I’m currently in the worst pain I’ve experienced in the better part of a decade and my boys are driving me crazy. While I’m more grateful than words can express that Emmett has found his voice, why couldn’t it have been his inside voice?
Collectively, they are screaming and fighting but Emmett is by far the loudest and the he has to climb all over me.
I’m so tired and every time I look away, a little bit more of my sanity sneaks away. I’m pretty sure that I don’t have much left. 🙁
This site is managed almost exclusively from my Samsung Galaxy Note 3. Please forgive any typos as auto-correct HATES me. 😉
Follow @Lost_and_Tired
“Like” me on Facebook
Visit the My Autism Help Forums
To reach me via email, please Contact Me
pain is awful. prayers is all i have for you on this one
Lost and Tired Sylvatine I don’t know what it’s like In your state and maybe you’ve already checked into it, but in NY kids with issues such as autism and Dev. delays, and would qualify for medicaid service coordination which offers among other services so many hours of respite time. Your local ARC probably offers respite hours too. I saw that you couldn’t put on your socks. I hope that changes but this is how I put mine on- http://carex.com/item/FGP22500+0000/Sock-Aid/#.UmHINRDYH4c
Sylvatine thanks. As far as respite goes, we’ve never had respite. The boys usually spend the night at their Grandparents on the weekend.
So Sorry, Rob! I have the same back issue and a kid that does not understand! I know exactly what you’re going through! Hoping and praying that your back’s in better shape very soon! Do you guys have respite services? You really need it!