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    Lymphadema

    Anyone here have lymphadema due to MS?

    #2
    My friend has lymphadema but not MS. Have you been told it could be due to MS?

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      #3
      My Nurse Practitioner granddaughter says it is due to immobility of the right limb. I have spms and hard to walk. I have Dr appt next Tuesday. My right side was paralyzed when I was dx 26 years ago. How is your friend doing with it.

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        #4
        My friend is doing fine. It has been many years now. At first he was self conscious about the size of one leg but I think he got used to it.

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          #5
          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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            #6
            I went off all salt, use Morton's lite salt and that helps a lot

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