#MeToo report suggests diluting male power
Geosciences professor Julie Libarkin doesn’t wear dresses in public.
It’s not because she has to get down on the ground to do her job — she doesn’t dig up rocks — but because she cannot stand the constant harassment that comes when she does.
“I don’t wear dresses any more because almost every time I have worn a dress, I have been assaulted,” said Libarkin, who is now a full professor at of Michigan State University.
That makes academia second only to the military in terms of rates of sexual harassment. Nearly 70 percent of military women say they’ve been sexually harassed.
Science, technology, engineering and medicine (STEM) fields are the worst, the report finds.
It lays down a road map for universities and other academic institutions to do something about it.
“Through our work it became clear that sexual harassment is a serious issue for women at all levels in academic science, engineering, and medicine, and that these fields share characteristics that create conditions that make harassment more likely to occur,” the study group’s co-chairs, Wellesley College president Paula Johnson and Massachusetts Institute of Technology professor Sheila Widnall wrote in the report’s introduction.
Concrete ways to help make it stop include sending a clear message that harassment will not be tolerated; supporting women who report incidents; making investigations clear and open; and diluting the power of male superstars, who often control the careers of everyone below them.
Libarkin approves of this proposal. Academic careers often hinge on a single mentor, and that’s not good for men or women, she said.
“I would suggest that even before entering STEM, (women) use social media to build a community of people,” said Libarkin, who heads the Geocognition Research Lab at Michigan State University.
“Expand your community and recognize that mentoring doesn’t come from one person.”
Academia is especially prone to sexual harassment because of the hierarchical nature of institutions, the report says.
“Research has consistently shown that institutions that are male dominated — with men in positions that can directly influence career options of women who are subordinate to them — have high rates of sexual harassment.”
And of course, most universities and colleges are male-dominated.
“Most department chairs and deans are men. Most principal investigators are men. Most provosts and presidents are men,” the report reads.
That doesn’t mean that all men harass all women, but it’s clear that when there’s a boy’s club atmosphere, with tacit signals that sexual harassment or discrimination will be winked at, bad behavior flourishes.
“An emeritus professor came up behind me at a public retirement party on campus, bent his knees, and humped me. And, yes, I was wearing a dress,” Libarkin wrote. "No one jumped in to rescue me, and no one seemed to have realized that I had just been assaulted.”
It’s so bad that women have started an online community to share their experiences.
Jen, who did not want to use her real name, said she suffered after she quietly asked a colleague to stop verbally harassing her.
“I was then taken out of the lab by senior members who said I was not to create a bad environment for everyone, and was sent to HR (human resources) by the PI (principal investigator) with the postdoc. I now see that everyone will lie to side with who is strong and no one will defend the lower ranking woman who is being wronged.”
“Lily” says she was raped and has suffered pervasive sexual harassment, but says her worst moment was when her academic adviser asked her to be ‘the estrogen in the room’ at a meeting.
“He didn’t ask me to go because of my strong communication and negotiation skills, or because of the work I’d done leading up to this moment, or because I was co-managing the project. He asked me to go because I was a girl,” she wrote.
“This isn’t going to force anybody to do anything.”
This kind of behavior must stop, the NASEM report says.
“Academic institutions should be as transparent as possible about how they are handling reports of sexual harassment,” the report reads. Cover-ups make things worse.
“Academic institutions should consider power-diffusion mechanisms (i.e., mentoring networks or committee-based advising and departmental funding rather than funding only from a principal investigator) to reduce the risk of sexual harassment,” it adds.
And women who report harassment should be treated as “honorable and courageous,” not as trouble-makers.
Having to battle sexual harassment is wasting time and money, the report said. And it’s costing society when women drop promising careers — or fail to even pursue them.
“What is especially discouraging about this situation is that at the same time that so much energy and money is being invested in efforts to attract and retain women in science, engineering, and medical fields, it appears women are often bullied or harassed out of career pathways in these fields,” the report reads.
Libarkin said she cannot even guess how much work she has lost because of the harassment she has experienced.
“This stuff takes an inordinate amount of time,” Libarkin said.
“Just dealing with sexual harassment, the emotional consequences take a lot of time. I lost several papers because I just didn’t work on them. I didn’t write them.”
Libarkin says the report is a good first step. Institutions also must address discrimination and harassment of ethnic and other minorities, she said.
