South-Carolina
Could SC expand Medicaid? New group says NC shows it can get done
COLUMBIA, S.C. (WIS) – South Carolina remains one of 10 states that have opted to not expand Medicaid since it became an option about a decade ago.
A newly formed coalition of dozens of nonprofits and organizations are now calling on lawmakers to change that, but they face substantial opposition.
Medicaid expansion has long been something of a third rail at the South Carolina State House.
But supporters point to another state with a Republican-dominated legislature to show how it can get done: North Carolina.
“It wasn’t easy. It took us 10 years to get there,” North Carolina Republican state representative Donny Lambeth said during a news conference Tuesday in Columbia.
Since last December, the state of North Carolina reports more than half a million people have signed up for coverage under its newly expanded Medicaid eligibility.
A report the group Cover SC recently commissioned found around 340,000 South Carolinians could benefit from Medicaid expansion.
“Most are workers who don’t qualify for Medicaid but make too little to afford private insurance,” Teresa Arnold, the group’s co-chair, said.
When states expand Medicaid eligibility, the federal government covers 90% of the cost, while states are on the hook for the other 10%.
South Carolina’s share for the first year is around $270 million, but by year 10, it is estimated to grow to more than $380 million dollars.
But North Carolina crafted a deal in which hospitals pick up that 10% through an annual tax.
“We’ve constructed this in a way that’s not costing the state of North Carolina a single penny,” North Carolina Republican state senator Kevin Corbin said.
Earlier this year, Governor Henry McMaster vetoed an effort to take a closer look at South Carolina’s healthcare market, including Medicaid expansion.
The Republican governor remains firmly opposed to the option.
“This is our state,” McMaster told reporters Tuesday. “We have to do the right thing in our state, and to be taking taxpayer dollars from our citizens and be giving them to able-bodied, childless adults, childless, able-bodied adults, is not a wise expenditure of that money.”
But South Carolinian Cliff Arnold said people like him would benefit.
He said he was working until two years ago when his kidneys started failing.
Arnold, who uses a wheelchair, said his disability check is too much to qualify for Medicaid but is eaten up by his medical expenses each month.
“I’m just sweating to see if I can make it to the next check,” he said. “Having healthcare would really make a huge difference in how much we actually would be able to — it would actually put food in our refrigerator.”
While both Carolinas are home to legislatures dominated by Republicans, a key difference between them is who leads the executive branch.
While McMaster is a Republican, North Carolina Gov. Roy Cooper is a Democrat and made Medicaid expansion a key priority.
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.
-
Detroit, MI8 minutes agoBest barbershop in Metro Detroit: Finalists for this year’s Vote 4 The Best
-
San Francisco, CA18 minutes agoHow to watch San Francisco Giants vs. Miami Marlins
-
Dallas, TX23 minutes agoDrivers in North Texas struggle with Friday floods
-
Miami, FL30 minutes agoThree wildfires burn more than 20,000 acres in Miami-Dade, force road closures
-
Boston, MA33 minutes agoMBTA, state transportation chief apologizes for ‘insensitive’ employee hair-pulling incident
-
Denver, CO38 minutes agoMan arrested on suspicion of murder in Denver shooting near South Park Hill, Hale
-
Seattle, WA45 minutes agoSeattle fans pack waterfront hours early as USA defeats Australia, advances in World Cup
-
San Diego, CA46 minutes agoNASCAR San Diego weekend revs up at Naval Base Coronado