I finally got Google to agree to repair it themselves but I never received a kit to send it in?? Anyway I haven't had a phone for months so

I've taken in my phone to this same place 3x, not counting the times they called me in and sold my part to some1 else, or WHEN THEY LOST IT

Since Dec I've been having issues with a phone repair I had and now screen is just lifting off and there's a burning smell

How TF are the other ppl who are losing vision doing this???? Do they all just relocate? Starve? Go nowhere ever?? HOW ARE THEY DOING IT

And it's like. I can't even get a GP bc nobody accepts my insurance nearby. I'm basically housebound and tbh it's not for the faint of heart

Discharged from PT bc of insurance and because I'm unable to go in 2x a week... Just been a nightmare. Pt says go back doc for in-home pt

They should have pushed it further and tried imitating me as much as possible as well, and led a secret double life as me

Does getting my art stolen to be sold mean I've finally hit the big time??

Spent last night in the ER with my boy. Have to go back in minutes from now. He seems much improved. It's really hard when this happens

The mind is willing but the joints are old and achy. I was having fun. Going to try and see if I can write instead w/o triggering pain

using pointer finger to do small motions is a rly bad habit kids, don't do that. hard to get rid of bad habits

got a lot of art stuff finished from last year over the past few months, but now my pointer finger rly hurts wah

girl are you kidding me my phone screen is busted AGAIN after two faulty repairs (NOT user error on my part), i am so over this

Really bad arm pain day. Good news though is I FINALLY, after 3 weeks, got a referral for a new pt who takes my insurance

It's hard to go up there bc they've reduced spending on public transit options for the disabled where I live, but idk what else to do

It's been 3 weeks of trying to contact the ortho's office with calls, texts, and emails and I still can't get anyone to respond

trying to function in this world with autism is miserable

Dr says no multifocal in sclerals but I don't understand why you can't?? Rly important for managing my degeneration so it's like. Why not??

At which point what is even the point of trying to get them? Prevention seems like the way to go??

My retinas are hanging on tho so that's good. Dr wants me in sclerals. Insurance won't cover unless I need cornea transplant