Cheerleading | Lessons from my daughter

Olympia

For the letter O, in our A to Z Challenge, Emil picked Olympia as in Cheer Olympia, Emily’s cheer club!

If you just started following our blog, you should have a look at some previous posts I wrote about cheerleading

Emily is still finding this writing challenge somewhat challenging 🙂 But after telling her that some of you have been asking for more from her, she sat down and wrote this:

Olympia is a cheer gym. I am a cheer leader. I have friends. I have a cheerleader uniform. I like cart wheels.

Once again, thank you Cheer Olympia… Thank you Lorraine and Colleen and many thanks to our wonderful coaches: Celine, Megan and Chloe. You ladies are the best!

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A to Z Challenge 2016 – Lessons from my Daughter (PR) #819

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We have a facebook page: If you want short updates and timely pictures of the little things that are happening in our life, please like and follow Lessons from my daughter‘s page.

You can also find me on Twitter at @plebrass

I am on Pinterest too: Lessons from my Daughter

Find more about about Cri du Chat syndrome at 5p- Society

Emily has a her own page in the family stories , you can find it here: Emily

February 29th is Rare Disease Day

In my own way, through writing about our experiences raising Emily, I continue to spread the word about Cri du Chat Syndrome (CdCs)

I do my best to share experiences that are positive, fun and inspiring. I don’t shy away from writing about struggles but I will always respect Emily’s need for privacy on some more personal topics.

Did you know…

Only 1 in approximately 50,000 born will miss that tiny part of their 5th chromosome…. chances of knowing or meeting another child with CdCs are really small.

Emily was diagnosed before facebook, the information available was outdated and scary. It took us 15 years before we met others with Cri du Chat Syndrome.

Now with facebook, association and blogs, our reach is far greater and parents find up-to-date information much faster.

That being said, it is essential to increase awareness to promote acceptance for any child with special needs.

I would love for Emily’s blog “Lessons from my Daughter” to reach as many people as possible…

Would you help me by sharing this post? Please help Emily and I raise awereness for Cri du Chat Syndrome!

Thank you for being part of our journey!

Find more about about Cri du Chat syndrome at 5p- Society

Emily has a her own page in the family stories , you can find it here: Emily

If you want short updates and timely pictures of the little things that are happening in our life, please like and follow Lessons from my daughter‘s page on Facebook.

You can also find me on Twitter at @plebrass

I am on Pinterest too… one day I will figure out what to do there other than finding cool recipes but meanwhile, you can find me here: Lessons from my Daughter