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Tag: Learning disorders

  • Toddlers with developmental delays are missing out on help they need

    Toddlers with developmental delays are missing out on help they need

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    CHICAGO — Alexander watches Paw Patrol with fervor, bowls his baby brother over with hugs and does everything with gusto.

    What the 3-year-old West Chicago toddler can’t do yet is speak more than a few words. His balance is wobbly and he isn’t able to let his preschool teachers know when he’s hurt or scared.

    When his mother, Hilda Garcia, had him tested, the youngster qualified for five therapies through a U.S. program dedicated to treating developmental delays in babies and toddlers — treatment designed to help Alexander develop the tools he needs to thrive.

    The relief she felt in identifying what he needed was short-lived.

    The federally mandated Early Intervention program is plagued by chronic staffing shortages nationwide, leaving thousands of desperate parents frustrated: They know their children need support, they’re aware of proven therapies that could make a difference, but they have to wait for months to get the help they need.

    After 14 months of phone calls, hours of research and pushing herself to the limit with work and childcare, Garcia finally landed an in-person early intervention appointment, but even then she couldn’t get Alexander all the therapies he needed. She tears up as she recounts how overwhelming the fight to secure access has been.

    “I didn’t have any support,” she said.

    Early Intervention was created in 1986 to address developmental delays in children like Alexander as soon as possible. About one in six children in the U.S. has at least one developmental disability or other developmental delay, according to the U.S. Centers for Disease Control and Prevention.

    Since all U.S. states and territories accept federal funding for Early Intervention, they are obligated to provide services to kids who qualify under the Individuals with Disabilities Education Act.

    But providers are scarce in almost all states. Some children wait months or years for the care they need, and many age out of the program before they access any services at all.

    The COVID-19 pandemic worsened chronic staffing shortages, in part because many providers didn’t want to risk infection by entering families’ homes, even when restrictions on in-person visits were lifted, according to Maureen Greer, the executive director of the Infant and Toddler Coordinators Association, which supports the Early Intervention system nationwide.

    For similar reasons, families were also less likely to request in-person help during the pandemic. But now the number of children seeking services has rebounded, and states are struggling to find the staff to meet the needs of families with young children with disabilities, according to Katy Neas of the U.S. Department of Education.

    Service delays in Illinois, where Alexander lives, nearly doubled in 2022, according to Chicago-based early childhood advocacy organization Start Early. Waitlists — technically not allowed since all eligible kids are entitled to Early Intervention — have increased dramatically and thousands of providers have left the field, according to the Illinois Department of Human Services.

    When children turn 3, the responsibility for providing special education services shifts from Early Intervention to school districts. But those systems are understaffed and booked up, too, according to speech-language pathologist Sarah Ziemba, an Early Intervention provider in Peoria, Illinois.

    Waiting means skipping precious months of development, while acting early saves money on special education and other services later in life.

    “Research really supports that the earlier, the better. And so when we miss those opportunities to help them at those younger ages, sometimes we are limiting their potential into adulthood,” said Ziemba.

    Families with private insurance can opt to pay for therapy appointments outside the Early Intervention program, but those without the means can be left behind, according to Ziemba.

    “In a way, Early Intervention is contributing to some social inequity,” she explained.

    Research supports her assessment. A report published this year by the National Institute for Early Education Research found that Asian, Hispanic and Black children are less likely to receive Early Intervention and Early Childhood Special Education services than white non-Hispanic children.

    “For Black children, the disparities in access to services are especially large and cannot plausibly be explained by differences in need,” the report says.

    Income also plays a role, said lead researcher Allison Friedman-Krauss.

    “Poorer states are serving a lower percentage of children, so really suggesting that there is a problem there,” Friedman-Krauss said.

    But there is no way to attract more providers without better wages, Ziemba explained. Early Intervention providers in Illinois are government contractors, meaning they get no health benefits or paid time off, and they can effectively double their salaries by working in other settings such as hospitals, schools or nursing homes.

    “People are just done with it, and it has gotten worse even in the last two months,” Ziemba said in late July. “I really feel like we’re kind of seeing the implosion of the whole program.”

    As families lose access to the free or reduced-cost therapies, pressure builds on schools to pick up the slack, but they’re short on special education teachers, too.

    “In the long term, we’re seeing kids fall farther and farther behind,” said Ziemba, who has done this work for nearly 25 years.

