In honor of the FOURTH ANNUAL Dravet Syndrome Awareness Day (June 23),
I’m holding my FOURTH ANNUAL
fundraiser to raise money for the Dravet Syndrome Foundation to help find a cure!
Our seven year old daughter, Luella, had her first seizure at nine months old. She was diagnosed with Dravet syndrome about a year later. Luella continues to have seizures and she needs a cure! You can read more about Luella on her blog - http://littleluella.blogspot.com/.
Donations will be accepted until midnight June 23 – Dravet Syndrome Awareness Day.
Donations will be accepted on this website OR cash or a personal check can be given to me. Please write checks out to “Dravet Syndrome Foundation” or "DSF". ALL of the money collected will be given to the Dravet Syndrome Foundation in honor of Luella. Over the past three years we've been able to send over $4,000 to DSF!! All of that money matters and we appreciate all your donations!
Find more details about this fundraiser on Luella's blog at https://littleluella.blogspot.com/2017/05/fourth-annual-cake-4-cure-fundraiser.html
If you'd like to follow Luella's Blog
please visit: http://littleluella.blogspot.com/
If you'd like to learn more about Dravet Syndrome
or the Dravet Syndrome Foundation
, please visit: http://www.dravetfoundation.org/