize with both sides. “There is logic to the current policy because MSM are the highest-risk population, but there is a danger of stigmatizing,” he says. “Every epidemic is a mosaic of smaller epidemics. Risk is contextual.” For instance, African Americans make up 41 percent of the 1.2 million HIV-positive Americans despite being only 12 percent of the population. In 2014, roughly a quarter of the nation’s 45,000 new HIV infections were black MSM. Poverty, access to housing and education, and geography matter, too. The South is home to 37 percent of the population but 44 percent of Americans with HIV. Yet there are no special donor questions or deferrals for black people, poor people, or Southerners.

Friedland says the FDA may have crafted its policy in deference to the hierarchy of medical evidence. “When we make guidelines for antiretroviral therapy, for example,” he says, “a strong recommendation will receive an ‘A’ if it’s based on two double-blind randomized control trials”—experiments in which neither the researchers nor the subjects know who receives the medication and who receives a placebo. A recommendation receives a “B” if it relies on observational studies, which Friedland describes as “lots of evidence but not randomized evidence.” (The studies from Australia and Italy would probably receive a “B.”) The third threshold, a “C,” is based on a consensus of expert opinion in situations where there are no good studies. (The idea of shrinking the MSM deferral to 30 days would get a “C” because it hasn’t been studied.) “Many decisions are made on this basis,” Friedland says. “There might have been a difference of opinion within the FDA that led to a less-than-forceful recommendation.” The apparent unwillingness of the medical community to undertake clinically relevant studies of a 30-day deferral for sexually active gay men—research many experts say could be conducted without endangering any transfusion recipients—leaves in place a somewhat arbitrary policy that feels discriminatory to many Americans.

Earlier this spring, I went to a Red Cross blood drive in New Haven, Connecticut, and found that the nonprofit had yet to implement the FDA’s “less-than-forceful” recommendations. Its laminated donor handouts still told gay men they could not donate blood, period. Dr. Dominick Giovanniello, the American Red Cross’ medical director for Connecticut, explains that the policy change is more gradual and complicated than media reports made it seem back in December. The new policy, Giovanniello says, was issued as a “draft guidance” back in May of 2015, which gave blood banks time to absorb the changes and get donation centers up to speed, rewriting and reprinting donor manuals, creating new programming for computer-based questionnaires, and retraining phlebotomy staff.

The American Red Cross, a private entity regulated by the FDA, is responsible for about 40 percent of the nation’s blood supply, more than 5 million pints every year, and it wants its policies and facilities to be “in sync” nationwide before it rolls out the changes. Donation facilities less strict than the FDA recommends can be cited or even shut down, so they err on the side of strictness. Yet more than a year has passed since the FDA issued the draft guidance, and the American Red Cross has yet to end the indefinite deferrals. “I’m a little surprised that it’s taken blood banks this much time,” Marks told me.

The ongoing deferral puzzles many LGBTQ advocates, given how vital blood is to the health care system. The Williams Institute, a think tank affiliated with the UCLA School of Law, found that the 12-month deferral forfeits as many as 300,000 pints of blood every year. Ending it, the institute wrote, could “help save the lives of more than a million people.”

Then again, the nation’s demand for blood is down significantly, falling by 27 percent from 2008 to 2013, due to the emergence of minimally invasive surgery and evidence that high-volume blood transfusion is risky and expensive. But the complex biology of blood means that even a slight expansion of the donor pool could save many lives. Although more than two-thirds of Americans have A-positive or O-positive blood, around 9 percent have O-negative and 3 percent have AB-positive, and these rarer types are highly versatile: You can transfuse any patient with O-negative blood cells, and AB plasma is accepted by any body. “There’s always a need for AB plasma and O-negative red blood cells,” Giovanniello says. Having these rare types on hand is especially important when time is short—say, in the aftermath of a mass shooting.

When I ask Marks about the Orlando attack and whether the FDA plans to respond to the renewed criticism of the 12-month deferral, he replies that the agency is “on a course to gather more data to move the policy forward” and that a new plan has “been in the works for weeks and weeks.” He and his staff would only hint about what such a plan might entail. Lorrie McNeill, Marks’ communications director, tells me that many in the LGBTQ community feel that any time-based deferral would be discriminatory. “The comments we heard back were overwhelmingly in favor of moving toward an individual risk assessment,” McNeil says.