    Illinois Gov. J.B. Pritzker signed a budget in June giving Early Intervention providers a 10% raise. That helps, Ziemba said, but likely won’t make up for the impact of inflation and may not be enough to slow the steady exodus of workers. She and another provider say wages were stagnant for years.

    In July, the administration announced a retention program designed to reward tenured Early Intervention providers, interpreters and service coordinators with payments of up to $1,300 to stay in the field.

    “We remain committed to giving our service providers the support and resources they deserve for caring for our state’s children,” said Alex Gough, a spokesperson for the governor’s office.

    The impact therapy can have is palpable. Lindsey Faulkner, a mother of four living in Peoria, got in-person speech therapy sessions for her 2-year-old daughter, Aria, within a month of her referral. She raves about the difference she has seen in her child after a year of working with therapist Megan Sanders.

    “She was an entirely different kid a year ago,” Faulkner said.

    Early on in their sessions, Aria zoomed around the room. Now, Aria can sit and engage with Sanders for most of the session. She looks Sanders in the eye more often, responds to her gentle guidance and is starting to use sign language.

    “We’ve come a long way,” Sanders said. “My goal throughout is just to make her more able to express herself.”

    When Aria was about a year old, Faulkner noticed that words the toddler had been using started to disappear. “She began screeching for everything that she wanted rather than asking us for help or gesturing.”

    Aria qualified for speech, developmental and occupational therapy, and was diagnosed with autism when Faulkner was finally able to secure an appointment with a developmental pediatrician, two and a half hours away in St. Louis. Although Aria started speech therapy promptly, she has been on the waitlist for developmental therapy for more than a year.

    Faulkner was “floored” when she learned about the wait times.

    “You need to get answers for your child,” she said. “But here, now you have to sit and wait.”

    Early Intervention providers and service coordinators, who connect families with therapists, are woefully underpaid, according to Darcy Armbruster, a physical therapist who serves DuPage County near Chicago and has worked in the Early Intervention program for 11 years.

    Armbruster said it would make more financial sense for her to quit Early Intervention, but she stays because she loves the relationships she builds with families. Still, she has a child of her own to care for, and a mortgage to pay. Passion and job fulfillment don’t pay the bills.

    “Every month I have to sit down and reevaluate where I am and if I can keep going and doing this,” she said.

    Hilda Garcia’s son, Alexander, qualified for five Early Intervention therapies in 2021 — physical, occupational, developmental, behavioral and speech. But the family waited more than a year before he received any of those services in-person.

    While they waited, Garcia signed Alexander up for virtual therapy, which didn’t start for more than six months. But virtual appointments weren’t effective, especially for physical therapy.

    Garcia tried to do the exercises with her toddler herself, but it never seemed to work. Finally, they were able to secure an in-person appointment through a private provider. They never made it off the Early Intervention waitlist.

    The therapist could tell much more by interacting with her son in their home.

    “His lips were not able to move the way they should so that speech can come out,” Garcia said.

    Garcia, meanwhile, was juggling childcare, work and the almost full-time advocacy needed to get Alexander what he needed. “It feels like another job,” she said.

    Garcia, who speaks English, is part of a primarily Spanish-speaking community in West Chicago, and she knows many parents can’t advocate for their kids in a second language.

    “I can’t imagine somebody else going through what I went through without speaking English,” she said.

    Translators are available, but that adds another layer of complexity to an already onerous process. Communication cuts into hourlong therapy sessions, leaving less time for actual therapy, she explained.

    Garcia worries about Alexander. She knows he’s missing vital tools. She is concerned about his safety because he struggles to communicate and has issues with balance.

    Just this summer, she said, another child pushed him off a playground set. A report from the school described his injuries as a scratch, Garcia said, but he continued to cry out “Mama, mama” and point to his back.

    She gave him Tylenol and asked about “pain” or “hurt,” but he didn’t understand. She called his pediatrician, who recommended a trip to the emergency room, where they took X-rays and tested Alexander’s urine for blood.

    When the results came back, they told her he’d had “a significant fall.”

    Garcia gently rocks Alexander’s baby brother in her arms as she tells the story. There’s a heaviness in her voice. If he had undergone speech and physical therapy sooner, would Alexander have been able to tell the other child to stop? Could he have kept his balance, preventing the fall?

    “I wonder if we would have had the Early Intervention in-person session earlier, if things would have been better by now,” Garcia said.

