!!!! The Launch of Our New Website !!!!
Lymphangiomatosis & Gorham's Disease Alliance
It is with great pleasure that we announce, effective immediately, the establishment of a new Foundation – the Lymphangiomatosis & Gorham's Disease Alliance (LGD Alliance), and the immediate transition to the new, permanent website for the worldwide lymphangiomatosis and Gorham's disease community.
Continuing the pioneering work began in Copenhagen, Denmark by the Veng-Petersen family, who have lost their little boy, Marcus, to Gorham's disease/lymphangiomatosis, the LGD Alliance is honored to host the new worldwide portal for patients and families, and our special partners: medical professionals, researchers/investigators, volunteers, and benefactors committed to helping find better diagnostics, improved treatments, and, ultimately, the dreamed-for cures.
Click now: http://www.lgdalliance.org
We are with you on the journey.
"Lymphangiomatosis & Gorham's disease Alliance is a not-for-profit foundation dedicated to patient support and advocacy for those affected by the rare diseases - lymphangiomatosis, and Gorham's disease."