Tuesday, January 17, 2017
Dollhouse
The dollhouse began as all stories do. Once upon a time. One time a long time ago a little girl like me...is the first line I write on a blank paper. In 1992 divorce was in my near future. I was blessed to have my sisters' little children in my care then, and having never put away my childlike awe, we played and learned from each other as hearty loving equals. I started the build of this dollhouse and finished the construction in 1994: the year the divorce was final, and I had a new home in my mind if not in real estate. In 1996 I was diagnosed with cancer. I needed a haven, respite and safe harbor from the world of disease. The outfitting of my alternate reality commenced in earnest. Most of the accoutrement in the house is art from life. The wreath in the bedroom stairway is a scaled reproduction of one I still own. The bedroom furniture is modeled on my set which is 120 years old in 2017. The Black Mariah stove is constructed to resemble my great-grandmother's, and there is a coffee grinder with real coffee in it. On the fireplace mantel is a miniature of the hand-tooled clock I bought for myself in 1980 which still keeps time and good company on my desk. As the years went by, I gifted the house. Last year was a plate of artisan-made springerle cookies.This year is the 20th anniversary of being cancer free, and I think this is the year to donate the dollhouse. My lovely friend Carol suggested C.S. Mott Children's Hospital in Ann Arbor. With that goal, I will chronicle the tale of the dollhouse here. Life is stories. Parents and ill children need good stories. And a place, path and passion to imagine.
Wednesday, January 11, 2017
Cancer In A Jar
January 1997. I no longer remember the exact day. We had to be at Harper Hospital at 5:00 a.m. Another woman was checking in as well, and we "no, please, you first" responded to the call for next. An O.R. was scheduled for 12 hours to get the cancer in my head out. In the room would be my surgeon, a maxillofacial prosthedontist (and his spare parts, including a nose, maxillary bone, eye socket) a back-up plastic surgeon, many other professional medical people. My sister said she couldn't imagine what I was about to live through. I told her it would be her who lives through those hours. I'd be awakened in post-op after it was all over. I awoke in recovery to a guy in surgical gear calling my name. First thing I said was there are duckies on your cap. He said it's in a jar. Do you understand me? It's in a jar.
That January day was preceded by a year of trying to get a surgical referral, of learning at high speed through a traumatic situation how to get what I needed. How to hurdle the gatekeepers, trample the stoppers. That was the year of Flat Alice: anyone who tried to get in my way. The year of Beckie being at my side for each encounter, of her agreement to hold my consciousness until I was ready to take it back, of her getting me to a chair before I passed out when I saw the room of face parts in the MP's office as I hung up my coat. Of sitting in her car in the freezing cold after the MP told me he could replace my eye, but he couldn't make it blink, and Beckie slamming both hands onto the steering wheel, shouting "Damn it! Why can't he make it blink?" Of her being my ears, my guide, as well as continuing to be my Best Friend in the Whole Wide World.
Of children who became my spiritual advisors. Of my mother, unaware she was going to die of cancer soon, trying to find a way to bond with me that did not include disease.
A year of fools and misogynists and incompetent famous doctors and ridiculous healthcare network rules and paperwork. A year of miracle workers, angels on earth, and family, friends, laughter and terrible pain.
There would be another six years of surgeries to repair and replace. Six years of deepening and new friendship and acute self-discovery. Six years descending into personal financial crisis, and ascending to gratitude and awareness. Six years of losing my mother and friends to that awful disease.
Through it all there would always be that day in January when Dr. John Jacobs said it's in a jar.
That January day was preceded by a year of trying to get a surgical referral, of learning at high speed through a traumatic situation how to get what I needed. How to hurdle the gatekeepers, trample the stoppers. That was the year of Flat Alice: anyone who tried to get in my way. The year of Beckie being at my side for each encounter, of her agreement to hold my consciousness until I was ready to take it back, of her getting me to a chair before I passed out when I saw the room of face parts in the MP's office as I hung up my coat. Of sitting in her car in the freezing cold after the MP told me he could replace my eye, but he couldn't make it blink, and Beckie slamming both hands onto the steering wheel, shouting "Damn it! Why can't he make it blink?" Of her being my ears, my guide, as well as continuing to be my Best Friend in the Whole Wide World.
Of children who became my spiritual advisors. Of my mother, unaware she was going to die of cancer soon, trying to find a way to bond with me that did not include disease.
A year of fools and misogynists and incompetent famous doctors and ridiculous healthcare network rules and paperwork. A year of miracle workers, angels on earth, and family, friends, laughter and terrible pain.
There would be another six years of surgeries to repair and replace. Six years of deepening and new friendship and acute self-discovery. Six years descending into personal financial crisis, and ascending to gratitude and awareness. Six years of losing my mother and friends to that awful disease.
Through it all there would always be that day in January when Dr. John Jacobs said it's in a jar.
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