Fundraisers

A Guide To Your Child's First IEP

by Michelle Sullivan September 18, 2017

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...

Posted in down syndrome, first IEP, IEP, IEP meeting, inclusion, kids with special needs, least restrictive environment, special needs

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Welcome To Holland

by Michelle Sullivan May 26, 2017

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...

Posted in autism, awareness, birth diagnosis, cerebral palsy, chd, chd awareness, children's hospital, Down syndrome, heart defect, holland poem, holland story, holland tour guide, kids with special needs, nicu, picu, prenatal diagnosis, rare disease, special needs, spread awareness, welcome to holland

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May 2017 Donation: The Confetti Foundation

by Michelle Sullivan May 10, 2017

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 ...

Posted in children hospital, hospital birthday party, kids with special needs, picu, special needs

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Lissencephaly Awareness

by Michelle Sullivan May 10, 2017

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

Posted in Lissencephaly, Lissencephaly awareness, special needs, special needs kids, spread awareness

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Harlequin Ichthyosis Awareness

by Michelle Sullivan May 09, 2017

Brenna was born in December 2011 and unexpectedly diagnosed with an extremely rare and severe skin disorder called Harlequin ichthyosis. Brenna ma...

Posted in A different Beautiful, A different beautiful book, Harlequin, Harlequin ichthyosis, Harlequin ichthyosis awareness, ichthyosis, kids with special needs, special needs, spread awareness

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The Littlest Warrior Story

by Michelle Sullivan May 09, 2017

Littlest Warrior Apparel was inspired by my son Eli who is my biggest hero. We found out when I was 20 weeks pregnant that Eli had a heart de...

Posted in av canal defect, down syndrome, Down syndrome awareness, heart defect, prenatal diagnosis, special needs, special needs kids, the lucky few, trisomy 21

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