More States Move To Phase Out Subminimum Wage

Chris Serres, Star Tribune/TNS • July 18, 2021
A man with Down syndrome picks up trash for his sheltered workshop job. (David Joles/Star Tribune/TNS)

MINNEAPOLIS — Krystal Halford recalls feeling jubilant after landing a job at an assembly plant in Eagan that employs people with disabilities.

But after opening her paycheck, Halford’s excitement turned to dismay. For two weeks of work, Halford discovered that she had made just $100 — amounting to less than $4 an hour. “It sent a message that I wasn’t valued, that I didn’t deserve what others have because I happen to be different,” said Halford, 32, who has Asperger’s syndrome, a developmental disorder.



Halford is among thousands of Minnesotans who have been paid less than the minimum wage solely because they have a disability. They work at dozens of centers across the state, known as sheltered workshops, that are allowed under a loophole in federal law to pay people with disabilities based on their productivity, rather than a fixed hourly rate. In many cases, their pay amounts to less than $1 an hour for basic tasks such as sorting and packaging merchandise, shredding paper or picking up garbage on work crews.


More than 8,000 Minnesotans with a range of disabilities, including Down syndrome, cerebral palsy and autism spectrum disorder, attend these cloistered workplaces — among the most of any state, according to federal workforce data.


Now, this separate and unequal payment regime is coming to an end. This month, after years of pushing by disability advocates, Minnesota became the latest state to move to abolish the practice of paying people with disabilities a subminimum wage. Tucked deep inside a 533-page budget bill is a measure that establishes a task force to develop a plan to phase out subminimum wages by August 2025.


Lawmakers also approved $14.1 million in grants to help disability service providers transform their business models and boost work options in the community.


The practice of paying subminimum wages began in the Great Depression as a way to give people with disabilities a chance to learn job skills. But in recent years, the practice has come to be seen as discriminatory, exploitative and a violation of civil rights under the Americans with Disabilities Act. A Star Tribune investigation in 2015 found that many of those in Minnesota’s workshops spend years toiling in poverty and isolation with little hope for advancement. At least eight states — including Colorado, Maryland, Oregon and Washington — have moved to prohibit subminimum wage employment in the hope of integrating more people with disabilities into the general workforce.


And early this year, President Joe Biden signaled his desire to end subminimum wages as part of his broader proposal to boost the federal minimum wage to $15 an hour for all workers, including those with disabilities.


“The world is moving in this direction,” said Jim Abeler, a state senator in Minnesota who chairs the Human Services Reform Finance and Policy Committee. “Everyone deserves a chance to be as independent as possible — and they shouldn’t be trapped in a subminimum wage job when they could work at a market wage.”


But the move to phase out subminimum wages is expected to force dramatic changes at approximately 80 centers across the state that provide a wide range of support services for people with disabilities. Many of these facilities — sometimes called “day activity centers” — have long struggled to find skilled workers for their clients. The demand for more staff is expected to intensify as centers transition more people to jobs in the regular workforce. People may require one-on-one job training, transportation and other services, providers said.


Many parents of adult children with disabilities have vigorously supported the alternative wage system, partly due to fears that their children will have nowhere to go if workshops close. In many smaller towns across Minnesota, workshops are bustling hubs of activity, where individuals make social connections and participate in crafts and learning activities. Many centers are the primary source of transit for adults with disabilities, shuttling them to and from work and activities in the community.


Each morning, about 60 adults with disabilities arrive at Options Inc. in Big Lake to do light assembly work, such as packing tools in boxes. These individuals are paid based on the number of products they sort or package each hour — a system known as piecework, which is allowed under a special section of the 1938 Fair Labor Standards Act.


Brenda Geldert, executive director of Options, said clients are asked several times a year if they would like to work in the community — and efforts are made to place people in mainstream jobs. Even so, many of the center’s clients prefer coming into the center, where they have developed strong friendships and “a sense of purpose,” Geldert said. “We have people who love it here and who absolutely do not want to pursue independent employment,” she said.


Jim Clapper, co-chairman of a grassroots coalition of Minnesota families with loved ones with disabilities, has been an outspoken supporter of subminimum wage employment. The system gave his 34-year-old son, Bob, who has Down syndrome, the opportunity to become accustomed to a structured work environment and build social skills, he said. After three years in a workshop, Bob gained enough confidence to transition to a mainstream job at a supermarket in St. Paul.


“My son’s skills and work ethic took a long time to develop, and he never would have gotten there were it not for the (workshop),” Clapper said.


