"One afternoon, I noticed how the late afternoon light was hitting the surface of my guitar. Sometimes I see something and realize I have to try to capture what I'm seeing before it passes.
Though it's a guitar, it really isn't (and isn't meant to be) a portrait of a guitar. I try to catch some angle, some perspective on things that isn't literal. I also strummed the strings in order to get the motion, some kinetic energy in the shot.
This has some particular meaning to me because I recently started to try to play music again, I played for years, music is what I studied in college, but I really couldn't with MECFS. But I'm trying again, and I have my instruments out in my living area where I can see them and have it be part of my life again."
- Michael Van Huffel
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Santa Cruz, CA
“I was in a tough state prior to this photography project. It brought an unexpected and deep relationship, and finally feeling productive again. Since I started, I feel much less like I am disappearing and it's given me much hope for a real future.”
Michael Van Huffel enjoyed a successful career as an artist, animator, Creative Director, and musician. His career got a jumpstart when he began working with the musician Prince, as a staff artist, and eventually Art Director. He also has also worked in motion design, TV and movies, and served as Creative Director for numerous projects in advertising and entertainment.
In 2007, Michael unexpectedly developed Myalgic Encephalomyelitis (ME/CFS) a devastating and poorly-understood neuroimmune condition. Michael began to face loss after loss. Unable to work and eventually housebound, his career, home, and the life he built were lost due to hundreds of thousands of dollars in medical co-pays. Life became very different and solitary. He relocated to a one-room studio outside San Francisco, and has been taking part in the largest-yet studies on his disease at Stanford. That room became his de-facto art studio.
Michael describes that his life for 8 years turned into an isolated existence, that most relationships had become virtual, except for home infusion nurses and very occasional visitors. The most recent transformation in his art career, and what you see featured on ArtLifting, occurred when he received an iPhone on a family plan, and an artist friend suggested they start a photo-a-day project. Michael describes that “this became a search to find beautiful or interesting things within an apartment that had only been accumulating painful associations using numerous physical and technical limitations as a means to a unique style and meaning. This also unexpectedly led to a relationship, a partner—something that had long seemed a lost part of life.”
In this past few years, his life has welcomed big changes and transitions. He got married and relocated to Santa Cruz. Michael can occasionally get outside for short walks and is now close to a lot of natural beauty. Nearly all of the photos use things he collects while outdoors. He then brings the objects, whatever they may be, back to photograph when he is feeling well enough. The photos are often expressionistic—an attempt to make things look like something other than what they are—such as paintings, sea creatures, or landscapes. He aims to convey emotions and feelings and for viewers to see and find interesting corners of his world.
To learn more about Myalgic Encephalomyelitis (ME/CFS), please visit the Open Medicine Foundation and follow the groundbreaking study mentioned in Michael’s bio. In addition, see the multiple award-winning documentary, Unrest, created by a woman living with the disease.
ArtLifting champions artists impacted by homelessness or disabilities through the celebration and sale of their artwork. Learn more here.