Marks has previously said that the FDA hopes to better understand why HIV-positive people would donate blood, which requires thinking about how and why people lie when answering donor questionnaires. “Most donors answer questions as if they’re asking ‘Is my blood safe?’ rather than what they actually ask,” he tells me. “If people feel like we have a fair policy, then they’ll be more likely to comply. There are certain questions that make people so embarrassed that they won’t answer truthfully.”

Marks is cagey about what an improved donor questionnaire might include. “If I could ask you your favorite kind of ice cream bar, and that would predict with 99.9 percent accuracy that you were safe to donate,” he says, “then that would work.” In any case, an FDA study on the effectiveness of a less invasive, more holistic donor history questionnaire would show that the agency is seeking evidence that could support an effective individual risk assessment.

But even if the FDA takes this step, the research would take years to complete, could be cut short by a Republican administration, and might deliver inconclusive results. In the meantime, queer men who want to give blood have to re-enter the closet for an afternoon. The FDA has thought through its policies with care, but its circumspection is lost on millions of gay men and their allies who view the deferral as a symptom of the same phobia that apparently brought a man with an assault rifle to a gay club. The current policy suggests that the federal government is more concerned with preventing injury than insult. With better evidence, it won’t have to choose one or the other.

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Gay Men Wanted to Donate Blood in Orlando. They’re Still Not Allowed To.

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Watch: Attacks on American Abortion Providers Over the Years

Mother Jones

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A new video from the Thomson Reuters Foundation shows a chilling timeline of violence against abortion providers over the past two decades, from the 1993 murder of Dr. David Gunn in Pensacola, Florida, up through the recent shooting at a Planned Parenthood clinic in Colorado Springs, Colorado.

But perhaps the most heart-stopping detail is that abortion providers are in increasingly short supply—Reuters reports that in 1982, there were 2,908 providers in the United States. In 2011, that number had dropped to 1,720.

Democrats in the House are calling for Rep. Marsha Blackburn to end the “witch hunt” of the Select Investigative Panel on Infant Lives, which was formed by John Boehner last fall to explore allegations that abortion clinics are selling fetal tissue for profit. (There has been no evidence thus far to prove this.) Democratic members have expressed concern that the aggressive allegations put forth by Blackburn and the Republicans on the panel endanger researchers and abortion providers.

You can watch the video below:

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Watch: Attacks on American Abortion Providers Over the Years

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Crude oil is flooding Texas rivers

Flooding in Brookshire, Texas, U.S. April 20, 2016. Handout via REUTERS TPX IMAGES

Crude oil is flooding Texas rivers

By on May 2, 2016Share

Dramatic, deadly flooding is the new normal for parts of Texas and Louisiana this past year. This weekend, a single flash flood killed six people. But the damage often doesn’t end when the skies are finally clear. In Texas — a state dotted with oil wells — extreme flooding can also mean contaminated water.

According to El Paso Times, chemicals and oil from overfilled wells and fracking sites have flushed into majors rivers. Texas officials have reportedly taken dozens of images of waterways polluted with crude oil and fracking chemicals, which show the “sheens and plumes spreading from tipped tanks and flooded production sites.” Affected waterways include the Sabine River on the Texas-Louisiana border, which flooded in March, and the Trinity, Red, and Colorado rivers, which flooded last year.

“That’s a potential disaster,” Dr. Walter Tsou, a physician and past president of the American Public Health Association, told the El Paso Times. “I’m sure it will get into the groundwater and streams and creeks.”

Fracking, of course, is the inherently toxic and increasingly common industry practice of injecting massive amounts of water laced with cocktail of chemicals into the earth to fracture underground shales with deposits of oil or natural gas. Crude oil spills are never pretty, least of all when they destroy habitats.

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Crude oil is flooding Texas rivers

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Shia Mob in Iraq Demands More Technocrats

Mother Jones

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Protesters stormed the Iraqi parliament today:

Baghdad Operations Command declared a state of emergency and said all roads into the capital had been closed….Iraq is in the grip of a political crisis, with Prime Minister Haider al-Abadi attempting to reshuffle his cabinet and meet the demands of the demonstrators, who have been spurred on by the powerful Shiite cleric Moqtada al-Sadr. But Abadi has been hampered by chaotic parliament sessions, where lawmakers have thrown water bottles and punches at one another.

