Skip to content
Welcome to our site!
Edwards Syndrome Association
  • About Us
    • Get To Know Us
    • About Us
    • Support Our Cause Today
    • ESA Brochures
    • Volunteer for Trisomy 18 Families
  • Programs
    • Cards of Hope: Brightening Your Child’s Day
    • Trisomy 18 NICU Care Packages
    • Meaningful 1st Birthday Gifts for Trisomy 18 Warriors
    • Bereavement Support for Trisomy 18 Families
  • Therapy
    • Pediatric Physical Therapy: Supporting Children’s Growth and Development
    • Occupational Therapy
    • Speech Therapy
      • AAC Devices
    • Vision Therapy
    • Specialized Therapy Services
    • Chiropractic Care
    • Therapy Toys
    • Trisomy 18 Educational Books: Resources for Understanding and Inspiring Hope
  • Parents
    • Trisomy 18 Family Directory
    • ESA Family Questionaire
    • Thriving Thursday
    • Thriving Thursday Submissions
    • Common Prenatal Questions
    • Parent Guide – Supporting your child
    • Family & Estate Planning
  • Medical
    • What is Trisomy 18?
    • Trisomy 18 Diagnosis Methods
    • Medical Articles
    • Trisomy 18 FAQ
    • Wilms’ Tumor and Its Impact on Trisomy 18
    • Understanding Cerebral Palsy: Resources, Support, and Care
    • CVI: Cortical Visual Impairment
  • Angels
    • Precious Angels
    • Honor Your Precious Angel
  • Events
    • Breaking Barriers: 3.18K Run for Trisomy 18
  • ESA Store
  • Contact Us
  • Toggle website search
Menu Close
Read more about the article Alejandro (Mosiac) 3 years old

Alejandro (Mosiac) 3 years old

  • Post author:Kelly Peterson
  • Post published:October 25, 2024
  • Post category:Mosaic

Continue ReadingAlejandro (Mosiac) 3 years old
  • Go to the previous page
  • 1
  • 2

If you do not see your registration password email in your inbox, please check your SPAM folders.

The Edwards Syndrome Association

6615 Grand Avenue #304

Gurnee, IL 60031

Email:  admin@edwardssyndrome.org
Edwards Syndrome Association

Useful Links

>About Us

>What is Trisomy 18?

>Prenatal Information

>Therapy Information

>Contact Us

Donate


Join our newsletter

Stay up to date with community news, interests, and much more…

Follow Us On:

Facebook Instagram Tiktok Youtube X-twitter Linkedin

© 2024 THE EDWARDS’ SYNDROME ASSOCIATION NFP. ALL RIGHTS RESERVed. SEE OUR PRIVACY POLICY & DISCLAIMERS. 

the EDWARDS’ SYNDROME ASSOCIATION IS A RECOGNIZED 501(C)(3) ORGANIZATION.

Close Menu
Verified by MonsterInsights