“My goal is… just to make the world dance.” -Ryan Morrissette

“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, Ryan1would 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

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Interview with Yesenia Peralta- Part 3

Part 3: “EVERYONE- the world- is helping me through this. You guys are my strength.”- Yesenia Peralta

(Click here to begin at Part 1 and Part 2)

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?

MS poster advertIn 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.

Continue reading