And the National Academies are highly respected, even if the organization is advisory only.
“One of my colleagues pointed out that of course the report has no teeth,” she said.
“This isn’t going to force anybody to do anything.”
June 13, 2018
rare virus found in rat droppings, health officials say. </p><p>The employee, who has not been identified, was found unconscious June 1 outside the stadium's housing unit in Belmont Park, just east of JFK airport, where they lived.</p><p>A preliminary investigation suggests the employee died from hantavirus, which is spread by mice.</p><p>The employee, who has not been identified, was found unconscious June 1 outside the stadium's housing unit in Belmont Park (pictured) where they lived. They died days later</p><p>Most hantavirus cases are transmitted when people breathe in rodent droppings in confined areas.</p><p>The New York Racing Association says it will overhaul its pest control practices in light of the suspected hantavirus death, which happened days before the Belmont Stakes, an annual horse race that attracts visitors from all over.</p><p>Hantavirus is rare and cannot be spread from one person to another. </p><p>Only 728 cases were reported in the United States between 1993 and 2017.</p><p>The virus is carried by deer mice, a type of rodent that can be found across the country, from the subway tracks in New York City to woodlands in California.</p><p>Humans can contract the virus by inhaling dust with particles of the mice' saliva, feces, or urine.</p><p>The virus can lead to hantavirus pulmonary syndrome (HPS), a condition that infects the heart, lungs and other organs by weakening blood vessels and causing them to leak.</p><p>The body attempts to fight the virus by creating inflammation, which combines with the organ infections and leads to intense damage throughout the body.</p><p>In the lungs, leaky blood vessels cause flooding in the air sacs, making it difficult for patients to breathe.</p><p>When the virus infects the heart, the damage reduces its ability to circulate blood through the body, causing critically low blood pressure and a lack of oxygen throughout the body, which can quickly lead to organ failure and death.</p><p> The views expressed in the contents above are those of our users and do not necessarily reflect the views of MailOnline. </p><p>Do you want to automatically post your MailOnline comments to your Facebook Timeline?</p><p>Your comment will be posted to MailOnline as usual.</p><p>Do you want to automatically post your MailOnline comments to your Facebook Timeline?</p><p> We will automatically post your comment and a link to the news story to your Facebook timeline at the same time it is posted on MailOnline. To do this we will link your MailOnline account with your Facebook account. We’ll ask you to confirm this for your first post to Facebook.</p><p>Part of the Daily Mail, The Mail on Sunday & Metro Media Group</p>
and pancreatic cancer: 'I'm not going home to die.' </p><p>Five years ago, Camille was diagnosed with pancreatic cancer - one of the most deadly forms of the disease.</p><p>The five-year survival rate for pancreatic cancer is just nine percent. Camille, now 58, is one of that tiny minority - and determined to use her second chance to remind other patients that they could be too. </p><p>She had an unheard-of 'total' response to the aggressive chemotherapy she was given and now has a new purpose to her life: being living proof that pancreatic cancer patients deserve treatments, funding for better ones and a chance to live.</p><p>Camille Moses was diagnosed with pancreatic cancer, one of the most deadly forms of the disease in 2012. Five years later, she is one of the very few to be in remission </p><p>Pancreatic cancer is one of the most lethal forms of the disease.</p><p>Around 95 percent of people who contract it die from it. </p><p>Steve Jobs, Joan Crawford, Patrick Swayze, and Luciano Pavarotti all died of pancreatic cancer. </p><p>It is the fourth-leading killer in the United States. </p><p>Around 10,000 people are diagnosed with pancreatic cancer each year in the UK, and 50,000 in the US.</p><p>It is caused by the abnormal and uncontrolled growth of cells in the pancreas - a large gland in the digestive system.</p><p>Most cases (90 percent) are in people over the age of 55.</p><p>Around half of all new cases occur in people aged 75 or older.</p><p>Other causes include age, smoking and other health conditions, including diabetes.