I really love seeing #CleanAirClub expand from focusing on infection control measures like masks and air filters, to also centering solidarity with people with long covid and ME/CFS. Connecting the dots.
This list of 50+ ways to show up for people with long covid and me/cfs is very good, despite being on Instagram:
Clean Air Club on Instagram: "Attention abled people: it's time to step up and support our loved ones and comrades who have Long Covid and ME/CFS!! There are over 400 million people living with Long Covid today, and many millions more living with ME/CFS. These are debilitating, energy-limited conditions that can make basic life functions extremely grueling. It's everyone's responsibility to make sure people with these disabilities are not left behind. PLEASE go through this list and pick one or two things that you can do on a recurring basis, then ask a friend or acquaintance with Long Covid and/or ME/CFS whether they would appreciate any of that help. The more specific, the better. You can also work in the other direction, sending this post to them and asking whether anything in particular would be most helpful! And to the folks with Long Covid and ME/CFS: what would you add to this list? We'd love to hear more ideas in the comments. It takes a village. Sending so much love to everyone dealing with these difficult disabilities. Thank you to @kd_kinetic and @coolgruel for providing feedback on this list! IDs in comments due to length."
1,694 likes, 30 comments - clean.air.club on October 30, 2024: "Attention abled people: it's time to step up and support our loved ones and comrades who have Long Covid and ME/CFS!! There are over 400 million people living with Long Covid today, and many millions more living with ME/CFS. These are debilitating, energy-limited conditions that can make basic life functions extremely grueling. It's everyone's responsibility to make sure people with these disabilities are not left behind. PLEASE go through this list and pick one or two things that you can do on a recurring basis, then ask a friend or acquaintance with Long Covid and/or ME/CFS whether they would appreciate any of that help. The more specific, the better. You can also work in the other direction, sending this post to them and asking whether anything in particular would be most helpful! And to the folks with Long Covid and ME/CFS: what would you add to this list? We'd love to hear more ideas in the comments. It takes a village. Sending so much love to everyone dealing with these difficult disabilities. Thank you to @kd_kinetic and @coolgruel for providing feedback on this list! IDs in comments due to length.".
