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action or later. Please see Debugging in WordPress for more information. (This message was added in version 6.7.0.) in /home4/robohara/public_html/www.LegsLikeMine.com/wp-includes/functions.php on line 6114Greetings!<\/p>\n
I get this question several times a day and decided it’d be more helpful if I wrote the reply out fully for everyone to see and then I can just share the link.<\/p>\n
So you think you have lipedema?\u00a0 There is help, welcome, and you are not alone!\u00a0 The first step is to check symptoms.\u00a0 I recommend looking at the professionals’ pages, like this one from the Lipedema Project<\/a><\/strong><\/span>, to get a comprehensive list of lipedema symptoms and details of the condition. This includes the different types and stages of lipedema, and will help you see pictures from their extensive galleries to use as a guide.<\/p>\n <\/p>\n If you’ve done some research and you’re showing symptoms of lipedema, your next step is to get to a doctor for diagnosis.\u00a0 Most doctors receive very little training on lymphatics and may not be familiar with the condition.\u00a0 However, I recommend starting with your normal doctor with two things in hand:<\/p>\n If your doctor will diagnose, your next steps are to find an occupational or physical therapist, familiar with lipedema, who can help you with manual lymphatic drainage and compression fitting\/training.\u00a0 If they cannot diagnose you, your next step is to find either a veinous specialist (they receive more training in lymphatics) or an actual doctor who is a lipedema specialist.\u00a0 See the provider directory<\/a> <\/strong><\/span>that the Lipedema Project maintains.<\/p>\n Things you can do on your own, now:<\/p>\n\n
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