Diana Leigh Waldron
@dianaleighwaldron.bsky.social
Wife, poet, dog and cat mom, retired civil servant, ethical vegan, chronic illness warrior. (she/her)
Profile pic: Me in bed with “Still Sick, Still Fighting” shirt and “Save Our Spoons” sign
Banner: Closeup of blue asters
Profile pic: Me in bed with “Still Sick, Still Fighting” shirt and “Save Our Spoons” sign
Banner: Closeup of blue asters
#SaveMedicaid #ACA
#MEAction
This is a very SCARY time! We are people with ME/CFS & Long COVID who stand against Medicaid cuts and ACA premium increases. Protecting the most vulnerable Americans is the only right thing to do.
#MEAction
This is a very SCARY time! We are people with ME/CFS & Long COVID who stand against Medicaid cuts and ACA premium increases. Protecting the most vulnerable Americans is the only right thing to do.
October 28, 2025 at 8:23 PM
#SaveMedicaid #ACA
#MEAction
This is a very SCARY time! We are people with ME/CFS & Long COVID who stand against Medicaid cuts and ACA premium increases. Protecting the most vulnerable Americans is the only right thing to do.
#MEAction
This is a very SCARY time! We are people with ME/CFS & Long COVID who stand against Medicaid cuts and ACA premium increases. Protecting the most vulnerable Americans is the only right thing to do.
<3 I had a black cat named Pyewackett and now have another black cat with Pyewackett as her middle name. <3
October 16, 2025 at 3:32 PM
<3 I had a black cat named Pyewackett and now have another black cat with Pyewackett as her middle name. <3
Post you from a different era:
Just adopted my first dog as an adult.
Just adopted my first dog as an adult.
September 30, 2025 at 1:49 AM
Post you from a different era:
Just adopted my first dog as an adult.
Just adopted my first dog as an adult.
#ShadesforMigraine 🕶💜
I've lived with migraine for more than three decades. You only see me on good days!
I've lived with migraine for more than three decades. You only see me on good days!
June 21, 2025 at 3:31 PM
#ShadesforMigraine 🕶💜
I've lived with migraine for more than three decades. You only see me on good days!
I've lived with migraine for more than three decades. You only see me on good days!
Erinnert mich an meine Kinder.
May 25, 2025 at 12:36 PM
Erinnert mich an meine Kinder.
May the spoons be ever in your favor! 🥄🥄🥄💙🩵💙
#BlueSunday2025 #MyalgicEncephalomyelitis #ChronicIllness #MEAwareness #VirtualTeaParty #MillionsMissing
#BlueSunday2025 #MyalgicEncephalomyelitis #ChronicIllness #MEAwareness #VirtualTeaParty #MillionsMissing
May 18, 2025 at 6:54 PM
May the spoons be ever in your favor! 🥄🥄🥄💙🩵💙
#BlueSunday2025 #MyalgicEncephalomyelitis #ChronicIllness #MEAwareness #VirtualTeaParty #MillionsMissing
#BlueSunday2025 #MyalgicEncephalomyelitis #ChronicIllness #MEAwareness #VirtualTeaParty #MillionsMissing
Quote this post with a picture of the airplane you’ll accept as a bribe.
May 15, 2025 at 12:43 AM
Quote this post with a picture of the airplane you’ll accept as a bribe.
I made this video for ME Awareness Day to illustrate how much my life has shrunk since I got sick. I am grateful every day for all I still have and can do. I also miss my old life, where I could be upright for 14 or more hours a day instead of one or two today. @meactnet.bsky.social
May 12, 2025 at 12:45 PM
I made this video for ME Awareness Day to illustrate how much my life has shrunk since I got sick. I am grateful every day for all I still have and can do. I also miss my old life, where I could be upright for 14 or more hours a day instead of one or two today. @meactnet.bsky.social
On ME Awareness Day, please consider a donation to @meactnet to help the #MillionsMissing fight for research and support.
COVID showed us how quickly we can develop treatments when the funding is there. ME patients just want their lives back.
COVID showed us how quickly we can develop treatments when the funding is there. ME patients just want their lives back.
May 12, 2025 at 11:43 AM
On ME Awareness Day, please consider a donation to @meactnet to help the #MillionsMissing fight for research and support.
COVID showed us how quickly we can develop treatments when the funding is there. ME patients just want their lives back.
COVID showed us how quickly we can develop treatments when the funding is there. ME patients just want their lives back.
I am one of the #MillionsMissing! We are sending out a #DisabilitySOS 🆘. Save our Support Systems💔. Save our Science 🔬. Save Our Society 🌍. #MillionsMissing #MECFS @meactnet Learn more: www.meactions.org/millionsmiss...
May 11, 2025 at 4:22 PM
I am one of the #MillionsMissing! We are sending out a #DisabilitySOS 🆘. Save our Support Systems💔. Save our Science 🔬. Save Our Society 🌍. #MillionsMissing #MECFS @meactnet Learn more: www.meactions.org/millionsmiss...