Mississippi Today
For this Delta State student with autism, ‘there’s always another wall to climb with no ladder’
For this Delta State student with autism, ‘there’s always another wall to climb with no ladder’
CLEVELAND — On a recent Thursday afternoon, Avery Williams hurried down an empty hallway in Kethley Hall with his mother, Deloris-Clay Williams. The 25-year-old was looking for a room he’d never been in before where, in less than five minutes, a meeting was scheduled to start that would determine the fate of his academic future at Delta State University.
His mother eventually found the sign, stamped on a window in sharp, black letters, that signaled they were in the right place: “College of Arts and Sciences — Office of the Dean.”
This was supposed to be Avery’s last semester. Avery has autism, a developmental disability that affects communication and learning, and he enrolled at Delta State two and a half years ago after getting his associate degree from the community college in his hometown of Moorhead.
By going away to college, Avery hoped to achieve two dreams: Become a cinematographer or video editor, and learn to live on his own. Deloris, who has lupus, was increasingly finding it harder to assist him.
But in the midst of the pandemic, Avery struggled to communicate with his professors via message board. His GPA steadily dropped. Over winter break, he was suspended. Nobody told him in person. All he got was an email.
Now he wouldn’t be able to graduate with the art degree he’d worked so hard for, and had taken out more than $30,000 in student loans to get.
Avery’s struggle to get through DSU is just one example of how universities in Mississippi are failing students with autism. While one state agency offers peer mentoring services, only one public university in Mississippi has an in-house program designed for students with autism. And there is no comprehensive data on the rate at which students with disabilities, including those with autism, enroll and graduate from college in Mississippi.
What was happening to Avery didn’t seem fair to Deloris. She decided to intervene. A retired public school teacher trained at DSU, she was used to standing up for Avery’s right to an education. It’d just been awhile since she’d had to do so.
On Jan. 9, the first day of classes, Deloris sent the dean, Ellen Green, a fiery email requesting Avery be readmitted to the art program. She signed it, “desperate parent.”
It got Avery a meeting. In the waiting room outside the dean’s office, Deloris looked over questions she’d prepared in a comprehensive notebook. Avery stood silently in the middle of the room, his arms crossed, anxious to know if he would be able to re-enroll and take classes. He just wanted to get the meeting over with.
At 4 years old, Avery could read, write his first and last name, and count to 100. He’d also cry at the sight of hair on the floor. If Deloris gave him a pencil and paper, she said he would draw circles “over and over.” The only food he’d eat was chicken nuggets.
Then he got encephalitis. It led to memory loss and intensified his repetitive behaviors. By the time Avery started elementary school, Deloris was certain he had autism. He was quiet and avoided playing with other kids unless it was basketball with his younger brother, Alex Williams.
Though Deloris begged Avery’s teachers to test him for autism, they wouldn’t. He wasn’t tested for any learning disabilities until fifth grade and only after Deloris said she wrote a complaint to MDE’s Office of Special Education.
That experience taught Deloris how to advocate for Avery, but it also foreshadowed just how much time and effort it would take to bend Mississippi’s school system in his favor.
It also set up a pattern that Deloris learned to expect any time she spoke up for Avery: Besting one hurdle usually brought another. Despite Deloris’s certainty, the first doctor to test Avery diagnosed him with an unspecified learning disability, not autism. Avery wouldn’t be diagnosed with autism until he was 15.
This is a common experience for Black children with autism. A 2007 study showed that at their first visit, Black children were 2.6 times less likely to be diagnosed than white children. ADHD was instead the most common diagnosis. As a result, they tend to receive treatment later in childhood when it’s less likely to be effective.
“As a parent, I have felt like I have failed him so many times,” Deloris said. “No matter how hard I work, it’s like there’s always another wall to climb with no ladder, so you gotta find a way around it, through it, over it — without help.”
Avery’s elementary school was down the road from Deloris’ house, right next to the levy his granddad helped build. She could keep a close eye on him. But middle school was another matter.
Deloris didn’t want to send Avery to the public junior high — it had a reputation for fighting. Instead, she enrolled him in a nearby private religious academy.
“It was supposed to be like a Christian school,” she said.
Avery said he was ignored by the teacher unless he did something wrong, like peeking at the answer key for tests, even if other kids did the same thing. This, too, is a regular experience for Black students with disabilities. According to the U.S. Department of Education’s Office of Special Education Programs, they’re more likely to be disciplined than their peers.
