Expanding Our Reach. Strengthening Our Impact.
LGDA is now the Lymphatic Malformations Alliance. Discover the next chapter of our mission.
Patients/Caregivers
Meet Emily who is living with Gorham Stout Disease. She was diagnosis before her 19th birthday. She shares her mental health experiences and solutions to help others living with a complex lymphatic anomaly.
Emily story was included in our Mental Health Webinar Series on September 21, 2023 with Dr. Kathleen Bogart.
Together, patients, families, clinicians, and researchers are changing the future of lymphatic malformations.
Your donation helps make that progress possible.
