Gastroparesis Pie Face Challenge

Gastroparesis Pie Face Challenge The official page of the Gastroparesis Pie Face Challnege. Smashing GP 1 pie at a time! Hi everyone! Since then, my symptoms have been under control.

My name is Andrew Belliveau and I am the creator and founder of the Gastroparesis Pie Face Challenge. Gastroparesis is something very near and dear to my heart as I was diagnosed with the disorder at age 10. In short, Gastroparesis is a motility that disorder that causes your stomach to become paralyzed meaning you cannot eat, digest or absorb nutrients. Although it affects millions, the condition

is widely unheard of. To make matters worse, there is no known cure and few effective treatment options available for those diagnosed. Personally speaking, my main symptoms were constant nausea, frequent vomiting (10-15 times per day), malnutrition, and severe weight fluctuations for years. Needless to say, my quality of life was pretty much non-existent. However, I was determined to continue on with my life the best I could. I often felt isolated because no one understood what I was going through. I rarely went out in public because I was so scared I would have to vomit and not know where the nearest restroom was. I couldn’t fully partake in social gatherings like holidays, dinning out, and parties because they tend to always revolve around food. In essence, life with Gastroparesis was mentally and physically draining. Luckily, in 2012, I received a gastric stimulator which works like a pacemaker for your stomach. However, the success rate of the device varies from patient to patient. Hence, there is still no known cure for Gastroparesis. Since I was extremely lucky to respond to the stimulator as well as I have, I decided to set out on a quest to raise awareness for Gastroparesis and hopefully, fund a cure. With inspiration from the Frates family and their work for ALS, I launched the Gastroparesis Pie Face Challenge on July 26, 2016. It took a while for the challenge to get off and running but once MLB pitcher David Price accepted my nomination, the challenge quickly caught fire. Since 2016, pies have been thrown across the globe by professional athletes from the MLB, NFL, and NHL celebrities, media personalities and plenty of GP warriors. Additionally, the challenge has even caught the attention of national media outlets like ESPN, People, Inside Edition, Bleacher Report, Sports Illustrated and even politicians. Most importantly however, over $12,000 has been raised for G-PACT, a non-profit working to support those with GP in addition to bringing hope to people who thought they were fighting alone. Bit-pie-bit, this once invisible condition, is slowly becoming noticeable. I encourage everyone to participate/donate and have fun with the challenge! Make sure to check out our celebrity participants as well as some of the most creative/funny pie faces! The rules are as followed:
1) Record yourself smashing a cream pie into your face
2) Challenge as many of your friends as you would like
3) Post your video on your personal social media accounts and on the official challenge page on Facebook https://www.facebook.com/gastroparesispiefacechallenge/ or Twitter/Instagram “”
4) Donate $1 to G-PACT, a non profit organization that helps Gastroparesis patients and conducts research on the condition. *(See information on how to donate below)
5) Have Fun and be creative!!! Donating to G-PACT: To donate to GPACT please follow this link https://www.g-pact.org . Once you are at G-PACT’s homepage hit the donate tab located in the top right hand corner. Questions? email me, Andrew, at [email protected]

Merch Link: https://www.zazzle.com/gp_pie_face

08/04/2026

Happy 1st Tik Tok Tuesday of awareness month!!

Some days, living with gastroparesis feels like I'm just making it up as I go. 😅

Every flare is different. The foods that worked yesterday might not work today. Plans get canceled, energy disappears, and sometimes the only thing keeping me going is electrolyte drinks, small sips, and hoping tomorrow is a little better.

The funny part is that people often think we have it all figured out. The truth is, a lot of us are just doing our best with the information our bodies give us that day.

So if you've ever gotten through a flare with nothing but vibes and electrolyte drinks... this one's for you. 💚

08/04/2026

And the pies keep coming, and coming and coming! 🥧

Let’s give it up for fellow warrior Tiago for his epic smash! 👏 💚

08/03/2026

Some people dream of having some delicious cake on their birthday🎂

Not us though…

We dream of smashing GP!!💪💪

What do you say… let’s get this pie party… STARTED!!

.

08/02/2026

**Please share**

Hi Drake and Ann-Michael,

My name is Andrew Belliveau. I'm 29 years old from Lynn, Massachusetts, and today, I'm challenging you to take on the Gastroparesis Pie Face Challenge.

Gastroparesis (GP) is a disease that affects millions, yet most people have never even heard of it. It's essentially paralysis of the stomach, meaning my body can't properly digest food or absorb the nutrients it needs. I was diagnosed when I was just 11 years old, and for the last 18 years, I've lived with relentless nausea and vomiting 10–15 times every single day. Needless to say, I can’t enjoy your favorite pizza or Ann-Michael’s amazing baked treats.

A few years ago, I was fortunate enough to receive a gastric stimulator, which has helped make my symptoms more manageable. But the reality is that it doesn't work for everyone. There is still no cure.