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    Savage is a corps member for the Associated Press/Report for America Statehouse News Initiative. Report for America is a nonprofit national service program that places journalists in local newsrooms to report on undercovered issues.

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    The Associated Press receives support from the Overdeck Family Foundation for reporting focused on early learning. The AP is solely responsible for all content.

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  • Bruce Willis has frontotemporal dementia. What is FTD?

    Bruce Willis has frontotemporal dementia. What is FTD?

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    Bruce Willis’ family has announced that he has been diagnosed with frontotemporal dementia.

    The announcement Thursday came about a year after his family said that Willis would step away from acting after being diagnosed with aphasia, a brain disorder that leads to speaking, reading and writing problems.

    Here’s some details on the condition:

    WHAT IS FRONTOTEMPORAL DEMENTIA?

    There are different types of dementia, and the frontotemporal form affects regions in the front and sides of the brain. Because it causes problems with behavior and language, aphasia can be a symptom.

    It’s caused by damage to neurons, the brain’s information carriers, but the underlying reasons for a particular case are often unclear. People with a family history of the condition are more likely to develop it. It’s rare and tends to happen at a younger age than other forms of dementia, between ages 45 and 65.

    The terms frontotemporal disorders and frontotemporal dementia are sometimes shortened to FTD.

    WHAT ARE OTHER SYMPTOMS OF FTD?

    Symptoms can include emotional problems and physical difficulties, such as trouble walking. Symptoms tend to worsen over time, though progression varies by person.

    The statement from the actor’s family said communication problems “are just one symptom of the disease Bruce faces.”

    CAN FTD BE TREATED?

    There are no treatments to slow or stop the disease, but some interventions can help manage symptoms.

    Some patients receive antidepressants or drugs for Parkinson’s, which has some overlapping symptoms with frontotemporal dementia. Many also work with speech therapists to manage communication difficulties and physical therapists to try to improve movement.

    People with the condition are more likely to have complications from things like falls, injuries or infections. The average life expectancy after symptoms emerge is seven to 13 years, according to researchers.

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    The Associated Press Health and Science Department receives support from the Howard Hughes Medical Institute’s Science and Educational Media Group. The AP is solely responsible for all content.

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  • Bruce Willis has frontotemporal dementia, condition worsens

    Bruce Willis has frontotemporal dementia, condition worsens

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    NEW YORK — Nearly a year after Bruce Willis’ family announced that he would step away from acting after being diagnosed with aphasia, his family says his “condition has progressed.”

    In a statement posted Thursday, the 67-year-old actor’s family said Willis has a more specific diagnosis of frontotemporal dementia.

    “While this is painful, it is a relief to finally have a clear diagnosis,” the statement read. “FTD is a cruel disease that many of us have never heard of and can strike anyone.”

    Last March, Willis’ family said his aphasia had affected his cognitive abilities. The condition causes loss of the ability to understand or express speech.

    In Thursday’s statement, his family said communication challenges were just one symptom of frontotemporal dementia.

    “Today there are no treatments for the disease, a reality that we hope can change in the years ahead,” the statement read. “As Bruce’s condition advances, we hope that any media attention can be focused on shining a light on this disease that needs far more awareness and research.”

    The statement was posted on the website for The Association for Frontotemporal Degeneration and signed by Willis’ wife, Emma Heming Willis, his ex-wife Demi Moore, and his five children, Rumer, Scout, Tallulah, Mabel and Evelyn.

    Over a four-decade career, Willis’ movies had earned more than $5 billion at the worldwide box office. While beloved for hits like “Die Hard” and “The Sixth Sense,” the prolific actor had in recent years primarily featured in direct-to-video thrillers.

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  • Pritzker calls for universal preschool in Illinois by 2027

    Pritzker calls for universal preschool in Illinois by 2027

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    SPRINGFIELD, Ill. — Illinois Gov. J.B. Pritzker called Wednesday for making preschool available to every 3- and 4-year-old in the state within four years, starting with a $440 million investment to bring 5,000 additional children into the program this fall.

    Details about the “Smart Start Illinois” program dominated the fifth annual State of the State and budget address by the Democratic governor, who easily won reelection in November and has hinted at an eventual presidential bid.

    “It will make our state the best place in the nation to raise young children,” Pritzker said in the speech to a joint session of the Legislature.

    He envisions a four-year plan in which annual increases in funding — although smaller than in the initial year — would make room for the approximately 20,000 children whose families desire pre-K but can’t because of a lack of space.

