← Return to Lymphedema - new support group: Let's connect

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@lilypilly

I think it is a wonderful idea. I have lymphedema of Mt face and neck from TO gue cancer. I am in therapy for it. It has also affected my tongue resulting on slurred speech. It has had a big affect on my day to day life. I have difficulty communicating so going out even to shop is rare.
I am swollen in the mornings that it takes 4 hours to get going.
So I am up very early each day.
I would love to be a part if a non breast cancer Lymphedema group.

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Replies to "I think it is a wonderful idea. I have lymphedema of Mt face and neck from..."

Have you tried a lymphedema pump? I use one made by Tactile Medical. My surgeon prescribed it and insurance paid for it. I also do massage. But the,pump really helps. I will try and find a link and post it.