Trey was born 19 minutes away from the leap year on March 1, 2004, his due date. Labour began early Saturday morning with Trey finally arriving in the wee hours of Monday, after a long and awesome labour. During the first hours of my labour, Ryan and I ate, went for walks, watched movies and anticipated the birth of our first baby. We were so excited. Trey's birth was originally planned to be at home, but 35 weeks into my pregnancy, Trey was found to have a Premature Ventricular Contraction (PVC). Although it was not serious, we were no longer comfortable giving birth at home. Trey was welcomed into the world at B. C. Children and Women's Hospital.
 
 
Life after Trey was born was great. Actually, it was the best time in my adult life. Watching Trey grow and just watching him see life for the first time was so amazing. Everything was new and fascinating. At first it was watching butterflies, feeling new textures, learning to crawl and walk.  Still now, nothing could be better than being a mom. We continue to play and explore - feeding squirrels at the park, splashing in water, and seeing how high and far Trey can jump. We have so much fun!
 
 
When Trey was just over a year old, and before we’d even heard of MPS, we found out that we were pregnant for the second time. On November 5, 2005, after a very short and easy labour, Avery was born at home. Trey woke up Sunday morning to a new little brother and welcomed him with big hugs and lots of kisses.
 
 
About Trey - Trey is an incredibly easygoing kid. He’s interested in whatever is going on around him and goes with whatever is thrown at him. He adjusted easily when Avery and Sadie were born and had no trouble moving into a new house.  Essentially, Trey makes parenting easy on us.
 
 
Trey also makes life fun because he loves people. I have met many new people because of Trey. He watches people, talks to people, smiles and waves at everyone we pass, and he always makes sure everyone is included. Whether we're out for a walk and someone is lagging behind, or I'm sharing a snack with Trey that Sadie is too young to eat, Trey will be sure to point out that someone is behind or make sure that Sadie gets a taste of whatever it is that's we're eating.
 
 
Trey also always has a ball or puck in his hand. Whether he's shooting hoops, playing soccer, throwing a football, or hitting a puck into the net, Trey is playing ball.  Water is another favourite of his. He loves to go swimming with our family on the weekends and could spend hours at the pool.  He loves jumping off docks into lakes and oceans, splashing in anything that resembles a puddle, and he loves bath time.
 
 
Picking berries, befriending animals, digging in the dirt, climbing and jumping off of everything and anything, reading Richard Scary books, playing hide and seek with Avery, drawing, and playing with our huge and awesome extended family are other favourite past times.
 
 
Life is just so much fun when you're around Trey. He shows you what it means to live, to have trust, and to love.
 
 
February 2006 was the first indication to us that anything was seriously wrong. Before that there had been minor concerns, but no red flags. Trey was a big kid, in the 99th percentile since birth, but he comes from a tall family, so we didn't think anything of it. We also took Trey to the pediatrician with concerns about a hernia and big head at around 9 months. Our pediatrician wasn't really concerned about either, as both are common childhood issues, but he said that we could do an ultrasound to investigate the head size if we wanted to. We did, and the ultrasound showed nothing wrong. Our pediatrician also assured us that the hernia would probably go away by the time he was three, and if it didn’t, a minor surgery would fix the problem.  Trey’s speech also seemed to be developing a bit slowly, so when he was 16 months, I contacted a Speech and Language Pathologist.  This led us to the Audiologist and an ENT who confirmed that Trey had hearing loss, probably due to recurrent ear infections and fluid in his ears. As a result, on January 17, 2006, Trey got tubes put in his ears and his adenoids taken out.
 
 
Around the same time, we began looking for a new pediatrician whose values more closely resembled ours. On Tuesday February 14, 2006, we had an appointment with Dr. Paul Thiessen, who came highly recommended. The appointment was going to be a quick stop for us. Afterwards, we planned to drop the kids off at home with grandparents so that Ryan and I could go out for a nice Valentines Day dinner.
 
 
It didn't turn out that way. I will remember the details of that appointment for ever. In short, we were told Trey might have an enlarged liver. Trey was scheduled for an ultrasound at Children's Hospital on Thursday, and on Friday, Dr. Thiessen called and told us that his liver and spleen were, in fact, enlarged. He had also booked us an appointment with a specialist at Children's Hospital for that Monday. Knowing how long it usually takes to get appointments at the hospital, we were scared that something was seriously wrong, but with no more information and no way of knowing what the results this far meant, we convinced ourselves not to think about it until Monday.
 