Toward the end of the 2014 school year, Avery and his brother were waiting outside when another student said the teacher wanted to see him.
“When he said that, I felt like something wasn’t right about this,” Avery said. “But I would just respect my teachers anyway, so I just went, despite the feeling.”
A second teacher came into the room and used a paddle on Avery while his teacher watched.
“I had no idea what was going on,” Avery said. “There was no explanation.”
When Deloris picked the boys up from school, she said that Avery, who never cries, was so angry he had tears streaming down his face.
They never went back to that school. But to this day, the experience shaped how Avery communicates with his teachers.
In summer 2020, Avery sat at Deloris’ kitchen table. Together they wrote a list of six accommodations they hoped he’d get at DSU that fall, including “extended time on projects/tests” and “daily life assistance with rules/ activities.”
Accommodations like these helped Avery get his associate degree at Mississippi Delta Community College.
With extra time for assignments, Avery went to MDCC’s tutoring center every day, braving rain and a neighbor’s pack of loud dogs. Algebra was his toughest subject, but with a tutor’s help, Avery was showing his classmates how to solve problems.
But when he got to DSU, the only accommodation Avery received was extended time on tests, according to a fall 2020 letter from the university.
This is not unusual. The laws that govern disability services in college — the Americans with Disabilities Act and Section 504 of the Rehabilitation Act of 1973 — are less extensive than those in K-12. Administrators have latitude to decline accommodations that would “fundamentally alter” a course or pose an undue financial burden to the university.
That fall, the university did not have a dedicated disability coordinator, according to budget documents. Kashanta Jackson, the director of the Office of Health and Counseling Services, filled the role until August last year when it became its own position.
In recent years, anywhere from just 14 students to 60 have requested accommodations each semester, according to a records request.
Jackson told Mississippi Today that since she started at DSU in early 2020, her office has never denied a student’s request for accommodation, though she signed the letter granting only one to Avery.
Deloris said, in retrospect, the partial denial was a sign that her alma mater might not be the place for Avery. It also bothered her that when she asked why Avery only received one accommodation, the university said his request was private under the Family Educational Rights and Privacy Act.
If Deloris wanted to talk to the school on Avery’s behalf, he’d have to sign a waiver.
FERPA is intended to protect students’ privacy, but for parents of students with disabilities, it can be a barrier, said Jerry Alliston, the assistant director of the University of Southern Mississippi’s Institute for Disability Studies.
It made Deloris feel like she wasn’t supposed to step in for Avery. But she knew that no one else on campus was advocating for him.
One incident at the end of Avery’s first fall semester demonstrated Deloris’ worry. The day she picked Avery up from his dorm, she went to his bathroom when he exclaimed, “don’t turn the light on!”
There was water dripping from the ceiling — it had been almost the whole semester. Avery didn’t know how he was supposed to request a fix because no one had shown him where to go.
DSU has been candid in the past about its shortcomings serving students with disabilities.
“I’m not saying students with disabilities shouldn’t come to DSU, but if accommodations are their priority, then they should look at universities that are able to be equipped to accommodate them,” Dr. Richard Houston, the former director of counseling, told the student newspaper in 2019.
Four years later, there’s still little programming and no clubs for students with disabilities. Disability Services mainly approves accommodations and relays students’ requests to their professors. But it doesn’t track the outcomes of the students it serves, according to a records request, such as if they graduated or not.
Jackson said she hopes to grow DSU’s services but that “it’s kind of hard to say what we’re gonna get more of without knowing specifically what students we’re going to have.” While funding is a limiting factor, she said her office is “doing pretty well with what we have.”
It’s not just DSU. The entire state of Mississippi is behind when it comes to serving students with disabilities. The state Department of Rehabilitation Services funds peer mentoring programs for students with disabilities in Mississippi, Alliston said, but just two universities – University of Southern Mississippi and Mississippi State University – have taken the offer. And MSU is the only university in the state with a case management program for students with autism.
Avery almost went to MSU, but it was too far away. A peer mentoring program would have benefited him, particularly with talking to professors. He’d email them a question about an assignment, only to be told to check the syllabus, which he had read and didn’t understand.
When Avery got to DSU, his GPA was a 2.88 GPA. That fall, he failed two classes and got a D in another. He did a little better in the spring.
One class in particular challenged him: 2-D design. He’d failed it repeatedly, but it kept getting put on his schedule. Deloris even tried to see if Avery could take a similar course at MDCC or Mississippi Valley State University.
