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Lymphedema Community - Support and Information for Lymphedema Patients
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  • Susan Smith
    Susan Smith is now friends with Marge Naab.
    • October 9, 2016
  • Sue Kenyon
    Sue Kenyon is now friends with Susan Smith.
    • August 7, 2016
  • Susan Smith
    Susan Smith Is there a forum somewhere?  I see the live chat, but I never seem to be on when other people are.
    • July 14, 2016
    • Susan Smith
      Lymphedema Community Staff Hi Susan,

      People certainly do visit the site at random times throughout the day. Most users have had success in meeting other users by sending a friend request. Once friends, they can message each other privately and share more personal information....  more
      Hi Susan,

      People certainly do visit the site at random times throughout the day. Most users have had success in meeting other users by sending a friend request. Once friends, they can message each other privately and share more personal information. Hope this helps.  
      • July 16, 2016
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    • Susan Smith
      Susan Smith So there is no forum area for open discussion?
      • July 16, 2016
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    • Susan Smith
      Lymphedema Community Staff There is general chat and users can create chat rooms which are essentially live forums.
      • July 16, 2016
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  • Susan Smith
    Susan Smith has just joined the community. Say hello!
    • July 10, 2016
    • Susan Smith
      Lymphedema Community Staff Welcome!
      • July 10, 2016
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Info

  • Classification Other
  • (detail) Other
  • Gender Female
  • Last Name Smith
  • First Name Susan

Friends

  • Sue Kenyon How do you know the amount of compression you need, I've just had a PT tell me I need to up my compression to 30-40 and use a flat stocking. I was in 20-30 Median sheer and comfort thigh high stockings. I just had a lymph node transfer and a bypass if that matters in the compression choice. I tried the Median forte in 30-40, and I can't keep them from rolling down my thigh and they're like impossible to put on. I worked up quite a sweat!!  
  • Marge Naab My lymphedema is in my left arm and I have carpal tunnel on my right hand. I need surgery but they can not give IV in left arm. My doctor said there is IV in right arm to give me nova cane and left arm would have IV to put me to sleep but because of lymphedema I have to have IV in my foot. Has anyone else ever have this done because of surgery? Would love feed back!
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