Our 1-on-1 support program connects you with a trained parent volunteer who has been through a similar diagnosis. It offers a dedicated space to share what you’re going through with someone who truly understands, and allows for an ongoing, individual connection.

Group support is also led by trained parent volunteers but brings together multiple parents at a similar stage of the journey, creating a sense of community and shared understanding.

You can choose 1-on-1 support, group support, or both. We generally recommend joining a group, and suggest adding 1-on-1 support if this is your first baby, if there are additional pregnancy complications, or if you have a history of birth or pregnancy trauma.

When you register, someone will be in touch to set up a quick initial chat. This is a brief and informal conversation, over the phone or on Zoom, just to learn a bit more about your situation and what kind of support would serve you best at this moment.

All our groups are facilitated by trained and experienced parent volunteers who have already been through a CLM diagnosis.

No. All our peer support services are always offered free of charge.

All peer support sessions are kept closed in order to protect the privacy, comfort, and trust of all the parent participants. No outside observers are allowed. Please get in touch with us for other ways to collaborate or learn more about the experience of going through a congenital lung malformation diagnosis.