Photographer Captures the Spark
By Sandi Bohle
This is the third in a series of posts about how many in the Lyme community turn to the arts as a way of supporting their healing and taking their mind off the daily struggle of dealing with Lyme disease. As someone who had a 30-year career in the arts before getting sick, I was interested in finding out how many of us, like myself, worked in the creative arts before getting sick. I was also curious about whether others have turned to the creative arts as a release, as I did with my photography, as a way to see the world outside of illness.
D.S. True (Devin True) is a Los Angeles photographer and artist. He was diagnosed with Lyme disease two years ago, but believes he has had it for over thirty years. He says he can’t remember a day without symptoms, and as he’s gotten older the disease became progressively worse.
“I’ve been starting to get a bit better over the past few months but I still have lingering symptoms,” he said.
Having studied photography and music production at Evergreen State College in Olympia, Washington, he worked in the music industry for many years, owning a club & promoting concerts in Olympia and Seattle during the 1990’s. He moved to Los Angeles in 2000, starting an audio rental company and recording studio. Around 2007, he started to get sicker and was unable to work, so he sold off his businesses to be able to care for himself.
“I often work on my photography, art, and writing music when I’m not feeling good as it offers a great creative outlet,” Devin explained, “Photography is story telling whether it’s commercial headshots or band portraits, and my goal is to capture the spark of the subject.”
Currently, he works independently as a commercial and headshot photographer and sells his artwork.
Of his journey with Lyme disease, Devin says,” be open, try as much as possible, don’t give up, and do your best to eat and be healthy.”
Devin’s photography can be seen here.
Devin’s artwork can be seen here.
Another life slowed down, ruined by Lyme, But still we can’t get treatment without spending our life-savings, then we are again left to suffer. Here is only Lyme warrior’s efforts to get signatures for awareness for Lyme. I signed already. Consider helping her achieve her goal. https://www.change.org/p/the-cdc-idsa-and-congress-stop-discrimination-against-individuals-with-chronic-lyme-disease-by-the-cdc-and-idsa?tk=Ou4EN-z6OXKs6iJGKnZ8qC3oTyqYRkdVt_cHNNy76GY&utm_campaign=fb_dialog&utm_medium=email&utm_source=signature_receipt&post_id=577303449086706_602321763251541#_=_
Lyme disease has made me a better actress that’s for sure! I have a wide range of emotions to pull from and I’m dying to play a real dark character.
I just hope you do not literally die to play that role. I understand what you are saying as most Lyme victims will. I do hope you get the roles to play, but I also hope you recover and only have the memories to draw from for your acting. If you become famous, be sure to support Lyme awareness.