South-Carolina
What SC is doing to combat rising rates of students missing school
COLUMBIA, S.C. — More students across the country and in South Carolina are missing school now than in the years before the COVID-19 pandemic.
The latest data, from the 2022-2023 school year, shows one in four students in the Palmetto State were considered chronically absent from school, just below the national average of 26%.
That state figure is nearly double from the 2018-2019 school year, when South Carolina’s rate was 13.1%.
A student is considered chronically absent when they miss at least 10% of the school year, so 18 days in a standard 180-day calendar.
Some education researchers call chronic absenteeism the greatest challenge facing American public schools post-pandemic, and South Carolina will soon put more focus on combatting it.
“Chronic absenteeism can really impact student achievement and student success academically,” Tenell Felder, communications manager for the South Carolina Education Oversight Committee, said.
The Education Oversight Committee oversees the accountability system for the state’s public schools.
It will soon launch a study and focus groups with South Carolina students to try to get to the heart of this issue and then develop recommendations later this fall.
“That could assist schools, teachers, principals, and parents in making sure that students are indeed present in school and ready to learn,” Felder said.
Studies have shown the negative impacts of chronic absenteeism include students being more likely to read below their grade level as well as later dropping out of school.
South Carolina School Report Cards indicate all districts grapple with chronic absenteeism but in varying degrees, ranging from a statewide low two years ago of 7.3% in Fort Mill to a high of more than half of all students, 51.9%, in Lexington School District Four.
On the higher end was Laurens County School District 56, where nearly one in three students were considered chronically absent.
“It’s just old-fashioned hard work and consistency and persistency, and not giving up,” Assistant Superintendent David Pitts said.
Pitts said the district has taken a hands-on approach to addressing absenteeism that includes making phone calls, not robocalls, for every absence, home visits, and even court orders if it rises to the level of truancy.
In one year, Laurens 56 cut its chronic absentee rate from 31.2% percent to 20.7%, which Pitts attributes to the work of school staff and principals.
“They just would not give up on a kid,” he said. “They would not accept, ‘I’m just not coming to school.’”
You can see the chronic absentee rates for all school districts across South Carolina for the 2022-2023 school year below.
Feel more informed, prepared, and connected with WIS. For more free content like this, subscribe to our email newsletter, and download our apps. Have feedback that can help us improve? Click here.
Copyright 2024 WIS. All rights reserved.
South-Carolina
Sickle Cell Day gathers advocates at South Carolina State House
COLUMBIA, S.C. (WACH) — Advocates, caregivers, patients, and community leaders gathered at the South Carolina State House on Friday for the inaugural South Carolina Sickle Cell Day.
Organizers said the event focused on raising awareness of sickle cell disease.
The South Carolina CBO Collective Caucus hosted the event at 10 a.m., coinciding with World Sickle Cell Day and Juneteenth.
Organizers said the gathering brought together healthcare professionals, legislators, advocates, and supporters from across the state to discuss education, support, and action related to sickle cell disease.
The program is designed to amplify the voices of individuals and families impacted by the disease and encourage conversations about healthcare access, advocacy, research, and community support, organizers said.
Attendees heard personal stories and learned about challenges faced by those living with sickle cell disease.
“World Sickle Cell Day is a powerful call to action for all of us,” said founder and CEO of The B Strong Group Brenda Green. She said the collaboration expands support, strengthens community response, and stands with affected families.
The B Strong Group, founded in 2017 and based in Columbia, is a nonprofit organization focused on sickle cell awareness, advocacy, and caregiver support.
The group organizes blood drives, caregiver workshops, and awareness campaigns under the motto “Educate, Advocate, Empower.”
South-Carolina
87-year-old South Carolina businessman says he has no plans to retire
An 87-year-old businessman in Columbia, South Carolina says he has no plans to retire.
Leonard Fabrizio works as a retailer at Brittons of Columbia, a locally-owned men’s clothing store.
“I’m not the type of person who can sit around by myself,” said Fabrizio. “I just enjoy the interaction and that’s the big thing, is the interaction with people. It’s always been the drive in this business for me, said Fabrizio.
Fabrizio’s retail career began as a college student when he worked at J.C. Penney. He has watched Columbia grow and has owned a store and managed several others.
His advice is to “Be patient. It takes time to build a business. It doesn’t happen overnight, but it’s rewarding. It’s fun. But you have to have compassion for the business.”
Fabrizio recently celebrated another birthday alongside those who have supported his career.
South-Carolina
South Carolina family raises awareness of rare Batten disease
(WPDE) — June 9 marked International Batten Disease Awareness Day, shining a light on a rare, inherited neurodegenerative disorder.
It primarily affects children and causes harmful waste material to build up inside the cells of the brain and nervous system.
One South Carolina family used the day to raise awareness as their 2-year-old son, Sam Stockton, lives with CLN2 Batten disease.
Sam was diagnosed at 16 weeks old, and his family says they travel every other week for enzyme-replacement therapy while also searching for clinical research opportunities.
Through Hope for Sam, the family is working to spread information about Batten disease and support other families facing rare diseases.
“Just the more you know about rare diseases, I never knew that over 300 million people worldwide live with rare diseases. And that means there’s less access to care because people aren’t researching it and not as many people have it. So the more information that’s out there, we feel is the better,” Jordan Stockton said.
There are 13 known types of Batten disease, and there is no cure. Researchers estimate the disease affects about two to four out of every 100,000 births in the United States.
The Stockton family says they have found support through the Batten Disease Support, Research and Advocacy Foundation, a nonprofit dedicated to helping families navigate the disease while providing resources.
More information and donation details are available at this link.
-
Wyoming10 minutes ago$1 million Wyoming home sale among the week’s top property transfers
-
Crypto13 minutes agoIreland Targets Crypto Assets in New Strategy to Disrupt Illicit Cash Flows
-
Finance17 minutes agoFinancial adviser warns, ‘stay away from the hype’ of an IPO
-
Fitness25 minutes agoThe Best Fitness Trackers for Your Lifestyle, Workouts, and Goals
-
Movie Reviews33 minutes ago‘Finnegan’s Foursome’ Review: Edward Burns’ Spiky-Quaint Sports Dramedy Is a Tale of Family Therapy Through Golf
-
World43 minutes ago‘X-Men’ Star Famke Janssen Says Marvel ‘Made a Mistake’ By Not Asking Her to Return as Jean Grey in ‘Avengers: Doomsday’
-
Lifestyle1 hour agoJames Burrows, director of classic shows ‘Cheers’ and ‘Friends,’ dies at 85
-
Technology2 hours agoNothing cancels this year’s CMF phone due to RAM prices