
Nothing About Us Without Us proudly serves as the welcoming home for Disability Community for Democracy, Inc., fostering a spirit of inclusion and collective voice.
| Platform | Pricing | Freemium | Publishes | Daily | |
|---|---|---|---|---|---|
| Issues | 233 | Founded | 2 years ago | Last Issue | 2 days ago |
| Active | |||||

Photo by Dan Meyers on Unsplash
In the 1990s, the American safety net forced my family into an agonizing administrative compromise. Medicaid was the only program that could fund my care. To receive the intensive mental health care I needed...
Photo by Stephen Wheeler on Unsplash
Yesterday was my birthday, and as I reflect on how far we have come, I want to begin with a heartfelt thank-you to our sustaining, paid members. You have kept this publication a bestseller since August,...
The image is a watercolor-style illustration with a strong narrative focus. At the top, a prominent banner with a distressed, textured background displays bold text in two lines. The top line, in a creamy yellow color with a subtle shadow,...
The image is a graphic design featuring text overlays and a portion of the United States Capitol Building. The color scheme is primarily dark blue and white, giving it a serious and official tone. In the upper-left quadrant, large white tex...
Photo by National ADAPT. A law enforcement officer stands near two people in wheelchairs. The officer is wearing a tactical vest and a cap.
After Monday's pavement theater at the Health and Human Services mobilization, the structural failu...
Subscribers, engagement, traffic and sponsorship for Nothing About Us Without Us.
| Subscribers | Engagement | 79 | Monthly Web Visits | ||
|---|---|---|---|---|---|
| Accepts Sponsors | Estimated Cost per Ad | ||||
The writers behind this newsletter.
CEO and Founder of Disability Community for Democracy, Inc. Publisher of Nothing About Us Without Us. Diversability’s 7th annual D-30 Disability Impact List honoree.
Sudden onset Myalgic Encephalomyelitis 1989. Advocating for adoption of ME-ICC to improve patient outcomes & quality research. Info includes ME/CFS, CFS, Long COVID. chronic Lyme & other marginalized diseases. Not to be considered medical advice.
Advocate for disability rights, outspoken chronic illness sufferer, veteran - founder of "Sick of this Shit Publications", "Banner & Backbone", and Director of Framing for "Disability Community for Democracy, Inc."
Writer, editor, child-wrangler, sometimes-filmmaker, Missoulian dropped on my head in NYC. Wandering Agent-lessly (She/Her)
Ryan Talley is a disabled LGBTQ creator and advocate using TikTok and Substack to speak out on disability rights, healthcare, accessibility, ableism, and justice. His work centers dignity, survival, and equality.
Jennifer Burss is a human rights activist, Disability advocate, Disability Rights Advocate, writer and performer living in Michigan.
Disability Community for Democracy Inc.'s Substack
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