
| This is a web site designed for people/kids with Lymphangiectasia (lym·phan·gi·ec·ta·si·a)(Dilation in the wall of a lymphatic vessel.); (Primary/Secondary) (Intestinal/ Pulmonary and/or any other version there of) and/or parents, caregivers, 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 in "our loved ones" section. Share your story or a loved ones story. Just send a few pictures and tell us your story or the story of your loved one and we will put in on Little Leakers. 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. |
| Camp is a blessing for kids with chronic illnesses. It gives them the freedom to be a kid. Help us support the camps that give kids a little freedom. |