WelcomeLiam's Lighthouse Foundation was founded in 2009 after Michelle and Chris Schulze were inspired by their son Liam to make a difference in the world of Histiocytosis and continue the fight against this horrific disease that he no longer could.
HLH (Hemophagocytic Lymphohistiocytosis) is is not well known among many doctors, so it continues to go undiagnosed or misdiagnosed, and many children have died before a diagnosis could be made due to its rapid, fatal nature. Parents are their children's best advocates and are part of the team to provide our children the best possible chance for early detection and survival. Liam's Light House was founded to help light the way for awareness, education, funding, and a cure. |
In Memory of Liam
Learn more about Liam Christopher Schulze and how his mother is going great lengths to help others save their children from an untimely departure.
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Our Mission
Liam's Lighthouse Foundation (LLF), a non-profit, tax-exempt organization, was established to create and provide educational material and awareness about Hemophagocytic Lymphohistiocytosis (HLH) including Histiocytic Disorders, and to distribute unbiased, factual information to physicians, hospitals, and the community regarding this disease. Our focus is also to bring families affected by HLH/Histiocytosis together and offer support through a variety of resources. We aim to raise much needed funds for continued education of physicians and research to develop safer and more effective treatment methods and ultimately a cure. LLF is also dedicated to bring awareness to the community about the importance of becoming a blood and bone marrow donor.
Get Involved
We are stronger together and we need your support to move forward. Please join us in learning more about Histio, spreading awareness, participating in annual fundraising events, and subscribing to newsletters. Every little bit helps pave the way for additional research and ultimately a cure.
