Tuesday, November 1, 2011

Cassidy

The month of November is Epilepsy Awareness Month.  For each day of the month I am hoping to profile the many faces of Epilepsy.  While this may not help find a cure, I am hoping it will get the word out that there are people living with Epilepsy and unfortunately, Epilepsy has taken loved ones far too soon.  Please read each story, look at their face and help spread awareness.

Cassidy


This is Cassidy.  She is 9 years old and is currently in the fourth grade.  She enjoys singing, dancing, reading and playing with her friends and sisters.  At the age of 7, Cassidy had her first Grand Mal seizure.  She was up early, ready for her first plane ride with her Grandma to visit family.  She was sitting on her mothers lap when her mother noticed a "weird noise" and her body stiffening up.  She asked if she was ok before noticing her lips were blue and her eyes were half rolled back in her head.  Within seconds her mother knew she was not breathing and as she shouted for help, Cassidy started shaking uncontrollably.  The seizure lasted for 3 minutes and she remained unresponsive for 30 minutes after.  After being taken by ambulance to a local Children's hospital and numerous tests later, she was diagnosed with Epilepsy.

Cassidy had a hard time after being diagnosed.  Her medication she was on was not working completely.  She had seizures at school and never felt like she was in control.  She was bullied at school and found ti hard to ignore the snickers and jeers from the other kids.  Within a year her medications were finally able to stabilize her and help control her seizures.  She has made some great friends who stick up for her when she needs it.

If you ask Cassidy about her epilepsy, she will tell you all you want to know.  She is not ashamed by it and wishes that everyone would treat her and others like her like normal kids.  Being left out o hurts, especially when her Epilepsy keeps her form doing some things the other kids can already do.  Cassidy loves being able to go out and spread awareness.  She has volunteered for The Danny Did Foundation and The Epilepsy Foundation of Greater Los Angeles. 

Cassidy is a child living with Epilepsy.  Please help spread awareness that Epilepsy is real and needs to be talked about!!!!




1 comment:

Launa said...

Great post K! Kind of weird to read it in third person but at the same time it's good to think that there are Cassidys everywhere!! Hugs to that sweet girl of yours. Miss you guys lots!

Related Posts with Thumbnails