Rebecca's Wish

Providing hope to children with pancreatitis

[Rebecca's Wish @RebeccasWishUS]

Here is Avery Winkelman, a Camp Hope camper walking you through ‘a day in the life’ showing us what a typical day looks like! We’re already planning for next summer.😀 #RebeccasWish #CampHope #PediatricPancreatitis #SummerCamp #NPF
https://t.co/p2i3XpgoXg

[Rebecca's Wish @RebeccasWishUS]

We were featured on @CBSEveningNews this week! So proud and inspired by our President, Christyn Taylor and Camp Hope, supported by the National Pancreatitis Foundation!

#CampHope #RebeccasWish #Inspiration #ChronicPancreatitis #SummerCamp

https://t.co/BARV1hhCsp

[Rebecca's Wish @RebeccasWishUS]

We're thrilled to have made national TV last night on @CBSEveningNews ! We're so grateful that others got to experience a glimpse into our mission and how we are providing hope to kids with #pediatricpancreatitis

[CBS Evening News with Tony Dokoupil @CBSEveningNews]

This mom started "Camp Hope," a free, week-long summer camp in San Antonio for kids with chronic pancreatitis, just like her 21-year-old daughter. The camp combines traditional activities with specialized medical care and support.

[Rebecca's Wish @RebeccasWishUS]

Check out yesterday’s segment that aired on @KENS5 news featuring this week, our incredible President, Christyn Taylor, and the Taylor family for continuing to bring this community together. #CampHope #Kens5News

https://t.co/VJ9bQ308GO

[Rebecca's Wish @RebeccasWishUS]

Carrying out our work in 30 states with the help of five top-tier physicians whom we have trained as #RebeccasWishFellows. We traveled to #Utah to highlight the impact and how we are making a difference nationwide as a nonprofit.
https://t.co/bjELdzZv1g

[Rebecca's Wish @RebeccasWishUS]

A video from our Fiesta party! Families share their experiences of a day filled with connection & support. From piñatas & egg hunts to delicious food trucks + face painting, this event was all about bringing our #pancreatitis community together. https://t.co/DE6uxJEkFN

[Rebecca's Wish @RebeccasWishUS]

We are a proud partner with Ariel Precision Medicine, a leading authority in the field of genetic testing, to provide a vital resource for families nationwide. A groundbreaking collaboration that revolutionizes the way families are supported & affected by rare + diseases.

[Laura Evans @lauraevansmedia]

How To Combat Medical Ignorance Of Rare Diseases. @RebeccasWishUS CEO and mom, Christyn Taylor, developed a kids' medical passport to help.
https://t.co/oN8mRYNfoD

[Rebecca's Wish @RebeccasWishUS]

Fiesta fun for families affected by #pancreatitis!✨ Nearly 200 pancreatitis families and helpers came together for an afternoon of piñatas, egg hunts, food trucks, dessert carts, face painting, crafts and more! Together, we've created a community of compassion and camaraderie.💖

[Rebecca's Wish @RebeccasWishUS]

Did you know that you can now access the Pediatric Pancreatitis Passport right from our website? This document is a game-changer for families battling pediatric pancreatitis. Learn more here: https://t.co/6NydMbWtMa

[Rebecca's Wish @RebeccasWishUS]

✨Calling all Volunteers and Medical Staff!✨Join us for an unforgettable summer! Camp Hope isn't just a week away from home—it's a haven where children can find comfort, support, and strength as they navigate the challenges of #pediatricpancreatitis https://t.co/gHRqKxRNUP

[Rebecca's Wish @RebeccasWishUS]

Our President Christyn Taylor was featured on @RadioHealthJrnl talking about strategies on how to combat the pervasive lack of awareness & understanding in the medical world regarding conditions. Listen to the full segment: https://t.co/Fy2V3pB7gB
#RebeccasWish

[Rebecca's Wish @RebeccasWishUS]

Get ready to make memories, forge friendships, and embark on unforgettable experiences with us! Camp Hope is back for another summer and we couldn't be more excited for June 10-14, 2024, at Morgan's Wonderland Camp in San Antonio, Texas!✨ Sign-Up now: https://t.co/gHRqKxRNUP

[Rebecca's Wish @RebeccasWishUS]

Myth Busted! Don't fall for the green peas hype when it comes to #pancreatitis. While they're a tasty addition to meals, they won't cure this condition. Remember, managing pancreatitis requires a comprehensive approach including medical guidance and balanced diet. #RebeccasWish

[Rebecca's Wish @RebeccasWishUS]

Thrilled to unveil the latest groundbreaking invention: the Medical Passport! A featured segment on @EWScrippsCo stations across the U.S., this digital document is a game-changer for children battling #pediatricpancreatitis and their families. Watch below! #MedicalPassport

[Rebecca's Wish @RebeccasWishUS]

Get ready to fiesta with us on 4/20! 🎉 Join Rebecca's Wish for a day filled with piñatas, spring egg hunts, games, treats, and amazing prizes! Don't miss out on the fun - RSVP by 4/16 via link! #RebeccasWish #PediatricPancreatitis #Fiesta #SanAntonio https://t.co/lbW4xsWATg

[Rebecca's Wish @RebeccasWishUS]

We're thrilled to announce our groundbreaking collaboration with Ariel Precision Medicine Together, we're changing the game for families affected by rare diseases. 💪
#RebeccasWish #ArielPrecisionMedicine #RareDiseaseAwareness #GeneticTesting https://t.co/nNJi2rn4CX

[Rebecca's Wish @RebeccasWishUS]

Camp Hope is back for the 3rd in-person session June 10-14, 2024, at Morgan's Wonderland Camp in San Antonio, Texas! Thanks to our amazing supporters, this opportunity is accessible to all + travel stipends. #RebeccasWish #CampHope #SanAntonio

https://t.co/2IhoxEZez5

[Rebecca's Wish @RebeccasWishUS]

With 450 attendees and 360 generous donations, we felt the power of our community coming together at last month's 3rd Fundraising Gala for #RebeccasWish. We raised over $500,000 - and donations are still pouring in for #pediatricpancreatitis patients! Another Gala success!

[Rebecca's Wish @RebeccasWishUS]

We're dedicated to shining a light on #PediatricPancreatitis advocating for those affected, and fostering a community of support. Let's empower each other and raise awareness for rare diseases like never before. #RebeccasWish #RareDiseaseDay