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My Story…
As Katie's parents we often wonder how we got here. It was not on our list of life goals or "5 year plan" to be campaigning and fundraising for epilepsy. In fact in 2010 we really didn't even know what epilepsy was until life took us on an unexpected journey and we watched, feeling helpless, as our girl's life spiraled out of control. We are very aware of the blessings of Katie's restored quality of life and experiencing what life is like seizure free again, and that is why we are compelled in our present strength of mind to do whatever we can to help "uncover the brilliance that will end epilepsy ~ forever"!!
Although we have little idea of all Katie has endured and all she fears for the future, we stand beside her as her support, in front of her as her advocates, and behind her as her encouragers.
We ask that you would consider joining us to do what you can to help all those living and trying to live well with epilepsy. Together we can make a difference.
Recent donors
| Donation date | Donor name | Donation amount |
|---|---|---|
| Jun 20 | Jim Little | $25.00 |
| Jun 20 | Rose Dennis | $30.00 |
| Jun 20 | Trudy Poot | $50.00 |
| Jun 20 | Louie Molenhuis | $10.00 |
| Jun 20 | Bonnie Hinschberger | Undisclosed amount |
| Jun 20 | Mike Grinnell | $25.00 |
| Jun 19 | Peter Smedema | $250.00 |
| Jun 18 | Martinus Otten | $100.00 |
| Jun 17 | Anonymous | $100.00 |
| Jun 17 | Jim and Karen Franko | $100.00 |
