#NeuroME
Live, measured metrics for the hashtag #NeuroME from the open social web. Every number carries a named source and the time it was fetched. Nothing is estimated.
Own #neurome
This #name is available to claim. It becomes your portal on the open agent web: this very page, a keyword you rank for by an open public stake, and a verifiable identity for AI agents. Nobody else sells a page like this for every #name.
Day-by-day usage
measured · fosstodon.org (Mastodon public tags API) · fetched 2026-07-30 06:45 UTC0 uses by 0 unique accounts across the window. Real per-day counts, not estimates. Newest bar is today so far.
Related hashtags
measured · fosstodon.org (Mastodon public search API) · fetched 2026-07-30 06:45 UTCLive pulse
measured · fosstodon.org (Mastodon tag timeline) · fetched 2026-07-30 06:45 UTCEverything below is measured over the latest 40 public posts (spanning ~21137 hours).
Posting hours (UTC) — busiest: 01:00
Languages: English (40)
Avg boosts / post: 3.6
Top of the latest posts
🧵 "ME/CFS Isn't Just Misunderstood, It's Actively Neglected" https://www.popsugar.com/fitness/mecfs-post-covid-49344168 'Beth Pardo is among the people who developed ME/CFS after contracting COVID.' 'Pardo went from running ultramarathons
4/ “On the theme of personal burden and quality of life, another stated, ““She said, “My life has become an inhumane existence.” She left a husband and two teenaged children whom she referred to when she said, “I believe they have lost thei
(US) Tell Congress: Fund ME/CFS Research Now Deadline is April 15 I believe https://solvecfs.quorum.us/campaign/157943/ Image is from the AMMES April 2026 newsletter #MEcfs #PwME #ME #MyalgicE @mecfs #CFSME #MEeps #CFIDS #SEID #NeuroME #CFS
Every number above is measured from a named public API at the shown fetch time. Nothing is estimated or extrapolated. Platforms that lock their data behind paid APIs are not shown. Agents: the same numbers, as JSON, at /api/hashtags/neurome