At Black Health Compass, we believe that informed communities are empowered communities. A crucial part of our mission is to provide clear, concise information on current health policies impacting Black Coloradans, and to champion advocacy for systemic change. Today, we’re highlighting a significant victory for health equity in our state: the new law designed to improve the lives of individuals affected by Sickle Cell Disease (SCD) in Colorado.
As many of us know, Sickle Cell Disease disproportionately impacts Black communities. In fact, nationally, Black Americans represent the largest minority group in need of organ transplants, and are three times more likely than White Americans to experience kidney failure, a common complication of SCD. Despite modern advances in treatment, access remains a critical barrier.
That’s why the recent signing of Senate Bill 24-042 (SB24-042) by Governor Polis is such a landmark moment. This new law, named after Arie Taylor—a pioneering Black politician and advocate—is a testament to sustained advocacy and community effort.
Why is this Law So Important?
Historically, individuals living with Sickle Cell Disease have faced significant healthcare disparities, including inadequate care and support. The Arie Taylor law aims to enhance resources and support for those living with this chronic illness by:
- Improving Access: Addressing barriers to innovative therapies and new medications that offer hope for managing SCD symptoms and complications.
- Targeted Support: Recognizing that SCD predominantly affects African Americans, this law is a crucial step towards ensuring our healthcare system serves everyone equally, with a focus on equity and justice.
- Honoring a Legacy: Naming the law after Arie Taylor, the first Black woman elected to the Denver City Council, underscores the enduring impact of Black leaders in the fight for civil rights and health equity.
As State Senator Janet Buckner emphasized, this legislation is
“crucial to health equity and justice, ensuring that our healthcare system serves everyone equally.”
This policy change helps pave the way for a healthier future for Black Coloradans affected by SCD.
What This Means for Our Community:
This law is more than just legislation; it’s a call to action and a reminder of what we can achieve when we work together. It highlights:
- The power of advocacy in driving meaningful change.
- The importance of understanding health policies and their direct impact on our lives.
- The continued need to support organizations like the Colorado Sickle Cell Association, who have been at the forefront of this fight for 50 years.
Stay Informed & Get Involved!
Policy changes like the Arie Taylor law are vital, but their full impact depends on our community being aware and utilizing the resources available. Black Health Compass is committed to keeping you updated on policies that matter most to our health.
Call to Action:
- Learn More: Visit the Colorado Sickle Cell Association’s website (cscadenver.godaddysites.com) for more information on SCD and how you can support their work.
- Advocate: Get involved with local organizations like the Colorado Black Health Collaborative (coloradoblackhealth.org) to participate in future policy discussions and community planning efforts that continue to address health disparities.
- Share Your Story: Your experiences matter. Connect with us in our community forums to share how health policies, or lack thereof, have impacted you and your family.
Together, we can continue to advocate for policies that create a healthier and more equitable Colorado for all Black individuals.
