Join us on September 27th from 11:00 a.m. to 1:30 p.m. at Hudson Gardens in Littleton, Colorado, as we come together to celebrate and honor the incredible individuals in our lives who have Turner syndrome.

Hunter’s story:

Hunter screened high risk for Turner Syndrome during an early pregnancy genetic screening test. We opted out of further invasive testing to confirm her diagnosis during pregnancy because it truly did not matter to us if she had it or not. God always had a plan for her to be on this earth.

During her month long stay in the NICU after she was born seven weeks early, we received her official diagnosis of Mosaic Turner Syndrome. Fortunately, Hunter has been very healthy since she was born and is thriving! She is a WILD two year old. She loves dancing, singing, swimming and spending time with her sister and cousins. She has a very beautiful personality to match her big beautiful smile. She is just like every other two year old girl! 

We are unsure what the long term effects that her diagnosis will have on her but we are extremely grateful to have a happy, growing, and beautiful girl. 

The Turner Syndrome clinic in Denver, CO has been incredibly helpful in helping us navigate what impact Turner Syndrome could have on our beautiful girl. This fundraiser means so much to us and are grateful to be part of such an incredible organization. We know times are hard so we are extremely grateful for any donation. 

“I will praise you because I am fearfully and wonderfully made; your works are wonderful, I know that full well.” - psalm 139:14

Family members, friends, and supporters are invited to make a donation in honor of their loved one with Turner syndrome. Every contribution helps support the vital programs and services of Turner Syndrome Colorado, including the eXtraOrdinary Kids Turner Syndrome Clinic, educational initiatives, community events, and family support programs.

After making your donation, you will be directed to the event registration page to reserve your spot and join us in person. We have an exciting day planned, including food trucks, family-friendly activities, community resources, and opportunities to connect with others in the Turner syndrome community.

Children are invited to participate in our Butterfly Parade, a special event celebrating the strength, beauty, and uniqueness of those with Turner syndrome. Costumes and creative butterfly-themed attire are encouraged!

We are also thrilled to feature new vendors and activities this year, including flash tattoos by BLK Sheep Studios and a Pop Claw trailer (sponsored by Resort 2 Kindness), along with other fun surprises for attendees. You don't want to miss it! 

After everyone has a chance to picnic, we will gather in teams to walk through the beautiful Hudson Gardens. Team signs, matching shirts, and creative displays of support are encouraged as we walk together in honor of our loved ones. 

We can't wait to celebrate with you and create another memorable day of community, awareness, and support.

If you are not automatically redirected to the registration page after donating, please use the link below to register for the event. TSCO will provide shirts for participants who have Turner Syndrome. Family and friends can purchase shirts on the registration page. The deadline to register and guarantee shirts is August  30th. 

Registration Link: https://donorbox.org/events/941361/steps/choose_tickets