The Story of a Bipolar Bear.

This is a photo of my sister at age one and me at five. This is the only picture I have where I am holding her.
She died a decade later after this photo taken. It shows the strength of a child who was born physically and mentally disable and her motivation to keep living. She never gave up till the day she died. She survived longer than the doctors predicted. Even on this day, she will always be the strength and courage my family needs to keep living.
She gave me something that no one could ever give me.
She kept battling what life thrown at her and she reminds me everyday I shouldn’t either.
I know there is a family out there that needs care and service for a child with disability.
I’m going to donate a penny for every reblog and like to the children with Microcephaly Foundation on March 18,2012 which is the day of her 17th birthday.
As much money as I can save goes to the foundation.
I also wanted this post to bring awareness and to remind everyone struggling with a love one who has microcephaly or is mental/physical disable know that they aren’t alone. I’m here if you want to talk. 
So please reblog to help a child that suffers from a neurodevelopment disorder and the many families that struggle everyday. 
Thank you.

This is a photo of my sister at age one and me at five. This is the only picture I have where I am holding her.

She died a decade later after this photo taken. It shows the strength of a child who was born physically and mentally disable and her motivation to keep living. She never gave up till the day she died. She survived longer than the doctors predicted. Even on this day, she will always be the strength and courage my family needs to keep living.

She gave me something that no one could ever give me.

She kept battling what life thrown at her and she reminds me everyday I shouldn’t either.

I know there is a family out there that needs care and service for a child with disability.

I’m going to donate a penny for every reblog and like to the children with Microcephaly Foundation on March 18,2012 which is the day of her 17th birthday.

As much money as I can save goes to the foundation.

I also wanted this post to bring awareness and to remind everyone struggling with a love one who has microcephaly or is mental/physical disable know that they aren’t alone. I’m here if you want to talk. 

So please reblog to help a child that suffers from a neurodevelopment disorder and the many families that struggle everyday. 

Thank you.

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    Happy birthday sis
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    This is a photo of my sister at age one and me at five. This is the only picture I have where I am holding her. She died...
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