Kristin Baird's Fundraiser:
Kick Epilepsy's Butt
Kristin
EVENT: Mozilla Firefox Challenge
HERE'S THE STORY:
Dylan was a healthy, active, sweet, fun and adorable little baby. When he was 16 months old he spiked a high fever resulting in a very prolonged seizure causing abnormal development on one side of his brain. After the seizure Dylan had to relearn all of the basic functions that he had already learned such as walking and talking. We spent about seven weeks in the hospital and as soon as we got home our sweet, loving, active, smart little guy returned. He started attending PT, OT and speech therapy weekly. He always went with a smile on his face and all the therapist commented on what a joy he was to work with as he never gave up.
About a year later (Nov. 2010) he started having simple partial seizures where he remained conscious and they usually lasted for a few seconds. These seizures aren't damaging to him, its more or less a disruption in his life. At first we saw a couple seizures a day. He was already on seizure medicine so we tried 3 more medicine's none of which worked. After a lot of discussion with the doctors we all decided surgery was the only option. Dylan had brain surgery in mid-Nov. 2011. He once again showed all the doctors that he's a fighter. They warned us that he might not walk for a couple of weeks to a couple of months. But not our Dylan he stood up and walked a few steps in the PICU two days post surgery and we were able to come home sooner than the doctors has originally anticipated.
Dylan continues to be a happy, energetic, sweet, smart and adorable little 3 year old. He still goes to therapy with a smile on his face and never gives up. We're amazed at his strength. We are about a month post surgery and Dylan is still having seizures, although drastically reduced in the number of seizures he's having daily. We're still optimistic that the seizures will stop.
It's frustrating to us that as advanced as medicine is today there is still so much we don't know about the brain and epilepsy. Our hope is that through research we can find a CURE for epilepsy.
$5,120
RAISED OF $10,000 GOAL| Stacey and Bobby Basso | |
| Linda Andersen | $25 |
| Sue and Grafton Jhung | $50 |
| Jamie Fierro | $100 |
| Chris and Jane Conway | $500 |
| Lori Conway | |
| Janet Evans Baker | $400 |
| The Belensons | |
| The Collins Family | |
| the Hamburgers | $75 |
| Amy and Cameron | $100 |
| Clay Lingo | $50 |
| Liz Scanlon | |
| Lyss + Chris | |
| Tracy and Ava Ciampi | $45 |
| the sorrells family | |
| The Cane's | |
| Tammy Plotkin-... | $100 |
| Rachel Heit | $25 |
| Johnson Family | |
| Libby Dafferner | $50 |
| kulkarni family | |
| Kaul Family | |
| The Miller Family | $100 |
| Kristin & Toby Baird | |
| Byron Jones | $50 |
| Lori, Brody and Audrey Kroll | $20 |
| Jodi and Mike Matula | $50 |
| Seidenst... | $75 |
| Fineman PR | $200 |
| Trisha Baird | |
| Jeff and Jen Lewis | $50 |
| Kristin and Scott Lineberry | $25 |
| Lynne and Mike Driscoll | |
| Lezlie Pearson | $15 |
| jeannie & Mike Hughes | |
| Nicole & Jason Hayes | $50 |
| Critter Care - Rich Anderson | $100 |
| John & Kath Murray | $100 |
| Sarah and Chris Muscolina | |
| Carolyn and Mike | $50 |
| Uncle Ty | |
| Tim and Joyce Baird | |
| Monique Johnson | $20 |
| The Valencia Family | $40 |
| Billy and Kendra Robins | $50 |
| Knox and Will Flynt | $25 |
| The Jeanguenat Family | $100 |
| Kellie and John Williams | $50 |
| Stacey Duncan | $30 |
| Candy & John Gooding | $50 |
| Frank and Margie Newell | $250 |
| Mindy Williams and Phil Polishuk | $50 |
| Karen Williams | $100 |
| John & Susan Ingram | $100 |
| The Maher Family | $40 |
| MacPherson Family | |
| Jane Finette | $90 |
| John Slater & Lane McNab | |
| Bob & Cathy Steuber | $100 |

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DONATION: $100