This is a web site designed for people/kids with Lymphangiectasia; (Primary/Secondary) (Intestinal/ Pulmonary and/or any other version there of) and/or parents, family members and friends. This is a private party site and has been designed to give support and share information. The information given is from personal knowledge and/or knowledge found through research and/or information given from health care professionals. We are not in anyway medical professionals nor do we claim to be. We advise everyone to talk with medical professionals in regards to ones health and well being or the health and well being of a loved one. Our medical professionals are our allies. We welcome anyone with IL to join us on our web site and our forum. Please feel free to send a picture and tell us a little about yourself or your child, we would love to put you on our site. Or if you have any questions or information you would like to share with us please let us know. We want people to know that like many other disorders of the lymphatic system this disorder has know preference and is a random condition. There is research being done right now that will help with our fight to help our loved ones live healthier lives. So please help us to bring more attention to this disorder and other disorders of the lymphatic system so we can find better treatments for our loved ones. And someday a way to correct this disorder. |
| We have had many offers of donations to littleleakers.com and would sincerely like to say Thank-You for thinking of us. We are a private site and would like any donations to go for research, where the funds can benefit everyone touched by a Lymphatic disorder or disease. littleleakers.com fully supports the Lymphatic Research Foundation. Our goals are the same and without LFR the lymphatic system would still be an unsolved mystery here in the States. LFR is able to reach heights that we would not be able. Thank-You LFR! May others follow in you're foot steps. |