#rarediseaseadvocate
Live, measured metrics for the hashtag #rarediseaseadvocate from the open social web. Every number carries a named source and the time it was fetched. Nothing is estimated.
Own #rarediseaseadvocate
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Day-by-day usage
measured · fosstodon.org (Mastodon public tags API) · fetched 2026-07-31 13:55 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 2026-07-31 13:55 UTCNo related tags with measured usage found for #rarediseaseadvocate.
Live pulse
measured · fosstodon.org (Mastodon tag timeline) · fetched 2026-07-31 13:55 UTCEverything below is measured over the latest 3 public posts (spanning ~2144 hours).
Posting hours (UTC)
Languages: English (3)
Avg boosts / post: 1.3
Top of the latest posts
Hello. I’m pretty quiet on here, but I would like to connect with other people in the Wilson’s Disease community. A hashtag yielded nothing, so I’m starting it here. If you see this, please amplify. #WilsonsDisease #raredisease #raredisease
This is a huge deal. I believe the condition that I have #HNPP is actually very prevalent but it's only ever tested if there are symptoms. In South Korea, however, it turned out there were 16/100,000 in a similar study. 100,000 babies to ha
I'm going to start the #hnpp tag as it's not here yet. I have it. It stands for Hereditary Neuropathy with Liability to Pressure Palsies. It's a rare degenerative neurological condition, closely related to #multiplesclerosis. It means I'm l
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/rarediseaseadvocate