    In the first year, $75 million would go toward the existing account funding pre-K, a 12.5% increase in the budget that currently serves 89,000 kids. That funds space for the additional 5,000 learners, all outside of Chicago. Chicago Public Schools have their own preschool program.

    But the plan goes beyond classroom learning. There’s $40 million for early intervention when a child is found with a learning impediment, such as a speech delay, and $5 million for Department of Human Services home visits to help families with parenting, school and more.

    “We’re attempting to cover the lowest income kids who don’t have spots available to them first, but it will also depend upon where the availability (of space) can be made in this fiscal year,” Pritzker said. “There may be places where it will take us a couple of years to build out the capability.”

    In a Tuesday briefing with news reporters, he insisted the time is ripe for opening the school door to more kids earlier in life, citing academic studies projecting that there’s a potential return of as much as $7 for every $1 invested in early education.

    “It’s a plan that will make our system more equitable, focusing in particular on children and families who have less ability to access quality programs, and investing in a workforce made up largely of women and people of color,” Pritzker said.

    The budget also includes $100 million to build facilities to house the expanded programs. There’s $70 million to expand participation in childcare for parents who need to work or attend school by increasing the income threshold, and $20 million to revamp the provider-payment system.

    Critically important is $130 million for what Pritzker says would be a first-in-the-nation “Childcare Workforce Compensation Contract” to lure providers to an understaffed field, give it stability and increase providers’ pay over four years to as much as $19 an hour.

    About 10 states offer universal preschool, including neighboring Wisconsin. Colorado is gearing up to offer it this fall, and Michigan Democratic Gov. Gretchen Whitmer last week proposed $300 million for schooling, hiring teachers and transporting 5,600 4-year-olds.

    Pritzker declined to discuss other initiatives he would propose in the coming year after a $50 billion budget in the current year. Other state leaders urging budgetary constraint did leave room for enhanced educational programs.

    “There are so many different programs that are meritorious but when you have limited funds… for this next year, they’re looking pretty good, but we always need to err on the conservative side of not spending everything,” Democratic Comptroller Susana Mendoza said. “Hope for the best, but plan for the worst.”

    Mendoza said education is an area where additional spending is called for, but she would like to see better funding of needs-based college grants.

    Republican Senate Minority Leader John Curran, of Downers Grove, warned of a coming fiscal cliff and the need for budget restraint, but called on Pritzker to expand help for working families — including in early childhood learning and childcare.

    He also bemoaned the underfunding of programs for the developmentally disabled. Despite a huge increase in 2021, it was still hundreds of millions of dollars short of what a federal judge ordered.

    “We can afford to do this,” Pritzker said “And as every provider, teacher and parent in this state will tell you, we can’t afford to wait.”

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    Follow Political Writer John O’Connor at https://twitter.com/apoconnor

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  • Faith leaders prep for border changes amid tension, hope

    Faith leaders prep for border changes amid tension, hope

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    REYNOSA, Mexico — Two long lines of migrants waited for blessings from visiting Catholic priests celebrating Mass at the Casa del Migrante shelter in this border city, just across the bank of the Rio Grande River from Texas.

    After services ended last week, several crammed around the three Jesuits again, asking about upcoming U.S. policy changes that would end pandemic-era asylum restrictions. That’s expected to result in even more people trying to cross the U.S.-Mexico border, adding to the already unusually high apprehension numbers.

    “All of you will be able to cross at some point,” the Rev. Brian Strassburger told the nearly 100 Mass goers in Spanish while a Haitian migrant translated in Creole. “Our hope is that with this change, it will mean less time. My advice is, be patient.”

    It is getting harder to deliver that message of hope and patience not only for Strassburger, but also for the Catholic nuns running this shelter and leaders from numerous faith organizations who have long shouldered most of the care for tens of thousands of migrants on both sides of the border.

    Migrants here — mostly from Haiti, but also Central and South America and more recently from Russia — are deeply mistrustful of swirling policy rumors. A judge has ordered the restriction known as Title 42, which only affect certain nationalities, to end Wednesday. But the asylum restriction, which was supposed to lift in May, is still being litigated.

    Faith leaders working on the border are wary of what’s to come. They expect tensions will keep rising if new restrictions are imposed. And if not, they will struggle to host ever larger numbers of arrivals at already over-capacity shelters and quickly resettle them in a volatile political environment.

