way to go jack attack!
We hope this makes you smile, Jack. You and your team are impacting the stories that our future generations will tell one day. Thank you for supporting in ways that keep on giving!
We put together team Jack Attack to show support for our youngest son, Jack, who was born with a complete unilateral cleft lip and palate. When we discovered that Jack would have a cleft at his 20 week ultrasound, we were quite rattled. Clefts are not something that we, and most other parents in our area, have been very well educated on. The unknown was and still is very scary for us! I’m hoping by doing the CleftStrong 5K, we can directly contribute to raising awareness for cleft and craniofacial abnormalities in our community as well as throughout the US.
Team Jack Attack will be participating virtually from Minnesota. Our team will gather at Jack’s house to run and/or walk the 5K route we have mapped out. Along with participating in the actual 5K, we will also be fundraising throughout the summer while spreading awareness! Crossing the finish line means a couple things for us, both symbolic and physical. Symbolically, it is us overcoming the hurdles that Jack will and has been facing as one united support group. Individually we are strong, but as a group we can accomplish anything! Physically, it is accomplishing a goal set out as a family to become healthier!
We are SO excited to be participating in the CleftStrong 5K this year!
Team Jack Attack
Every month, we will feature our leading fundraising team of individuals and their efforts to raise awareness and funds in support of creating a world where those born with oral cleft and craniofacial conditions THRIVE. Create your team or donate toward an existing fundraising team here! Thank you for your support.
Dedria Noll Kelm
3/31/2022 01:27:55 pm
Congratulations Jack! And Congratulations to your amazing family! You are all so loved!
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As hard as you fight, we will strive to fight alongside you.