Happy #PrideMonth! 🏳️🌈
Inclusive healthcare means creating environments where every patient feels respected, heard, and empowered to seek care.
We're proud to support LGBTQ+ members of the pancreatitis community and remain committed to advancing care that works for everyone.💙
Living with pancreatitis can mean holding a lot of mixed feelings at once, sometimes all on the same day. There's no "right" way to feel. It’s a bit like learning to surf the rough waves!
Which one resonates the most? Or, you can also share your own mixed bunch👇💙
Some days, just getting through is enough. But if you've found something that helps, a small reset, a comfort, a routine, a ritual, a prayer, we'd love to hear it.
What do you do to recharge on or after hard days? 👇💙
If you've ever tried to explain pancreatitis to someone who doesn't have it or doesn’t get it... here’s your validation card deck.
Swipe through and tag someone who genuinely gets it. 💙
If you or someone you love has been affected by pancreatitis, we'd love to hear your story too. Sharing your experience can make a real difference to someone who's just been diagnosed or feeling alone. 💙
Share your story: https://t.co/PHXXyf6Hb4
Amanda spent months being misdiagnosed before learning she had chronic pancreatitis.
“I found Mission: Cure while I was in a very dark place during my battle with pancreatitis. It helped knowing that I wasn’t alone"
🔗 Full story here: https://t.co/iJSMsDVTE5
Reminder: our free pancreatitis nutrition webinar is this Wednesday, May 13th.
🕛 12:00 PM Eastern | 11 AM Central | 9 AM Pacific
💻 Free to attend. Registration is quick. Recording sent upon registration, even if you can’t attend live.
Register now: https://t.co/3wEtoVpsEi
May is #MentalHealthAwarenessMonth 💚
Living with pancreatitis doesn't just affect your body — it affects your mind, your relationships, your sense of self. This month, we're sharing new mental health resources for people living with pancreatitis.
On May 13th, we're bringing in Kevin Walton, MS, RDN, a registered dietitian who specializes in working with patients with pancreatitis.
Register now: https://t.co/3wEtoVpsEi
Diet advice for pancreatitis is complicated.
On May 13, Kevin Walton, MS, RDN (Mass General) is joining us for a free webinar on getting the right individualized nutrition support for your condition
🔗 Register here: https://t.co/3wEtoVpsEi
Just two days away! 💙
Thursday night, pancreatitis patients, caregivers, families, friends and researchers come together for the Moments of Hope Gala — free, virtual, and open to everyone.
We hope you join us: https://t.co/PFZG1Teirn
Living with recurrent or chronic pancreatitis can change your daily routine in ways people don’t always notice: meals, energy levels, plans, pain management…
What’s one change you’ve had to make in your day-to-day life to accommodate your new needs?
What’s one small win you’re proud of lately?
Some days, getting through is the win. Other days, it’s something a little more. Either way, we’d love to hear 💬
💙 We made our gala virtual for a reason. Mission: Cure’s community spans the country and the world, and with pancreatitis, plans aren’t always predictable.
Save your spot → https://t.co/FwNBL2LD8M
Our annual gala is back, and registration is open! 🎉
Join us Thursday, April 30 at 8:45 PM ET | 5:45 PM PT for Moments of Hope, Mission: Cure's free virtual gala bringing the entire pancreatitis community together for one night.
Register today → https://t.co/8uQ6dsU5FO
#MondayMotivation: Mondays can come with pressure to “reset” or “catch up.”
But with pancreatitis, some weeks start with symptoms, fatigue, appointments, or just trying to feel okay.
If today is a “keep it simple” day, you’re not failing, you’re listening to your body. 💙
Progress isn’t always linear, it curves, dips, and doubles back.
With pancreatitis, you can do everything “right” and still have a rough day. You can feel steady for a while, then get knocked off course. That doesn’t erase what you’ve learned or how far you’ve come.
We're sharing an opportunity for people living with IgG4-related disease (IgG4-RD) or Type 1 autoimmune pancreatitis to contribute to research by sharing their experiences.
👉 Take the survey: https://t.co/Vl3Y5u2QeK
A reminder for anyone starting the week feeling tired.
Rest isn’t a reward; it’s part of taking care of yourself.
If you needed a gentle nudge to go slow today, consider this is it. 💙
Drop a 💤 if your body is asking for a slower Monday.
Today is Rare Disease Day.
“Rare” should not mean harder to diagnose, harder to treat, or harder to be taken seriously.
For everyone navigating chronic pancreatitis and other rare conditions, you deserve:
• Timely answers
• Coordinated care
• Meaningful research investment