Interview with Alicia – Let’s meet Natalie!

Let’s continue our interviews!  Today, we chat with Alicia! 

1.  Can you tell me about your family?

There is just the 4 of us. We live in Hamburg, Arkansas. Natalie was born June 21, 2008 and Dillon was born June 23, 2004.   

 

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

Natalie Grace Wilson, born June 21, 2008 after a somewhat hectic pregnancy. We got her diagnosis when she was less than 2 weeks old. We got the speech of not being sure what she would be able to do. She has overcome so much. She loves to watch nick jr and Disney jr. Her favorite color is purple. She loves to fight with her dad and brother. Loves bubbles and playing outside. Loves animals and most people. She loves shopping. She’s a very social loving little girl who will say hi and smile at anyone. 

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

Now, not so many. We just do sick visits and check ups. We’ve been to cardiologist, Ent, audiologist, geneticist, general surgeon, etc. 

She goes to school at noble elementary in Hamburg Arkansas where she is in the 1st grade. She is in special education classes and does pullouts (pe, art, music, etc) with her regular class. She also has PT, ST, and OT all twice a week. They also work in groups and one on one. 

4.  Tell me a success story. 

She has learned to walk, run, climb, etc. Physically, she has no limits (except being clumsy). She has learned to count out loud to 5. She can count and identify up to 10. She can tell you all the colors and shapes. Her main restriction is that she has limited speech, but we are working on this. But she has come a long way. πŸ˜ƒ 

 

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

This sweet sassy stubborn loving little girl has made it where we look at the world a different way and made us more appreciative of the little things. She doesn’t believe she has any limits and I believe this has been a major influence in how far she has come.

  

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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