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After her daughter died from Sickle Cell Disease, one woman created fund to help patients cover everyday expenses

Posted: 8:13 AM, Nov 14, 2019
Updated: 2019-11-14 17:46:20-05
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CLEVELAND — The MCS Fund offers $150 to Sickle Cell patients who need help covering any kind of cost, if they apply through a social worker or the Kincaid's Kindred Spirits nonprofit.

For more than 20 years, Glinda Dames-Fincher has been getting blood transfusions because of her Sickle Cell Disease. She needs new blood often just to stay healthy, making staying healthy expensive.

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Glinda gets ready for a blood transfusion at University Hospitals to help treat her Sickle Cell Disease.

"So I've ended up with a lot of medical debt because of the co-pays," said Dames-Fincher.

Her career was only periodically interrupted by the disease, making her ineligible for medicaid. She says patients who aren't able to work might qualify for better healthcare coverage but it also means they don't have much money left over for anything else.

"Those that never worked tend to be more in poverty," said Dames-Fincher.

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The MCS Fund is named for Meesha C. Saxton, who died at 14 months because of complications from her Sickle Cell disease.

It's a common problem in the Sickle Cell community and can destroy a family's finances.

"Even when mom and dad are both working jobs, a lot of those people end up, if their kids are sick a lot, a lot of them end up in bankruptcy multiple times before the child is 18," said Dames-Fincher.

Roughly 100,000 people in the United States have Sickle Cell Disease but MCS Fund Founder Teresa McCurry says the disease often gets overlooked.

"With Sickle Cell Disease, there isn't a lot of research, there isn't a lot of studies and things done for it because it does primarily affect the African-American community," said McCurry.

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McCurry says she's carrying on her daughter's memory by helping Sickle Cell patients cover small costs so they can focus on feeling better.

McCurry has spent the last 20 years helping Sickle Cell patients after her 14-month-old daughter, Meesha C. Saxton, died because of the disease. While some nonprofits can help cover medical bills, they often aren't allowed to help patients with the long list of other expenses they have.

That's where the MCS Fund, named after Meesha, comes in.

"Our sole existence is to collect unrestricted funds to be able to be a blessing to people affected with Sickle Cell," said McCurry.

Unrestricted, because patients can use the $150 the fund awards them for any expense as long as they qualify after applying through a social worker or another nonprofit. By covering a week's worth of groceries, a utility bill, or a credit card bill, the MCS Fund tries to take a little stress off of patients so they can focus on feeling better.

"Any kind of stress, physical or emotional stress, can kick off a sickle cell crisis," said Dames-Fincher.

Dames-Fincher gets her transfusions at University Hospitals , which is one of only two locations in Ohio offering this clinical trial regarding patients with sickle cell disease.

Patients will need to be referred by a sickle cell doctor and are seen by a transplant physician.