Clearwater Marine Aquarium

I am worried my words can’t do justice to the day we spent at the Clearwater Marine Aquarium.

After 2 years and 8 months working on this, on Monday May 5th, I woke-up and took this picture.  My girl slept like a rock the night before.  I thought the excitement would keep her awake but I guess the flight and shopping tired her.

I got us all dress in matching outfits. That’s a sight you will not see that often!


We rented a car and started driving from Orlando to Clearwater.

We saw this!


Eventually, this!

And finally these!

    

It was a gorgeous day in Clearwater.

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We were VIP’s πŸ™‚

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This is Emily looking at Winter.   She had tears in her eyes.

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Emily relates to Winter in a way that none of us can see or feel.

None of us!

Which is why I’m worried my words can’t express the magic we witnessed that day.

Since the very first movie preview…

Emily wanted to know more about Winter the dolphin that never gave up.

Winter who, against all odds, survived and now thrives.

Winter, the dolphin who inspires thousands to move forward.

We took a behind the scene tour… We learned about the history of the place, we saw the turtle intensive care unit, Emily asked questions and contributed to the tour.

When Emily heard Winter whistled, it was as if the whole world made sense.  She was so happy.  She had stars in her eyes.

I probably have a couple of hundreds of pictures of our day.  Picking the ones included in this post was challenging.

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Here is Emily getting ready to meet Hope (Winter’s buddy) and finally, Emily listening to Mallory and playing with Hope.

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I cried while taking these pictures.

I can try to explain why I cried…

When Emily was diagnosed with cri du chat syndrome, we were told she would do nothing.

Never walk, talk, not recognized us, not show or even comprehend emotions.

When I saw her listen to Mallory and reach out to Hope I was slightly overwhelmed.

New parents assume their kids will do things and experience life.

After Emily’s diagnosis, all of our hopes and dreams were crushed.

All those new experiences, small or big, they are all big wins for us!

So, I cried.

Just a couple of tears really.

One tear for my baby girl who struggled with everything from drinking, to gaining weight, to sleeping…

One tear for my 24 year old self who cried so much.

One tear for all the doctor and therapy appointments who took over our lives.

One tear for our crushed dreams who are slowly coming true.

Thank you Becca for your help in making this dream come true.

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We saw Winter getting her tail put on.

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Emily received the cutest USB key ever made.

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Our visit continued at the museum.

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And concluded with a Sea Life Safari tour.

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Thank you Sunshine Foundation of Canada and Thank you Clearwater Marine Aquarium

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Interview with Amy – Let’s meet Nellie!

It’s Sunday night and Emily asked me to watch the Billboard  Music Awards with her. 

So here I am, on the couch, feeling slightly guilty for having spent the last 2 days sitting around, enjoying my family, watching Netflix and eating. 

Tomorrow is a holiday in Canada… Tomorrow will be laundry, cleaning, organizing and everything I should have done already. 

Maybe I can start writing about our trip to Florida… I have so much to tell you. 

But for now, here is my newest interview. 

Let’s chat with Amy

1.  Can you tell me about your family?

We are a family of 5. My husband Jay and I have Colin 17, Nellie 15 and Braley 11. Nellie has CDC. We live in upstate NY. We are a busy family, always on the go. Our children are all involved in sports and that takes a lot of our time

2. Tell me about your loved one with cri du chat syndrome.  

 Nellie is super sweet and has blessed our family in ways we could never have imagined. She has taught each of us about being kind, patient and understanding. Nellie attends a life skills class at our local high school and she knows everyone. She enjoys many of the same things that all 15 year old girls enjoy. She always has her iPhone in hand, loves music and you tube. She enjoys her bike riding and swimming. She plays on 2 basket ball teams, baseball, football and bowling. Most of her sports are played through our local miracle league. She also spends a lot of time playing littlest pet shops. Above all I would want to tell you that Nellie is a gentle, sweet, very funny, well behaved little girl who is adored by all who know her. 

3. Tell me about doctor appointment, therapies or school. 

When Nellie was little our life was a whirlwind of doctor & therapy appointments. We saw every type of specialist imaginable. Nellie was sick as young child and spent a lot of time in the hospital. She had open heart surgery and palate surgery. She had a spinal fusion done at age 13 for scoliosis.  Now, at 15 she is very healthy and rarely even gets a cold. She had failure to thrive as a baby so weight was always a big issue but she outgrew that too. Nell has always had a ton of therapy and I believe it made all the difference. Speech has always been a big issue so she has always had speech every day, she has taken sign language since she was baby and still has a sign teacher at school, she speaks pretty well but we always wanted to give her every opportunity to communicate. Music therapy was fantastic for Nellie. She has also always had PT & OT. She gets all her therapy through school and they are amazing. She works with her high school class for 2 hours a day at different local businesses. I have to say that playing sports, Sunday school and Girl scouts were all important too. 
4.  Tell me a success story. 

Our CDC are always amazing us so it is very difficult to pick one success story. A few stick out. 1. Getting the training wheels off her bike. 2. Learning to read! She can read hundreds of words, thanks to finding the right reading program for her. 3. It may be strange to hear a parent say this but being able to use a iphone. It gives her a way to communicate with all of us. I feel so much better knowing she has a phone with her to reach me. She knows how to use a smart phone better than I do. She keeps it charged and is actually really responsible with it. And it is typical for her age!!!!

5.  What else would you like the world to know?

I would like people to know that with a lot of support these children are capable and will continue to amaze us. We were so lucky to have access to great therapy & medical care. I never believed in the “it takes a village theory” but I do now!  Without wonder teachers, therapists, programs & doctors I do not know where Nellie would be. We have also been blessed with a loving & supportive family. We could never have gotten this far without “our village”.

Thank you Amy for taking the time to chat with me. 

Here is Nellie and her brother before homecoming dance