One of the more frustrating experiences for long-term Lyme patients can be that they feel too sick to exercise. They read in Burrascano’s guidelines and elsewhere that exercise is critically important for healing. Yet, many are too debilitated to get up out of a chair, or in some cases, even out of bed. When merely crossing the room requires Herculean effort, the concept of exercising for health can seem utterly unobtainable.
A new book called “Sunlight Chair Yoga” may help.
It’s written by Stacie-Saraswati Dooreck, a long time yoga instructor who some years back experienced her own bout of serious illness. Unable to exercise or do yoga the way she used to, she decided to try adapting her yoga practice so that she could do her poses sitting down.
“The first time I tried chair yoga for 10 minutes,” she recalls, “I felt some of the healing energy I used to feel during a full yoga practice before I got sick.”
Encouraged by that experience, she continued with her chair yoga practice as she convalesced. She has since gone on to teach these adaptive yoga strategies to people who are too sick, injured, or otherwise limited to undertake regular yoga poses. What she learned in this process is now incorporated into the book.
She advises anyone who is quite ill and hasn’t exercised in a long time to start slowly.
“Some yoga and exercise or meditation—even a minute—is better than none,” she says. “I learned to let go of comparing how I used to exercise, and listen to the limits of what my body and mind is comfortable doing in that moment.”
Although the book is called “Chair Yoga,” some of the exercises can be done lying in bed. There are breathing techniques, hand movements, even yoga for your eyes.
Breathing exercises alone can bring more oxygen to the body and promote feelings of vitality, Stacie points out.
“With simple meditations, breathing exercises and gentle movements you can help restore your body and mind to wellness.”
Click here for Stacie’s website, with information about how to order the book.
TOUCHED BY LYME is written by Dorothy Kupcha Leland, LymeDisease.org’s VP for Education and Outreach. Contact her at firstname.lastname@example.org.
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