    “People are coming because it’s not long before the bridge will be opened. But I don’t think that the United States is going to say, ‘OK, all!’” said the Rev. Hector Silva. The evangelical pastor has 4,200 migrants packed in his two Reynosa shelters, and more thronging their gates.

    Pregnant women, a staggering number in shelters, have the best chance of legally entering the U.S. to apply for asylum. It takes up to three weeks, under humanitarian parole. Families wait up to eight weeks and it can take single adults three months, Strassburger explained at Casa del Migrante, where he travels from his Texas parish to celebrate Mass twice a week.

    Last week, the shelter housed nearly 300 people, mostly women and children, in tightly packed bunk beds with sleeping pads between them. Men wait in the streets, exposed to cartel violence, said Sister Maria Tello, who runs Casa del Migrante.

    “Our challenge is to be able to serve all those who keep coming, that they may find a place worthy of them. …Twenty leave and 30 enter. And there are many outside we can’t assist,” said Tello, a Sisters of Mercy nun.

    Edimar Valera, 23, fled Venezuela with family, including her two-year-old daughter. They crossed the notoriously dangerous Darien Gap, where Valera nearly drowned and went without food. After arriving in Reynosa and escaping a kidnapping, she found refuge at Casa del Migrante, where she’s been since November despite having a sponsor ten miles away in McAllen, Texas.

    “We need to wait, and it could be good for some and bad for others. One doesn’t know what to do,” she said, finding some comfort in Mass and daily prayers, where she begs God for help and patience.

    So does Eslande, 31, who left Haiti for Chile. She is on her second attempt to cross into the U.S. after not finding there the right help for her young son’s learning disability. At Casa del Migrante just a day, she read the Gospel aloud in Creole during Mass, a reminder of happier times when her father distributed Communion.

    “I have faith that I will be going in,” she said in the Spanish she’s learned en route. Like many migrants, she only gave a first name fearing for her safety.

    Tensions are rising faster than hope as it’s unclear who will be able to cross first.

    “Any change could grow the bottleneck,” said the Rev. Louie Hotop, dropping off hygiene donations at one of Silva’s shelters — a guarded, walled camp with rows of tents pitched tightly together.

    Even if Title 42 is lifted and thousands more are allowed to enter the U.S., asylum seekers would still face enormous backlogs and slim approval chances. Asylum is granted to those who cannot return to their countries for fear of persecution on specific grounds — starvation, poverty and violence don’t usually count.

    It’s a long, uncertain road ahead even for the roughly 150 migrants at a barebones welcome center in McAllen, Texas, where the Jesuit priests stop after their Reynosa visits. Families legally admitted to the United States, or apprehended and released, rested in the large Catholic Charities-run hall before traveling to join sponsors.

    Lugging their Mass kit and heavy speakers, the priests offered migrants spiritual and practical help– like writing “I’m pregnant. Can you ask for a wheelchair to bring me to my gate?” on a paper for a Honduran woman eight months pregnant with her first child and terrified about airport travel.

    “It’s a way of listening, of supporting, it’s not so much resolving the immediate problem,” the Rev. Flavio Bravo said. “They bring stories of trauma, of life, that we must give value to.”

    Sister Norma Pimentel, a prominent migrant rights advocate who first helped border crossers four decades ago and now runs Catholic Charities of the Rio Grande Valley, said religious people should push for centrist reform to help migrants — not make them political pawns.

    “Policies don’t respond to the realities we’re facing,” said Pimentel, who opened the welcome center in 2014 for the first big asylum surge of this century. “It’s impossible to help everyone … but who are we to limit the grace of God?”

    Now, the busiest crossing is some 800 miles away in El Paso, Texas, and neighboring Ciudad Juarez, Mexico. Ronny, 26, turned himself into U.S. authorities there and was flown to McAllen because “around Juarez it was collapsing,” he said last week at Pimentel’s shelter.

    He and his family left Venezuela on foot in September because he opposed his country’s regime and his wages were too low to afford food. He has a U.S. immigration appointment next month in New York where his sponsor lives, but no money to get there.

    On his first free night in the U.S., he turned to God, following Mass from a distance so he wouldn’t leave the thin mat where his children slept.

    “We ask God for everything. Always,” he said.

    ———

    Associated Press religion coverage receives support through the AP’s collaboration with The Conversation US, with funding from Lilly Endowment Inc. The AP is solely responsible for this content.

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