If you find anything, lemme know. Ménière's disease sucks, and my left ear is pressurized currently.
Lemmy411 - Don't know where to find what you're looking for?
As with /r/411 this is where you ask what Community you're looking for but not finding. Perhaps a bit more helpful now that some communities are only found on certain instances.
Found/new community announcements - there are numerous "announcement type communities - see https://lemmy.ca/post/612532
There is also !wowthislemmyexists@lemmy.ca
Before you request There are several resources available to find communities and resources and these have been pinned to the top.
- there are community search engines at https://browse.feddit.de/ and https://lemmyverse.net/communities
- there are numerous other "find a community" and "community announcement" .. communities (list stickied; if you find another, comment pls)
- we will publish a Community Listing (at an as-of-yet-undetermined schedule)
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Rules
- Don't be a jerk or be deliberately unhelpful
- Please post a clear easy to understand request for a community (or instance!)
- Pls no NSFW requests - if you want to create /c/NSFW411 go ahead.
- No posting of personal information
- Please refrain from suggesting users should use search engines or directories.
- No joke, troll or misleading suggestions or requests
- No spam
It most certainly does suck. It's be great to have a place where we can vent, talk about what triggers attacks and what helps prevent/soothe attacks. There was a sizeable community on Reddit, and I miss that resource.
If you don't mind me asking, how long have you had symptoms/been diagnosed? It's been an eight year struggle for me, but only recently diagnosed after moving states and seeing a new ENT.
it's been roughly 7 years on the diagnosis, maybe 8 or 9 for the symptoms. I had a pretty good ENT.
I didn't know there was a subreddit for it, that may have helped me lol
I've been mostly managing with magnesium and hydration, but for some reason this last couple of weeks, it's really kicked in hard
Hydration is super underrated!
Sorry to hear you're having it tough lately. I have been too, and that's why I was trying to find the right group here to chat it out lol. I'm honestly surprised there's no community that's remotely relatable for what we're going through.
Coincidentally, finally released today after about 3 weeks of variable plugged. Yay for vertigo! Wasn't too bad today, because it released slowly. Hope yours works out soon.
I made !chronicillness@lemmy.world which is decently active, but a bit more general.
I’m functionally deaf due to a chronic illness, so I can relate a bit, sorry to hear you have Menieres.
Thank you! Subscribed!!