Connective tissue & cell walls are up to several hundred times thicker in people who have Lipedema. Again, there is NO cure at this time, so you can only manage it as best you can.
Hopefully, there will be a cure in the near future. I do not want to have this disease progress to the stage where I might lose mobility or have my legs amputated!
To find out more info about Lipedema (known as Lipoedema in the UK) and my personal journey with this disease, please visit my blog Lippy Legs & All at http://lippylegs.blogspot.com
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