Mission: Cure (@Mission_Cure) header
Mission: Cure (@Mission_Cure) profile picture

A new model for curing disease, starting with pancreatitis.

New York, NY
Joined September 2017
Photo by Mission: Cure (@Mission_Cure)Photo by Mission: Cure (@Mission_Cure)Photo by Mission: Cure (@Mission_Cure)Photo by Mission: Cure (@Mission_Cure)Photo by Mission: Cure (@Mission_Cure)Photo by Mission: Cure (@Mission_Cure)Photo by Mission: Cure (@Mission_Cure)Photo by Mission: Cure (@Mission_Cure)Photo by Mission: Cure (@Mission_Cure)Photo by Mission: Cure (@Mission_Cure)
It’s Pancreatic Disease Awareness Month. Too often, people with pancreatic diseases like pancreatitis have to fight just to be understood and taken seriously. Mission: Cure works every day to change that.
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Only 2 days away! ⏰ Is there a mental health question about living with pancreatitis you haven’t found the right place to ask? Bring it to our free live Q&A with mental health experts Lara Govendo and Julie Wells this Thursday at 12 PM ET. 🔗 Register: buff.ly/1ny7kMV
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For many patients with pancreatitis, being truly listened to by a doctor or health care provider isn't a given, and it can shape everything from diagnosis to daily care. What's something a medical professional has done that made you feel heard? 👇💙
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Joshua Henderson, our Chief Cure Strategy Officer, presented Mission: Cure’s poster “Measurement Instruments for a Core Outcome Set in Pediatric Recurrent Acute and Chronic Pancreatitis“ at #PancreasFest2026! 📄 Read the poster: buff.ly/zh0yCl5
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“A good day for me looks like ______” Fill in the blank in the comments. 👇💙
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Where are we headed in the fight against pancreatitis? Explore our current strategies, learn about our 2026 projects, and see where we’re headed next. Explore the roadmap → buff.ly/Z7iDibd
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Researchers from the Engle Lab at the @salkinstitute grew pancreas organoids, tiny models of the pancreas made from patients' own cells, from 37 people with chronic pancreatitis. Learn more about organoids and what this research means: 🔗 buff.ly/StNEKBj
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#MondayMotivation Rest is not a setback. It's part of the process. With pancreatitis, rest isn't giving up or being unproductive; it's part of managing a serious condition, even when it doesn't feel that way. 💙
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“I wish more people understood ______” Fill in the blank in the comments. 👇💙
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On June 24, 2026, Ionis Pharmaceuticals announced that the FDA approved a new treatment to lower triglycerides and reduce the risk of acute pancreatitis in adults with severe hypertriglyceridemia (sHTG). 🔗 Read more: buff.ly/w0soLoL
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Ever wondered how clinical trials work, or what’s happening in pancreatitis research? 🤔 Join us for a beginner-friendly webinar, "Your Guide to Pancreatitis Research & Clinical Trials," on Thursday, August 27 at 12 PM ET / 9 AM PT! Register here: buff.ly/PlRnOWK
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Living with pancreatitis means constantly listening to your body, and making judgment calls most people never have to think about. How do you know when it's a rest day versus a push-through day? 👇💙
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On Thursday, August 27 at 12 PM ET, join Joshua Henderson, our Chief Cure Strategy Officer, for a one-hour live session on how clinical trials and observational studies work, and how you can take part. 🔗 buff.ly/pm9EtNr
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When you live with pancreatitis, success doesn't always look like big milestones. What's one small win you're celebrating today? Share it below. 💙👇
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#MondayMotivation Today doesn't have to be a good day to still be a meaningful one. Getting through a hard day is its own kind of strength, even when no one else sees you carrying it. 💙
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With pancreatitis, progress doesn't always look big or scream loudly. Sometimes it's getting through the day with a little more energy, taking a walk, or just feeling a little better than you did the previous week. What's a small victory you've celebrated recently? 👇💙
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That's a wrap on #PancreasFest26!💙 It's one of the few places where clinicians, researchers, patient advocates, and nonprofits are all in the same room with one goal: better lives for people with pancreatic disease. Thank you to @CAPERpancreas for another great event!
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“My hardest symptom to manage is ______” Fill in the blank in the comments. 👇💙
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Small acts of care can make a big difference on hard days. What's the most helpful thing someone has done for you during a flare? 👇💙 You can also tag them and share your gratitude and love!
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