Welcome to HoPE
We welcome you into our fellowship of families affected by holoprosencephaly (HPE).
Learn MoreAbout Us
Families for HoPE, Inc. is a 501(c)(3) nonprofit organization formed to address the needs of families and children diagnosed with holoprosencephaly (HPE) and related brain malformations.
Learn MoreContact Us
This form is for requesting general information or establishing contact with Families for HoPE without registering in our Child and Family database.
Learn MoreAmbassadors for HoPE
Thank You for Your Support
THANK YOU 
THANK YOU for blessing other HPE families with your compassion, commitment and support every day. You help build a community that is a refuge for families who would otherwise face the journey of caregiving alone.
THANK YOU for supporting people in need overcome the challenges of raising a child diagnosed with HPE. Many have gained information, resources and added confidence -thanks to you.
Most of all, THANK YOU for giving to Families for HoPE. YOU make a huge difference to empower, support, educate, encourage, and advocate for holoprosencephaly families.
WE ARE BETTER TOGETHER! Please share with others and encourage them to make a donation of any amount to support families touched by HPE, during our year-end fundraising campaign. Every dollar makes a difference!
Ambassadors for HoPE
Two Vibrant, Young People with HPE Join Us as Ambassadors for HoPE
Families for HoPE, Inc. is honored and grateful to have two young people with HPE join the ranks of our organization’s Ambassadors for HoPE to help raise awareness of holoprosencephaly.
Ambassadors for HoPE
AMBASSADOR FOR HoPE – Kal-El Wright
Seventeen-year-old Kal-El Wright enjoys many things, including going to school.
Ambassadors for HoPE
AMBASSADOR FOR HoPE – Brianna Bixenman in Her Own Words
Hi everyone. My name is Brianna. I was born with lobar Holoprosencephaly.