Laura Mungo

Why I walk for Apraxia Kids!

Recently my son was diagnosed with Childhood Apraxia of Speech. While there is a lot of relief in getting a proper diagnosis, one that reflected my observations and gut feelings at home, there is a lot of uncertainty about the long-term prognosis. Will he ever be able to hold a conversation like I can see he desperately wants to? What is the best therapy and treatment options for him? Am I doing the right thing? There wasn't a lot of literature about Apraxia. I did not go home with a packet of print outs and info sheets like I had with other diagnoses. I walked out of the therapy office empty handed.

This is why I'm walking to raise awareness and funding for Childhood Apraxia of Speech.

I walk to support all children diagnosed with apraxia of speech - our Apraxia Stars. To show these children they are not alone and to acknowledge all the hard work they must do to overcome communication challenges that affect their day-to-day lives.

I walk to raise funds for the mission of Apraxia Kids – to strengthen the support systems in the lives of children with apraxia of speech by educating professionals and families; facilitating community engagement and outreach; and investing in the future through advocacy and research.

Please help me meet my fundraising goal by making a donation now or by joining our team. You, too, can make an impact for children and families affected by apraxia!
I believe, “Every child deserves a voice”.