Has your child been diagnosed with a neurological condition, such as Cerebral Palsy, Autism, or Traumatic Brain Injury?

Have you been told all of the things your child won’t or can’t do...and then set your sights on what your child can do and would do?

Has he or she--perhaps through complementary treatment methods, nutrition, and environmental changes--found recovery and an improved quality of life?

Is your child’s story one that needs to be told… to let other families know what is possible for their child?

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Since you know my family's story, I would love to hear yours! I truly believe each and every one of you are so inspiring. If you are open to it, I'd be so excited to read and hopefully feature your story and/or family’s treatment journey on our website. It is my hope that hearing your story will motivate and inspire others who are just starting out with their own journeys and have begun following The Brain Possible.

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Technology--especially the internet--has made a tremendous impact on philanthropy. Read 10 (plus) simple but powerful ways technology has changed the way we give.

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The COVID-19 Pandemic has changed the way we do nearly everything: Work, attend school, spend time with friends and loved ones, and even the way we volunteer. When areas first went into lockdown in early 2020, we were no longer able to volunteer at our local food pantry or attend civic club meetings. Organizations and their faithful volunteers had to look for new ways of fulfilling volunteer opportunities and continue the important work they provide to their communities.

SO WHAT DID THEY DO? GO ONLINE, OF COURSE.

It hasn’t been easy, but nonprofit organizations and their volunteers have stayed flexible and made changes that have allowed vital services to continue well into the Pandemic.

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What is mindfulness, and how can it help my child? Practicing mindfulness is simple--in its most basic form, no tools, books, or supports are needed--just a little time, a quiet place, and the intention to care for yourself.

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On the evening of Friday, April 9, 2021, around 170 guests from as far away as Miami gathered at The Bardot Event Space in the Crossroads. This group came together--with multiple precautions in place to prevent the spread of COVID-19--to honor the legacy of a little boy, Carter Abbott, and look to the future possibilities that this one-of-a-kind nonprofit is creating.

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In November 2019, the Who Is Carter Foundation hosted its second annual gala and auction in Kansas City, Missouri. There were hundreds of people in attendance who were all there because they support Who Is Carter and The Brain Possible's mission, which is to change the conversation around children with brain injuries from one of limitations to one of hope and possibility.

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Podcasts are a great way to gather information, news, and perspectives on just about anything these days. (And a great way to pass the time while folding laundry or waiting for an appointment!) There’s a growing library of popular parenting podcasts out there, which can make them challenging to sift through. So we took some time to find11 of the best podcasts for parents of children with special needs. We’re sure you’ll find a few that inspire and inform you!

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In case you missed it, Who Is Carter and The Brain Possible made the news in 2020.

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The Coronavirus Pandemic has affected all aspects of life in 2020, including charitable giving and how we report those charitable gifts on tax returns. Here are a few clarifying questions and answers to support you as you navigate filing your 2020 taxes and reporting your 2020 charitable gifts in the coming weeks.

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The Who Is Carter Foundation and The Brain Possible are excited to share a triple-whammy approach to holiday gift shopping in 2020: 1) Find everything you need for the special kids and adults in your life, 2) all while shopping online, from the safety of your home, 3) and you’ll be making purchases that give back!

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What is complementary medicine? And why is it important to children’s health?

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Out of all of the things we do at the Who Is Carter Foundation and The Brain Possible, some of the work we are most proud of is our “Stories of Hope” series, which showcases real stories from real families who are overcoming adversity and focusing on hope and possibility while raising differently-abled children.

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2020 has been a challenging year for everyone. We know that supporters of the Who Is Carter Foundation are generous individuals and companies who hold a number of charitable causes close to your hearts, so we wanted to provide you with a snapshot of the nonprofit landscape in 2020.

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It’s clear that every sphere of our society has been impacted by the COVID-19 crisis: our healthcare system, schools, businesses. Everyone has had to make adjustments in 2020, and nonprofit organizations are no exception.

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Have you noticed more and more butterflies in your area in recent days?

They seem to be everywhere, and their return is a welcome sign that Spring is here. Nature’s cycle of life continues, punctuated by these fluttering, colorful messengers all around us.

You may have also noticed that the logo for Who Is Carter is a butterfly, so we thought that this time of year is perfect to share the story behind that symbol.

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Even though the Coronavirus Pandemic is impacting our lives in significant ways, the staff, board, and volunteers at the Who Is Carter Foundation are still ramping up plans for this year’s Gala, and we’d love for you to join us!

There are a few key volunteer roles that you can fill, and the great news is, you can fulfill these roles from the safety of your home!

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Cooper's mother, Adrienne, says she noticed things were a little different with Cooper from a young age. He struggled with fine and gross motor skills, and he had constant ear infections. When he grew a little older, around the second grade, she noticed he didn't run the same way his peers did and that it was more challenging for him to complete basic tasks, like tying his shoes.

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I was beyond nervous to hand my non-verbal toddler over to a bunch of strangers. What if he wandered off and couldn’t tell anyone his name or answer when people were calling his name? The very idea kept me up at night. He needed this help, but sending him to school was terrifying to me.

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