</p><p>There is no screening method for pancreatic cancer. </p><p>Pancreatic cancer typically does not show symptoms in the early stages, when it would be more manageable. </p><p>Sufferers tend to start developing the tell-tale signs - jaundice and abdominal pain - around stage 3 or 4, when it has likely already spread to other organs. </p><p>For all stages of pancreatic cancer combined, the one-year survival rate is 20 percent. </p><p>At five years, that rate falls to just seven percent. </p><p>If the cancer is caught in stage 1A, the five year survival rates is about 14 percent and 12 percent for 1B. </p><p>At stage 2, those rates are seven and five percent, respectively. </p><p>For a pancreatic cancer in its third stage, only three percent of people will survive another five yaers. </p><p>By stage IV, the five-year survival rate falls to just one percent. </p><p>The only effective treatment is removal of the pancreas. </p><p>This proves largely ineffective for those whose cancer has spread to other organs. </p><p>In those cases, palliative care is advised to ease their pain at the end of their life. </p><p>When her long daily walks with her three big babies - her beloved dogs - started hurting her back and leaving her winded, Camille figured that at age 53, it was about time menopause came calling. </p><p>But when her pain intensified, she went to the ER where CT scans revealed spots on her pancreas, liver and lungs in March 2012. </p><p>The doctor ordered blood tests and a biopsy of her liver. Camille's heart sank. This was a similar sequence to what had preceded her mother's death from pancreatic cancer when Camille was just 24. </p><p>A few days later, she was back at the hospital for her results. Her diagnosis was the same one that had been the death of her mother: stage IV pancreatic cancer. </p><p>Camille started to panic and was given Valium to calm her down. When she came to, an oncologist walked briskly, unceremoniously into her room. </p><p>'When I woke up, I knew I was in trouble. Once the staff oncologist came in, I asked him what that next step was,' she recalls.</p><p>'He said, "there's no hope for you. You'll be gone by November."</p><p>'My first thought then was Christmas, I thought, "I'm not going to be here for Christmas." It was devastating. And then he just left, left me with that news.' </p><p>Pancreatic cancer strikes 55,000 people a year and 44,000 of them will not survive. </p><p>Camille was, of course, convinced she was going to die. But her boyfriend of 17 years, Peter Catallo, daughter Jessie and her friends were not going to let her go so easily. They convinced her to get a second opinion.</p><p>When she drove from her home in Hollywood, Florida, for a consultation at the University of Miami's Sylvester Comprehensive Cancer Center, Camille was paralyzed by anxiety.</p><p>'Coming into that building was petrifying. I couldn't walk to the appointment, I was wheeled in, having been told I was going to die and having never heard of anyone surviving it.' </p><p>When she did make it into the exam room, she met Dr Caio Max Rocha Lima and his nurses, Jessica and Terri.</p><p>'Once they walked into that room, I felt immediately like I knew I was in the right place,' Camille says. </p><p>Dr Rocha Lima plotted out an explanation of her cancer, why options like surgery were out of the question and what approaches were left for her on big pads of paper. </p><p>He was honest and direct, but he wasn't giving Camille a death sentence. There was one option they could try: a very aggressive form of chemotherapy, called Folforinox. </p><p>Camille's (second from right) boyfriend of 17 years, Peter Castallo (left), and daughter, Jessie (right), urged her to get a second opinion when her first doctor told her she would die of pancreatic cancer as her mother and dog, Bear (center) did</p><p>She feels like she has been given a second chance and a new purpose, Camille has become a tireless advocates for pancreatic cancer research through the Pancreatic Cancer Action Network, including appearing on ABC News with her 'crush,' Ron Claiborne (left)</p><p>Camille (center) was treated at the University of Miami, where the athletics helped her celebrate being 'living proof' the beating pancreatic cancer is possible </p><p>Folforinox is a combination of five chemo drugs, given to patients like Camille who have pancreatic cancer that has spread to other nearby parts of the body. </p><p>She started treatment immediately. Over the course of 17 months she was to receive 34 rounds of the potent drug. </p><p>'When I went on it, no one really knew what was going to happen. But in the first three months I was really lucky. We started seeing shrinkage,' Camille says. </p><p>She was still very sick, weak, weighed less than 100lbs and could barely do a lap around her coffee table, but the hope the drug was giving her was even more important than her physical strength to Camille.