bathrooms should be accessible for all.
tysm fatigue
Receive message, be too busy/tired/stressed to respond right away
???
It has been long enough that responding without preamble would now be Weird
never speak again.
Terrarium Life collection~
I painted these way back during the pandemic (hence the hoard of toilet paper and Switch that I wish I had, but they were all sold out) No pandemic now but the chimney smoke from all the neighbors have made the air unbreathable and I'm stuck inside again 😭 cuddling my dog, drinking tea
tending to my fish tank and my plants
lately if im not constantly occupying my brain i spiral.
my mind is exhausted from the constant stimulation but i dont know what else to do.
yes. yes. yes.
honestly i get so excited when i see someone switch over to the “i could never” response because so many people do the “lucky you, you get to be lazy” and that one just really hurts.
so when i see even a small step in the direction of understanding my life is not glamorous, even if its still a response i hate, i feel excited dkdhks
i really cannot understand how people see disabled life as this glamorised lazy life. i genuinely cannot wrap my head around this.
how could ANY of what i go through be seen that way i just dont get it.
I feel like most able bodied people see wheelchairs as the worst thing that could happen to a person. When I discuss my want to have a wheelchair for various reasons, most peoples first reaction is to be surprised that I could voluntarily consider that.
But what they fail to consider is that, unlike them, I very much hate walking. It causes me pain and fatigue, it is a miserable experience.
So to any able bodied person reading this, yes some wheelchair users like walking, some want to gain that ability back, but that does not invalidate the feelings of wheelchair users who absolutely hate walking.
agreed, making things i need pretty?? instantly changes my perspective on it.
decorating my feeding pump and using fun tube tape has done wonders for my mental health and not being able to intake much besides water by mouth. making things your own when you're disabled is such a necessity for me. 
i want my life back fuck being ill.
gave up on home care and went to hospital on day 15 😭
on day 5 of a migraine get me out of here
healthy coping looks different for everyone right, but i really wish it was easier to figure out what was right for me without all this trial and error stuff 😭