Idk new post bc the last lost traction, no donations in a week. We need 450 for the rest of February, 450 for a deposit, and 950 for March, 50 for the rest of the utilities. We were homeless since Aug 2020 excepting 4 different months whose places fell through for various reasons, have to get rid of the van we were living in because it's falling apart, Collie got FFS December 28th, she's recovering well and maybe could do something with a car if we had a better car, given her ability to drive. I still haven't found much work but I'm still looking. Anything helps.
paypal.me/NoraEstherRose
venmo: nora-esther-rose
venmo: Leah-Esther-Rose
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Hey babes, sorry I've been dead, but I coulda been literally dead if I had not gone.
I didn't hurt myself and we're still figuring things out. I would love to share but I've already forgotten what I've learned. I hope I get more guidance and time for healing and learning on how to lead my life in a better direction than where I was. But that takes time and effort.
I hope to get some rest, get some support, and get it together. But right now, I don't think it's healthy for me to worry about art in the way I do now. I may not express it here, but trying to maintain my art endeavors/projects while there's so much bullshit going on backstage is not helping me. Especially since I'm not even obligated to do so. But trying to force myself to do something I am currently unable to do will just make me feel worse. I'll follow my dreams and passions one day, but I've been putting off the healing process for years.
So I guess it's better to get better now so I can get the ball rolling again. Why drive on a flat tire?
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SO saw the cardiologist again (np but it was a followup so), cardiologist changed my diagnosis from neurocardiogenic syncope to POTS. not much difference in the lifestyle "changes" they'd want me to make but because it was switched they're prescribing me midodrine, already picked it up from the pharmacy gonna take first dose today (unless i forget)
looking it up on reddit and tumblr it does seem to help a lot of people so hopefully it helps me too :)
kinda scared of being diagnosed with POTS since there are so many people online who have such a horrible time with it but at the same time i'd be having these symptoms whether i was diagnosed or not, i've been having them for a couple years now, and even if the med doesn't work now i know it's not just all in my head
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I want to apologise in case you already tried it. But I've seen many people with ehler danlos say that shapewear helps. Do you think it's something you could use?
Ive tried pretty much every otc method of keeping my joints in place including shapewear, with the execption of like 1 or 2 that has slightly too many steps for me to muscle thru the executive dysfunction and do (ring splints -_-). I dont actually know if there is a way to keep my joints from subluxating or dislocating with almost every movement but if there is its gonna have to be like. Complete imobilization except in the direction that said joints are actually supposed to move.
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