</p><p>'I thought: "somebody has to beat this cancer. Why not me?"' she recalls. </p><p>Inspired, she resolved to live her life normally. Even on her way to treatments, Camille did her hair and her makeup and dressed in the clothes she loved. </p><p>'I never let cancer interfere with who I was,' she says. </p><p>Camille kept getting treatments, and her scans kept coming back cleaner. </p><p>She finished the 17 months of treatment. Her doctors told Camille she could take a 'chemo holiday,' and give her body a little break from the assault of cancer fighting drugs. </p><p>That was July 2013. Almost five years later, Camille is still on 'holiday' and still cancer free. She no longer even takes pain medication. </p><p>Alongside her daughter, Jessie (left) Camille (left) appeared on Good Morning America with Ron Clairborne (center) to talk about pancreatic cancer research </p><p>Camille has been in remission for five years and is back to walking and biking to raise money for pancreatic cancer research </p><p>'Basically, the fact that I'm alive is a miracle, and I'm hoping that because I'm not on chemo, I can be the voice for someone who is sitting in that chemo chair, or has passed away,' Camille says. </p><p>Since going into remission, Camille has gotten her purple belt in Brazilian Jiu-Jitsu, gone back to riding her bike, walking her beloved dogs and has become a tireless advocate for pancreatic cancer research. </p><p>'It's so important to get research on why [treatment] worked on me, and why it doesn't work for everyone,' she says. </p><p>Currently, only one percent of national cancer research funding is allocated to pancreatic cancer research. </p><p>This week, she attended a national advocacy day in Washington, DC, where she spoke with politicians and met 150 pancreatic cancer survivors. </p><p>'Pancreatic is the cancer that's been left behind, the bad horrible cancer that killed my mom in 1984. The stats have not changed much since then,' she says. </p><p>Camille says that people still treat the diagnosis like a guarantee of death.</p><p>'They make this face and I would say, "don't go to my funeral before I'm there." Everyone assumes you will die, and that's why [advocacy] is so important,' she says. </p><p>'I just don't want people to have a cancer and be told "go home and die,"' she says. </p><p> The views expressed in the contents above are those of our users and do not necessarily reflect the views of MailOnline. </p><p>Do you want to automatically post your MailOnline comments to your Facebook Timeline?</p><p>Your comment will be posted to MailOnline as usual.</p><p>Do you want to automatically post your MailOnline comments to your Facebook Timeline?</p><p> We will automatically post your comment and a link to the news story to your Facebook timeline at the same time it is posted on MailOnline. To do this we will link your MailOnline account with your Facebook account. We’ll ask you to confirm this for your first post to Facebook.</p><p>Part of the Daily Mail, The Mail on Sunday & Metro Media Group</p>
ns of students struggling to read fluently, write and spell — and being stigmatized for it — because of an often undiagnosed learning disability called dyslexia, died on June 15 at her home in Lakeville, Conn. She was 90.</p><p>The cause was complications from several falls, her son, Christopher, said.</p><p>Ms. King, whose uncle was dyslexic, taught, tutored, founded camps and trained teachers in education programs that were replicated around the world.</p><p>“The time to diagnose dyslexia is before the child has a chance to fail at reading,” she said.</p><p>She was instrumental in transforming the popular perception of people with dyslexia from being backward or unteachable to being often highly intelligent despite their learning difficulties. Often they were endowed with keen powers of observation and original thinking, innate charm, a sense of balance and high energy.</p><p>“We continue to see the tragedy of a bright child coming home from school in the second or third grade in tears — ‘I’m the dumbest kid in all of the second grade’ — and getting stomach aches before they go to school, and all of this totally unnecessary and totally preventable, ” Ms. King said in a videotaped interview with the International Dyslexia Association in 2013. “It drives me crazy.”</p><p>She said that dyslexia affects as many as one in five people and can be detected by age 4. (A child’s saying “washerdisher,” for example, or “flutteryby” can be symptomatic.) But through intensive tutoring, she maintained — learning a few letters at a time, and integrating spelling and handwriting into their curriculum — students can pass standardized tests or even surpass their peers by the fourth grade.</p><p>“I am aghast at the lack of training teachers get,” she said.</p><p>Her own formal scientific training was limited to a botany course, but she developed an expertise in learning disabilities as a teacher at the private Sidwell Friends School in Washington, where she had a number of mentors, including Anna Gillingham, a pathologist who pioneered methods of remediating difficulties in reading and processing language in collaboration with Dr. Samuel T. Orton, a neuropsychiatrist.</p><p>Diana Hanbury was born on Sept. 2, 1927, in London to Anthony Hanbury, who worked in finance, and Una (Rawnsley) Hanbury, a sculptor.</p><p>In a 2014 interview with the founders of Camp Spring Creek in North Carolina, she recalled “those few moments when someone expressed confidence in me and my ability to learn.” She was nine when a neighbor, a Royal Air Force pilot, taught her long division.