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Join us on Tuesday, November 14th for Hope for HIE’s video support group session for extended family members.
➡️ Led by Hope for HIE’s licensed social worker, Haley, extended family members will be engaged in a space of healing and hope, no matter where their journey may take them, talking with others to build connections and support.
This support group event will be co-hosted with one of our peer mentors, Dee Talty. Dee is a retired high school teacher and mother of 3 who is currently raising her grandson who has many diagnoses along with HIE. She could not get through this without help and have been fortunate enough to have an amazing village.
➡️ This event will be hosted on a closed Zoom meeting experience and is scheduled for 10 a.m. EST.
➡️ Register using this link.
**Hope for HIE will convene a video support call for extended family members who are supporting a family member diagnosed with HIE. This support group is for extended family members ONLY to children diagnosed with neonatal or pediatric-acquired Hypoxic Ischemic Encephalopathy. By registering, you attest that you are connected to Hope for HIE’s support network as an extended family member. If you do NOT meet the demographic criteria to attend this group, we have many other options for support, and welcome you to reach out to Haley Thomas, LMSW, Hope for HIE’s social worker to get connected – email@example.com. Thank you for your interest & understanding!
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