Angelina Namiba serves as a possibility model for effective and sustained engagement with those vulnerable to HIV. When she was diagnosed in the early 90s, she immediately set to work to understand why Black women were being left out of national efforts to combat the spread of the virus, and she participated in and assembled groups of women committed to raising the voices of women living with HIV globally.

She is a titan within England’s HIV advocacy movement and she has worked for almost 25 years to promote and advocate for the involvement of women living with HIV in forming and informing local and national HIV strategy and policy. Today, we explore the resilience required to sustain our advocacy when our lives are systemically undervalued and the ongoing need for cultural competency within the NHS, which despite being built on the backs of Black women, still leaves so many Black women to suffer in silence.

Angelina shares the mnemonic device she created to help women remember their rights when engaging with healthcare practitioners, and the role literature, storytelling and book clubs have played in bringing her and others like her together to effect systemic change. Angelina reminds that in the face of anti-Blackness, homophobia and misogynoir, it has always been us looking after us.

Recommended reading:

Our Stories Told by Us by Angelina Namiba

Queer Footprints by Dan Glass

Thank you

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