“I would hate to see these choices evaporate.”


Yet some individuals with disabilities describe the experience of working in sheltered workshops as dehumanizing.


Alex Jaffe, 33, who has Asperger’s syndrome and attention deficit hyperactivity disorder, recalled the tedium of spending his days packing zip ties into plastic bags at a workshop. When orders were slow, they would sometimes empty the bags and redo the work just to stay busy. Because Jaffe was paid based on his productivity, he received no income when orders stopped or a machine broke down.


Jaffe, who is now employed as a security guard at $19 an hour, said no one ever asked him about his career ambitions or told him he was capable of working in the community at a higher wage. “It was a whirlpool of despair,” said Jaffe, who left the workshop and eventually received a bachelor’s degree in criminal justice. “It’s the mind-numbing nature of the work that leaves you wondering, ‘Will I ever get a slice of the American dream?'”


Noah McCourt, a disability rights advocate with autism spectrum disorder, recalled feeling “hurt and confused” when he received his first paycheck at a workshop in Watertown, where he sorted recycled garbage on a conveyor belt. His total earnings for two weeks were a mere $18. It was only later, when McCourt went online to research federal wage laws, that he discovered that America had a separate pay system for people with disabilities.


“Looking back on it, there was no expectation that you could ever amount to anything better,” McCourt said.


Despite recent efforts to expand work opportunities, Minnesota still has one of the lowest rates of integrated employment in the nation for people with intellectual and developmental disabilities. A 2020 state survey found that only 57% of adults with developmental disabilities report having a job with income — largely unchanged from a decade ago. Only 17% of Minnesotans with developmental disabilities believed their employment prospects would improve in the next two years, the survey found.


“It saddens me to say this, but there is still a strong institutional bias in Minnesota against hiring people with disabilities,” said state Sen. John Hoffman.


Halford said she has tried to forget the 18 months she spent at a sheltered workshop. The pay was so low that she would regularly skip meals to save money and could not afford outings with friends. Since leaving the facility, Halford has founded her own online jewelry and gift business and landed work at a Cub Foods supermarket for nearly $13 an hour.


“I still feel like part of my life was taken from me,” Halford said. “You can’t treat grown adults like children and expect them to be happy.”


