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

06/02/2026

Here’s to another month full of raising awareness and laughs!

In this week’s Tik Tok Tuesday, I depicted how quickly those with Gastroparesis experience bloating.

One bite, and all of a sudden, you’re a bowling ball 😅

Living with gastroparesis often means spending so much energy managing symptoms, appointments, medications, and daily re...
06/01/2026

Living with gastroparesis often means spending so much energy managing symptoms, appointments, medications, and daily responsibilities that self-care can feel like an afterthought. But your health, your well-being, and your needs matter too.

Self-care doesn't have to be elaborate. Sometimes it looks like resting without guilt, staying hydrated, preparing safe foods, setting boundaries, or simply giving yourself grace on a difficult day.

This week, remember that taking care of yourself isn't selfish, it's necessary. You deserve the same compassion and care that you so freely give to others💚

Living with gastroparesis comes with challenges that many people never see. From canceled plans and unpredictable sympto...
05/30/2026

Living with gastroparesis comes with challenges that many people never see. From canceled plans and unpredictable symptoms, to the daily balancing act of managing food, medications, and energy levels, there’s so much happening behind the scenes.

Today, I want to hear from YOU! 💚

What’s one thing you’d wish
more people understood about living with Gastroparesis?

Share your answer in the comments below!

05/26/2026

✨ Tik Tok Tuesday ✨

Sometimes living with Gastroparesis feels like a full-time job with no reward.

You try the “safe foods,” eat smaller meal, take the medications, track symptoms, avoid trigger foods, stay hydrated… and somehow you can still end up feeling sick anyway. It can be frustrating putting so much energy into managing your symptoms just to have your stomach completely ignore the plan 😑

Gotta love the GP life 😅

Happy Memorial Day! 🇺🇸 ⁣⁣On behalf of the  , we’d like to remember those that have served and sacrificed their lives for...
05/25/2026

Happy Memorial Day! 🇺🇸 ⁣

On behalf of the , we’d like to remember those that have served and sacrificed their lives for our safety. ⁣

Thank you🇺🇸⁣

05/24/2026

Splish, splash, smash! 😆 🥧

We’re going into the vault on this fine Sunday to re-share an awesome video from 2023 in which mighty Tyler gave his dad one pie face, he’ll never forget 😂

05/19/2026

Hey, hey, hey It’s Tik Tok Tuesdayyyyy 😂

In this week’s episode I depicted what it’s like trying to convince Gastroparesis that one little snack won’t hurt anything…

Why doesn’t Gastroparesis ever feel our love for food the way we do? 😭💀

One minute I’m confidently eating and the next it’s spent by the toilet
Anyone else feel this?!

Monday Motivation Gastroparesis may challenge the body, but it cannot break the spirit. 💚This Mental Health Awareness Mo...
05/18/2026

Monday Motivation

Gastroparesis may challenge the body, but it cannot break the spirit. 💚

This Mental Health Awareness Month, remember to give yourself grace on the hard days and credit for every battle you fight silently. Your soul is stronger than your surroundings. 🌊

You know what they say…April showers, bring May.. pies?? 😳 🥧 As we work to raise awareness all year round, who’s ready t...
05/17/2026

You know what they say…

April showers, bring May.. pies?? 😳 🥧

As we work to raise awareness all year round, who’s ready to “spring” into action and help Smash GP?

05/12/2026

Oh we’re backkkkk 😁

Happy Tik Tok Tuesday!!

In this week’s episode I decided to depict one of the most alarming feelings those with GP have: feeling nauseous while out in public 😬

The second even the littlest wave of nausea hits in public, its a full out emergency 😭

Living with gastroparesis means constantly wondering if one small symptom is about to turn into a whole flare.

If you know, you know 😅💚

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