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Bringing disabled perspectives to the forefront

Hello Lelu was born out of the need for honest, accessible conversations about disability and chronic illness, grounded in lived experience. It’s a space where journalism meets personal reflection, and where systemic issues blend with everyday realities.

Who I am

I'm Madison “Lelu” Rodriguez, a disability advocate living with hypermobile Ehlers-Danlos Syndrome (hEDS), postural orthostatic tachycardia syndrome (POTS), and endometriosis. My writing is informed by both research and firsthand experience, so you’ll get reporting rooted in disability justice as well as what it actually means to live with chronic conditions.

What you’ll find here

  • Journalistic reporting on disability justice, health science, education law, policy, history, and more

  • Personal essays reflecting the day-to-day and emotional landscape of chronic illness, bigger concepts involving disability rights, and more

  • Product reviews, tips, recipes, etc. from mobility aids to health-tech and self-care tools

  • Embedded videos that complement written pieces and expand their reach

Expect a mix of casual entries and in‑depth exposés centering disabled perspectives.

Who this is for

Whether you're disabled, chronically ill, a caregiver, medical professional, or curious ally, if you want critical, compassionate insights around disability and how societies treat it, you’re in the right place.

My commitment

I publish thoughtfully and consistently; not always on a fixed schedule, but always with purpose. I’m committed to maintaining journalistic integrity, centering disabled voices, and using this platform to inform, educate, and advocate. Your support and feedback help shape this evolving space and community.

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Hello Lelu is a space for reporting and reflections that center disabled and chronically ill experiences.

People

26 | Chronic Illness & Disability Advocate | POTS | hEDS | Endometriosis