When I was 20 years old I spent the summer with my mother in
the house I lived in as a child. I
had only been away for less than a year.
It had been a very hard year.
I felt very alone. I was not doing very well in college. I was falling. I was failing. I went home to my mother’s embrace.
But I am unable to sit still for long.
Soon I was volunteering for the local community
theatre. I only had one year of
college but that was deemed sufficient training to be in charge of costume
design and stage construction for the production Oliver. Every spare moment I was building
costumes or building sets on the local high school stage. I scheduled a work call to build the
set and only person showed up to help.
Fortunately he was a contractor, so we got quite a bit done. The next day I began hauling 50 lb drums
of drywall mud to the set, when I felt my back go out. Once I could breathe through the pain I
went to the office and called my Mom.
She came in her car to get me. I could barely walk. Going to the doctor was out of the
question since we had no insurance, so she placed me on her bed to rest with an
ice pack on my back. She rolled me
over as needed, because I could not do that myself.
I lay within the room upon the softest white sheets. In the center of the sheet my mother
had embroidered a peacock in a sacred tone of blue. I would run my hands over the hundreds of French knots that
marked the plumage. An occasional gentle breeze would blow in from the open
window and the window sheers would billow like the wings of angel. My mother cared for me.
Soon the show's director called wanting me to come in to work
on the set. Now, my Mother is the
sweetest, kindest person you could ever meet. I had never seen her raise her voice outside the
family. But that night she yelled
on the phone at the director of the show, and I smiled. I knew my mother had my back, even if I
had broken it.
Perhaps this story is the reason I loved Tiffany Peterson
since the moment I met her. She is
an amazing advocate in the Lupus community and she orchestrates great deeds
from far away, often while laying in a bed in pain.
Tiffany is an older child in a large family. For many years her mother depended on
her help with the younger children.
Then one day Tiffany was sick.
For quite a long time no one knew what was wrong with Tiffany. She moved down from her upstairs room
because climbing became too much for her.
She was placed near her mother who became her caregiver.
This is Tiffany’s jacket: Tiffany and Lupus.
I painted this in New York at Social Media Week NYC in
February 2012. I painted this at
the easel while Tiffany told me her tale and a crowd swirled around us. The strangers laughed and spoke with a
slightly maniacal tone that accompanies the second glass of wine. Occasionally, someone would jostle my
easel or make a witty remark about live painting at a cocktail party.
But within the spiraling conversations, there was a pool of
stillness where Tiffany and I stood.
For beautiful, quiet Tiffany was pouring out her heart and I was wetting
my brush in her soul.
In this painting Tiffany lies within a darkened room. In the far background her father is
represented only as a silhouette.
He is leaving her. He does
not believe her pain, after all she
doesn’t look sick.
In the foreground Tiffany rests on purple sheets, the color of Lupus. Her mother holds her as she holds her mother. The love between them is palpable.
In Tiffany’s hand she holds her laptop. It is her window to the wider world. It represents all of her online friends who support her in her disease and on her journey.
In the foreground Tiffany rests on purple sheets, the color of Lupus. Her mother holds her as she holds her mother. The love between them is palpable.
In Tiffany’s hand she holds her laptop. It is her window to the wider world. It represents all of her online friends who support her in her disease and on her journey.
Tiffany is beautiful, brilliant and she has so much to look forward to. She has such a powerful voice online and in person. But she suffers still. She gets tired. She watches what she eats. She wears a hat in the sun. No matter what she does to stop it, the disease can still assail her. Tiffany does all she does while in pain. When all of the other advocates have gone to sleep; it is just Tiffany staring at the blinking cursor. Just Tiffany and Lupus.