Hi friends! I was just thinking about MLD this morning while I was in the bathtub and I began to wonder if I’ve shared info on this for my followers who may be early in the learning process about managing their lipedema. At this point in time, self care is by far the biggestContinue reading “Manual Lymphatic Drainage – Where do YOU MLD?”
Tag Archives: mld
There are Amazing Professionals Providing More info on Lipedema than Ever – Meet Kathleen Lisson
Hi friends! I want to share with you an amazing resource to the lipedema and lymphedema communities. If you haven’t met her yet, please meet Kathleen Lisson, a certified massage and lymphedema therapist, who’s written numerous books that will aid in our treatment and self-care. And even better, she shares SO much information that willContinue reading “There are Amazing Professionals Providing More info on Lipedema than Ever – Meet Kathleen Lisson”
My New Book, Aqua Therapy for Lipedema and Lymphedema is Available!
Link to buy it: https://amzn.to/3z8DxYF Hi friends! Whew! I did it! Just in time for swimming season, Aqua Therapy for Lipedema and Lymphedema is out on Amazon! After some late nights of editing and reviewing I’ve finished the aqua therapy book and I’m really excited to share what I’ve learned with you all! It turnsContinue reading “My New Book, Aqua Therapy for Lipedema and Lymphedema is Available!”
Does your Face Puff Up When You Get a Lipedema Flare? I’m Doing a 30 Day Test to See if I can Un-Puff
Hi friends! I’ve noticed lately that when I get a lipedema flare up (which to me, looks like significant swelling and nighttime pain, sometimes even with added dislocations in the knee, ankle and hip), that my face also gets puffy. I started doing some research in medical stuff and learned how the lymph nodes ofContinue reading “Does your Face Puff Up When You Get a Lipedema Flare? I’m Doing a 30 Day Test to See if I can Un-Puff”
Celebrating the Medical Professionals Who are Dedicated to Making Lipedema Patient Lives Better
Hi friends, If you follow many of the facebook support groups for women with lipedema, you’ve probably seen a new movement in our ranks: We are doing writing campaigns to educate doctors and clinicians who have not responded well to our requests to diagnose or discuss lipedema. In the first weeks alone, I completely depletedContinue reading “Celebrating the Medical Professionals Who are Dedicated to Making Lipedema Patient Lives Better”