Oddly, the “firebrand cleric” Sadr (remember when that practically used to be his first name in news reports?) is demanding that…the current hacks running government ministries be replaced with nonpartisan technocrats. “More bean counters in the cabinet!” isn’t the usual rallying cry of a populist uprising, but there you have it.

Needless to say, the sectarian hacks currently in charge have been resisting this change for the past month. In the meantime, Iraq is in chaos. Again.

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Shia Mob in Iraq Demands More Technocrats

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How an Anti-Vax Scientist Helped Inspire the Planned Parenthood Videos

Mother Jones

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After Theresa Deisher received a doctorate in molecular and cellular physiology at Stanford, she worked in a lab that studied heart muscle cells. One day, representatives from a biomedical company came to her workplace to sell fetal heart tissue. Deisher asked them how and where they got the tissue. “They told me ‘miscarriages,'” Deisher says. I was like, ‘Woo hoo!'” But later she was confronted by one of the research assistants.‘How can you be so naive?'” Deisher remembers the assistant saying. “‘You know that’s not from miscarriages; think about it, you’re better than that.'”

She did think about it, and eventually her previous ease with a woman’s right to choose was replaced by a conviction that the fetus was a human being and that, therefore, both abortion and the use of fetal tissue for research were morally wrong. “I don’t care what someone’s opinion is on abortion or women’s reproductive rights,” she says. “I just don’t believe that people really could support a living baby harvested like that for their organs.”

She founded Sound Choice Pharmaceutical Institute, a small nonprofit in Seattle dedicated to finding alternatives to vaccines that she describes as “manufactured in cell lines that were derived from electively aborted babies,” and she became a prominent activist in the anti-abortion and anti-vax movements. She is also credited with inspiring and educating David Daleiden, the self-proclaimed “citizen journalist” who now faces a second-degree felony charge of tampering with a government record and a misdemeanor charge of illegally offering to purchase human organs from Planned Parenthood doctors in his now infamous—and discredited—undercover video recordings.

How the stories of Theresa Deisher and David Daleiden intersected, and how her work as an anti-abortion activist aligns with her work in the anti-vax movement, reveals a great deal about the attempts by the movement opposing abortion to marshal science to support their agenda. An interview with Daleiden in the National Catholic Register characterized it this way: “Theresa Deisher helped to prepare Daleiden for his role as a biomedical representative, teaching him the ins and outs of the field.” Deisher’s company links to the National Catholic Register story on its website, and its newsletters repeatedly tout Deisher’s connection to Daleiden. “It was the work of Sound Choice that brought the human exploitation of biomedical research to the attention of The Center for Medical Progress,” the December newsletter states. Children of God for Life, an anti-vaxxer organization that warns against “aborted fetal vaccines” like Gardasil, has been cheering on Daleiden’s Center for Medical Progress from social media. Not long after the videos went viral, the group posted a link on its Facebook page to Daleiden’s interview with the National Catholic Register: “God bless Dr. Deisher for her help in exposing Planned Parenthood!” The group’s website identifies Sound Choice as one of its partners, and in January it posted a petition to clear Daleiden of his pending charges.

In the past, anti-abortion organizations focused on moral arguments to justify their position. But scientific research, much of it discredited, has been increasingly used to legitimize their opposition. For example, the American Association of Pro-Life Obstetricians and Gynecologists (AAPLOG)—a counterpart to the American Congress of Obstetricians and Gynecologists (ACOG)—maintains through “international studies” and some marginal scientific research that there is a link between abortion and breast cancer. (The National Cancer Institute has since disputed this claim.) Another popular anti-abortion position that has come up in subsequent congressional hearings regarding Daleiden’s videos is that fetuses developed past 20 weeks are “pain capable.” The medical consensus is that the fetus must be nearly full-term before the systems necessary to sense pain are developed enough.

In an interview with The Church Boys podcast, Deisher explained that although she was not involved with shooting or editing any videos for the Center for Medical Progress, she had spoken to Daleiden regularly over the years and advised him in his research. “Just to make the Center for Medical Progress aware of how the material was being described, how the harvest was being described, and, most importantly, my suspicions that some of these babies were alive when they were being harvested,” she said.

