Hope for HIE – Hypoxic Ischemic Encephalopathy Hope for HIE – Hypoxic Ischemic Encephalopathy

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Early Fall eNewsletter

Early Fall eNewsletter

October 8th, 2021

Our Early Fall Newsletter is now available! Topics: NICU Awareness Month wrap-upLeadership UpdateFocus on HIE Research

Board of Directors Change

Board of Directors Change

October 8th, 2021

After her tenure of serving her two year term, we want to express our most sincerest thanks to Jennifer Kegyes for her dedicated service to our Board of Directors. During her tenure, Jennifer created extensive changes in our organization by implementing the Newly Diagnosed Family Box program (you may remember seeing a photo of a stuffing party she had taking […]

Call for Board of Directors Members

Call for Board of Directors Members

September 17th, 2021  | News

In continually planning out organizational leadership, we are looking to learn the talents of our community, and those that may be interested in serving the organization on our Board of Directors lending various areas of expertise. Hope for HIE’s Board of Directors has a long standing tradition of being made of HIE parents to guide the growth of our organization. […]

Hope for HIE collaborates with Families’ Bridges to Caring Hands

Hope for HIE collaborates with Families’ Bridges to Caring Hands

September 14th, 2021  | News

As we work to improve care, communication and connection for families facing HIE in the NICU, we are excited to share that we are expanding our reach by sharing access to our educational materials and support connections for HIE families through Families Bridges to Caring Hands. About Families Bridges to Caring Hands Families’ Bridge to Caring Hands ® is designed […]

Hope for HIE Recognizes NICU Awareness Month

Hope for HIE Recognizes NICU Awareness Month

September 13th, 2021  | Advocacy

Every September, we come together with hundreds of other support organizations, partners, and professionals to recognize NICU Awareness Month. We work to share stories of our community, and focus on advocacy to improve care, communication and connection for our HIE families. Historically, the NICU has been painted as just a place where premature infants go, but we know that half […]

SHARE YOUR HIE STORY

One of the ways many HIE families work through the trauma of their journey is sharing their story to help other families who will find us in their own HIE journey. We hope you’ll take a few minutes and share yours with us. We’ll publish it to our Family Stories blog!

Share Your Story

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