By summer 2021, Avery’s GPA had dropped to 2.39. He received a warning from the financial aid office for not making satisfactory academic progress.In order to get more financial aid, Avery had to file an appeal form. He wrote that the reason he failed some classes was because online learning was “giving me trouble to figure out what the teacher is looking for in an assignment.”
“If things continue to look up in the future and we can get back to attending class in person, I believe I will do a lot better,” he wrote.
The meeting with the dean lasted 45 minutes.
There was a process for Avery to get re-admitted to the art program, Green had told them, and it was easy. If the adviser was available, he could help Avery make a plan that day and the suspension would be lifted.
Avery and Deloris walked out of Green’s office with palpable relief. Deloris had tears in her eyes, and Avery’s posture had relaxed.
But the more Deloris thought about the meeting, it started to bother her. If the process was as easy as Greensaid, why did it take Deloris and Avery so much effort to make it happen?
They’d soon see it wasn’t going to be easy.
The next day, Avery and Deloris drove back to DSU so he could sign up for classes. When they got to his adviser’s office, the re-admittance plan was written and printed out. His adviser had already signed it. All Avery had to do was sign it too.
Other elements of the plan spoke to the lack of input from Avery: His schedule once again included 2-D design.Nobody mentioned course substitutions, a common type of acommodation, as an option.
Deloris was confused. She thought they were going to create the plan together. It reminded Deloris of a dynamic she’d seen before between Avery and authority figures: “They lead the conversation,” she said, “and give you little to say.”
Still, at least Avery was no longer suspended.
Then on Jan. 19, Avery received a puzzling letter from financial aid after he’d emailed them with a question. It read: “Avery, We are showing that you are currently on suspension for the Spring 2023 semester.”
He’d have to go through another appeals process to get his federal financial aid, including the Pell Grant and student loans, reinstated. Otherwise, Deloris would be on the hook for tuition — all $9,000, a sum she can’t afford. Avery would have to drop out.
No one had mentioned there’d be a second process for financial aid, Deloris said. Just like every success, there was another yet another roadblock.
If Avery can stay in school, he’ll graduate next year. But he won’t know for another month if he’ll get financial aid this semester or not.
Deloris and Avery’s brother, Alex, said they think he is holding back from sharing how disappointed he is with his experience at DSU because he doesn’t want to get anyone in trouble.
She thinks about just how much noise it took her and Avery to get help from the dean, and how quickly and easily the university fixed the issues in comparison.
“If I didn’t say anything, then what would happen? He would’ve just been left out,” Deloris said. “What if I was in one of those stages where I’m really sick and I’m in the bed and I can’t go nowhere. Then what? I want to trust that if I can’t come with him, he’s still going to be treated fairly. And given time. And effort.”
This article first appeared on Mississippi Today and is republished here under a Creative Commons license.
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https://www.biloxinewsevents.com/?p=205853
Mississippi Today
On this day in 1997
Dec. 22, 1997
The Mississippi Supreme Court upheld the conviction of white supremacist Byron De La Beckwith for the 1963 murder of Medgar Evers.
In the court’s 4–2 decision, Justice Mike Mills praised efforts “to squeeze justice out of the harm caused by a furtive explosion which erupted from dark bushes on a June night in Jackson, Mississippi.”
He wrote that Beckwith’s constitutional right to a speedy trial had not been denied. His “complicity with the Sovereignty Commission’s involvement in the prior trials contributed to the delay.”
The decision did more than ensure that Beckwith would stay behind bars. The conviction helped clear the way for other prosecutions of unpunished killings from the Civil Rights Era.
This article first appeared on Mississippi Today and is republished here under a Creative Commons license.
Mississippi Today
Medicaid expansion tracker approaches $1 billion loss for Mississippi
About the time people ring in the new year next week, the digital tracker on Mississippi Today’s homepage tabulating the amount of money the state is losing by not expanding Medicaid will hit $1 billion.
The state has lost $1 billion not since the start of the quickly departing 2024 but since the beginning of the state’s fiscal year on July 1.
Some who oppose Medicaid expansion say the digital tracker is flawed.
During an October news conference, when state Auditor Shad White unveiled details of his $2 million study seeking ways to cut state government spending, he said he did not look at Medicaid expansion as a method to save money or grow state revenue.
“I think that (Mississippi Today) calculator is wrong,” White said. “… I don’t think that takes into account how many people are going to be moved off the federal health care exchange where their health care is paid for fully by the federal government and moved onto Medicaid.”
