What We Do

At the core of our organization is the desire to help families struggling with the emotional downfalls associated with childhood pancreatitis. We offer support to parents through various outlets including, public and private support groups, links to personal and professional blogs related to “living with pancreatitis” as well as providing contact information for pancreatic specialists and hospitals across the country.

We believe in having the most up-to-date information so that families can make informed decisions regarding the care of their child or loved one. Families just like yours share their stories, dreams, emotions and love for the world to see. We believe in the H.O.P.E. (Hold On, Pain Ends) testament and we support each other every step of the way.

Why We Do, What We Do

Because no child should have to endure the debilitating pain associated with pancreatitis. And no parent should have to watch helplessly as their child suffers through such unbearable pain as that associated with pancreatitis.

“It is not enough to sit back and go through the motions to help your children. There are other kids, just like mine, who are suffering and who need help. Their parents just don’t know where to find it.” – Founder & President, Sheila R. Williamson