even though I’m pretty sure offering money for votes is very illegal I’d rather #VoteForCount than anyone else at this point
truer now than four years ago
miku!
throwing something new on an old tumblr just to see what happens
wow
exactly seven years and seven days ago I started this little tumblr! holy moley. still gonna keep going because at this point why not right?
love y’all! be good, be safe, drink some water!
now it’s eight years and twelve days ago! gosh
The fact that Selma Blair, a successful, wealthy, white actress, “cried with relief” when she was diagnosed with MS. After YEARS of suffering, not being believed or taken seriously by her doctors (who I’m sure were some of the ‘“best” doctors available) and being left to suffer as her illness worsened should really shed a light on the systematic issues chronically ill people are facing. It’s 2019. It shouldn’t be this hard.
Stuff That A Person With A Chronic Illness Wishes You Knew - Fibromyalgia Animation
In this short and light-hearted animation, Rosie and their wonderpup Brodie explore what it’s like to live with a chronic illness like fibromyalgia - through Rosie’s personal experiences, rather than a lot of statistics that can be easily found elsewhere.
This is just one narrative of many for those with chronic conditions, and it does not mean to try to encompass all possible experiences. Every story is different, and they’re all equally valid.
does anyone still follow me here? go find me on instagram or even twitter instead I use those infinitely more. @asundayraine on those things too. thanks bye
matching icons for u and ur crew
oops i’m all bald now
(I don’t think my new office job 🙌 would have appreciated the fashionable asymmetry)
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