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American Focus > Blog > Health and Wellness > Why this activist is putting her body on the line for Americans with disabilities
Health and Wellness

Why this activist is putting her body on the line for Americans with disabilities

Last updated: July 2, 2025 2:26 pm
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Why this activist is putting her body on the line for Americans with disabilities
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Latoya Maddox, a disabled activist, found herself at the center of a heated debate as lawmakers discussed the future of Medicaid, a 60-year-old health care plan that provides crucial services to millions of Americans. Alongside her friends, Maddox raised her voice in protest, shouting, “No cuts to Medicaid! No cuts to Medicaid!” The passionate demonstration quickly caught the attention of Capitol Police, who escorted Maddox and her fellow activists out of the House Energy and Commerce Committee meeting.

The protest was organized by American Disabled for Attendant Programs Today (ADAPT), a group dedicated to advocating for the disability community. Since its inception in the 1980s, ADAPT has been at the forefront of major actions, including the iconic “Capitol Crawl” where protestors with physical disabilities climbed the Capitol building’s steps to highlight the challenges they face in a world not designed for their needs. This action played a significant role in the passage of the Americans with Disabilities Act.

Despite their efforts, Maddox and other disabled activists are facing a daunting challenge as conservative lawmakers push for significant cuts to Medicaid funding. Vice President J.D. Vance recently cast a tie-breaking vote in the Senate, paving the way for a $4.5 trillion tax-cut bill that includes drastic reductions to Medicaid. These cuts could leave nearly 12 million people without access to essential health care services.

For Maddox, who relies on Medicaid for 24-hour care due to her arthrogryposis multiplex congenita and other disabilities, the proposed cuts are a direct threat to her well-being. Without Medicaid, she fears she would struggle to afford a wheelchair, essential medications for her son, and the support she needs to navigate daily life.

As a seasoned activist, Maddox has been involved in numerous protests and actions over the years. She has witnessed firsthand the impact of grassroots advocacy and the power of collective action. Despite facing challenges and physical risks, Maddox remains committed to fighting for the rights and dignity of the disability community.

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In a conversation with STAT, Maddox reflected on her journey as an activist and the challenges she faces as a disabled mother advocating for herself and her community. She shared her experiences of witnessing the deplorable conditions in nursing homes and finding inspiration in the collective power of grassroots movements like ADAPT.

As the battle over Medicaid funding continues to unfold, Maddox and her fellow activists remain determined to make their voices heard and protect vital health care services for millions of vulnerable Americans. Their courage and resilience serve as a reminder of the ongoing fight for equality, inclusion, and justice for all.

Living with a disability, navigating the complexities of the healthcare system, and advocating for rights can be a daunting task. For individuals like myself, who have dedicated their lives to helping others with disabilities, the potential cuts to Medicaid funding pose a significant threat to our well-being and independence.

As a parent of a 13-year-old son who relies on daily medications to function in school, the prospect of losing Medicaid coverage is terrifying. Without access to these essential medications, my son’s ability to thrive in an educational setting could be compromised, potentially leading to serious consequences such as expulsion. Ensuring that he receives the necessary care and support is a top priority for me, and any disruptions to our healthcare coverage could have devastating effects on our lives.

Engaging in activism and advocacy work, such as protesting at government hearings, comes with its own set of challenges and risks. The recent arrest of myself and other members of ADAPT during a protest at the House Energy and Commerce Committee hearing highlights the ongoing struggle to bring attention to the needs of disabled individuals in the face of looming policy changes. Despite facing legal repercussions for our actions, the fight for disability rights and access to essential services remains a top priority for our organization.

With the Senate passing their version of the tax bill, the focus has now shifted to working with state governors to mitigate the impact of potential Medicaid cuts on disabled adults and seniors. As a grassroots nonprofit organization, ADAPT relies on the dedication and passion of its volunteers to drive change and advocate for the rights of disabled individuals across the country. The financial constraints of our organization make it challenging to mobilize large groups for protests and advocacy efforts, but our commitment to creating lasting change remains unwavering.

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Balancing activism with the responsibilities of caring for my son adds another layer of complexity to my daily life. The fear of being arrested and potentially separated from my child weighs heavily on my mind, highlighting the sacrifices and risks involved in fighting for disability rights. The misconception that disabled individuals are simply seeking attention or financial gain undermines the genuine commitment and passion that drives our advocacy work.

As we continue to push back against potential Medicaid cuts that could force disabled individuals into nursing homes or institutions, the fight for community-based living and independence remains a central goal for ADAPT. Deinstitutionalization is not just about relocating individuals from facilities to community settings; it’s about recognizing the inherent right of all individuals to live and thrive in the community of their choice. The dignity of risk, the freedom to make choices and take risks, is a fundamental principle that should guide our approach to supporting individuals with disabilities.

Ultimately, the fight for disability rights is about more than just access to healthcare and services—it’s about the right to live a full and independent life, free from institutionalization and discrimination. By standing together and advocating for change, we can create a more inclusive and equitable society for all individuals, regardless of their abilities.

The Impact of Missing Medications and Services Due to AWOL Status

When someone goes missing for two days without notifying anyone, it is often assumed that they have gone AWOL. This term, which stands for Absent Without Leave, is typically associated with military personnel who abandon their duties without permission. However, in civilian life, going AWOL can have serious consequences, especially when it comes to receiving necessary medications and services.

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Imagine a scenario where someone with a chronic illness or mental health condition goes missing for two days. During this time, they are unable to contact their healthcare providers or pick up their prescribed medications. As a result, they may experience a decline in their health and well-being, putting them at risk of harm.

The impact of missing medications and services due to being labeled AWOL is a serious concern. Without access to the right medications, individuals may struggle to manage their symptoms and maintain their health. Similarly, without the necessary services and support, they may find themselves in dangerous situations that could have been prevented.

It is important to emphasize the dramatic impact of this issue. While it may not lead to immediate harm for everyone, depending on the individual and their specific needs, the consequences can be severe. Without the proper medications and services, people may struggle to regulate their lives and protect their health and safety.

In light of this, it is crucial for healthcare providers, support services, and organizations to have systems in place to address situations where individuals go missing or are unable to access their medications and services. By ensuring that there are protocols in place to prevent gaps in care, we can help protect the well-being of those who are most vulnerable.

Ultimately, the loss of access to medications and services due to being labeled AWOL is a serious issue that needs to be addressed. By recognizing the potential risks and taking proactive steps to mitigate them, we can help ensure that individuals receive the care and support they need to maintain their health and well-being.

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