As the Soaring with Hope for PD Parkinson’s project took off, one of the team members for that project, Clara Kluge came up with yet another way to engage People with Parkinsons (PwPs) for the World Parkinson Congress(WPC). Because she loved to dance and was involved in dance classes for PwPs, she envisioned having PwPs and the community at large create dances using cranes as the theme. Her dream became thePD Crane Dance Project. David Leventhal, the co-founder of Mark Morris Dance Group’s Dance for PD® Program, became her mentor on this endeavour; he calls Clara “the force behind this project.”
And she truly was a force, inspiring so many to participate in the project. Clara invited People with Parkinson’s from around the world to submit a 2 minute video of an original dance inspired by the origami cranes that she folded and sent to those who requested them. Expecting to receive about 50 videos, she received 147 from 17 countries. This added up to a whopping total of 5 hours of video! Over 1800 dancers participated from around the world. The two videos were shown on a continuous loop at the WPC at the Soaring with Hope exhibit and the Dance for PD® Program Booth.
Some of the spin offs from the project are that it inspired dancers to:
Learn how to fold origami cranes
Write poems about the experience
Dance more, move more
Tap their inner creative spirit
Make stronger connections
Feel connected with other dancers from around the world
Collaborate with fellow dancers
Not feel alone
Get excited about doing something positive for themselves
Get a tattoo of an origami crane
This project was such a success that Clara is looking into making a documentary of the whole experience with the many dancers and dance groups who participated in the original creation of this project.
Origami Dance Japan Parkinson’s Disease Association Fukuoka
Invertigo Dance Theatre, Los Angeles, California
To view more of these inspiring dances, go To YouTube and search Crane Dances Parkinson’s and a number of dances will appear. I will keep you posted when and where you can see all of the dances.
Last month I had the chance to interview two more women with PD. Since each of us experiences our PD differently, it is always interesting to hear how each person approaches her diagnosis and finds a way to move forward with her life. We can learn so much from each other, finding our way on this lifelong journey with each other’s support and encouragement.
Linda and Gail
Linda
Linda was a dancer. When she was in NY several years ago, she discovered that Mark Morris Dance Studio, the premier modern dance studio in NY, has classes for people with Parkinson’s. She went in and there were about 50 people at all levels who were dancing. It is such a beautiful program. We know that exercise is good for us. It brought in music, imagery and creativity and it was so much more fun than slogging away on a treadmill for exercise.
Mark Morris dancers trained Invertigo Dance Theater to run the program. It must be run by professional dancers, because they really understand strategy of how the body works.
“A doctor told me 10 years ago when I was diagnosed that dance is going to help me stay well. And I am doing pretty well. Maybe it is the dance. We don’t make any medical claims. It is just a real dance class that is modified for PD.”
Linda thought her first symptoms were just the aging process, even though her mother had died years earlier from PD. “I thought it was age. I was taking jazz classes but I couldn’t turn all of a sudden. I was getting dizzy when I turned on my left side. I thought, that’s unusual, since turns were always easy for me, and I wasn’t quite as flexible and I was stiff. It wasn’t till I was on vacation and I started getting a tremor in my left leg and I got worried. It started and stopped at the beginning and then eventually it just wouldn’t go away. It only bothered me when I was resting. And that’s when I went to a doctor.”
She knows she had symptoms before. She had a couple of falls and other symptoms 5 years prior that she attributed to age. “When you look back it kind of resonates. I always had a reduced sense of smell. I broke my nose when I was 10 and so I never thought of that as a symptom.”
Initially she went to her internist who said “You don’t have Parkinson’s”. “I said maybe I have Parkinson’s since my mother had it. My mother had been bedridden for a number of years with Parkinson’s before she died. Then Linda went to a general neurologist and he said ‘I don’t know, you need to go to a movement specialist.’ I was going to NY to visit my children, so he suggested I go to a movement specialist in NY, which I did , and then I went to UCLA afterwards. They said time will tell. And they were right. It took 2 years to find the right doctor to treat her.”
She gets her info about PD from groups like ours, and from her doctors who have also given her a lot of information. Because she goes back and forth to NY so often, she also sees a doctor in NY who is one of the premier PD doctors in the US. All of her doctors have agreed on a course of action, and progression, which is comforting to know that the best doctors think along the same lines.
Linda started with Azilect, then the Neupro patch, which they recalled. Then Requip. And now Sinimet. It is the same medicine her mother was on. “I do see a difference after several years. It wears off sooner, I have to take it more often, but I am still on a relatively low dose.”
She is in a telemedicine study with the University of San Francisco. She thinks it is terrible, it has a long way to go to make it work. She is interested in the exercise study at USC, but travels too much to participate.
So what keeps her going? Linda is doing the things she likes, like volunteering to teach this dance program. It is satisfying and keeps her going. She takes dance classes that are not so hard, but she is still dancing. And her grandchildren are her vitamins. She travels often to see them.
