I was hoping this update would have been as easy and neat as one of my many #DisabledChronicles posts: a dramatic retelling of my true life events leading to an ultimate revelation. Succinct. Deep. Raw. Instead, in the days since my procedure, I’ve found myself near tears, touched by the outpouring of magick woo, prayers and love from those whom I share community with, who love and support me. I’ve been moved by the protection and care from those who
I was one of those kids who was sure that No ONE was the boss of me; not even my Momma. I remember the very first time I was ever angry with her, being five or six years old and how I glowered at her as she tied my dark brown orthopedic shoes and tried to push me to do more physical therapy when I just didn’t want to. As she lifted her head after tying my shoes, she was
That one time you ask your aide to make you multiple servings of the new Cream Of Rice cereal you found and that was purchased along side Bethany’s Cream Of Wheat… And though they were bagged together but in separate containers, your aide managed to grab the wrong box (and you didn’t even think to triple check to ensure she grabbed the correct one) and proceeded to make a whole 12 mini containers worth of the Cream Of Death so
The amount of advocating I’ve had to do for myself (and with some help) this past week has been astronomical. This has been on top of the normal fuckery people bring on the daily. It’s also made me weary. The landscape of my main condition has been shifting… for some time, if I’m honest. This past week was the reckoning. I advocated for new equipment, new services and other things besides. These recent days behind me, have been my main
New-to-Me doctors are an interesting bunch: They either discount everything I say and treat me like any other typical patient (never a good idea) or they are so determined to peg me into some kind of category that they miss things. That is never good either. So it was with a leery mind that I followed my PCPs recommendation to follow up with an allergist after things took a left turn for me earlier this year. That horrible blood draw
Hi, my name is Sandra and so… this blog will be about my writings, my existence as a writer, my living as a disabled person, my thoughts on being a creative and my book and self publishing exploits. But mainly? It will be about my writings.
Disabled Chronicles, No.2 
Fight ME! 
Celiac Chronicles, No.7465 
Disabled Chronicles, No.8 
Disabled Chronicles, No.7
Recent Comments