Software that can understand images, sounds, and language is being used to help people with disabilities such as deafness and autism in new ways

https://goo.gl/zVzdor

CC rules require TV stations to provide closed captions that convey speech, sound effects, and audience reactions such as laughter to deaf and hard of hearing viewers. YouTube isn’t subject to those rules, but thanks to Google’s machine-learning technology, it now offers similar assistance.

YouTube has used speech-to-text software to automatically caption speech in videos since 2009 (they are used 15 million times a day). Today it rolled out algorithms that indicate applause, laughter, and music in captions. More sounds could follow, since the underlying software can also identify noises like sighs, barks, and knocks.

The company says user tests indicate that the feature significantly improves the experience of the deaf and hard of hearing (and anyone who needs to keep the volume down). “Machine learning is giving people like me that need accommodation in some situations the same independence as others,” says Liat Kaver, a product manager at YouTube who is deaf.

Indeed, YouTube’s project is one of a variety that are creating new accessibility tools by building on progress in the power and practicability of machine learning. The computing industry has been driven to advance software that can interpret images, text, or sound primarily by the prospect of profits in areas such as ads, search, or cloud computing. But software with some ability to understand the world has many uses.


Six charts that illustrate the divide between rural and urban America

https://goo.gl/OfS5Ow

3. Disabilities are more common in rural areas

Disability matters in rural America. Data from the American Community Survey, an annual government poll, reveal that disability is more prevalent in rural counties than their urban counterparts.

The rate of disability increases from 11.8 percent in the most urban metropolitan counties to 15.6 percent in smaller micropolitan areas and 17.7 percent in the most rural, or noncore, counties.


3 Facts About Mental Health and Down Syndrome

Let us not forget substance use disorder and IDD either.......

https://goo.gl/aHybgT

Have you ever thought about the mental health concerns of people with down syndrome? Perhaps not. However, I truly believe that it is important to think about the unique mental health issues faced by some of the most vulnerable people in our communities, including people with disabilities. Not to say that people with Down syndrome are not strong or kickass individuals. But it’s no secret that they face a lot of hurdles, including infantalization by people without the disorder. In honour of tomorrow, which is World Down Syndrome Day, I thought I would share some information to enlighten you about the personal experiences of people with Down syndrome.

People with autism, intellectual disabilities fight bias in transplants

https://goo.gl/CXLxhb

Paul Corby needs a new heart. On that there is no dispute. The same rare disease that killed his father at 27 is destroying his left ventricle. While there is no cure or surgery that might repair the damage, a heart transplant could extend his life considerably.

But Corby, who lives in Pottsville, Pa., is autistic, suffers from several psychological conditions and takes 19 medications. When he applied to the transplant program at the University of Pennsylvania in 2011, he was rejected because of his “psychiatric issues, autism, the complexity of the process . . . and the unknown and unpredictable effect of steroids on behavior,” according to the denial letter sent to his mother.

“I couldn’t even believe this would happen,” Karen Corby said, “that this would be the reason in this day and age.”

In fact, mentally disabled people are turned down for organ transplants often enough that their rights are a rapidly emerging ethical issue in this corner of medicine, where transplant teams have nearly full autonomy to make life-or-death decisions about who will receive scarce donor organs and who will be denied.


Losing Friends to Ableism

https://goo.gl/EGVGEW

“I would’ve made sure it was accessible if we were closer friends.” An ex-friend said this after I expressed hurt over his party being held in an inaccessible venue. I wasn’t even mad at him initially since it was a surprise planned by his family; they knew I couldn’t get inside, and ignored guests offering alternate, accessible spaces. When this ex-friend told me of the event, all he said was “sorry you can’t come.” That was it.

I wouldn’t have been too upset if this person offered to visit for a mini celebration with mutual friends. I wouldn’t have been angry if he gave a sincere apology rather than defensiveness and silence. Making accessibility a privilege offered only to closest friends or family is horrifically ableist. This person was someone I hung out with regularly, so I assumed we were good friends. But even if we were acquaintances, what he said was dehumanizing. To make things worse, he spouted that quote above knowing I was going through an emotionally vulnerable time in my life. I’m glad I ended that friendship, especially after realizing he was toxic in other ways.

This was not the first time folks invited me to parties that were not accessible.One of my best friend’s mom hosted a party at a local VFW, and we all assumed it was wheelchair accessible because, you know, veterans. But when I got there, there was a flight of stairs. Those friends were as upset and shocked as me, so we partied on another day at home – with ice cream cake. Compassion and following through to solve a problem make all the difference.