© 2021 Star Tribune
Distributed by Tribune Content Agency, LLC


Image from https://www.ridehirta.com/invisibledisabilities
By JT Moodee Lockman February 10, 2025
BALTIMORE -- A proposed bill in Maryland would allow residents to disclose "nonapparent disabilities" on their driver's licenses or identification cards. Eric's ID Law, or HB707, [01] would require the Motor Vehicle Administration (MVA) to add a certain symbol to licenses, ID cards or moped permits indicating that the applicant has a nonapparent disability. The idea was proposed by a Maryland family during an appearance on ABC's "The View," The Baltimore Banner reported. [02] The Carpenter-Grantham family had the idea after the 2020 murder of George Floyd [03] which sparked protests across the nation. "I realized that I have an African American son with an invisible disability," mother Linda Carpenter-Grantham said during the TV appearance. The bill was introduced in the state Senate during the 2024 legislative session but missed a deadline in the House. The proposed bill would require the MVA to establish public outreach programs to educate the public about the new symbols or notations. The MVA would work with disability advocates to design the symbols. The MVA would be prohibited from sharing information about an applicant's disabilities. The bill would also prevent the MVA from asking an applicant to provide proof of their disability or reject an application because the listed disability does not match other documents associated with the applicant. Under the bill, the Maryland Police Training and Standards Commission and Department of State Police would have to immediately implement training for police interactions with those who have nonapparent disabilities noted on their IDs. The bill will be the subject of a hearing on Feb. 13 at 1 p.m. What is a nonapparent disability? According to the proposed bill, a nonapparent disability is a health condition that is not immediately obvious or visible, this could include developmental or intellectual disabilities. According to a study by the National Institutes of Health (NIH), [04] common nonapparent disabilities are anxiety and depression, Alzheimer's, deafness, post-traumatic stress disorder (PTSD), attention-deficit hyperactivity disorder/attention deficit disorder (ADHD/ADD), and diabetes among others. People with developmental disabilities are about seven times more likely to encounter law enforcement than neurotypical individuals, according to a 2001 study by the Department of Justice. [05] Citations: [WEBSITE] Legislation: Eric's ID Law , or HB707: https://tinyurl.com/4r5s8ntp [ARTICLE] Maryland mom and her autistic son pitch a disability safety bill on ABC’s ‘The View’: https://tinyurl.com/4nzukspm [ARTICLE] George Floyd's death sparks large protests, confrontations with police: https://tinyurl.com/263hk9sk [STUDY] Living with invisible medical disabilities: experiences and challenges of Chilean university students disclosed in medical consultations: https://tinyurl.com/bdexd9js [ABSTRACT] Contact with Individuals with Autism: Effective Resolutions: https://tinyurl.com/56d6yd44 [ORIGINAL ARTICLE] Proposed bill would allow Marylanders to disclose nonapparent disabilities on their IDs: https://tinyurl.com/9k7z6nyh 
Advocates and members of the developmental disability community rallied Monday to demand legislators
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Advocates and service providers on the Eastern Shore are joining Maryland’s disability community to call for rollbacks on projected cuts to funding for developmental disability services. Scott Evans, executive director of the Benedictine School in Ridgely, said the near $200 million in cuts to Developmental Disabilities Administration funding outlined in Gov. Wes Moore’s proposed budget would be the worst he’s seen in his 25-year career. “Bottom line, these proposed cuts of close to $200 million in state funds would be catastrophic to the community service providers, as well as the people we support and our employees,” Evans said. “It would literally set us back years in funding.” The proposed cuts come as the state faces a near $3 billion deficit. Some advocates from the Eastern Shore note they could reduce the choices available for families and people with disabilities. Jonathon Rondeau, president and CEO of The Arc Central Chesapeake Region, says families and people with developmental disabilities on the Eastern Shore already have a limited number of options. “There are less agencies providing services for people with disabilities on the Shore,” Rondeau said. “So if there is instability in the system, it can potentially reduce choice for people with disabilities.” Evans echoed the same sentiment, and added that the cuts could hurt Benedictine’s ability to stay competitive when hiring employees. In recent years, the nonprofit school and service provider has raised wages in an attempt to attract quality employees. “All that has been an investment we’ve made because of the funding that we have received,” Evans said. “Now to wipe that funding out basically overnight means that we’re stuck in a holding pattern.” THE CUTS In Moore’s budget proposal, his office notes that in addition to the $1.3 billion set for the Developmental Disabilities Administration in fiscal year 2026, the state will “better leverage federal funding and align Maryland’s program more closely with federal guidance and practices across other states.” Evans says it’s not clear how DDA would implement the cuts, though his team at Benedictine team is working to crunch the numbers. Evans said it would cost the school hundreds of thousands of dollars of funding at the very least. Specific cuts that worry advocates include reductions in “dedicated hours” funding for those in community living programs, as well as a $14.5 million blow to self-directed services funding. “Someone who is in their late 60s and retired and chooses to stay home every day rather than going to a day program won’t necessarily have that choice anymore,” Rondeau said regarding the dedicated hours cuts. “There won’t be the funding available for that. It’ll be difficult for providers such as The Arc to support someone who may have significant health issues and need to go to the doctors.” Karenna Jones of Salisbury worries that cuts to self-directed services will impact the ability for her family to take care of her 26-year-old son, Kenneth, who has a traumatic brain injury and lives at home. Jones says as long as she lives, she “would never put (her) kid in a provider home.” But large cuts in funding may leave her with no choice. “We might be forced to do that,” Jones said. “It’s not fair.” RALLY IN ANNAPOLIS With the uncertainty swirling, hundreds packed Lawyers Mall in Annapolis Monday night, protesting for legislators to reject the proposed cuts. Leaders at the Benedictine School and The Arc Central Chesapeake Region attended, as did Jones. “I’m always amazed at how quickly the folks within the disability community can rally around a cause, and a cause that means so much to them,” Evans said. “And also, to some extent, the positive response we’ve gotten from legislators about these cuts.” Jones said the rally — organized with just three days notice by a developmental disability coalition — was inspiring and beautiful. “We were saying, ‘Save our DDA services. Save it. Don’t leave us behind,’” Jones said. Citations : [ORIGINAL ARTICLE] ‘Catastrophic:’ Eastern Shore advocates share impacts proposed disability cuts may bring: https://tinyurl.com/5ahffbu8
