My Protest to Live - a Pre-Obituary Sounds Right!

This writing has been featured in Positively Aware magazine as a resource/tool to speak out against public health funding attacks throughout the country. Read more about it here.

Kamaria Laffrey, born with Black Girl Magic and Chronic Optimism, lived a life deeply rooted in her faith in the power of the people and in the science that saved her life since her HIV diagnosis in 2003. A mother, a widow, an advocate who led with a smile, curiosity for solutions, and endless ideas for liberation.

When the Florida ADAP changes were proposed in January 2026, outside of the rules-making process that the state is supposed to follow for such changes to the Federal Poverty Level and drug formulary, she joined in activating community members to help as many people be informed as possible, navigating insurance program deadlines and patient payment assistance programs. Speaking with the media and traveling to the state capitol to hear from legislators was a tactic Kamaria supported and often drew inspiration from because she wasn’t alone in doing it and was joined by many of the 16,000 people impacted by the proposed changes. 

Even with the response to that collective advocacy and pending lawsuit to the state filed by AHF, the lack of transparency still infiltrated Kamaria’s life like an additional diagnosis, one that doctors couldn’t screen for or test. Without access to her treatment, her body succumbed to the inadequacy of leadership in securing the health and well-being of others like her.

Kamaria died not because her treatment failed, but because the very systems meant to sustain her life decided she was too expensive and risky to keep alive. She lived and thrived with HIV, and because of ADAP, lived well, until coverage gaps, formulary exclusions, state violence, and bureaucratic indifference replaced medicine with uncertainty, confusion, and anger. She leaves behind unfinished work, a body of advocacy that insisted people living with HIV deserve stability, not substitutions or having to sacrifice their integrity to live, and a reminder that “cost-saving measures” decisions led to a quiet death sentence. 

She also leaves behind proof that policy choices are never neutral, and that denying stable, transparent access to care is an administrative decision but a lethal one. Her death was not inevitable; it was engineered. She should have outlived the politics that failed her. Her life did not end from a lack of science, but from a lack of prioritizing humanity and political will. 

Kamaria Laffrey is survived by the science that could have kept her alive, the treatment that worked until it was taken away, and a movement that warned what would happen when care is rationed by indifference. She is survived by her only daughter, family, and friends who were inspired by her, supported her, and gave her the encouragement she needed to leave behind the very empowered legacy she fought to help others have through embracing healing, giving inspiration, and living victoriously. She lived with HIV, virally suppressed and strong, until coverage gaps broke the promise that treatment equals life. What she leaves behind is not just advocacy, but a critical truth: when access is interrupted, survival is too. 

May we all remember this as a regret for what we chose not to protect and a reminder that we can know our history but tend to repeat it at the detriment of our own lives.