CDH Support

    Dealing with CDH is hard. It changes our lives forever. Grieving families mourn always. Families of survivors struggle and grieve over the loss of dreams. Family and friends aren't quite sure what to do. CHERUBS is run by volunteers - parents, grandparents, survivors and medical care providers who have personally dealt with Congenital Diaphragmatic Hernia. We haven't read it in a book or on a blog - we have personally lived it and when we say that we understand, we truly do.  

Expecting Parents

We know it's overwhelming learning that your child has Congenital Diaphragmatic Hernia. You're not alone. CHERUBS is here to help you through your journey.

Expecting Parent Resources

Grieving Parents

CHERUBS offers grieving parents a safe place of support where we understand what a broken heart feels like.

Grieving Parent Resources

 

CDH Survivors

CHERUBS has the world's largest long-term database, as well as a wealth of information and support through our over 3000 members.

Survivor Resources

Honor Your Cherub

Positive ways to honor your cherub's memory and ways to help other CDH families as well.

Honoring Your Cherub

 

 
Join the Angel Club and make a monthly or annual donation in honor or in memory of your cherub.

Donation Amount Options
In honor or memory of who?