As parents of children with Down syndrome, we often hear about the challenges—delayed milestones, low muscle tone, sensory sensitivities. But what if we could shift our focus from limitations...
Transforming
Hope
Into Action
We Inspire
And
Empower one another
Welcome to The Down Syndrome Action Plan
Transforming Hope into Action
Welcome to The Down Syndrome Action Plan, where we inspire and empower one another to not just embrace a new normal, but to create New Extraordinaries. We cultivate a curious and collaborative community dedicated to changing mindsets and redefining the reality of what Down syndrome will mean for our children and our families. Our focus on integration, neurodevelopment, functional health and wellness approaches, epigenetics, and neuroplasticity as well as drawing inspiration and information from specialty areas outside the world of Down syndrome allows us begin turning hope into action together.
Key Services

Join Our Community
The Down Syndrome Action Plan Community Platform is a collaborative place of education, empowerment, inspiration, and possibility. Some features of the platform are:
Live educational webinars with me as well as experts from both within and outside the world of Down Syndrome
Live Q&A sessions
Live Open Forums that are community driven for brainstorming, calls to action, open discussion
Direct access to me during all live events and exclusively through the platform for questions, suggestions, and brainstorming
Live events like book clubs
Community Challenges
Initiative forums where we come together to identify big questions and work collaboratively to create big possibilities
Collaborative development of new and progressive services for our community members
The resources offered are an accumulation of information over the past 14 years
of the Down Syndrome Action Plan FB Group. These resources will be richly
enhanced with new information, downloads, and e-books that can play a crucial
role in the creation of our children’s unique and individualized action plans.
A very special project aimed at sharing our stories of rejecting the new normal
and shining a spotlight on all of the New Extraordinaries mothers around the
globe have created. These stories are inspirational and powerful and they ignite a fire within all of
us for creation and change. It honors the women we are, spotlights our
endeavors, and inspires more women to join us.
This book offers you the same opportunity: to create a new extraordinary. It’s more than just information; it’s a movement that challenges the status quo and equips you with the tools to unlock your child’s full potential. Whether you're just starting your journey or looking for new ways to support your child's growth, this book will inspire and empower you to take action, find real answers, and redefine your reality.
Our New Extraordinaries podcast will be coming soon.
The New Down Syndrome Action Plan Blog
Want to know more?
Contact Us Now!

The New Down Syndrome Action Plan Blog
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Thoughts From The DSAP Community
"This is a book that every parent of a child with Down Syndrome needs to read. It opened my eyes to so many possibilities that lit a fire in my soul to do the most for my son. Not only did this book teach me things I was completely unaware of that will benefit my son, It gave me the hope I needed. Without having completed research of my own yet, Geralyn’s book gave me just the springboard I needed. I am hopeful to give my son the life he deserves. Down Syndrome isn’t what we’ve been taught - it is so much more than that!”
"DSAP has helped set the tone for us on our journey. I have always been a go-getter - don’t settle for status quo - let’s set the bar high and get after it… but I didn’t exactly know HOW to do that with my girl. So many areas need attention/direction…All very heavy and I want to do my very best for her!
Having hundreds of other like-minded mommas, many of whom are ahead of me on the journey, has been a gift. DSAP is a place to seek information, experiences, and advice. A place to LEARN and GROW and to keep my mindset right, especially when I may question myself or our path!"
"The resources & information are invaluable, but it’s really the feeling that we are a community that helps me the most. Even though each of our kids are different, it is about the journey & doing it together. That is what DSAP means to me. Celebrating, inspiring & supporting one another."
"I truly feel that there is no better time to have been born with Down syndrome than right now. I appreciate the perspective of the ‘take action’ parents who are further down the path than I am that are willing to take the time to share their experience, and insights.
I appreciate that there is room for differences of opinion and an acknowledgment that ‘one size’ doesn’t fit all children with T21.
If you’re wondering what you can do to maximize your child’s unique genetic potential while looking for out of the box strategies and have found that traditional approaches tend to leave you wanting more, DSAP is a great place to land."
"I have learned a lot from this group and I love that there are other like minded moms/families doing different approaches to help their children that are different from the status quo. No one is doing it where I live. It is great to be able to ask questions, get advice, and support. This is not an easy journey and it helps me know I am not alone."
"What I love most about DSAP is that it is safe and respectful. They supported our family in taking a very holistic and neuroplastic approach to neurodevelopment. It prevented isolation from choosing the path less traveled and provided comfort and support from other families who have chosen a similar path for their children. I have been blessed through this group to unite with like minded mothers across the globe who’ve become wonderful friends over the years."
"Finding a community of Take-Action moms is so important, even though everyone’s journey is different, is inspiring to me. I love the fact that the group believes in setting the bar high and not accreting “that’s just DS.” I know many parents take the traditional route but this group really inspired and saved me right after the birth diagnosis when things were feeling very dark and gloomy."
Check out our Youtube channel Filled with videos that inform, educate, empower and inspire parents and practitioners to Redefine the Reality of Down Syndrome and create true action plans for development and learning.
DISCLAIMER
The information provided on this website is for educational and informational purposes only and should not be considered as medical, health, or professional advice. The content is intended to empower individuals with knowledge and insights, but it is not a substitute for professional medical consultation, diagnosis, or treatment. Always seek the advice of your physician, healthcare provider, or a qualified professional regarding any questions you may have about a medical condition or before implementing any information, recommendations, or techniques shared on this site. Never disregard or delay seeking professional advice because of something you have read here. The Down Syndrome Action Plan and it’s founder Geralyn Spiesz do not assume responsibility for any decisions made based on the information provided. Reliance on any information appearing on this website is solely at your own risk. Please consult with a healthcare professional before starting any new health, nutrition, or therapeutic programs, especially if your child has specific health conditions. In case of a medical emergency, contact your doctor or emergency services immediately.