From the moment I met Joan at Danzaire Studio, I noticed a unique energy about her. At first, it seemed like a kind of quiet, friendly, charisma on the outside. But the more that we talked, the more I understood that there was an even bigger and ‘louder’ depth of character looming inside of her. And boy was I right. I soon learned that there was remarkable story of strength and resilience behind Joan and her dancing, a story of courage and inspiration that I am so honoured to be able to feature in the form of an interview here on Dance Me Free.
“Those who say it cannot be done shouldn’t interrupt the people doing it.”
– Chinese Proverb
This is definitely one of my favourite quotes because it continues to remind me of the power of our own inner strength, despite the obstacles we might face. But what I love the most is meeting people who prove to be amazing examples of this- those individuals who, because of their own will, passion, and courage, manage to go beyond what they might normally be thought capable of doing, and then often inspire others to do the same.
Little did I know that one of these individuals, who I had the pleasure of meeting recently, would be a young teen- Ryan Morrissette. Ryan, a member of the hip hop crew Freshh, is a talented, charismatic dancer whose energy is well, … contagious, to say the least. His hard hits, quick and clean moves, and overall enthusiasm on stage definitely draw the attention of his audiences. But even off stage, Ryan seems to often be found smiling and sharing a positivity with friends and strangers alike that is truly refreshing. So when I heard that this young dancer has been dealing with a serious health condition since the age of two, I couldn’t believe it. You’d just never know that Ryan has Cystic Fibrosis if you saw him out there – the way he always seems to be giving it his all- whether on stage dancing, or co-emceeing and event, or just hanging out with his friends.
But that’s what Ryan does- he gives his utmost to this passion he has for dance, and to life in many ways, it seems. In fact, rather than letting CF stop him from pursuing his love of dance, Ryan uses dance as a way to heal his condition and to reach others out there to remind them to live life to the fullest. “I wasn’t supposed to be able to do a lot of cardiovascular exercise,” says Ryan. But if you saw him out there, training, leaping, doing flips and tricks- well, Ryan has pushed through many physical obstacles that might otherwise cause another person in his shoes to not even attempt any of it. And that kind of perseverance is extraordinary . Continue reading
“The way I got into dance was through watching movies and TV shows. I’d see all the mainstream dancing and I thought it was really cool. So I started dancing and training. And sure, it sucks sometimes when I make plans with my friends from school and then I remember I can’t hang out with them because I have dance practice. But then, once I come to dance, well, I kind of forget about those other plans because dance is so much fun.
The feeling I get from dancing, well, I can’t really explain it. It’s always different. I could be happy, I could be sad. But each time I dance, it makes me feel really good about myself. It just makes my day. And in our crew, we get to share that feeling with each other, as a family. It’s hard work, but it’s worth it. Because even though we’ve reached a high level, there are others out there who are better than us. And we don’t want to just stay at the same level. We want to get better too and be good role models. ”
– Justin Nicolas – Age 15- member of The Freshh Crew
“I started dancing, as a bboy first. Back then, in 1984, there was no Youtube, nothing like that. We would just see something on commercials or on TV – some breakdancing moves- and dancing looked like a positive way for us to channel our energy.
That’s how we got started, and maybe also because we thought it would help us get the girls at first (laughs). But later, you realize there is so much more to it. And when you get into dancing so deep, it becomes your passion.
I love dance, but it is the pioneers of Hip Hop who really inspire me. Crazy Legs, The Rock Steady Crew, and all the others who, despite the criticism they faced from everyone that didn’t believe in hip hop and breakdancing at the time, just kept going with it.
If it wasn’t for those guys who paved the way for us, those artists who constructed the highway for us, we wouldn’t be enjoying what we enjoy right now.”
-Cezar Tantoko- dancer, coach and choreographer
Creator of Fresh Groove Productions
Part 3: “EVERYONE- the world- is helping me through this. You guys are my strength.”- Yesenia Peralta
I found out about your health condition when your brother sent me an invite to the fundraiser that was put on for you earlier this year. I was shocked. I had no idea you were even suffering through anything, let alone multiple sclerosis. How did the diagnosis come about for you?
In 2007, I had tingling in my arms and my legs. And the tingling got worse. I went to Singapore with my brother, but I wasn’t being very social there, and I wasn’t dancing as much as I used to. I didn’t know why, but I just wasn’t feeling good. When I came back from Singapore, it got worse. It went from my hands to my arms and to my legs. The tingling got so bad that I couldn’t unbuckle my belt, I couldn’t brush my hair, and I couldn’t write the receipts for my students. Eventually, I couldn’t teach!
I had to go to three different hospitals before I got admitted because nobody could figure out what was going on. So I finally get admitted and they released me five days later, without telling me what was wrong, because they said they didn’t know. And because I didn’t have insurance, they couldn’t continue to just keep me there. So they let me go. And then little by little, I got better, so I just thought, “Oh, it’s gone. All right. Back to work!” I opened up another school and didn’t think twice about what had happened.
Then, in 2010, I get this feeling again- tingling, numbness, and all that stuff. And then finally, I got diagnosed in August of that year. But when we finally saw the paperwork from 2007, it said ‘possible Multiple Sclerosis’ on it! 2007! Why couldn’t the doctors have just mentioned that word to me then? But no, they didn’t. And that’s how I found out three years later.
It is my pleasure to share a special photo feature this month involving three fellow dancers and friends from our very own Vancouver dance community!
Carlos Molina and Nicole Chan are captured here in a beautiful moment of dance by photographer and dancer Elina Sumichan. The photo was taken at a recent event in Vancouver called Kizomba Temptation. Thank you Elina for hosting and organizing such a magical night, and special thanks to Nelda Sumichan for providing us with such an elegant, intimate venue in which to get our Kizomba dance on! It definitely proved to be a great night of mingling, music, and fun memories. I am thrilled to be able to share one of those moments here as Elina’s shot of Carlos and Nicole will be our new header photo for this season.