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Robert F. Kennedy Jr. testifies before the U.S. Senate Committee on Finance concerning his nominatio
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rom left, Laura Howell, CEO of Maryland Association of Community Services; Ande Kolp, executive dire
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Pixabay Stock Photo
By Zoe Beketova, Yale University December 11, 2024
People with disabilities (PWD) make up 25% of the U.S. population. They face elevated mental health concerns and are more likely to utilize mental health services compared to non-disabled individuals. Yet, PWD also report higher unmet mental health service needs and barriers to accessing care. Dr. Katie Wang, Ph.D. '14, associate professor in the Department of Social and Behavioral Sciences at the Yale School of Public Health (YSPH), and colleagues recently examined the experiences of PWD who engaged in mental health services. The study is published in [ 01 ] the journal SSM - Qualitative Research in Health. "We interviewed 20 U.S. adults with a wide range of visible and invisible disabilities," said Wang, a social psychologist and the study's lead author. "Participants identified ableism as a major concern when they talked about their experiences in seeking mental health services ." Ableism is prejudice and discrimination against people with disabilities, based on the belief that people without disabilities are superior. It can be conscious or unconscious and is embedded in institutions, systems, and society as a whole. It manifests in many forms, including harmful stereotypes, misconceptions, and generalizations. This can include the belief that people with disabilities are less able to contribute and participate in society; and the belief that people with disabilities are to be pitied or viewed as inspirational rather than just as normal human beings. Participants in the qualitative study [ 02 ] ranged in age from 22 to 67. Their disabilities included chronic health conditions (e.g., epilepsy), mobility disabilities (e.g., spinal cord injury), sensory disabilities (e.g., blindness) or, for a majority, a mixture of different disabilities alongside mental health conditions. Upon speaking with the participants about their experiences with mental health care providers, the researchers identified several recurring themes. A common experience cited was providers holding misplaced assumptions about the impact of disability on mental health as well as a general lack of knowledge about disability, either overlooking the connection between mental health and the disability or minimizing the role of disability in a person's life. Many participants also described providers not believing their lived experiences, being stereotyped, or ignored. "These results underscore the importance of emphasizing disability competency when training the next generation of mental health providers," Wang said. Care is a challenge for people with multiple minority identities The study also explored the quality of mental health care received by individuals with multiple minority identities, including having a disability. Such individuals often struggle with receiving professional help, yet little research exists on the issue. One of the participants, when discussing an unhelpful provider, said that it's hard for them, as a person with many minority identities, "to know which identity it is and why it triggered them [the provider]." The researchers found that having intersecting minority identities—such as being Black or transgender and disabled—presents additional barriers to receiving quality care. Systemic ableism undermines good intentions Another major point raised by participants was the systemic ableism within mental health care systems. "What struck me in particular is the findings pertaining to systemic ableism, specifically, how even well-intentioned mental health care providers can perpetuate ableism, given that they are working in a fundamentally ableist system," Wang said. "None of the people … want to hurt us, but the structures are built to hurt us and so they always will," one of the participants stated. Participants raised this point when discussing the emotional pain providers often unwittingly caused them during a mental health session. A need for better access to care A final point identified in the study was that physical accessibility barriers also present obstacles for PWD accessing mental health care. Telehealth, a form of online health care support, has been praised for mitigating some of the physical barriers that people face, but not all participants in the study could navigate virtual interactions. For example, lip reading is particularly difficult behind a virtual screen, some deaf or hard of hearing participants said. "I think what we want to be careful of, and what a lot of participants were warning against, is we should not be thinking of telehealth as a silver bullet," Wang said. "It does not fix accessibility across the board. It does not remove all access barriers. But having telehealth as an additional tool in the toolbox is definitely a benefit for the disability community." In response to the findings, the researchers are calling for systemic structural reforms such as increased training on disability competency for providers as well as the recruitment and—vitally—retainment, of disabled faculty and students to normalize discourse. For practitioners, the study recommends self-education on disability awareness and more of a focus on improving accessibility to their care, whether through increased flexibility, universal design practices, or openness to learning about disabilities. Wang stressed that ableism is more than just an interpersonal phenomenon: it is deeply embedded in health care systems. With YSPH's focus on addressing inclusivity, intersectionality, and belonging in public health and health care, studies such as Wang's shine a light on the experiences of PWD across different conditions and identities when seeking mental health support. More information: Katie Wang et al, Ableism in mental healthcare settings: A qualitative study among U.S. adults with disabilities, SSM - Qualitative Research in Health (2024). DOI: 10.1016/j.ssmqr.2024.100498
Special Olympics World Winter Games Turin 2025 Logo
December 11, 2024
The President will host a dinner honoring Special Olympics athletes as they prepare to compete at the upcoming Special Olympics World Winter Games in Turin in March 2025.
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