Annabelle

Annabelle may only be two years old, but she has conquered more in her short life than many do in a lifetime! She was born with Trisomy 21 and Unilateral Left Clubfoot. She did not let the weekly trips out of state to get new leg casts hold her back and even began rolling over at just a month old! Every single milestone that doctors predicted she wouldn’t be able to accomplish for months (or even years!) she was able to accomplish in weeks. At 12 months old, Annabelle was named Zulily Cutie 2017 and was flown to Seattle for several photo shoots with her family. Appearing on their social media pages and on their website, Annabelle was well on her way to changing the way the world views Down syndrome. Just weeks after the cross-country trip, Annabelle was diagnosed with Acute Lymphoblastic Leukemia. She spent many months in the hospital, but thankfully achieved remission in September of 2017. With only a few months of treatment left now, Annabelle is rocking the world once again. She became an ambassador for the Children’s Miracle Network in 2018 and is so excited that she’s been given the opportunity to represent Nothing Down as a 2019 ambassador! Even with all of these complex issues, as well as being profoundly deaf in one ear, Annabelle has already shown the world that there’s absolutely Nothing Down about Down syndrome! To learn more about Annabelle’s journey, follow her on Facebook at www.facebook.com/TravelWithAnnabelle/

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It is with a heavy heart that we announce the closure of the Nothing Down organization. After much careful thought and consideration, we have made the difficult decision to bring this chapter to a close.
Since our founding in 2016, we have achieved so much together—making a meaningful impact in the Down syndrome community and connecting with incredible individuals along the way. We are immensely proud of the work we've done and deeply grateful for the opportunity to have been part of such a positive and supportive network.
We would like to extend our sincerest gratitude to every donor, participant, volunteer, and supporter who helped bring Nothing Down to life. Your contributions have been invaluable, and none of our accomplishments would have been possible without you.
Though our organization is closing, Nothing Down's Facebook page will remain where new and expectant parents can find hope and inspiration from our past projects and awareness content. We are so grateful for all the wonderful years.
Thank you, from the bottom of our hearts, for everything.

It is with a heavy heart that we announce the closure of the Nothing Down organization. After much careful thought and consideration, we have made the difficult decision to bring this chapter to a close.
Since our founding in 2016, we have achieved so much together—making a meaningful impact in the Down syndrome community and connecting with incredible individuals along the way. We are immensely proud of the work we've done and deeply grateful for the opportunity to have been part of such a positive and supportive network.
We would like to extend our sincerest gratitude to every donor, participant, volunteer, and supporter who helped bring Nothing Down to life. Your contributions have been invaluable, and none of our accomplishments would have been possible without you.
Though our organization is closing, Nothing Down's Facebook page will remain where new and expectant parents can find hope and inspiration from our past projects and awareness content. We are so grateful for all the wonderful years.
Thank you, from the bottom of our hearts, for everything.