Happy World Down Syndrome Day! Just over six years ago I rarely thought about Down syndrome, I didn't know anyone with Down syndrome and if I did see someone, I never went out of my way to interact with them. I was uninformed and scared. Today it's different, I'm a new person and a little bit of an expert when it comes to Down syndrome! Beckett has changed everything, in a good way.
I often wonder if some people think I'm full of it when I say that Beckett has changed our lives for the better. In my experience, I was told so many negative things about Down syndrome and constantly reminded of what Beckett wouldn't do...of course I was sad in those early days. Actually, I was terrified, and why wouldn't I be? I was bombarded with so much unnecessary garbage, all the photos I looked at of children with Down syndrome in pamphlets were outdated and unflattering. I get it, Beckett won't drive, have children, live on his own - blah, blah, blah. When people heard of Beckett's birth most were inclined to say "sorry" instead of "congratulations"...there is nothing to be sorry for, we are the lucky ones. We really are.
I can't tell you how many new parents I have spoken to over the past six years, honestly I have lost count. I have talked to women in their hospital beds holding their hours old baby, women who have just found out they are carrying a baby with Down syndrome, women crying because their husbands had one foot out the door....you name the situation - I have talked to them. I tell them all the same thing...it's going to be okay - I promise.
It will be okay and I really do promise. Down syndrome does not cross our minds on a daily basis, yes Beckett is a slower to develop when it comes to speech and toilet training and a few other things. We have had more appointments for this sweet boy than we ever imagined but we're used to it. We know what it's like to be on a wait list, and I'm clear on what it means to be an advocate. We can't imagine life without his bright smile (toothless right now), his hearty laugh and his charismatic glow. Beckett is empathetic, smart and ambitious. We love him so much our hearts could seriously burst.
Some may look at Beckett or another child with Down syndrome and think they are not perfect, they are flawed. Here's a news flash, perfect doesn't exist and even if it did - how terribly boring. If you are looking for perfect, you will be looking for a long time. What a shame to miss the real beauty in life, we are all unique - we all have a story to share.
It really would have been nice if in those early days someone told me all the wonderful things Beckett will do and what an amazing person he will become. I get why 90% of women who find out they are carrying a baby with Down syndrome terminate the pregnancy (this number is widely reported), there is so much negativity and fear.
It's 2014 and we have come a long way. We don't throw a child with Down syndrome into an institution anymore (at least not where I live) - although it wasn't long ago in Canada that we did. A child that is loved and nurtured like their typical siblings thrives. I find at times there is still a bit of negativity when meeting with some health care professionals, we have crossed paths with a few who are stuck in the sixties - the good news is, we just move on and find someone new. We find someone who sees what we see, a beautiful, charming, bright boy....who happens to have an extra chromosome.
Of course there are challenges, there always are - with every child. I'll never forget our first meeting with our Geneticist, he said to me "Tamara, in the grand scheme of things Down syndrome is not a big deal" - it was to me and I was very confused by his comment. I get it now, compared to the thousands of horrific diseases and challenges a person can have - Down syndrome is not so bad. He was being kind and trying to let me know that we were going to be fine and we are.
So today on March 21st (everyday for our family) we celebrate that extra chromosome with World Down Syndrome Day, a day to raise awareness of what Down syndrome is, what it means to have Down syndrome and most importantly - how people with Down syndrome play a vital role in our lives and communities. Next time you see someone with Down syndrome say hello, I guarantee they will say hello back and smile.
For more information on World Down Syndrome Day please click here.
Showing posts with label down syndrome. Show all posts
Showing posts with label down syndrome. Show all posts
happy world down syndrome day
Friday, March 21, 2014
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beckett's 6th birthday party
Friday, December 20, 2013
The photo in the middle is Beckett & his best friend Finn. Seriously, how cute is that? Finn is in the other grade one class at school, the boys find each other at lunch & they love spending time together. Finn also happens to have Down syndrome. My heart is full when I think of the boys going through their school years together.
My sweet friend Denise made the cake (again), she really is the queen of cakes. Sonia at Sugary Sweet Things made the cookies. We set up two major HotWheels tracks in the backyard & the kids raced cars all afternoon.
The only chance we have of getting a family shot is during the cake...we have til the end of Happy Birthday to sneak in a five-shot. There are lots of hugs, many kisses and too many smiles to count. It was nice to do this post five months after the party....such a great reminder of a fantastic day. xx
a sigh of relief
Friday, July 23, 2010
This photo breaks my heart. Poor little bug, he's getting his blood test and didn't cry but wow was he sad. It's routine that each year as we near Beckett's birthday he goes through a series of tests and appointments. In the last two weeks we have been to the lab at Children's Hospital for his complete blood work, Audiology for a hearing test, the Ophthalmologist for an eye check-up (he has cataracts) and then to the Paediatrician for his yearly check-up.
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| photo by ka davidson |
I'm happy and relieved to report that all is good with Master Beckett. It's quite stressful waiting for results, I can't help but go through the worst case scenario as I'm laying in bed trying to fall asleep. So when the eye doctor says his eyes look good and the cataracts haven't grown, I smile and sigh. When the audiologist checks B's ears and says that his hearing is "normal", I feel relief. The big one is the blood results, we head to the doctor's and when we learn that his blood is good, I'm so grateful I could cry.
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| photo by ka davidson |
When you have a child with special needs there are a lot of tests, you're always watching and noticing and like any parent you are always worrying. We have a lifetime of tests ahead of us, unfortunately I was born a worrier, my worrying is far more intense since I have had children. I try to keep it under wraps, control it....I don't want it to rule my life. Right now, as we approach Beckett's 3rd birthday, I'm happy and so thankful that my babes are well.....may all our babes be well. xx
love
Sunday, April 25, 2010
I have a great husband. He's kind, funny, generous and full of love. What I love best about D is that he's an amazing dad. When I married D I knew he would be a great dad - he really is incredible. Nothing melts my heart more than when D is with our kids. They adore him, the sweet sounds of their giggles while playing with their dad is almost too much for my heart to handle.
When Beckett was diagnosed with Down syndrome, we were tested. We had never been faced with such fear and pain before. You see a person's true soul when together you are challenged. I'll never forget the moment the doctor said the words, the tears that D and I cried and then the strength we gave each other. There's no one else on earth that I would rather be with for this incredible journey.
When Miss Zoë was born I saw the father-daughter connection immediately, love at first sight - sigh. I never had that relationship with my own dad, so to see such love was beautiful. Zoë definitely has her daddy wrapped around her finger - and she knows it. Her favorite word is "Daddy" and she's not afraid to use it.
Beckett and his dad are two peas in a pod, best pals forever. Zoë is the apple of her daddy's eye, a sweet connection. Soon Number Three will be here and a new journey will begin, what fun that will be! xx
When Beckett was diagnosed with Down syndrome, we were tested. We had never been faced with such fear and pain before. You see a person's true soul when together you are challenged. I'll never forget the moment the doctor said the words, the tears that D and I cried and then the strength we gave each other. There's no one else on earth that I would rather be with for this incredible journey.
When Miss Zoë was born I saw the father-daughter connection immediately, love at first sight - sigh. I never had that relationship with my own dad, so to see such love was beautiful. Zoë definitely has her daddy wrapped around her finger - and she knows it. Her favorite word is "Daddy" and she's not afraid to use it.
Beckett and his dad are two peas in a pod, best pals forever. Zoë is the apple of her daddy's eye, a sweet connection. Soon Number Three will be here and a new journey will begin, what fun that will be! xx
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