The Weight of Lipedema
by Crystal Ellingsen
Over the previous three years before starting CDT, I had lost some weight through pain management strategies. I was in a pretty good place, although I did have to give up some of the things I loved, such as sports, vigorous exercise, projects, and pushing myself in loads of capacities in general. I’d been pushing through incredible pain for years, and my disproportionate/uncooperative body was more prone to injury.
I was naïve, no question. How does one know until they need access to healthcare that it is incredibly ill-equipped to help them? Not only was a very common women’s health issue being completely ignored and women are being mistreated and discriminated against, but even when I knew what was wrong, I found professionals who want to assist me manage my pain and manage my swelling, therapists especially, and they were very willing to learn, but quickly they discovered until the underlying issue of lipedema is addressed, there therapies are cannot be as effective and are definitely not long term solutions. I’m not afraid to be honest and ask the questions and still the system works to deny access to the treatments both conservative and surgical.
Never have I ever dreamed I would be seeking legal advice in Canada to get a much needed surgery. Never have I ever had to consider remortgaging my family’s home to secure healthcare. Never have I ever really questioned that fat people, myself included, lacked two things; knowledge of how to get thin and/or the resolve to follow through. Never did I ever think it could be anything other than my failure. But I did it! I cracked the code, I have lipedema.
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