Deisher and Daleiden’s relationship began about four years ago, when Daleiden called her asking for some help. Deisher said Daleiden had not been aware of “the day-to-day pervasive way” fetal tissue is used in biomedical research before he encountered her work—she can’t recall whether he’d heard her speak or had read one of her papers—and he wanted to know more. Together, they pored over articles in scientific publications, and Deisher explained the terminology. “What I did was translate science to him,” she said. “In many publications, it was very clear that especially the heart and brain research—where the stated optimal gestational age is 22 to 24 weeks for the best material, and those are times when babies are viable outside of the womb—it was very clear that some of these babies might have been alive when they were harvested.”

Viability has been a hotly debated subject since 1973, when the Supreme Court essentially legalized abortion in Roe v. Wade. One of the central points of the ruling concerned the “viability” of the fetus, arguing that state governments cannot prioritize the interests of a fetus over the interests of a pregnant woman until a time at which the fetus could survive outside the womb. Put simply, this has been interpreted as meaning that as long as a fetus could not exist outside its mother’s womb, it was basically not an individual person, and abortion remained a woman’s choice up until that imprecise point.

Since that time, medical technology, access to health care, and subsequent Supreme Court decisions about abortion have complicated the question of viability. A study published last year by the New England Journal of Medicine found that a very small number of 22-week-old babies could survive outside the womb, but it’s impossible to prescribe a blanket term of viability to a gestational age because survival depends on an array of factors. Researchers at Advancing New Standards in Reproductive Health, or ANSIRH, say viability can only be determined when taking into account the health of the pregnant woman and her fetus. Determining factors include “chromosomal abnormalities, the sex of the fetus, the conditions of a woman’s health, and the availability of sophisticated neonatology care.”

Deisher says her ideology is backed by science that works with her Catholic faith rather than against it. She takes issue with the use of fetal material for any scientific work on a moral basis, but scientifically the heart of her argument against vaccines is this: “When we use an animal- or a plant-based system to manufacture vaccines, there are animal- or plant-based contaminants that will be in the final product, and we mount an immune response to them and eliminate them from our body. In the case of the human fetal cell lines, those contaminants are human, and they could trigger an autoimmune attack, or what is called insertional mutagenesis.” Her nonprofit’s website has pages dedicated to the theories that vaccines cause autism and the use of fetal stem cells can cause cancerous tumors.

Dr. Paul Offit, director of the Vaccine Education Center at the Children’s Hospital of Philadelphia, says autoimmune theory is not plausible. “It’s like throwing a pingpong ball off the top of the Empire State Building and hoping that it lands in one of 7 billion little fishbowls.” In this analogy, the genetic material in vaccines represents Offit’s “pingpong ball,” and the “little fishbowls” are the cells in our bodies that are protected by cellular membranes, which would have to be penetrated by the DNA. Additionally, the DNA in the vaccine would have to do so without damaging the cell membrane to effectively contaminate it the way Deisher claims. Vaccines do contain some genetic material from the fetal cell lines they were derived from decades ago, but the amount is incredibly tiny— nanograms, which are roughly one-billionth of a gram. The material is highly fragmented to boot, and for genetic material to make its way into a cell, it would require an extraordinary chemical process. Offit notes that if what Deisher claims were actually true, “it would be the best news for gene therapy ever.”

Deisher disagrees with the previous Mother Jones article that reported the hindrance of life-saving research involving fetal tissue as a side effect of Daleiden’s videos. “It’s not true that there is no substitute for fetal tissue,” she says. “We have a very nice technology now called induced pluripotent cells that more effectively model what a postnatal heart cell does.”

Tim Kamp, the co-director of the University of Wisconsin-Madison’s Stem Cell and Regenerative Medicine Center, said it’s impossible to make pluripotent cells (also known as iPS cells) develop in a petri dish the way humans develop in utero—for that, and for the research on heart disease pioneered by his colleague Gail Robertson, they need fetal tissue. “There are aspects of developmental biology that can’t be done using iPS cells,” Kamp said. “There are different tools used for different research. You want to have access to all the different tools you can, but taking fetal tissue off the table will slow progress. It’s pretty straightforward.”

Deisher’s overall goal—to find alternative vaccines that weren’t developed using fetal cell lines—is not an impossibility. But Offit says it’s complicated, and the process of developing a new vaccine, putting it through clinical trials, and obtaining all the proper licensing along the way could amount to “hundreds and hundreds of millions of dollars” in costs. “In the world of things we need to worry about and prevent, this is not one of them,” Offit said. “It’s more a perceptual problem than a physical problem; there’s nothing unsafe about that vaccine.”

