Anyone here have lymphadema due to MS?
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I was dx'd 20 years ago with PPMS. I continued progression with my right side involvement. I have had lymphedema for many years on the right side, and recently developed some on the left due to large amounts of IV fluids. I need to use leg wraps to compress them during the day, and a lymphedema machine at night. I can no longer walk or bear weight to transfer.
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