For patients and family
How can we help you?
Have you or has a family member been diagnosed with lymphangiomatosis or Gorham’s disease? You must have a million questions. Or none because you don’t know where to start. We are here to help you and your family finding the support you need, providing you and your doctors with knowledge and to have hope for the future.
Please take a look at our website or send us an email at firstname.lastname@example.org. We will offer you the best help we can.