Deisher believes the claims put forth by Daleiden’s videos—that Planned Parenthood has been “harvesting” fetal tissue to sell for profit. Twenty states so far have either cleared Planned Parenthood of wrongdoing or decided to not investigate, and five congressional committees have also failed to find any evidence of wrongdoing. Still, Deisher maintains that the videos from the Center for Medical Progress reveal a dark truth. “A picture says a thousand words,” Deisher said. “As a scientist, I can talk clinically ’til I’m blue in the face. When people see the pictures—it doesn’t matter if you’re religious or not—I think it really cuts to people’s hearts.”

The Planned Parenthood sting videos have had an undeniable effect on both the abortion debate and the questions around vaccines. As I previously reported for Mother Jones, the political controversy surrounding Planned Parenthood has undermined medical research and poses a potential threat to the safety of scientists. Further exacerbating this effect is a GOP-led House committee that recently issued subpoenas to eight medical institutions, demanding the names of researchers, students, and doctors. Democrats are calling this effort a “witch hunt;” committee chair Marsha Blackburn (R-Tenn.) insists the group is simply trying to “get the complete picture,” as she told the New York Times. Five states have banned research on fetal tissue—Indiana, North Dakota, South Dakota, Ohio, and Oklahoma. Arizona bans the transfer of fetal tissue for research, and Florida bans the “purchase, sale, or transfer of fetal remains.”

For Deisher, her faith continues to be the final word when it comes to the debate surrounding Planned Parenthood. “You know, we get so caught up in pro-choice or pro-life, and if we throw the politics aside and really think about it, wouldn’t we all like a world where a woman didn’t have to make that choice?” she says. ” I think most people would; I think we’re all pro-life.”

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How an Anti-Vax Scientist Helped Inspire the Planned Parenthood Videos

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This is What It’s Like to Be an Abortion Provider in the Bible Belt

Mother Jones

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In Dawn Porter’s latest documentary, Trapped, a 19-year-old sits in an Alabama abortion clinic, recovering from her procedure. A white blanket surrounds her slight frame, and her hair is pushed back with an olive head wrap. She speaks frankly, but her internal conflict is clear.

“I want to go to heaven,” she says to the camera. “It’s like, what if I never have a little girl? What if I don’t get married? What if this happens, what if that happens, all because I had an abortion and that’s my payback?”

This scene is only one of the powerful moments viewers witness as Porter navigates the grim reproductive rights landscape in the South, with its complex relationship between religion and abortion. For some who live there, religion dictates that abortion is wrong—an unforgivable sin. For others, including the documentary’s protagonists, providing abortion care is one expression of Jesus’ commandment to love one another.

Porter was first introduced to the region in 2010, while hanging out with a group of idealistic young public defenders working in the Deep South. Her interest in them eventually led to her debut film, Gideon’s Army. “I was like a lot of good Northerners—prejudiced,” Porter says with a laugh. “A lot of people there were very generous in not being suspicious, and a lot of people I’m interested in are misunderstood by people they live with. These characters have thought a lot about who they are, as people, as Southerners.”

After Gideon’s Army, while Porter began working on her second film, Spies of Mississippi, she stumbled upon some unexpected inspiration. Whenever she’s on location, Porter picks up the local newspapers, and when she was in Mississippi, the Jackson-based Clarion-Ledger featured an article about the last remaining abortion clinic in the state.

“I just felt like how could it be that a pro-choice woman who pays attention to politics and reads the paper doesn’t realize there’s only one clinic in Mississippi?” she asked.

So she did what any good documentarian would do—she called up the clinic and asked if she could stop by for a visit. After meeting Dr. Willie Parker—a Harvard-educated OB-GYN in his 50s who’s from Alabama and has been providing abortions full time since 2009—and seeing the conditions for staff members at the facility, she decided to work on a documentary that eventually became Trapped. The film’s name comes from insidious laws known as TRAP laws—Targeted Regulation of Abortion Providers—that target abortion providers through unnecessary regulation.

“For better or worse, the right to have an abortion is a protected right by the Constitution. How could it possibly be that states could be intentionally, without any subterfuge, aiming to take away that right?” she asks. “I think a lot of people don’t like people to do things that are underhanded. And I think that these laws are underhanded. Straight up, come at me! You want to overturn Roe v. Wade? You should do it straight up.”

