Gastroparesis Pie Face Challenge

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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

10/07/2026

Our Tik Tok video of the week this week is for our pretty little liar fans out there..

Apparently I got a little too confident after feeling good for five minutes. 😂

Gastroparesis said, “Oh, you thought you were having a good day? That’s adorable.” 💀
Anyone else with a chronic illness know better than to get too excited about a good day? 😂👇

Monday MotivationLiving with gastroparesis can sometimes feel like your body has written a story you never asked for. Th...
10/05/2026

Monday Motivation

Living with gastroparesis can sometimes feel like your body has written a story you never asked for. The pain, nausea, unpredictable symptoms, food challenges, exhaustion, and setbacks can make it easy to believe that this is simply how your story
has to go.

But it doesn’t have to define the ending.

Some days, rewriting your story looks like pushing forward. Other days, it looks like resting without guilt, asking for help, advocating for yourself, trying something new, or simply making it through the day.
Gastroparesis may be part of your story, but it is not the whole story.

Your diagnosis does not get to decide your worth, your strength, your dreams, or what comes next.

So this Monday, remember: you can pause, you can pivot, you can start again, and you can keep believing there is more to your story.

10/04/2026

Psst… hey you!

Do you know the secret to a cure? 🤔

It’s simple… take the challenge & donate to G-PACT!!

Well, it may not be as simple as it sounds but seeing a “pie” face from Puerto Rico 🇵🇷 is awesome to see!!

10/01/2026

Of course we had to do our weekly TikTok to one of Taylor’s new songs!

Living with gastroparesis means sometimes your stomach treats food like a toxic ex… it knows it should let go, but apparently it’s just not ready. 😂💀

One meal can turn into hours of fullness, bloating, nausea, discomfort, and wondering why my stomach has decided to hold onto it for dear life. Meanwhile, I’m just trying to exist and pretend my digestive system isn’t actively plotting against me. 🫠

If you have gastroparesis, you already know the struggle. And if you don’t… just know that “let it go” is apparently not in my stomach’s vocabulary. 😂

Chronic illness humor is sometimes the only way to laugh at the ridiculousness of it all.

Monday Motivation Living with gastroparesis can sometimes feel like facing a dragon that nobody else can see. 🐉There are...
09/28/2026

Monday Motivation

Living with gastroparesis can sometimes feel like facing a dragon that nobody else can see. 🐉

There are days when eating is difficult, symptoms take over, plans have to change, and simply getting through the day feels like an accomplishment.

But maybe the point isn’t pretending the dragon isn’t there.Maybe it’s remembering that the dragon doesn’t get to write the ending. ❤️

Gastroparesis may be part of our story, but it doesn't have to be the whole story.

Some days we fight.�Some days we rest.�Some days we adapt.�And some days, putting one foot in front of the other is enough.

Whatever kind of day today is, you’re still here. You’re still trying. And that matters. 🥧💚

Happy Monday, Gastroparesis warriors.�One bite, one breath, one day at a time.

09/27/2026

Shock? ✅�Laughter? ✅�A dramatic “MY GOD!”? ABSOLUTELY. 🤣🥧
Yep… we think it’s safe to say this pie face was one for the history books! 😂

A massive shoutout to our friend from across the pond, Ian, for stepping up to the plate (quite literally) and helping us SMASH GP!! 💥🥧

09/25/2026

Happy (a very late) TikTok Tuesday! 😂🎥

Yes… it’s Thursday. I know. 😂 I apologize for being a couple days late! With school starting back up, this week got away from me. So, better late than never!

This week’s TikTok is for all my fellow gastroparesis warriors who know that sometimes “What did you do today?” is actually a VERY complicated question. 😂

Sometimes the answer is basically: rotated between the couch, heating pad, bathroom, and staring at the ceiling while waiting for your stomach to decide what it wants to do. Because apparently our stomachs process food like it’s stuck in airport security. 💀✈️

Gastroparesis can take so much out of us, even when it looks like we’re “doing nothing” from the outside. The fatigue, nausea, fullness, pain, brain fog, and unpredictable symptoms can make even a normal day feel
like a full-time job.

So here’s your reminder that resting is still doing something. Surviving a flare is still an accomplishment. And if your biggest achievement today was simply getting through the day, that counts.

09/16/2026

Gastroparesis really has a talent for keeping me humble. 😂

I can find a food that my stomach seems to tolerate, eat it several times without a problem, and start thinking, “Okay… maybe we finally figured this out!”

And then, out of absolutely nowhere, my stomach decides that same food is now public enemy #1. 💀

That’s one of the most frustrating parts of gastroparesis there’s no guarantee that something I tolerated yesterday will cooperate today. Sometimes it feels like I’m constantly trying to solve a puzzle where the pieces keep changing. 🫠

So if you’ve ever wondered, “But you ate that before… why can’t you eat it now?”—trust me, I wish I had a better answer. 😂
Just out here playing gastrointestinal roulette and hoping for the best. 🎰💀

Monday MotivationFor those of us living with Gastroparesis, this quote can hit differently.Because the load isn’t always...
09/14/2026

Monday Motivation

For those of us living with Gastroparesis, this quote can hit differently.

Because the load isn’t always something we can simply put down. It can be the nausea, the pain, the unpredictable symptoms, the exhaustion, the food struggles, the appointments, the cancellations, and the constant uncertainty of what our bodies will allow us to do today.

But maybe the goal isn’t to carry it all perfectly.

Maybe the goal is to carry it differently. 💚

Give yourself permission to slow down.�To rest without guilt.�To change your plans.�To celebrate the tiny victories.�To ask for help.�To listen to your body instead of fighting it.

Your Gastroparesis is part of your story, but it does not get to define your worth, your strength, or your future.

This Monday, don’t worry about carrying the whole week.

Just carry today.�
One moment. One breath. One small victory at a time. 🌱

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Boston, MA

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