By David Owens, Contact Reporter

The governor on Friday formally announced his plan to expand housing opportunities and services for people with intellectual disabilities.

Gov. Dannel P. Malloy included $3.8 million in his proposed budget for what he termed the “intellectual disability partnership initiative.” The goal is to reduce the waitlist for people with intellectual disabilities who need state-funded housing and to find new ways to address the need.

Malloy also proposed $1 million in bonding funds to convert group homes to supportive housing units, residential care homes or community care homes for people with intellectual disabilities. Continue reading →

Advocates for the more than 16,000 people with intellectual disabilities who are served by the state are reacting favorably to some aspects of Gov. Dannel P. Malloy’s proposed budget, including an increase of about $4 million to, among things, help create more community settings for people now living in state facilities.

They also applauded the closing, at a savings of $1.6 million, of the on-campus fire department at the Southbury Training School — a unit that has hung on year after year as the population has dwindled to fewer than 250 residents and the unused portions of the complex are being mothballed.

But there was despair over the lack of funding for day programs and job training for high school graduates in 2017 and 2018 — as many as 600 young people who are turning 21 and will have completed their federally mandated schooling. For decades, these graduates went fairly seamlessly into the social, recreational, and skill-building programs for young adults. In the last few years, funding cuts have restricted these opportunities. Continue reading →

Julie Swanson, of Durham, is the mother of a grown son with autism and a special education advocate. She is part of group that has joined with the state in its appeal of a Superior Court judge’s ruling that would radically change the way public education is funded in Connecticut. Swanson and advocates across the state were stunned by Judge Thomas Moukawsher’s suggestion that school districts could deny educational services to profoundly disabled students. (Cloe Poisson)

Parents and advocates have joined in the state’s appeal of a judge’s ruling striking down Connecticut’s school-funding formula, seizing on language that described some children with profound developmental disabilities as possibly incapable of learning and unworthy of local education dollars. Continue reading →

By Adam Liptakjan

WASHINGTON — In a case that could affect the education of 6.7 million children with disabilities, the Supreme Court on Wednesday struggled to decide whether it should require public schools to do more under a federal law that calls for them to provide a free education that addresses the children’s needs.

Justice Samuel A. Alito Jr. said the court was being asked to choose among several finely shaded formulations. “What is frustrating about this case and about this statute is that we have a blizzard of words,” he said.

The court appeared uneasy with a standard used by many appeals courts, which have said that providing a modest educational benefit was enough. But some of the justices indicated that they were concerned about the costs that any changes could impose. Continue reading →

By Ken Byron

As with other pageant competitions, the title of Ms. Wheelchair Connecticut comes with a sash. But it also comes with responsibility.

The event uses a twist on the idea of a traditional beauty pageant to give women who rely on a wheelchair more visibility. And that is what the newly crowned Ms. Wheelchair Connecticut, Shannon Mazurick of Avon, liked when she heard about the pageant.

Mazurick, 30, has cerebral palsy and uses a wheelchair to get around. It’s difficult for Mazurick to speak so she uses a computer program to put words she types on a keyboard into speech.

“Advocacy has always been a huge part of my life,” Mazurick, wearing a red dress with the sash draped across her chest, said in a recent interview. “I feel it is so important. And Ms. Wheelchair, the organization or the pageant, deals with advocacy.” Continue reading →

The White House hosted its final National Disability Employment Awareness Month event Thursday and celebrated the strides we have made to create a more inclusive federal workforce. I’m proud to announce important progress toward that effort.

In 2010, President Obama challenged the federal government to hire 100,000 people with disabilities within five years. Not only did we reach the goal between 2011 and 2015, we surpassed it. Since then, the federal government has hired more than 154,000 permanent and temporary employees with disabilities, and more than 109,000 of whom are permanent hires. Continue reading →

Thanks to a grant focused on encouraging professional development for individuals from diverse backgrounds in human services, three Goodwin College students will have a rare — and challenging — educational experience that can profoundly shape their careers and benefit the clients with whom they will work.

The source of this unique opportunity comes from a grant that the University of Connecticut University Center for Excellence in Developmental Disabilities (UConn UCEDD) received from the U.S. Department of Health and Human Services, Administration For Community Living, Administration on Disability (AOD) Excellence in Developmental Disabilities National Training Initiative. The funds support the recruitment and retention of trainees from culturally and linguistically diverse backgrounds to participate in a fellowship experience at the UConn UCEDD in Farmington, Connecticut. Continue reading →

By Ben Mattlin, author of the memoir “Miracle Boy Grows Up”

In midsummer, I learned of the death of Laurie Hoirup, a prominent 60-year-old disability rights advocate in California. Laurie drowned in the Sacramento River after a July 4 celebration. She was well-loved and accomplished. She’d served as a chief deputy director of the State Council on Developmental Disabilities for five years and wrote books about living with a disability.

Laurie’s sudden and tragic death was not directly caused by her S.M.A., but it is a stark reminder of the vulnerability of disabled lives. She was deboarding a pleasure boat when the ramp to the dock shifted. The weight of her motorized wheelchair — and the fact that she was strapped into it — pulled her down into the water too rapidly for rescue.

Laurie’s death had extra significance for me, a 53-year-old husband and father of two, in part because we shared a diagnosis: spinal muscular atrophy.

S.M.A. is a congenital and progressive neuromuscular weakness akin to muscular dystrophy. Until recently, half the babies born with it would die before their second birthdays. Their hearts and lungs became too weak to continue. Medical care and understanding have improved the odds somewhat. Continue reading →

By Matt Flegenheimer and Amy Chozicksept, New York Times – September 21, 2016

ORLANDO, Fla. — Of all the attacks that Hillary Clinton and her fellow Democrats have tried against Donald J. Trump since he captured the Republican presidential nomination, one has stood out for its emotional force and persuasive power: No one, it seems, can abide Mr. Trump’s mockery last year of a reporter’s physical disability.

And as Mrs. Clinton strains to make a more affirmative case for her own candidacy, after a summer focused largely on hammering Mr. Trump, her campaign believes that a focus on an often-overlooked constituency — voters with disabilities — can accomplish both goals at once.

On Wednesday, without mentioning the Trump episode, Mrs. Clinton discussed her vision for an “inclusive economy” with expanded job opportunities for what she called “a group of Americans who are, too often, invisible, overlooked and undervalued — who have so much to offer, but are given far too few chances to prove it. Continue reading →

By Susan Campbell, Contact Reporter, Hartford Courant

When he was a kid, Nick Glomb watched his mother prepare food for the family in her kitchen. He knew enough to stay out of the way — this was his mother’s kitchen, after all — but it was inspiring in the way his mother made so much from scratch, and her preparations planted a seed.

Now Glomb is putting his dream into action. He wants to open a hot dog stand, using only the best ingredients, and he has a GoFundMe account to help him raise the cash. Right now, he’s at just over $6,500, a few thousand short of his $10,000 goal.

He has a name for the cart already, Family and Friends Roadside Cart.

Continue reading →