Fibromyalgia and Lupus's Starter Pack
Created by
@fibroandlupus.bsky.social
@lupusdnadoc.bsky.social
Global lupologist, pediatrician, mother, avid reader. Writing good science and bad poetry. Citizen of earth. Runner. Seeking truth and excellent ice cream. Views are my own and do not reflect my employer #Rheumsky
@lupuswarrior69.bsky.social
#LGBTQ #LovelsLove #BLM #ChronicPainSucks #CancerSucks #Lupus 🛑 NO DMS! 🛑 NO FOREX/BITCOIN 🛑 💙 I'm a blue 🔵 in a red state. Don't judge my GoFundMe unless you know me! https://www.paypal.me/RenateTurner https://gofund.me/9856991e NO Lists please
@lupusandme.bsky.social
Wife🏳️🌈Mom.Retired Nurse Practitioner, CNS Lupus, et al. Warrior.💜Mental Health Matters💚Grateful🥰Poet💕Advocate For The Underdog
@lupus.org
Lupus Foundation of America is the only national force devoted to solving the mystery of lupus while giving support to those who suffer from its brutal impact. 💜
@mecfs.at
💛 Österreichische Ges. für #MECFS ⚡ NEWS zu #MECFS #pwME #myalgicE 👇 Informationen, Spenden, Kontakt http://linktr.ee/oeg_mecfs https://mecfs.at/
@dgmecfs.bsky.social
ME/CFS ist eine schwere körperliche Erkrankung, die bisher kaum erforscht ist. Wir setzen uns für die Interessen der Erkrankten und mehr Forschung ein. mecfs.de
@andrewgiffordphoto.bsky.social
Hello, welcome :) This Invisible Illness: my first long form photography project, about ME/CFS a complex & challenging health condition - like Long Covid. https://linktr.ee/andrewgifford.photography Bristol, UK. 335.42 ppm. He/him/oi.
@dialoguesmecfs.bsky.social
https://www.dialogues-mecfs.co.uk Website with videos created by Natalie Boulton & Josh Biggs with a Wellcome Public Engagement Fund Award. Professionals and patients explain key aspects of #ME/CFS and a longer film explores the wider context and history.
@probablyacryptid.elikwake.com
36, AuDHD, asthmatic, trans male, aro, demi, EDS, IBD, CFS. Apparently a dire threat to the American way of life. Still wearing masks. Keybard author he/him Discord: (mutuals only, DM me) Ko-fi book and music shop: https://ko-fi.com/orpheusandeli/shop
@me-cfs.bsky.social
Disabled by very Severe Post-COVID ME/CFS. Not always able to use phone. Bedridden. Unable to Speak. I care. My ME/CFS News Aggregator: @me-cfs.mastodon.social.ap.brid.gy Ⓐ💚, (FR/DE/EN, but posts in english) Clinging onto the ledge above the abyss.
@duvelfella.bsky.social
F** Russia- F** the orange 🤡, Putin, Orban and the rest! Vatnik destroyer- democracy shall prevail https://savelife.in.ua/. 🇺🇦💙❤️🇧🇪💙🥰 #nafo #fella
@soisfibroreal.bsky.social
Beating #fibromyalgia one day at a time, taking my power & my life back. Join me! The- So Is Fibromyalgia Real? What I Know Is Real -Blog #Fighter Canadian #Resister #ElbowsUp #ClimateActivist soisfibromyalgiareal.com
@mynameisfibro.bsky.social
Our official account. Raising awareness and helping fibromyalgia warriors find the help, support, guidance and advice they need 24 hrs a day worldwide
@marting8177.bsky.social
RAF Veteran Fibro Warrior Everyone is welcome here Mental Health & Suicide Awareness Matters I Support Small Businesses Please be kind and love yourself Your life is so special 💕 Please Follow Your Dreams Sorry, No DMS or Cripto Mwaaah xxxxxxxxxxxx
@fibroandlupus.bsky.social
A place to create an online support community for Fibromyalgia and Lupus