Right to Know – Peer Support & Webinars for DCP, NPE, and MPE Community
Nationwide
Right to Know is a nonprofit focused on the needs of people with misattributed parentage experiences (MPE) — including donor-conceived people (DCP) and non-paternal events (NPE). They provide weekly peer-led support groups, mental-health resources, and expert-led webinars for their community.
Programs
- Weekly Peer-Led Support Group: Online community and connection group facilitated with mental-health professionals and community experts. Members share experiences, offer mutual understanding, and provide emotional support in a safe, confidential setting. Preregistration required; participant info is never shared.
- Webinar Series: Regular sessions featuring specialists on aspects of misattributed parentage, adoption, donor conception, and NPE experience.
- Access to mental health professionals: Curated list of therapists familiar with DCP, NPE, and MPE experience.
Who it’s for
Donor-conceived adults, people with misattributed parentage experiences, NPEs, late-discovery adoptees, and their loved ones. Virtual programming with participants across the U.S. and beyond.
More info and registration at righttoknow.us/support/