$191

Raised of $1,000

Sara Miceli

Participating in DS ACT Step Up Walk 2025

Team Captain of sMILES for Santino

sMILES for Santino's Mission

Welcome to my Connecticut Step Up for Down Syndrome Walk fundraising page!

My name is Sara. I am the mom of two boys, Salvatore and Santino. Santino has Down Syndrome.

We are walking for our 4th year in order to show support for individuals with Down syndrome. Every dollar raised brings us one step closer to ensuring that each individual with Down syndrome will have the opportunity to reach his or her potential.

My fundraising efforts will support local programs and services that benefit all individuals with Down syndrome. DS ACT has provided our family with an immeasurable amount of love and support even before Santino was born. I love bringing people in the community together, whether that be through social events, fundraisers, or even if it means just connecting with other parents or individuals with DS in any type of setting.


Here are a few things about DS ACT:

  • Our Literacy Education Center provides one-to-one literacy tutoring for individuals who have Down syndrome.

  • We hold and sponsor workshops and training for parents, educators, and medical professionals to share up-to-date medical research, best educational practices, and long-term planning information.

  • Our First Call program supports new parents of babies with Down syndrome and those who receive a prenatal diagnosis. First Call conducts outreach and educational services for medical professionals and students who are pursuing healthcare degrees.

  • Our Siblings First Call program provides peer support to school-age brothers and sisters of children with Down syndrome.

  • We continue to sponsor social activities for families so they may share information and support one another.

  • We provide grants to schools and other organizations to support the inclusion of people with Down syndrome.

  • We collaborate with other organizations to educate parents about their child’s IEP and their legal rights.

  • The Advocacy Avengers is the DS ACT teen and young adult support group for individuals who have Down syndrome that meets monthly.

  • We fund a camp grant program to benefit individuals with Down syndrome.

Make your tax-deductible donation today and take the first step toward helping me achieve my goal. Thank you for your support!

About the Event

Oct 4, 2025

10:00 am

230 John Karbonic Way New Britain, CT 06051 US

Donations 2

Support us today, and you’ll give strength & connection tomorrow

The Down Syndrome Association of Connecticut is 501(c)(3) organization

EIN #06-1176478