Vascular Birthmarks Foundation Forum - View Single Post - Lymphangioma of the leg
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Old 05-08-2013, 05:59 PM
JMR00 JMR00 is offline
Junior Member
Join Date: Aug 2010
Posts: 4

Are you part of a Facebook group for LM? They are pretty active and people (parents and people with LM) have lots of good advice. Search for 'Lymphatic Malformation Awareness Group'. There is another 'secret' group which does not show up in a search - if you post on the one above someone will be able to add to you to it.
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