</p><p>She earned a bachelor’s degree from the University of London and a master’s from George Washington University. Her marriage to James Cecil King ended in divorce, but they remained lifelong friends. In addition to their son, she is survived by three grandchildren and her sisters, Jillian Poole, Anna Larkin and Josephine Coatsworth. A daughter, Sheila King, died earlier.</p><p>Ms. King spent time in Southern Rhodesia (now Zimbabwe) on her uncle’s farm, realizing only later that he and his daughters were dyslexic. By chance, she was hired as a teacher at Ruzawi, a boys’ boarding school, and immediately developed a passion for teaching.</p><p>After emigrating to the United States in 1950 and teaching at Sidwell, she became a naturalized citizen. In 1955, she opened Camp Dunnabeck in western Pennsylvania, offering a six-week program for dyslexic children. She was soon stunned by how much they could progress in a matter of weeks.</p><p>“They never had to experience failure or feel they were stupid,” she said. “That one summer changed my life.”</p><p>Ms. King also established a program for learning-disabled prison inmates.</p><p>She retired from teaching at 85. In 2016, she received the Lifetime Achievement Award from the National Teachers Hall of Fame.</p>
moke at much higher rates than men or women in any other ethnic group — and deaths from lung cancer among them have soared.</p><p>In its video, various men pose with their children, or in the arms of wives or girlfriends. Then, slowly, the men fade away into wisps of gray smoke.</p><p>“Every cigarette puff reduces your years shared with your loved ones,” the announcer says in Mandarin. “Stop wasting your precious life, and quit smoking now.”</p><p>Lung cancer deaths among Asian men in the city have increased 70 percent in the last 15 years, and smoking rates among them have risen even as they have declined among other ethnic groups, the health department said.</p><p>Two factors push up smoking rates among Chinese men in New York, said Regina F. Lee, who chairs the Asian-American Smoke-Free Community Partnership.</p><p>Cultural norms from China persist in the city because many Chinese residents are foreign-born, she said: “Sixty percent of men there smoke, while there is a stigma to women smoking.”</p><p>Also, it has long been hard for Chinese-speakers to get the help the city offers to smokers, including free nicotine patches and gum. Anyone calling the quit-smoking hotline usually got an English-speaker and had to wait while a translator was found.</p><p>“So we were delighted when the health department proposed this,” Ms. Lee said.</p><p>The hotline mentioned in the ad (1-800-838-8917) is part of the national Asian Smokers’ Quitline, which is funded by the Centers for Disease Control and Prevention and offers help in Mandarin, Cantonese, Korean and Vietnamese.</p><p>But antismoking efforts in China face a delicate political situation. More than 7 percent of the government’s revenue comes from its monopoly ownership of the Chinese National Tobacco Corporation.</p><p>“The health department did focus groups and decided to start with a slightly softer approach,” Ms. Lee said. “No one knows how the community will react.”</p>
the nation’s largest provider of hospice care, dominating a rapidly growing — and controversial — business. </p><p>Death has always been lucrative enterprise, whether it involves mahogany caskets or teams of estate and tax lawyers. But hospice, the business of caring for those who are nearing death, has become a booming multibillion-dollar industry that is attracting more and more for-profit companies, including one of the nation’s major insurers. </p><p>In short, Humana, which provides Medicare Advantage plans to about 3 and a half million people for their medical needs, also wants to dominate care for those at the end stages of life, whether it provides aid in a home setting or in a facility. </p><p>“We need to make sure quality is front and center,” she said. </p><p>Government officials had accused Chemed and its hospice unit, Vitas, of aggressively billing Medicare for “crisis care,” even when patients did not require intensive services. One nurse who worked for Vitas described being sent to patients’ homes during a so-called crisis only to find the patients “were at church, the beauty parlor, or playing bingo.” Vitas, which was the nation’s largest hospice chain at the time, went ahead and billed for crisis care, according to the government’s lawsuit. </p><p>Kindred, whose hospice business Humana hopes to buy, was penalized $3 million in 2016 by federal officials and closed some facilities after the government said it could not ensure that it was not overbilling Medicare. The hospice outfit now owned by Kindred had paid $25 million in penalties in 2012 to settle accusations of improper billing.</p><p>United’s hospice unit, known as Evercare, was accused of enrolling patients who did not qualify, setting “aggressive census targets” for enrollment and paying employees bonuses if they met those targets. The company employed a team to “troll nursing homes, hospitals and other care facilities to obtain new Evercare hospice patients,” the Justice Department said. </p><p>The flood of lawsuits has discouraged some companies from getting into this field. “There’s a lot of risk,” said Paul Keckley, an independent health care analyst. </p><p>Home health care, including hospice, is a critical component of Humana’s strategy, analysts say, which is to offer an array of services for people as they age. The insurer may also be betting that hospice care in the home eventually becomes a part of what private Medicare plans must cover in the future. </p>
