I can't remember if I have already posted this link? This is a slide show of a little boy that also has Doose syndrome like Lauren. There is a great yahoo group for families with Doose syndrome that we belong to. His parents started a non-profit foundation to help all families dealing with epilepsy. I think November is Epilepsy awareness month so they are trying to get the word out.
http://epilepsyoutreach.org/emmetts-story.html
Lauren
4 comments:
I'm glad that you've found support through other families who are living with seizures. We continue to pray for your whole family. (We'll get the word out in RS :)
What a touching video and reminder of what Lauren has to go through. We love you all very much!!!
Love, The Starbucks
I had no idea things were so hard recently! You are such amazing parents. Lauren is lucky to have been born into such a great family. Thanks for letting me a part of your kids lives!
What a great video! You know, we always support the American Cancer Society every year in their fundraising and "walks", we should change our focus to what would help Lauren. Tell us what the best organization to research would be.
I'm sorry things have been so difficult (understatement, I'm sure!). Everyday I think I should call and get an update, especially since your blog hasn't been updated recently. I kept telling myself that no news is good news and never remembered when I thought it would be a convenient time to call. I need to be better about keeping in touch with you guys, I'm so sorry! We are still remembering Lauren and her family in every prayer! Keep going...you're doing an awesome job! Kim
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