Yoga and The Hypermobile Yogi – Managing Chronic Pain and Stabilizing Joints with Ehlers-Danlos syndrome (EDS)
“Yoga is dangerous for EDS.”
“I was told not to do yoga.”
“Yoga will make you end up in a wheelchair.”
I’m sure that you’ve heard all these phrases before, and many people feel that that all three are absolute truths. While we all are entitled to our opinions, the fact is there is no black and white factual statement that has come out about doing yoga when you have Ehlers-Danlos Syndrome. Usually, our ideas stem from personal beliefs, from what we have been told by someone we trust, or from our experiences with yoga. We are all different, and the truth is what works for someone else, does not work for you and vice versa. This applies to the practice of yoga.
There are countless people with hypermobility/Ehlers-Danlos syndrome, who have been practicing yoga for years and have done well. There are also those who tried it and did not have the strength, nor were self-aware enough to know how to protect their hypermobile joints when practicing yoga. In their defense, extreme hypermobility used to be glorified, not just in yoga, but dance, gymnastics, and other sports where being able to bend and twist your body in extreme ways was viewed as a value and helped give you that edge over others who could not do the same. You take that same person who is not aware of how to protect their hypermobile joints when practicing yoga and pair that with an instructor who may not be aware of the damage that can be done long-term to the body when pushed to those extreme positions, and you can see why many EDSers were told not to do yoga.
When you learn more about the philosophy of yoga and the various types of yoga, it becomes apparent how much more there is to yoga than what is perceived by many as a form of exercise where you need to push poses to the extreme. Yoga is quite the opposite. My feelings on the topic of yoga and EDS probably come as no surprise to anyone who reads what I post or sees my Instagram yoga challenge pictures. However, I have not always liked yoga, nor thought it was beneficial to me. I felt that yoga was quite annoying, but I never questioned if it was good or not or not for me once I was diagnosed with EDS. Then again, I was also told to not workout at all and didn’t listen. So, it’s likely anything I was told about yoga would have gone in one ear and out the other as well.
My opinion about yoga changed when I bought a Bryan Kest’s power yoga tape (a VHS tape to be exact!) when I was in college. I purchased this video because I’ve always done intense workouts and wanted something like yoga to help balance out my workouts. I also wanted to do something when I didn’t feel like working out. I liked the idea of yoga, but a traditional class was way too slow and tedious for me. I wanted more intensity and the pace to move slightly fast, which is how I learned that there are different types of yoga practice. From what I read, vinyasa flow yoga and ashtanga yoga seemed to be more up my alley. Bryan Kest’s power yoga tape was the perfect blend of ashtanga and vinyasa flow yoga practices, and it soon became a regular in my workout routine. I even worked out to Bryan’s video the morning of my wedding. Because I’ve always followed the Just 5 Minutes rule and have done it for years, that still applied on my wedding day. Plus, I needed a way to calm my butt down.
Yoga – One woman’s story on managing chronic pain from EDS
Christine is a friend that I met via her Facebook page and her article. She also submitted a story for Our Stories of Strength – Living with Ehlers-Danlos Syndrome.
The Healing Power of Yoga: How Practicing Helped Me Cope with Pain
“Many of us have dealt with a painful injury or illness at some point in our lives—some more serious than others. But for Christine Spencer, a 30-year-old from Collingswood, NJ, dealing with severe pain is an ever-present fact of life.
Spencer was diagnosed at 13 with Ehlers-Danlos Syndrome (EDS), a debilitating connective tissue disorder related to fibromyalgia. It causes hyper-mobility, muscle tension, constant pain, and in some cases, death.
When her symptoms worsened and caused her to withdraw from college, doctors wrote her a prescription for a cocktail of medications, including painkillers. ‘This was the only way Western medicine knows how to deal with disease,’ Spencer says. ‘I did some physical therapy, but no one gave me a long-term plan to help me heal.’ For months, she was completely disabled and unable to carry on with any semblance of a normal life.”
Yoga and EDS links and resources:
– This post was originally written for Strength/Flexibility/Health/EDS “Yoga and Hypermobility – Managing Chronic Pain and Joint Stabilization with Ehlers-Danlos Syndromes/Hypermobility Syndromes;” however, StrengthFlexiblityHealtheds.com is currently being prepared to relaunch as the first and ONLY digital wellness magazine for those living with Ehlers-Danlos syndrome, other hypermobility syndromes, and related conditions. Relaunch is planned for May 2016.
– Bryan Kest’s Power Yoga Video – Sweat
– Rodney Yee’s Yoga for meditation
– Yoga Gypsey Blogspot
– Our Stories of Strength – Living with Ehlers-Danlos Syndrome – anthology of over 50 stories from those living with Ehlers-Danlos Syndrome and how have found ways to persevere
– Move your DNA – Book
Disclaimer: Yoga may work for some and not for others. This post is for your information only and should not be substituted for proper medical care, or viewed as a directive for those who have hypermobility syndromes, such as Ehlers-Danlos syndrome. To read the full disclaimer, go here.