omputer science professors swapping ideas over a meal a quarter-century ago.</p><p>“Jim and I were at lunch one day and we decided to plan on doing some research together,” one of the professors, Peter Olivieri, related.</p><p>Dr. Olivieri suggested that they come up with a list of 100 projects; his colleague, James E. Gips, thought that was overly ambitious. They zeroed in on a couple of things.</p><p>“The first item on the list was to look at ways in which the brain itself might be used to control a computer,” Dr. Olivieri said by email. “At this time, the technology to do so was a bit daunting. Item 2 on the list was to develop ways in which you could control the movement of the cursor on the computer screen just by using your eyes.”</p><p>From that initial brainstorming session in 1992, the two men and a colleague in the psychology department, Joseph Tecce, who had been studying eye blink rates, came up with EagleEyes, a technology that uses electrodes placed around the eyes to allow a user to control the computer with eye movements.</p><p>Dr. Gips’s daughter, Amy Gips, said the cause of death was not clear, although he had recently had surgery related to his pancreas.</p><p>In the program, he acknowledged that he had not thought much about people with disabilities previously, although every day he would walk by a school on the Boston College campus where children with disabilities were taught.</p><p>“They were not in the center of my mind when we developed the technology,” he said. Rather, the prototype was being used to play video games. But once it was demonstrated at a technology conference, others could see its potential for people with disabilities.</p><p>One of those was Kathy Nash, who stumbled upon a brief report about EagleEyes on television and realized it could help her teenage son, Michael, who was born with spastic quadriplegic cerebral palsy, was nonverbal and had no voluntary muscle movement below the neck. The family had been told that his intelligence level was below that of a 2-year-old.</p><p>Hoping to try EagleEyes on her son, she called Dr. Gips, who was resistant, since the technology was still in a developmental stage. But Ms. Nash was determined.</p><p>“About her third or fourth telephone call on that phone there,” Dr. Gips says in the documentary, “I said, ‘O.K., let’s try.’ ”</p><p>“It was clear to me within a minute of his getting on the system that he was perfectly intelligent,” Dr. Gips continues. The “Turning Point” episode ends with footage of Michael’s high school graduation ceremony in 2003.</p><p>James Elliot Gips was born on April 3, 1946, in Queens. His father, William, was an accountant, and his mother, Helene Sally Rosenthal Gips, was a teacher.</p><p>He grew up in Larchmont, N.Y., where he was an excellent bridge player, winning the Westchester County scholastic pairs championship. He graduated from nearby Mamaroneck High School in 1963.</p><p>He received a bachelor’s degree from the Massachusetts Institute of Technology in 1967, a master’s degree at Stanford University in 1968 and a doctorate in computer science at Stanford in 1974.</p><p>Dr. Gips worked at the United States Public Health Service’s psychophysiology laboratory and as an assistant research computer scientist at the University of California, Los Angeles, before joining the Boston College faculty in 1976.</p><p>The Camera Mouse system, developed around 2000, did away with the need for electrodes by using a camera to track the computer user’s head or finger movements. For several years it was licensed to a start-up company that marketed it at $395, but it did not generate enough sales to be profitable, so in 2007 the college decided to make it available as a free download.</p><p>Asked if he regretted not making a lot of money off the technology, Dr. Gips said: “I’m very pleased with the way this has all turned out. I’m richer in spirit.”</p><p>Dr. Gips’s first marriage, to Patricia Biggiani in 1973, ended in divorce in 2000. In addition to his daughter, Amy, his survivors include his wife, Barbara (Thompson) Gips, whom he married in 2007; a sister, Kathy Gips; a son, Jonathan; his stepmother, Joan Gips; a stepdaughter, Caitlin O’Connor; and a grandson.</p><p>Among Dr. Gips’s other areas of research was the effects of technology and new media on consumer behavior. For instance, a 2008 study by him and a colleague, S. Adam Brasel, found that television viewers using video recorders to fast-forward through commercials may actually be influenced by those commercials anyway, even if seeing a brand image for only for a fraction of a second.</p><p>In the “Turning Point” episode, Dr. Gips reflected on the unexpected direction his career took when EagleEyes proved useful for people with disabilities, and on the personal change in perspective that resulted.</p><p>“I thought EagleEyes was a technology project,” he said. “It’s not a technology project. It’s a people project.”</p>
