As many of you know, we started our journey to end epilepsy and save lives for very personal reasons. We lost our sweet 9-year-old son, Kaden, to the disorder on August 3, 2010, and we also have a 22-year-old daughter who is diagnosed with epilepsy as well.
As we’ve moved along this journey, our fight to end epilepsy has evolved. We’ve grown as we’ve seen and learned so much from so many who have shared personal stories with us! And I will say, the fight is not over! We will never bring Kaden back, but we can continue to fight for so many others in his sweet honor!
Here are just a few things the Epilepsy Foundation is able to do because of your generous support! .…
· They provide funding for research to develop better medications and treatments.
· They provide access to medical assistance for families or individuals who don't have resources to get the treatment they need.
· They host Camp Brainstorm annually where children with epilepsy can experience summer camp in a very safe environment! These children get to be with other children who are similar to them and face similar challenges – they aren’t “alone” any longer! Some develop new life-long friendships!
· They provide training for first responders at schools and many other places so individuals can recognize seizures and know what to do and what not to do to keep that child or adult safe while they are experiencing a seizure.
· They also provide support groups for families to share their experiences and gain a better understanding of epilepsy and the resources available to them.
PLEASE consider showing your support by either donating, volunteering, sponsoring or attending one of our events!
Thank you so much for taking the time to read this!!! Big, bug hugs from the Smith family and many blessings to all of you!! We couldn’t do it without each of you! It definitely takes a village! xoxo
