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Playing With Disease

Words: Paul Jenulis

Image: Jenny Jimenez

Lesli Wood

 

Lesli Wood has had her hand in the Seattle music scene since 1997. She leads the four-piece known as Ms. Led and performs in the melancholy and low-key Saeta with her good friend Matt Menovcik and cellist Bob Smolenski. Where Saeta will calm and ease you, Ms. Led wants things “to be like a mini-revolution every time we play,” says Wood. She also performs with Menovcik in an accordion and guitar two-piece known as Roxy & Clark, attends law school at the University of Washington and works at the Public Defender’s office. One can see how busy Lesli Wood is and how getting Multiple Sclerosis out of the blue could seriously fuck up her life.

“I have a lot of issues with MS,” says Wood. “The fact that I have it is my first one.” In January, Wood noticed numbness in her hands and went to the doctor. By that Sunday, she could barely walk or roll over in bed; it was like her whole body was asleep. The following day her MRI revealed white spots spread over her brain, indicating lesions: patches of neurons stripped of their myelin, a fatty protein. Neurons, billions of them, communicate signals within the central nervous system, as well as the rest of the body, and, when stripped of their myelin (which insulates neurons and is responsible for increasing the speed of nerve signals), the neurons cannot function efficiently and may be damaged. Symptoms of MS vary from person to person, but may include fatigue, vision and memory problems, dizziness, slurred speech, bladder dysfunction, and difficulty walking.

The week Wood was diagnosed, Roxy & Clark had a show at Seattle’s Green Room. “It was a big deal for me to do this show,” says Wood. She still hadn’t come to terms with MS. “I’m thinking, ‘What does MS stand for? I didn’t even know. MS to me at the time was like a foundation. People do walks for MS. People do fundraising for MS. MS wasn’t something that I would have.”

But she did have it, and she endured three-day steroid treatments to fight the symptoms. “I was so drugged up. It was over the top. I would stand up and I could feel the steroids whoosh through my body…. All you do is sit around and think about how your life is going to change because you have MS and you can’t do all this shit, and you’re fucked up on steroids. Are you ever gonna get your hands back? Are you ever gonna play music again? How are you gonna tell people? I couldn’t even fucking play guitar.”

She couldn’t play guitar because she had one of four types of Multiple Sclerosis: relapse and remitting, meaning new symptoms could appear and old ones worsen. Slowly, she accepted she had MS and it would be with her for life. Still, “I wasn’t going to change anything,” she says. “I wasn’t going to cancel a single show.” She played piano that night at the Green Room. Five songs. At the end her hands had locked up; she couldn’t walk down stairs without help. She also pulled off a huge show for Saeta (playing with Low) during that time, as well. “Biggest show of our career,” she says.

“I don’t think I’ve seen her encounter anything that she couldn’t handle,” Menovcik says. Drummer Stephanie Hasselman says Lesli “sees a sense of urgency more than ever to get out there and play and tour and see and do things with the band.” The only real difference now for Ms. Led, Menovcik says, is that at times, the band may have to carry more of the weight if Wood encounters MS-related difficulties. Guitarist Peg Wood has learned many of Lesli’s guitar lines in case Lesli has to resort to just singing for the night because her hands won’t allow her to play guitar. Lesli Wood has been told she can’t do a lot of things, but her drive (and medicine) still allow her to play guitar and piano, hold things, and type notes during class. As long as she can do that, she’ll keep doing what she’s been doing her whole life: playing music.

“What,” she says, “I just have to sit in my home waiting to be in a wheelchair one day? Fuck it, I can do whatever I want. Music is what I want to do.”

Ms. Led’s new album will be out this summer. Thanks to mult-sclerosis.org for additional information.




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