a surprising and somewhat horrifying diagnosis: they were made by a worm.</p><p>The 32-year-old woman likely caught the worm, a type of nematode, when she was bitten by mosquitoes in a rural area outside Moscow, her doctor said.</p><p>“She had first noted a nodule below her left eye. Five days later, it had moved to above her left eye, and 10 days after that to the upper lip,” Dr. Vladimir Kartashev of Rostov State Medical University in Russia wrote in a letter to the New England Journal of Medicine.</p><p>“She documented these changes by taking photographs of her face (i.e., ‘selfies’),” added Kartashev, who wrote in to describe the case along with parasitologist Fernando Simon of the University of Salamanca in Spain.</p><p>“The nodules occasionally caused a localized itching and burning sensation, but otherwise she had no symptoms.”</p><p>Doctors pulled the worm out and identified it as Dirofilaria repens, a type of nematode that usually affects animals such as dogs and cats. But mosquitoes can pick it up and carry it to people on occasion.</p><p>The parasite, a cousin of heartworm, is found in Europe, Africa and Asia and can grow to as long as six inches. It's usually harmless, although it can cause an allergic reaction in animals.</p><p>The patient in Russia fared better. “After removal of the worm, the patient had a full recovery,” Kartashev and Simon wrote.</p>
cutting back on insulin use because of cost. The consequences can be deadly.</p><p>Everyone with Type 1 diabetes needs to take insulin, while about a third of those with Type 2 diabetes do. Not getting enough insulin can have severe consequences for someone with diabetes who does not produce enough of the hormone, which regulates levels of glucose in the blood. Within a week or so without insulin, people with Type 1 diabetes die. </p><p>The Yale team launched the recent study to assess how many people are affected by the rising prices. They surveyed 199 patients in the New Haven area who had either Type 1 or Type 2 diabetes, asking them six questions about their ability to afford insulin, including “Did you use less insulin than prescribed because of cost?” and “Did you not fill an insulin prescription because of cost?” A positive response to any of the six questions counted as insulin underuse. </p><p>The researchers also used medical records to determine participants’ HbA1c level, a measure of blood sugar control. Unsurprisingly, those who reported underusing insulin because of cost were more likely to have dangerous blood glucose levels compared with those who said they did not underuse. </p><p>The new study focused on a single clinic, but researchers said it likely reflects what is happening nationwide. </p><p>Last year, Alec Raeshawn Smith, who had Type 1 diabetes, reduced his insulin dosage to stretch out his medicine. He was 26 and had recently been removed from his parent’s insurance plan. Mr. Smith was found dead in his home in Minneapolis last June.</p><p>His mother, Nicole Smith-Holt, said he had been shopping for health plans but could not find one he could afford. When he went to pick up his insulin and glucose strips, he was told it would cost $1,300.</p><p>“He realized maybe too late, or he never realized he was in such danger and couldn’t make a rational decision to even call for help,” she said. </p><p>Sara Theeler, a 41-year-old mother of three in Akron, Iowa, with Type 1 diabetes said she started rationing insulin after her divorce in 2010, when she lost her health insurance. She cut back on insulin and tried to manage her blood sugar levels by eating less. </p><p>A spokesman for Eli Lilly, which makes the drug, said that the firm offers several reimbursement plans, but some patients do not have good options because they do not have insurance or they have health plans with high deductibles.</p>
