Thursday, February 19, 2015
liplyp sisters introduction
My name is Sandra,my sister is Tammy we are creating this blog to share our discoveries,experiences, challenges, opinions,and journey with both Lipedema and Lymphedema. We have just begun this journey are newly diagnosed and will be learning as we go. We both are in therapy and are currently wearing wrappings on our legs awaiting delivery of our customized compression garments. These conditions are obviously hereditary but Lymphedema can be caused from trauma to the lymph nodes and or system due to cancer treatment or surgery. My sister and I both have primary Lymphedema which is inhereited, as we are learning we can see how many relatives must have had these conditions but were never diagnosed to our knowledge. These conditions are more common than most may realize but are not as publicized as other conditions. My (Sandra's) objective is to raise awareness with this blog and find support and encouragement throughout this journey. I will let Tammy make her own statement as to her objective. Please google Lipedema and Lymphedema to get a better and more thorough definition of these diseases, their symptoms, causes and available treatments. You may also want to print the information for your doctors benefits if you feel it applies to you most have heard of them but may not have not dealt with them. There is no cure but many treatments available to minimize the pain and suffering and research is being done to find cures. Sandra is older (51) and more advanced with the progression of the conditions than Tammy. The earlier you are diagnosed and treatment begins the better so please don't wait your mobility and quality of life are at risk, I will wait for Tammy's opening statement before going further.
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