Digital Punk Girl
@digitalpunk.bsky.social
Angelle Kingston
She/Her • Xennial
ME/CFS • POTS • MCAS • Fibromyalgia
Disabled COVID Long Hauler
Artist. Photographer. Gardener.
X Files nerd. Coveter of books, strange art, & vintage wares.
Baby monitors would work, that way you can at least sleep in your own bed.
April 19, 2025 at 2:27 AM
Baby monitors would work, that way you can at least sleep in your own bed.
Reposted by Digital Punk Girl
Our invisibility as a group of people doesn't help.
Our ability to be part of everyday society is often very limited.
It's hard for us to be advocates for change.
And power concedes nothing without a demand.
So we need allies.
Our ability to be part of everyday society is often very limited.
It's hard for us to be advocates for change.
And power concedes nothing without a demand.
So we need allies.
February 5, 2025 at 1:52 PM
Our invisibility as a group of people doesn't help.
Our ability to be part of everyday society is often very limited.
It's hard for us to be advocates for change.
And power concedes nothing without a demand.
So we need allies.
Our ability to be part of everyday society is often very limited.
It's hard for us to be advocates for change.
And power concedes nothing without a demand.
So we need allies.
Very well said.
The most common advice I lend to fellow LC sufferers who ask, is to remember to be kind to yourself. Amidst the relentless cycles of grief, I know that’s been an ever present struggle for myself in my 5yr journey with this disease.
The most common advice I lend to fellow LC sufferers who ask, is to remember to be kind to yourself. Amidst the relentless cycles of grief, I know that’s been an ever present struggle for myself in my 5yr journey with this disease.
February 6, 2025 at 4:09 PM
Very well said.
The most common advice I lend to fellow LC sufferers who ask, is to remember to be kind to yourself. Amidst the relentless cycles of grief, I know that’s been an ever present struggle for myself in my 5yr journey with this disease.
The most common advice I lend to fellow LC sufferers who ask, is to remember to be kind to yourself. Amidst the relentless cycles of grief, I know that’s been an ever present struggle for myself in my 5yr journey with this disease.