or redistributed. ©2018 FOX News Network, LLC. All rights reserved. All market data delayed 20 minutes.</p><p> Haywood claims she was discharged from the hospital despite exhibiting symptoms of an infection, which led to a debilitating stroke. (SWNS) </p><p>A new mom was left brain damaged after suffering a stroke caused by an infection she reportedly caught at hospital following the birth of her daughter.</p><p>Sarah Haywood, 44, collapsed just days after doctors discharged her with new daughter Mila, even though she was suffering symptoms of an infection.</p><p>On October 3, 2010, Haywood was rushed back into hospital and doctors discovered she had suffered a stroke which left her brain damaged.</p><p>Haywood, of Baddeley Green, Stoke-on-Trent, has spent the last seven years battling University Hospital North Staffordshire NHS Trust claiming they were negligent in her care.</p><p>Medical negligence lawyers Irwin Mitchell, who acted on her behalf, have revealed the NHS Trust was liable for causing her stroke following a trial in December 2016.</p><p>She has received an interim payment to help fund part of her rehabilitation but the case is ongoing and she has not received an offer of settlement.</p><p>Haywood said she still suffers with strength and mobility problems down the right side of her body and has difficulties with her speech, memory and coordination.</p><p>Haywood, who lives with her partner Mirko Budimir, 44, and their daughter Mila, now 7, has been unable to return to her job as a manager of a clothes shop.</p><p>“The effects of my stroke have a huge impact on my life," she said. "Even things like dressing myself, brushing my teeth or making myself a hot drink are a problem now. Sometimes when Mila wants to do something, I can’t do it with her and I feel broken inside."</p><p>“Whenever we want to do something as a family we have to think ahead and look at how practical it will be," she said. “I try to keep upbeat and do my absolute best to get on with life the best I can. Mirko helps me more than I could ever ask or hope for; he has been amazing.”</p><p>Investigations revealed Haywood contracted an infection which triggered a huge stroke after having an emergency caesarean section birth at the hospital on September 17, 2010.</p><p>She was transferred to a ward following the c-section, which was deemed to be straight forward, without complications.</p><p>But on the evening of September 17, regular monitoring showed she had a high temperature and an increasing heart rate – a tell-tale symptom for having an infection.</p><p>Her heart rate continued to increase the following day but when it started to fall she was discharged on September 19, and told her high pulse would continue to settle.</p><p>On September 22 she went to her doctor complaining of feeling unwell and was prescribed antibiotics, as the incision which was made during the c-section had become infected.</p><p>She visited hospital three days later to have her wound drained and again on September 28 for a consultation.</p><p>On the morning of October 3, she suffered a stroke at home and was rushed back to hospital.</p><p>A judge agreed that if the hospital had fully investigated Haywood’s high heart rate, staff would have considered she had contracted an infection and received antibiotics which would have avoided the resulting stroke.</p><p>Almost eight years after suffering her stroke, Haywood said she still struggles with everyday activities.</p><p>“I am trying to move forward but it’s hard to get over the fact that a failure to take a few reasonable steps has caused so much damage and turned my life upside down," she said. “I try to keep upbeat and do my absolute best to get on with my life. Mila is my savior and my whole world revolves around making the most of life with her and Mirko.”</p><p>“Sarah was badly let down in the standard of care she received, which meant she experienced a life-changing moment for all the wrong reasons," Jenna Harris, a specialist medical negligence lawyer at Irwin Mitchell, said. “It is important that there is not a loss of confidence in the NHS but it is also important that the NHS Trusts learns lessons from the care it provided Sarah so no other families don’t have to suffer the years of hurt that Sarah and Mirko have."</p><p>“We also call on the Trust to accept responsibility for its mistakes," Harris said. "Despite strong evidence presented against it, the Trust tried to fight this case. Eighteen months from a Judge ruling Sarah’s care was negligent, the case is still ongoing.”</p><p>This material may not be published, broadcast, rewritten, or redistributed. ©2018 FOX News Network, LLC. All rights reserved. All market data delayed 20 minutes.</p>
estriction and potential downsides that comes with detoxes and cleanses, clean up your eating with these nutritionist-approved tips instead.</p><p>To reboot your diet and reset your gut, remember to eat the three P's: prunes, pulses and pears.</p><p>When I need to give my diet a reboot, I focus on having two nourishing, planned snacks per day.</p><p>“When I need to give my diet a reboot, I focus on having two nourishing, planned snacks per day, like a pear and pecans, or grape tomatoes and string cheese, or berries and yogurt. And I put the snacks on a plate, sit down and enjoy them.” This part is especially key. When you graze or snack mindlessly, you don’t register those foods as well as when you plate them. No plate? No problem! Use a paper towel, napkin, cup or whatever is available to you to help you eat more mindfully.</p>