This is KCNQ2 Awareness Week and I’m helping to raise money for KCNQ2 Cure Alliance.
Teagan Marie is our precious granddaughter who was born with a rare genetic disorder called KCNQ2 Developmental and Epileptic Encephalopathy. The beginning of her life was difficult and she continues to face challenges every day. Teagan is now six and growing into a beautiful little girl. Her smile and laugh can brighten your day and her hugs will warm your heart. She is our miracle girl!
March is Developmental Disabilities Awareness Month and March 1-7 is KCNQ2 Awareness Week. March 2 is KCNQ2 Awareness Day so today I'm participating in Team KCNQ2, a fundraiser supporting KCNQ2 Cure Alliance. I’m passionate about this cause and am asking for your help. Every donation—big or small—helps me reach my fundraising goal and directly impacts this important cause.
Here's how you can help:
Donate: Contribute whatever you can. No amount is too small!
Spread the Word: Share my fundraising page with your friends and family. By spreading awareness, we can raise more money.
Thank you for your help in this effort. Your support is greatly appreciated.