Instead of letting GP define me, I wanted to turn my struggle into something bigger. So in 2016, I created the Gastroparesis Pie Face Challenge to spread awareness and raise money in hopes of one day finding a cure. Together, we've raised more than $20,000 for G-PACT, a nonprofit dedicated to supporting the gastroparesis community. People around the world have joined the challenge from fellow GP warriors to media personalities, celebrities, and professional athletes across the MLB, NHL, and NFL... including some Patriots legends in Julian Edelman and Rob Gronkowski.

First, Drake, you've become my favorite Patriots player.

Second, you wear No. 10, and this year marks the 10th anniversary of the Gastroparesis Pie Face Challenge.

And third, wheather I'm watching the
Patriots on Sundays or seeing what incredible treat Ann-Michael is baking next, the two of you have given me something priceless: moments where I can forget, even if it's just for a little while, that I'm living with this debilitating disease.

As a diehard Patriots fan, it would truly mean so much to see you both continue carry on the legacy that past Patriots have helped build by joining the fight to smash gastroparesis.

So here's my Hail Mary.

Drake and Ann-Michael, I hope you'll accept the Gastroparesis Pie Face Challenge.

You fan,
Andrew Belliveau



New England Patriots annmichaelhmaye drake.maye

G-PACT (Gastroparesis Patient Association for Cures and Treatments, Inc)

08/01/2026

Us for the next 30 days…

Happy awareness month!!💚

.

08/01/2026

🚨2026 GP Pie Face Challenge Awareness Month PSA 🚨

August is Gastroparesis Awareness Month💚

For millions of people living with gastroparesis, every day begins with a challenge they never chose.

This year's PSA, *"The Challenge They Didn't Choose,"* is dedicated to every patient, caregiver, family member, and friend who faces this disease with strength and hope.

Gastroparesis is more than an upset stomach. It can mean chronic nausea, vomiting, pain, malnutrition, feeding tubes, surgeries, and countless moments that most people never see.

But while we didn't choose gastroparesis, we choose to keep fighting. We choose hope. We choose awareness.

As we celebrate the 10th anniversary of the Gastroparesis Pie Face Challenge, we're inviting you to stand with our community.

🎥 Watch the video.
🥧 Take the challenge.
📢 Share it with others.
💚 Help make the invisible visible.

Because awareness leads to understanding.
Understanding leads to compassion.
And compassion helps bring us one step closer to better treatments—and one day, a cure.

Music: I do not own any of the music in the video. Please credit 'Ascension' by Scott Buckley - released under CC-BY 4.0. www.scottbuckley.com.au

G-PACT (Gastroparesis Patient Association for Cures and Treatments, Inc)

07/31/2026

⏳ 24 hours to go...

Gastroparesis Awareness Month begins tomorrow! 💚

For the next month, we'll be raising awareness, sharing stories, breaking misconceptions, and standing with everyone living with gastroparesis. Every voice matters, and every story helps make a difference.

LET’S GOOOOOO!!

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07/30/2026

August is Gastroparesis Awareness Month!

💚 Here are 5 ways you can make a difference and help raise awareness for the GP community:

1️⃣ Take the Gastroparesis Pie Face Challenge 🥧
2️⃣ Register for the Dash 'N Smash Virtual Run/Walk (Aug 29–30) 🏃‍♂️
3️⃣ Share your personal story to educate and connect 🗣️
4️⃣ Pitch your story to local media 📰
5️⃣ Stay active—share infographics, participate in our GP Bingo, or contact your legislators! 📄

We are tired of being sick and tired. Let’s make our voices heard this August! 👇

Which one are you doing first?

Extra, Extra! Read all about it! 🗞️In an effort to highlight patient voices, we will be featuring the stories of several...
07/29/2026

Extra, Extra! Read all about it! 🗞️

In an effort to highlight patient voices, we will be featuring the stories of several GP Warriors throughout Gastroparesis Awareness Month!

This week, we get to meet the incredible
Sabrina! 💚

After years of symptoms and inconclusive testing, Sabrina finally found answers at Mayo Clinic. Today, she not only continues to navigate life with gastroparesis, but also gives back by supporting others through a Facebook support group and volunteering with G-PACT. Her story is a powerful reminder that while GP may change our lives, it doesn't define who we are.

Thank you, Sabrina, for sharing your journey and inspiring others in the GP community!

07/29/2026

🎬 TikTok Tuesday 🎬
Today's trend: "Me getting ready for the Netflix documentary about..."

Mine? "...the organ that clocked out without notice." 😅

I promise there were no stomachs harmed in the making of this documentary… because mine already gave up 🤷‍♂️

To everyone living with an invisible illness: I see you. And if your stomach also decided to quietly quit, this one's for you. 🤍

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Boston, MA

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