Skip to main content

Skydiving

Sing it with me..."I went skydiving; I went Rocky Mountain climbing; I went 2.7 seconds on a bull named Fu Manchu..." 

Hell to the yeah!  It was an awe-inspiring, balls-to-the-wall, scream-worthy, boundary-pushing event! A not-to-be-denied booster shot to my ego. It was so far out of my formerly staid domestic life. Nobody saw it coming...not even me!

Following the implosion of my marriage with the requisite accusations, grenade-lobbing of insults, splitting of the money, bills, furnishings and paraphernalia of a married life, I was an empty shell walking. Alternately filled to bursting with anger, bitterness, rage, self-loathing, and terror, without a support system, I turned to alcohol, men, and anything that took me out of me.

Oddly, it was a man, my paramedic, who appeared following a suicide attempt, that introduced the idea of skydiving. He described his experiences and the idea took root and quickly came to fruition. One beautiful, sunny desert day, I awoke to the thought that today was the day. I was alone, lonely, with 24 hours stretched in front of me and I was sick to death of doing what I was doing.

"You don't know how to risk!" was one of the invectives backhandedly lobbed at me, that echoed in my head. (That's okay, I told him that he had a small penis. I figure one of us got to prove the other wrong.) I jumped for my life that day. I jumped for my self esteem; for my freedom; for my future. I had many more obstacles to overcome; I would not discover Alcoholics Anonymous for another two years.  And, I would amass a trainload more wreckage.

But that act, performed without the knowledge of my friends or family, was as close to God as I would get, before sobriety. That day I risked. That day I stepped out in faith. That day I overcame.

Amen. .

Comments

Popular posts from this blog

I Remember...

I remember catching fireflies,  putting them in a jar, as a girl of five. I picked pears off a tree that overhung an alleyway on my route home from school, then enjoyed the forbidden fruit. .I had a golden cat who chased a gray mouse through our living room sending my mother, 3-year old sister, and me screaming atop the sofa and chairs. We lived in a farmhouse and I watched Romper Room. A daddy longlegs skittered across my dirty kid legs as I teeter-tottered on a broken kitchen chair back. I played grocery store and laid out a bedroll for group nap time in preschool. We lived in an apartment attached to a bakery. My maternal grandparents visited and a photo was snapped. Grandma held Dawn and Grandpa held me. I held Grandpa's chin. Walking through the back of the flour-caked kitchen, I saw scrumptious pastries and colorful toys stuck in the cupcakes with my hungry kids eyes. We lived in a two-story apartment building next door to a large farmer's field.  That field was my...

On-the-job Sass

I continue getting sass from one particular caregiver. He says, "You need to communicate with us." he continues to completely miss or dismiss the concept of I would if I could . It is part and parcel to having ALS, I am losing my ability to communicate and it is his job to assist me. Part of helping me, like it or not, is to learn my routine and anticipate needs, when possible. He misses the fact that I'm failing more every day and night time is when I'm weakest. It is extremely insensitive and arrogant to expect me to cater to his needs and expectations. Pushing me to repeat words or expound on a simple one word suggestion is physically taxing on my system, adding stress which further depletes me. Cuing is supposed to be caregiver's domain, not the patient's. Here is the situation, I am being changed. In the midst of the action, as seems to be his practice, he is sidelined asking me trivial, meaningless, but energy-sapping questions. Do I want my legs raise...

Managed

Managed care, do not get me started. It is the bane of my existence and my savior. If quadriplegia has curtailed my activities, and it has, then being in a home has curtailed even more. I've had to dumb it down and set my standards low. Gone, are the halcyon days of getting in my wheelchair to go for a stroll or sit in the sun, or even sit in the sun room. Neither the nurses, nor patient care technicians, know how to put me in my wheelchair. Seriously. My chair has head controls and it is a bafflement. Most caregivers don't even realize I have head controls. First, they hit the left head pad when they lift the armrest which turns the chair on. Next, they sling me over and place me in the chair. The problem? My head, naturally, rests on the headrest, which accelerates and drives the chair and is beyond my control. Running over a caregiver or running myself into an obstruction are very real consequences of their ignorance. What could be worse? The caregivers remain clueless abo...