It isn’t just about meeting accessibility needs, either. In this guest post by Noemi Martinez, she writes on friends ghosting when our disabilities present themselves in ways that make abled friends uncomfortable:

“Recently, friends went out of my life after . . . we went through some pretty life-changing health scares. Just like we often don’t make conscious decisions on who ends up being our friends, we can’t change when friends feel they are no longer part of the flow of a friendship. We are often left wondering if we were too much.”


Syphilis Rate Among Newborns Reaches Highest Level in Years

https://goo.gl/D3lvi8

The disease was nearly eradicated around 2000 but has been on the rise since 2012. Health officials partially blame the opioid epidemic.

Congenital syphilis is when syphilis is passed down from a mother to her fetus. The disease can cause miscarriages and stillbirth. For newborns, it can result in brain and nerve problems, bone deformities, meningitis and death.

California has the third highest rate of congenital syphilis, after Georgia and Louisiana. Outbreaks vary in size and scope, but health officials agree there are at least two common factors contributing to the problem everywhere: the opioid epidemic and lack of prenatal care.

“If someone is actively engaged in substance abuse, they’re not thinking about their health care,” says Kern County's Smith.

Women who use drugs, particularly opioids like heroin and methamphetamine, are more at risk of contracting syphilis because it can be transmitted through needles as well as sex. Karen Landers, medical director for communicable diseases at the Alabama Department of Public Health, says that pregnant women using drugs are less likely to seek prenatal care and therefore learn they have syphilis. Unless treated with antibiotics early in a pregnancy, syphilis has a 50 percent chance of infecting a baby.

CDC data shows that overdose deaths involving opioids began to rise sharply in 2013, the same year congenital syphilis started to come back. Before that, overdoses were actually steady after years of gradually increasing.


Stanford researchers show we’re sending many children to school way too early

Always thought this.....

https://goo.gl/BgqVVu

“We found that delaying kindergarten for one year reduced inattention and hyperactivity by 73% for an average child at age 11,” Thomas Dee, one of the co-authors and a Stanford Graduate School of Education professor, said in a release.

Dee did his research with Hans Henrik Sievertsen of the Danish National Centre for Social Research, who told Quartz that the impact was strong and lasted a long time: “We were a bit surprised at how persistent the effect was.” The effect of delaying school on hyperactivity and inattention didn’t diminish over time, as they expected, but increased: in fact, waiting one year virtually eliminated the chance that an average kid at age 11 would have higher-than-normal scores on those measures.


Shain Neumeier - For Your Own Good: Coercive Care in the Lives of Marginalized People

Youtube video....

https://goo.gl/6NGAF2

Shain M. Neumeier is an autistic attorney who has a number of other disabilities including ectodermal dysplasia and a cleft lip and palate. Shain is also a survivor of coercive treatment. This background has led Shain to be involved in disability justice advocacy for the past 7 years. During that time, Shain has worked with a number of organizations including other statewide protection and advocacy agencies, self-advocacy organizations and a law firm, with a focus on addressing and preventing abuse and neglect in institutional settings.

How Murder Victims With Disabilities Get Blamed For Their Own Deaths

https://goo.gl/I2oFON

Alex Spourdalakis was 14 when his mother and godmother decided to kill him.

The women tried to poison the boy, who had autism, with sleeping pills. When that failed, Dorothy Spourdalakis stabbed her son four times in the chest with a kitchen knife, twice hitting his heart. She slit one of his wrists so deeply she nearly severed his hand, according to court records. Then she handed the knife to Jolanta Agata Skrodzka, who used it to kill the family cat so it wouldn’t have to live in a shelter after their arrests. 

A year later, 11-year-old Raashanai Coley, another child in Illinois, died from a stomach rupture after her mother, Nicholette Lawrence, punched her repeatedly. The autopsy revealed scars and old injuries indicating previous physical abuse.

Alex was killed in River Grove in 2013. Raashanai died in Waukegan in 2014. Both were slain by people entrusted to protect them. But the respective outcomes of these first-degree murder cases ― one involving a child with disabilities, the other involving a child without medically documented handicaps ― speak volumes about an insidious bias in the justice system.

Alex’s killers pleaded guilty to involuntary manslaughter, and served three years each before they were sentenced to time served and released. Raashanai’s killer, meanwhile, was convicted of murder and is serving 43 years.

Advocates for the disabled say such disparities are common in a legal system that seems to treat accused killers less seriously when the victim was a person with special needs who depended on the person charged with murder for care.

On average, at least one disabled person is killed each week by a parent or caregiver, according to a Ruderman Family Foundation report that documented more than 200 deaths from 2011 to 2015.