The heroes of her film are the women who run clinics in Alabama, Mississippi, and Texas, as well as Parker, who works with several clinics in the Southeast to provide the procedure. After nearly every legislative session, a new law threatens to close down these clinics, and all the owners struggle to remain open as they make their way through anti-choice protests and daunting piles of paperwork. It’s hardest of all to answer the phone calls from desperate women who must be denied services because the clinics are overbooked and, in some cases, have only one doctor.

“Women who have had abortions are so stigmatized, and so made into caricatures,” Porter says. “There’s the Jezebel and the irresponsible co-ed, so seeing the range of folks was a big deal.”

The film is steeped in religion, and Parker’s faith occupies a central role in his personal story. Parker is filmed singing hymns with his family at a Baptist church and praying at a meal with other clinic workers. He says he wants to talk to the church about abortion because he thinks the church is missing a ministry opportunity by condemning it. Callie Chatman, a recovery room assistant at Reproductive Health Services, agrees. “No woman has ever told me that she feels it’s alright to have an abortion, but they have told me that, ‘This is the only decision I can make at this time,'” she says. Chatman is later seen praying with a patient in recovery.

Porter says the issue of religion kept coming up organically. “The patients would say, ‘Dr. Parker, am I going to hell?'” she remembers. “It struck me how often he was counseling people, telling them they aren’t going to hell, and talking about his own beliefs.”

In another scene, the clinic workers say “The Lord’s Prayer” together as they prepare to endure an Operation Rescue anti-abortion demonstration in front of the Reproductive Health Services clinic in Montgomery, Alabama. The demonstration has all the hallmarks of abortion protests from small towns to the steps of the Supreme Court: children holding signs depicting fetuses with such messages as “I’m a child, not a choice,” and yelling, “Jesus Christ saves!” The clinic workers have erected signs—one says, “Jesus never shamed women”in front of the building.

While filming, Porter and her team experienced some of the safety concerns that many abortion providers must face on a daily basis. Protesters looked Porter up and began posting her name on their websites. They screamed at her as she visited the clinics. Trapped premiered at Sundance mere weeks after a man in Colorado brought a gun into a Planned Parenthood clinic and started shooting, killing three people and wounding nine others. Porter learned from Parker to not let fear dictate her life. In one of their final interviews, he tells her that he doesn’t wear a bulletproof vest. She later asks him if he had any concerns about her including that fact in the film.

“And he was like, ‘You can and you should. Because I don’t, I’m not going to, and that’s not going to keep me safe. Me being vigilant and responsible will keep me safe,'” she continues.He said, ‘I’m not foolhardy. I don’t want to die, but I’m also not going to live as if that’s around every corner.'”

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This is What It’s Like to Be an Abortion Provider in the Bible Belt

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DIY Laundry Hacks to Save Money & the Planet

Don’t you wish you were as happy about your laundry as this baby is?

Irecently talked with Eco Karen (aka Dr. Karen Lee) about getting greener and less toxic in the laundry room. Listen to this fun Green Divas @ Home podcast then read on for more DIY laundry hacks. . .

Most commercial brands of laundry detergent contain a myriad of known and potentially harmful toxic ingredients. Even the so-called cleaner ones aren’t always so clean. Here’s a helpful chart of laundry chemicals to avoid. One way to know exactly what is in your laundry detergent is to make your own!

1. Make your own Borax-free laundry detergent

While there are a lot of simple DIY laundry detergent recipes out there, many of them include Borax, which can be rough on sensitive skin, so Karen offers us a great Borax-free laundry detergent recipe that she tested herself.

1 TbspWashing Soda(you can make your own, did you know that?)
1 Tbsp Baking Soda
1 Tbsp Grated Castile Soap (see alternative option below)
1 C Distilled White Vinegar in the Fabric Softener Compartment
1 TbspCitrus Enzyme Cleaneror Citric Acid

Scoop the powder separately without mixing them, makingsure to use the right amount for each.

If you have extra stains, you canspot clean it with peroxide/water mixture or Oxyclean first, before throwing the garment in the washer with the rest of the laundry, like you would with other types of detergent.

As an alternative togratingcastile soap, you can substitute with 1 Tbsp ofliquidcastile soap.

