The Lymphatic Malformations Alliance's Peer-to-Peer Program connects individuals affected by complex lymphatic anomalies (CLAs) and isolated lymphatic malformations (LMs) with others who understand the journey firsthand.
Whether you're an adult (18+) living with a CLA or isolated LM, or the parent of an affected child, you'll have the opportunity to connect with a peer who has shared similar experiences. Our program provides a supportive space to ask questions, share experiences, and find encouragement from someone who understands the unique challenges of living with a rare condition.
The program is open to participants worldwide.
By completing our Peer-to-Peer Matching Form, you'll be matched with an individual or family who shares a similar experience based on the information you provide. Whether you're looking for a one-time conversation or an ongoing connection, the relationship is guided by your comfort level and mutual preferences.
Before signing up, we encourage you to review our Program Guidelines. These guidelines help create a respectiful, supportive, and positive experience for everyone by outlining expectations for confidentiality, sharing personal experiences, and respecting each participant's unique journey.
If you have any questions or need assistance, we're here to help. Please contact the Lymphatic Malformation Alliance Support Team.
Thank you for being part of our community and for helping ensure that no one has to navigate a lymphatic malformation journey alone.
