Angela S. Davis
Rare Disease Patient Advocate and Writer, Stiff Person Syndrome Patient Advocate
@cureclcn6.bsky.social
We are a 501c3 dedicated to raising awareness of ultra rare neurodegenerative mutations on the CLCN6 gene, providing support and advocacy to impacted families, and funding the research and development of treatments for these devastating diseases.
@jacquelineraposo.bsky.social
Freelance writer exploring bodies + food folk. Author. Sick crip. Nature nerd. Reluctant hermit.
@altnps.bsky.social
The official "Resistance" team of U.S. National Park Service. Our website: www.ourparks.org
@goldenhourcomms.bsky.social
Working my way back to one name. #staygolden
@ohnoshetwitnt.bsky.social
~* Jewish American Disney Princess *~ I’m from N-E-W Jerz
@bsky.app
official Bluesky account (check username👆) Bugs, feature requests, feedback: support@bsky.app