From #meactionnetwork:

#MillionMissing 2023 is 3 weeks away! Take a look at our Activism From Home Kit & plan how you can join in! In order to get a greater amplification of these efforts and to get THE MOST press attention for this event, we will need help from those at home. https://docs.google.com/document/d/1-JBHY9C6xrm1iP6sGgjlXdz9lnLQQ3H3BkybEpDKGdA/mobilebasic

@mecfs @cfs #MyalgicEncephalomyelitis #ChronicFatigueSyndrome #mecfs #cfs #pwme #PwMEs #cfsme #cfids

RT @[email protected]

Il me restait 2 mois sans le savoir "à vivre " avant d'être frappée par une maladie incurable, invivable, méconnue : l'em/sfc
Incurable car trop peu de recherche ,0 en france malgré les entre 150000 et 300 000 personnes atteintes.
( + que la sclérose en plaque )
#millionmissing

🐦🔗: https://twitter.com/Emilie33037871/status/1550550989224263680

Star Wars Rebellion pill dispenser commission o/

Having a chronic illness is hard. Having an invisible one is even harder because you can disappear without anyone noticing.

Start the rebellion now, take your pills, be proud and may the force be with you x

In the memory of Carrie Fisher, she brought hope to so many other spoonies like me, we will always miss her.

#pills #chronicilness #invisible leillness #MastoArt #chronicpain #fibromyalgia #millionmissing #MEaction #StarWars #Rebels