 
Monday is the day our world came crashing down. What I remember about that day is: before the appointment I was not able to make eye contact with Ryan. Any time we did, we would cry. During the appointment when were told that our child likely had something called Muchopolysaccharidosis (MPS).  We were told that this would affect every part of his body.  Specifically, we were told that Trey's hands would curl, his bones wouldn't grow properly, his organs would start to fail and his life span would likely be shortened significantly. For about 2 weeks, we cried.  We cried and cried until we were so exhausted, we didn’t have the energy to cry anymore. After a while, all the testings at the hospital became a blur. Everything became divided into before "the appointment" and after.
 
Trey was eventually diagnosed with MPS Type II, also known as Hunter Syndrome (For more information, see www.hunterpatients.com). Our life has turned 180 degrees since that Valentines Day. Everything has changed. What it means to have children, what it means to have "healthy" children, what it means to live, what it means to have family and community, what it means to be different. Our relationships have changed, with each other and with the people around us.
 
Very little is the same, but at the same time, it all is. What I have realized is that life is life. Nothing is guaranteed, and as a result, we must appreciate every moment of it. We love Trey. We loved him before and we love him now. That has not changed, but what has changed is the realization that we love him no matter what. He is our baby and none of the other stuff matters.
 
 
We have also learned to take information with a grain of salt. We have been told that Trey has a severe form of Hunter’s Syndrome - that he will be mentally impacted and will be lucky if he lives into his teenage years. But we’ve also been told that he will likely not be mentally impacted because he is doing so well developmentally and in general.  His hearing aids have helped dramatically with his speech and he uses the toilet at two and half.
 
MPS is a rare disease (or difference as we like to call it). Most people have no idea what it is, and many of the specialists we see also have never seen a person with MPS.  Some things are known about the disease, but not everything. So what we have decided to do is believe and hope. We believe in Trey, we believe in his body’s ability to find a way to work around his lack of enzyme, and we believe that he is going to be okay.
 
We believe that through nutrition, alternative forms of medicine, and Enzyme Replacement Therapy (a treatment developed for Hunter Syndrome and other related diseases), Trey will live a happy and fulfilled life. We celebrate that Elaprase has been approved by Health Canada and are excited that it has been funded for Trey here in BC.  We continue to talk with him about what he wants to be when he grows up. And we hope that with the help of fundraising, awareness, and research, we will find a cure so that Trey and other children with MPS will not be limited by this difference, and so that families will not have to go through the devastation that we have.
 
Things are still not back to the "normal" they were before diagnosis. I don't think they will ever be. We are forever changed, but we have found a new “normal” for our family. Living with MPS is Trey's version of normal, and we will walk his path with him just as we will walk Avery's path with Avery and Sadie’s path with Sadie. We love Trey because of it, for it, regardless of it.








THE FACTS
Birthday:   March 1, 2004
Height: 21 inches 
Weight: 8 Lbs 14 oz








MY FAMILY
Mother:   Deb Purcell
Father:    Ryan Purcell
Brother:  Avery Purcell
Sister: Sadie Purcell

I also have a large extended family who I’m close with.


 






MY HOME
I live with my family in Vancouver, BC, Canada. 











FAVORITE FOODS
Anything and everything











FAVORITE ACTIVITIES
 Throwing a ball.  Kicking a ball. Anything with a ball.
  
I also really enjoy playing in all things related to water, cooking and baking with my mom and brother and showing my brother cool stuff that I’ve just discovered.









I DON’T REALLY LIKE
Sitting still for long.












MY DIFFERENCE
MPS II - Hunter’s Syndrome









HOW MPS AFFECTS ME
I have mild-moderate hearing loss.  I have hearing aids that help me hear, and we are learning to sign.

I get weekly Enzyme Replacement Therapy at BC Children’s Hospital.











About Trey     TREY ARTHUR CEHAK PURCELL But MPS doesn’t affect my glowing personality, kind heart and great sense of humour.
   www.treypurcell.com  dcehak@telus.net   .   
604.222.2767
Envisioning a hopeful future for families with MPShttp://www.treypurcell.commailto:dcehak@telus.netshapeimage_6_link_0shapeimage_6_link_1
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