My 11 year old daughter has epilepsy. Found out about this group in the year 2012, My daughter got to go to Camp Neuro Revolution in July 2012,her first and really enjoyed it and then got to go to it again in 2013. She has made many who have epilepsy just like her. Epilepsy foundation of Utah is great they are always there for my daughter and always leave sweet thoughts. They will be helping me do a presentation at my daughters school for the whole 6th grade about epilepsy and what to do. I love being part of this great and wonderful epilepsy foundation of Utah if it wasn't for them my daughter and I would be lost. They have useful information about epilepsy.
Never in my life would I have ever thought I would be a part of such a wonderful organization. As scary as my son's first seizure was, his second was devastating because now it mean it wasn't just a fluke. We moved to Utah to find help for him and within a year, I was on the Board of the Epilepsy Association. I saw the wonderful support they provided to people and I had to help! I can unabashedly say: They are the BEST group of people I have ever known...and I have been around the block a few times. The services they provide to individuals with epilepsy are fabulous: Transportation Assistance Program, Scholarships, Medication Assistance Programs, statewide Support Groups, Camp for teens, Political Awareness among others. There is almost nothing these folks can't do and I am honored to be a part of it!
Now in it's 40th year the Epilepsy Association of Utah is growing and helping thousands of individuals in Utah every month. They are growing all the time and expanding to new areas in Utah all the time. I have loved Camp Neuro Revolution for teens with Epilepsy. Crop Because you care annual Scrapbook fundraiser and Artilepsy (art exhibit) for those who are touched by epilepsy as just the beginning of the things I love about the Epilepsy Association of Utah.