White is not the only Mississippi politician who has expressed concern that if Medicaid expansion were enacted, thousands of people would lose their insurance on the exchange and be forced to enroll in Medicaid for health care coverage.
Mississippi Today’s projections used for the tracker are based on studies conducted by the Institutions of Higher Learning University Research Center. Granted, there are a lot of variables in the study that are inexact. It is impossible to say, for example, how many people will get sick and need health care, thus increasing the cost of Medicaid expansion. But is reasonable that the projections of the University Research Center are in the ballpark of being accurate and close to other studies conducted by health care experts.
White and others are correct that Mississippi Today’s calculator does not take into account money flowing into the state for people covered on the health care exchange. But that money does not go to the state; it goes to insurance companies that, granted, use that money to reimburse Mississippians for providing health care. But at least a portion of the money goes to out-of-state insurance companies as profits.
Both Medicaid expansion and the health care exchange are part of the Affordable Care Act. Under Medicaid expansion people earning up to $20,120 annually can sign up for Medicaid and the federal government will pay the bulk of the cost. Mississippi is one of 10 states that have not opted into Medicaid expansion.
People making more than $14,580 annually can garner private insurance through the health insurance exchanges, and people below certain income levels can receive help from the federal government in paying for that coverage.
During the COVID-19 pandemic, legislation championed and signed into law by President Joe Biden significantly increased the federal subsidies provided to people receiving insurance on the exchange. Those increased subsidies led to many Mississippians — desperate for health care — turning to the exchange for help.
White, state Insurance Commissioner Mike Chaney, Gov. Tate Reeves and others have expressed concern that those people would lose their private health insurance and be forced to sign up for Medicaid if lawmakers vote to expand Medicaid.
They are correct.
But they do not mention that the enhanced benefits authored by the Biden administration are scheduled to expire in December 2025 unless they are reenacted by Congress. The incoming Donald Trump administration has given no indication it will continue the enhanced subsidies.
As a matter of fact, the Trump administration, led by billionaire Elon Musk, is looking for ways to cut federal spending.
Some have speculated that Medicaid expansion also could be on Musk’s chopping block.
That is possible. But remember congressional action is required to continue the enhanced subsidies. On the flip side, congressional action would most likely be required to end or cut Medicaid expansion.
Would the multiple U.S. senators and House members in the red states that have expanded Medicaid vote to end a program that is providing health care to thousands of their constituents?
If Congress does not continue Biden’s enhanced subsidies, the rates for Mississippians on the exchange will increase on average about $500 per year, according to a study by KFF, a national health advocacy nonprofit. If that occurs, it is likely that many of the 280,000 Mississippians on the exchange will drop their coverage.
The result will be that Mississippi’s rate of uninsured — already one of the highest in the nation – will rise further, putting additional pressure on hospitals and other providers who will be treating patients who have no ability to pay.
In the meantime, the Mississippi Today counter that tracks the amount of money Mississippi is losing by not expanding Medicaid keeps ticking up.
This article first appeared on Mississippi Today and is republished here under a Creative Commons license.
Mississippi Today
On this day in 1911
Dec. 21, 1911
Josh Gibson, the Negro League’s “Home Run King,” was born in Buena Vista, Georgia.
When the family’s farm suffered, they moved to Pittsburgh, and Gibson tried baseball at age 16. He eventually played for a semi-pro team in Pittsburgh and became known for his towering home runs.
He was watching the Homestead Grays play on July 25, 1930, when the catcher injured his hand. Team members called for Gibson, sitting in the stands, to join them. He was such a talented catcher that base runners were more reluctant to steal. He hit the baseball so hard and so far (580 feet once at Yankee Stadium) that he became the second-highest paid player in the Negro Leagues behind Satchel Paige, with both of them entering the National Baseball Hame of Fame.
The Hall estimated that Gibson hit nearly 800 homers in his 17-year career and had a lifetime batting average of .359. Gibson was portrayed in the 1996 TV movie, “Soul of the Game,” by Mykelti Williamson. Blair Underwood played Jackie Robinson, Delroy Lindo portrayed Satchel Paige, and Harvey Williams played “Cat” Mays, the father of the legendary Willie Mays.
Gibson has now been honored with a statue outside the Washington Nationals’ ballpark.
This article first appeared on Mississippi Today and is republished here under a Creative Commons license.
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