2. Soap nuts?

Soap nutsare an effective, truly non-toxic, cheap and easy way to do laundry. I tried this when I was in California for a couple of weeks and was impressed with how well these things work. Why don’t we all use these things all the time? In fact, why am I not using them now?

Here’s what you do: put 4 – 6 nuts in a natural muslin bag that ties shut. Remove them from the laundry after you are done and let them dry. These can be used several times before you have to ditch them for new ones. When the shells start to get soft and gray, toss them in the compost.

3. Dryer balls from lonely old socks

This is an excellent idea for making use of those solo socks to make your laundry fluffy and naturally scented. Go here to get ecoKaren’s detailed tutorial on making dryer balls from socks!

BONUS:

Listen to the latest Green Divas Radio Show . . .

Disclaimer: The views expressed above are solely those of the author and may not reflect those of Care2, Inc., its employees or advertisers.

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DIY Laundry Hacks to Save Money & the Planet

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5 Ingredients to Avoid in Your Hair Products

Many Americans are working to reduce their exposure to harmful chemicals and toxic ingredients. Few industries have faced more criticism for their ingredients than the cosmetics industry, and lately, it seems that more and more brands arereleasing organic or all-natural personal care lines.

Shampoos and conditioners, in particular, contain a lot of toxic ingredients. Some health-conscious consumers have taken to making their own haircare products, but others still prefer to use ready-made, expert-developed shampoos and conditioners. If this is you, rest assured that you have plenty of options. You dont necessarily have to spend a fortune, either! A quick glance at a products ingredient list can tell you a lot about its safety. Here are five toxic ingredients youll want to be sure to avoid when picking out a shampoo or conditioner:

Sulfates

Youve probably heard of sulfates by now; pretty much every natural hair care brand states proudly on itspackaging thataproduct is sulfate-free. But what are sulfates, and why should you avoid them?

The main thing to keep in mind when thinking about sulfates is that they are chemical detergents. That in itself isnt necessarily a bad thing, but it means that sulfates are extremely effective at removing dirt and oil … in fact, theyre a little too effective. Sulfates are harsh on the hair and scalp, so they can strip away that natural moisture that keeps your hair shiny and soft.

On a deeper level, they may carry some hormone-disrupting agents along with them. According to Natural Society, many sulfates contain traces of dioxane, a known carcinogen. Dioxane is also thought to disrupt kidney function.

Parabens

Parabens are another widely hated group of chemicals that youve probably been told to avoid in your beauty and personal care products. Parabens are xenoestrogens, which means that they have a similar composition to hormones found in the human body. Xenoestrogens are thought to disrupt hormones and could even post a cancer risk.

Real Simple even noted that British scientistsfound evidence of parabens in samples of breast cancer tissue. Though this doesnt necessarily mean the parabens caused the cancer,most natural-minded folks try to avoid parabens completely.

Fragrance

Fragrances are bad, bad, bad. If the fragrance in your product comes from a natural essential oil, it will say so on the packaging. If all the manufacturers have chosen to tell you about the ingredient is that its a fragrance, thats generally bad news.

The term fragrance allows manufacturers to opt out of including a list of the ingredients used to create that fragrance, as the term is not regulated by the FDA. So really, if fragrance is listed on an ingredient list, theres no telling whats in there. Natural Society even notes that there are more than 3,100 chemicals used by the fragrance industry to concoct these suspicious-sounding additions to your shampoos and conditioners.

Triclosan

Triclosan is an antibacterial agent thats often added to personal care products as a preservative. Dr. Ben Kim notes that we still dont have enough conclusive evidence to say for sure whether or not triclosan is safe for use, but there have certainly been some warning signs to the contrary.

Triclosan is thought to be an endocrine disruptor, which means it can be harmful in the same fashion as xenoestrogens. Its also been linked to immune system problems, weight loss and uncontrolled cellular reproduction, according to Dr. Kim.

Polyethylene Glycol

Polyethylene glycol, or PEG, is also thought to interfere with the body. According to Natural Society, the state of California has classified the chemical as a developmental toxicant, which means that it may interfere with human development. Its also known to be contaminated by the aforementioned cancer-causer dioxane.

If youre looking for shampoos and conditioners that are made with safe, reliable, natural ingredients, you have lots of options at your fingertips. And if youre feeling more adventurous, of course, you could always try making your own homemade hair care products!

