For those who don’t know, March is Cerebral Palsy Awareness Month and it is a time to celebrate and educate! I know that it might sound weird to celebrate a disability right? But the reality is for those of us who live and breath the disability on daily basis, we see progress in our loved ones or ourselves and being able to educate others is definitely reason to celebrate.
Throughout the whole month of March, all of my posts will be about CP in one way or another. I hope by doing this I can spread awareness but also find ways to celebrate! So for today, I wanted to talk about how important it is to share and talk about different disabilities with your young children. The more we talk about them and educate our young children, the more accepting they will grow up to be as well as accommodating.
For example, yesterday while at my Gracie’s and Ricky’s softball/ baseball practices, a little girl who had been playing with Grace and her friends took notice of Olivia and started asking me questions. Mind you this is a very common thing that I have become used to. And I love it! I love that children ask me questions about her and they should. They usually ask me questions like, “why can’t she walk?”, or “can she talk?”, or “why can’t she hear?” or “why does she have that walker?”. All very valid and perfectly fine questions to ask me. I do my best to always sit down and explain in the most simplest way I can (depending on the age) to help answer their questions honestly.
There have been times that I actually had a parent come up and say, “Omg, I am so sorry!” and pull their child away. I get it, it’s more taboo right to ask up front what is wrong with someone? However, I find it as a learning opportunity and I highly encourage any parent of a non-disabled child to ask questions and let the parents or child explain. Because honestly, after I tell the children why she cannot hear or why she cannot walk, they sit and play with her. They engage her, and don’t treat her any different. Guess what happens next after that?! They meet another person in a wheel chair or with hearing aids and they don’t stare or make comments, they may go up and talk to them or they will do nothing because they understand and it’s not ‘strange’ or ‘different’ to them anymore.
One of my best friends here in Austin recently told me how blessed she was to have Olivia in her family’s life. She said not only did she love her but she loved how humbling her own children became after meeting Olivia. They protect her, talk to her, check in on her, help her and most importantly try to include her. I am so happy that Olivia was able to make such an impact in some kids lives, and I know that because of her they will grow up to respect those who may need a little extra help.
So please, please, please do not discourage your young children to ask questions about disabilities! It will greatly help all of us parents with disabled children as they grown up, to live in a less judgmental world. Well at least one can hope:)


