In a better world, I'd be able to meet my monthly expenses, which after house stuff are: 820€. My priorities are: meds (165), food (250), psychiatrist (75) + physiotherapy (330), which should be every day, but 3x a week already costs a lot & that's my minimum need for my MS to be properly managed, so that's what I'm setting as my goal even tho I didn't meet it 100% last year. I'm very grateful for the help I've had because without it I wouldn't be here. You're helping me survive, y'all! Ty!
🏳️🌈♿ She/Her; They/Them. Neurodivergent (ASD & ADHD). Ambulatory wheelchair & cane user since #MultipleSclerosis dX in '16. Previously an Anthropologist student, now just someone fond of photography, AiArt, writing, moderating online communities & some beta-testing. On Fedi: @eloisa@masto.pt
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Hi! I'm an immunocompromised neurodivergent (ASD & ADHD) 36 yr old disabled queer with Multiple Sclerosis and I need your help! The goal I've placed is what I spend just so I can keep surviving and managing my mobility and balance issues and chronic diseases (Multiple Sclerosis, GAD, Depression, Chronic Pain and Chronic Fatigue, among others) in 2022. I do so mostly through physiotherapy, psychiatry, medication and, ofc, some food. Donations & gifts are always welcome and very appreciated! 💖 The fight is not over, yet! As per usual, I'll update you through here, Fediverse & Twitter! Thank you in advance for any sharing of this among your social media and/or donation/s! Every cent helps! Yes, really. <3, Eloísa
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