Related
How to Choose Natural Ingredients for Beautiful Skin8 Natural Mosquito Repellents

Disclaimer: The views expressed above are solely those of the author and may not reflect those of Care2, Inc., its employees or advertisers.

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5 Ingredients to Avoid in Your Hair Products

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This Law Just Took Abortion Pseudoscience to a New Low

Mother Jones

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Utah Gov. Gary Herbert on Monday signed a bill that makes the state the first in the nation to require doctors to anesthetize fetuses before performing abortions after 20 weeks of gestation. Previously, fetal anesthesia for abortion after 20 weeks was optional in Utah.

Supporters of the new law, called the Protecting Unborn Children Amendments, say fetuses can feel pain starting at about 20 weeks, so anesthesia or analgesic should be administered to “eliminate or alleviate organic pain to the unborn child.” But scientists have rejected the fetal pain claim, saying there is no conclusive evidence to back up such legislation.

Still, 12 states ban abortion after 20 weeks post-fertilization on the grounds that the fetus can feel pain. The 20-week mark is several weeks before the point at which the fetus is considered viable and abortion is no longer legally protected by Roe v. Wade. Utah already bans abortion after viability.

Republican State Sen. Curt Bramble initially planned to introduce a 20-week ban, but attorneys in the state advised him the law would not pass constitutional muster, according to the Salt Lake Tribune.

“The process of a child being born is a natural process. There’s nothing natural about abortion. In fact, it’s barbaric,” Bramble said, adding, “In this quote ‘medical procedure,’ let’s call it what it is: It’s killing babies. And if we’re going to kill that baby, we ought to protect it from pain.”

Dr. Sean Esplin, a Utah-based physician, told the Associated Press that in order to comply with the law, the anesthesia will have to go through the woman to reach the fetus. Doctors can give the woman general anesthesia, which would make her unconscious, or a heavy dose of narcotics, neither of which were previously necessary for the procedure.

According to the American Society of Anesthesiologists, side effects of anesthesia include nausea, confusion, chills, and rarely more serious symptoms like delirium or long-term memory loss. “You never give those medicines if you don’t have to,” David Turok of the University of Utah’s obstetrics and gynecology department told NBC.

Utah is the only state in the country with an anesthesia requirement during abortion. The Montana Legislature passed a similar law in 2015, but it was vetoed by the governor.

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This Law Just Took Abortion Pseudoscience to a New Low

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Clinton Says She’ll "Put a Lot of Coal Companies and Coal Miners Out of Business"

Mother Jones

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Just one day after Hillary Clinton issued a lengthy apology for a controversial comment she made about Nancy Reagan’s contribution to the fight against AIDS, the Democratic front-runner made another unforced error during a CNN town hall event on Sunday night.

Speaking in Ohio about her plans to revitalize coal country, Clinton said, “We’re going to put a lot of coal companies and coal miners out of business.” That comment was immediately preceded by a promise to invest in the clean-energy economy in those places, and immediately followed by a pledge to “make it clear that we don’t want to forget those people.” But it’s not hard to guess which comment will end up as a sound bite in attack ads in coal states during the general election.

Clinton’s statement likely referred to her support for President Barack Obama’s Clean Power Plan, the cornerstone of his climate policy, which will require states to reduce their coal consumption in favor of natural gas, renewables, and energy efficiency. It garnered a quick rebuttal from Sen. Rand Paul (R-Ky.).

Obama’s climate regulations have little to do with the coal industry’s decline over the last decade. For one thing, they are currently held up in court, and they wouldn’t take effect for several years anyway. More important, coal is getting hammered by competition from natural gas made cheap by fracking, as well as the exploding solar and wind industries. In the last town hall, Clinton said that under her administration, “I do not think there will be many places in America where fracking will continue to take place.” Since a widespread decline in gas consumption would most likely lead to an increase in coal consumption, it’s possible that Clinton’s energy policy could be just the opposite of the “war on coal” Paul describes.

Although Bernie Sanders is also a vociferous proponent of clean energy, Clinton is so far the only candidate in the race to produce a specific plan for supporting coal communities affected by the transition to a cleaner energy economy. Still, Sanders appears to be crushing Clinton in coal states that have had primaries so far. So it probably doesn’t serve her campaign well to remind people that for a small number of communities, the fight against climate change could mean the end of a traditionally important field of employment.

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Clinton Says She’ll "Put a Lot of Coal Companies and Coal Miners Out of Business"

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