What makes her experience so unique? Her mother had PD. She sees how different her life is than her mother’s was with PD. Her mother wasn’t active, so the trajectory of her disease was very different. She had a different life and wasn’t well. Linda says “I see all of us making the most of a situation that can make you want to crawl up into a ball and do nothing. But we are not letting it. We are trying not to let it.
Her one piece of advice for others is to keep moving. It really makes a difference.
Gail
Gail was diagnosed about 4 years ago. In about 2005 she noticed her foot bouncing occasionally at odd times. She got a referral to a neurologist who said it was something neurological, but he didn’t know what. If it gets worse come back. In 2008 she thought it was getting more frequent and went to Dr. Steven Sykes at Cedars, who also said he didn’t know what it is, but if it gets worse come back. November, 2011, while at a movie, she realized she had a tremor in her left hand and whispered to her husband “I have Parkinson’s.” I went to Dr. Sykes in December, who said he had good news and bad news. The bad news is that she did have Parkinson’s, but the good news is look how long it took to get to this point. In 2008, he had written in her record Parkinsonism. Something like, but he couldn’t make the diagnoses at that time. He thought I would have a slow progression and I think I have. I went on Azilect right a way. Started Sinimet about a year ago when I realized that my balance was off and I was stiff and I wasn’t moving. I could look in the mirror and see that it wasn’t me. The Sinimet really helps.
She goes to 3 support groups. She has made wonderful friends and learns a lot in the groups. The doctors don’t experience the weird little things that happen to us. We can always ask in the groups “does anyone have????”
Apathy has never been a problem for her. She goes to exercise classes and has so many activities to choose from. She loves the exercise class at the Westside Pavilion. When she first started she could barely do many of the movements and has seen a big improvement in what she can do.
What makes her story unique? Loving support groups. If you reach out and use the support groups, it is very valuable. The thing that is really exciting to her is that she is on the board of the new PD organization that is starting in LA.
Her advice to the newly diagnosed: find all of the kinds of exercise and do the things that you enjoy and go to support groups.
I hope to continue to interview more people with PD in the coming months and post their stories here. Guys, that includes you, too. Please contact me directly if you would like to share your PD story.
April is Parkinson’s Awareness Month. Join the Parkinson’s Disease Foundation Team During Parkinson’s Awareness Month Friday, April 1- Saturday, April 30 (Online & around the US)
What will you do to help raise awareness this April, Parkinson’s Awareness Month? Join the team to #EndParkinsons with PDF and help make a difference in the PD community!
Last month, my Movement Disorders doctor, Indu Subramanian, asked me to write about my experiences with yoga and PD for the Brian Grant Foundation’sPower Through Project. She worked with a yoga instructor to produce videos for the website about the benefits of yoga for People with Parkinson’s. My story and Dr. Subramanian’s videos are now up on the Power Through Project website.
Sunday, we had another great meeting for Women living with PD in Los Angeles. Invertigo Dance Theater’s Sofia Klass and Linda Berghoff (also a PWP) teach Dancing Through Parkinson’s in various locations around LA. They led us through dance sequences designed specifically for people with Parkinson’s Disease. Special thanks to the The Wallis Annenberg Center for the Performing Arts in Beverly Hills for hosting us. I had the opportunity to interview 2 more women about their experiences with Parkinson’s. This has been a great way to share our journeys with other women and to help all of us better understand this disease that is changing our lives. I will post their interviews later this week.
“Never be afraid to try something new. Remember amateurs built the ark. Professionals built the Titanic.”
–Unknown
I recently attended one of these classes. If there is a Dance for Parkinson’s Class in your community, check it out. It is a lot of fun.
I run the Dancing Through Parkinson’s program in Los Angeles through Invertigo Dance Theatre (www.invertigodance.org/parkinsons) and we have had many people with other neurological diseases attend our classes because they help improve their lives physically and emotionally. Just like people living with Parkinson’s, people who have Multiple Sclerosis, Dystonia, and even those who are recovering from a stoke all benefit from the challenges of a dance class like balance, mind-body connection, moving fluidly, hand-eye coordination and gait. Dance classes are not only good for exercise but they also create strong community and help connect people with one another which can be super important for those dealing with the isolating effects of neurological conditions. We encourage all our students, whether they have Parkinson’s or not to find creativity and joy through movement and I think that is so empowering for someone who is grappling with any kind of issues that inhibit their ability to move. The act of changing the focus to what you cannot do with your body, to what you can do, and to do it gracefully, is such a good experience for people dealing with neurological conditions. So I will end saying that if you ever wanted to try dance, feel free to come to any of our 5 classes in Los Angeles whether you have Parkinson’s or not. We have both weekly and monthly classes through out the city.
designed specifically for people with Parkinson’s Disease. Special thanks to the The Wallis Annenberg Center for the Performing Arts in Beverly Hills for hosting us. I had the opportunity to interview 2 more women about their experiences with Parkinson’s. This has been a great way to share our journeys with other women and to help all of us better understand this disease that is changing our lives. I will post their interviews later this week.
