I'm dumbfounded.
Speechless.
At a loss for words.
That doesn't happen very often, by the way.
I was planning to let y'all know that you have until midnight tonight to enter the mega prize pack, and the winner will be announced tomorrow.
But this is more important.
Nicole lives in Canada. Over the past year, I have followed her journey of sending her young child to school with diabetes. It feels like a nightmare when I compare what she has gone through to the 504 protections that my child has here, in the United States. She has worked tirelessly, writing letters to lawmakers, organizing educational events, connecting with other families. Her efforts are inspirational, to say the least.
She posted THIS last night.
Read. it. now.
Respond to it.
And let's show the world that children with TYPE 1 DIABETES everywhere deserve to have their lives protected at school, regardless of what country they live in.
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THE STORY OF ONE FAMILY'S JOURNEY WITH TYPE 1 DIABETES AND CELIAC DISEASE.
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While I'm happy to share our experiences with what works, and what doesn't work, for the management of Type 1 Diabetes and Celiac Disease in our house, please do not mistake anything you read here for medical advice. Decisions regarding your/your child's health care should be made only with the assistance of your medical care team. Use any information from this blog at your own risk.
Thank you SOOO MUCH for re-posting and for the wonderful words...you have touch my life in a way I can't even start to express xoxox I love my blogger family :)
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