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Monday, August 10, 2026
Get The Scoop On Why Blacks Have A Cure for Sickle Cell Anemia But Few Can Access it
Help Us To continue to inform and empower our community please Donate. Get The Scoop Weekly On the Global Black Community and Southeast Queens, NY. Subscribe to Our Mailing List. Receive the Latest Events, News, Jobs, and Top Community Economic Development Stories Like this one Click Here | Reach up to 1.3 million people Promote
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Sickle Cell's Quiet Revolution: A Cure Exists - So Why Can't Black America Access It?
By AiSha | Digital Green Book and Kamau Austin for Southeast Queens Scoop
According to Pharmacy Times, "In a historic medical breakthrough, 21-year-old Sebastien Beauzile from Laurelton, Long Island (Queens, NYC) , has become the first New Yorker to be cured of sickle cell anemia. This life-changing transformation was made possible through Lyfgenia (in Spring 2025) , a pioneering gene therapy that corrects the genetic defect responsible for the disease. Sebastien's journey offers hope to countless others battling this debilitating condition."
Pharmacy Times also added "Sebastien's battle with sickle cell anemia began at just four months old, leading to years of excruciating pain and frequent hospitalizations. Traditional treatments provided little relief, making daily life a constant struggle. However, with the advent of Lyfgenia, a therapy that introduces healthy genes into stem cells, Sebastien's life has been transformed. He now enjoys activities previously hindered by his condition, such as working out, traveling, and pursuing his education.
The success of this treatment not only marks a personal victory for Sebastien but also signifies a monumental advancement in medical science. By effectively curing sickle cell anemia without the need for bone marrow transplants, Lyfgenia paves the way for new therapeutic approaches to genetic disorders. This breakthrough offers renewed hope to millions affected by similar conditions worldwide."
Sebastien and Cohen Children's Medical Center weighed in "A new birthday, a new beginning! After living with sickle cell anemia for over two decades, Sebastien is now disease-free thanks to Lyfgenia — a groundbreaking genetic treatment.
“Growing up with sickle cell, it’s kind of been over all my life,” Sebastien said. “So now that I’m cured, I’d say it’s my new birthday because now nothing’s going to stop me.”
Sebastien was the first patient in New York to receive this life-changing therapy, and with the generous $100,000 donation from civil rights attorney Ben Crump, we will continue advancing sickle cell care for more patients. We are so happy to celebrate Sebastien’s incredible journey and the future of sickle cell treatment!
Article On How Blacks Now Have A Cure Available for Sickle Cell Anemia But Few Can Access it Continues After Sponsor's Messages Below...
Article On How Blacks Have A Cure Available for Sickle Cell Anemia But Few Can Access it Continues Below...
A Disease Born in Black Bodies, Funded by Other Priorities
Sickle cell disease has a long history of receiving less research funding relative to diseases affecting predominantly white populations. The National Institutes of Health has historically allocated less per patient to sickle cell research than to comparable genetic diseases like cystic fibrosis. Advocates have raised this disparity for decades. The arrival of these new therapies represents genuine scientific progress - and it arrives in a context where the healthcare system's relationship with Black patients carries deep historical weight. Trust, access, insurance coverage, and proximity to the specialized treatment centers equipped to deliver gene therapy all shape who actually benefits. thegrio.com
What Needs to Happen Now
Community advocates, Black medical associations, and patient organizations currently push on several fronts simultaneously. The Sickle Cell Disease Association of America works to expand insurance coverage and reduce administrative barriers. Black physicians and researchers call for investment in treatment infrastructure at HBCUs and community health centers in cities with large Black populations. Federal legislators have introduced bills targeting gene therapy affordability through outcomes-based payment models, where insurers pay over time tied to patient outcomes rather than upfront.
The cure for sickle cell disease exists. Science delivered its part. Now the healthcare system, policymakers, and the broader public carry the responsibility of making that cure reach the people who need it most - the Black families who have carried this disease for generations and deserve to see it end.
The sickle cell disease expense issue may be the most clear illustration for the need for a more responsive health care system overall to the Black community. Ultimately, it makes a points for a need for a Medicare for all health care system. Blavity.comhas more basic info on sickle cell disease.
Checkout the 60 minutes Video on The Discovery in Sickle Cell Disease Treatment Below...
Sponsor's Messages Below
Author Max Miller Releases New Self-Help Book “Blame It on the Feel of Pain” About Detangling From Past Pain
Get ready for a transformational journey toward inner peace as indie author Max W. Miller’s new self-help release, Blame It On The Feel Of Pain, inspires readers in a witty, down-to-earth book. Truth and compassion are foretold, using poetic frames called ‘The Wises,’ and the help of opinionated little emojis bringing laughter and thought-provoking conclusions throughout.
The author encourages her readers, whom she also calls partners, to stop wrestling with the hard knocks of the past. She expresses how voluntarily walking back into time precedes trauma healing. Confronting lingering pains is a step toward strength and hope for the future. ‘Blame It’ delves into the author’s life experiences, bringing to life the importance of using Full Circle Moments to find resolutions.
Throughout Blame It On The Feel Of Pain, the reader grows to understand through a unique interpretation that what we are destined to become grows out of the years we’ve already traveled. Further, our future hinges on how we address the pains of the past. Other expressions focus on how desires in the present are carved out of having a clear vision that old, lingering strongholds must be defeated. A history of suffering is a prerequisite for becoming fed up enough to demand enjoyment now!
New Children’s Picture Book Honoring A Mother-Son Bond And Black Hair Pride
See How Author Shellice Beharie pays tribute to the memory of her loving son in her debut picture book, "PRINCE AND HIS MOTHER’S CROWN: Tales Within my Mother’s Hair."
This read-aloud narrative communicates that in their early stages of childhood boys can find comfort and creativity in their mother’s tresses. Checkout this is very uplifting reading for our challenging times: Click Here. Or to order: Click Here
While there are brilliant persons on the Autism Spectrum celebrated today, very little media stories focus on people, especially women of color. Our co-publisher's new bio-pic "nZinga's Spectrum In 3D," is a moving and inspirational documentary on how a young Black woman RISES to overcome her challenges.
nZinga Austin is also the Co-publisher of Our Black News Scoop and Southeast Queens Scoop. The documentary of about 1/2 hr long is getting rave reviews.
Checkout Nzinga's Spectrum in 3D now Click Here. Please share
Posted by community events coordinator, Nzinga Lonstein Austin, is a prolific blogger who writes on the entertainment industry and issues for people with developmental and physical challenges.
She is presently in high school looking to have a career in video, film, and media. You can see more of her entertainment writing on Lonstein Movies.
About the Southeast Queens Scoop - is the premier website and only publication offering daily news and updates on the events, culture, issues, and is dedicated to the business and economic development in this largely black historic community.
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