My Nonprofit Reviews

My son has born with a rare deformity of his lymphatic system. He has been suffering from the effects of it for 14 years. The research and awareness the The Lymphatic and Research Network has done in just a few short years has meant everything to Lane and his family. For many years we had no known diagnosis.We have been able to try different treatments and see Doctors that specialize in Lane's condition that we would not have otherwise known. Lymphatic diseases are debilitating and the medical world is just now starting to understand them and that is mostly due to the work of this non profit.