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Halloween Costumes For Kids With Special Needs

Halloween Costumes For Kids With Special Needs

Halloween is just around the corner and I'm blown away by the creativity of some parents! It's no secret that I love taking things that some people...

A Guide To Your Child's First IEP

A Guide To Your Child's First IEP

I know how you feel. You've got therapies and doctor appointments, not to mention all the typical things that moms of toddlers need to worry abo...

Tripp Trapp Highchair

Tripp Trapp Highchair

Eli is 3 and he is having feeding issues. His diet hasn't changed much since he was a baby - he still eats mostly puree's and drinks from a bottle....

Forest Home Family Camp

Forest Home Family Camp

We just got back from an awesome week at Forest Home Family Camp!  A week filled with no cooking, unplugged, relaxing with my family is like hea...

Heterotaxy Syndrome Awareness

Heterotaxy Syndrome Awareness

Heterotaxy Syndrome affects 1 in 10,000 babies and can cause any of the internal organs to be misplaced, malformed, multiplied or missing. There i...

How Do Siblings of a Child with Special Needs Feel?

How Do Siblings of a Child with Special Needs Feel?

Do you ever wonder how siblings of kids with special needs feel? Sometimes I wonder how the girls have processed everything that has happened sinc...

Welcome To Holland

Welcome To Holland

When I was pregnant with Eli we found out that he has Down syndrome and a heart defect. I read Welcome to Holland (a short story/poem for anyone w...

Williams Syndrome Awareness

Williams Syndrome Awareness

Sweet Dahlia was born full term, but only 3 lbs and 4 oz, despite full medical care the entire pregnancy.  She had some heart problems, really ba...

Meet A&E Born This Way's Newest Cast Member: Rocco

Meet A&E Born This Way's Newest Cast Member: Rocco

  The Emmy award winning show, Born This Way, has a new cast member - 3 year old Rocco! Eli and Rocco have known each other since they were one an...

Syndromic Craniosynostosis Awareness

Syndromic Craniosynostosis Awareness

Avery was born with syndromic craniosynostosis. There are over 200+ known craniosynostosis syndromes that can be confirmed through geneti...

May 2017 Donation: The Confetti Foundation

May 2017 Donation: The Confetti Foundation

Happy May! This month we'll be donating 10% of sales to The Confetti Foundation // The Confetti Foundation is a non profit that supplies birthday ...

Lissencephaly Awareness

Lissencephaly Awareness

Hi everyone! Meet Harper. She's 2.5 years old and continues to prove her doctors wrong most days despite the odds. Harper was diagnose...