ginger

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did I read somewhere that you should not eat/take    ginger. 

 i'm stage IV with bone mets, ER/PR+

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  • wishiwere
    wishiwere Member Posts: 3,793
    edited August 2008

    I've never heard that.  IN fact, I read here to use ginger for n/v after chemo and such.  I can handle the snaps and cookies and what not, but COULD not even stand the smell of it in tea.  But my smeller was way out of whack, more so than my taste buds :(

  • cp418
    cp418 Member Posts: 7,079
    edited August 2008
  • bomber410
    bomber410 Member Posts: 564
    edited August 2008

    I have heard nothing contrary to ginger.  In fact, over on the Lymphedema board, we've discussed ginger as an anti-inflammatory that may help relieve LE symptoms. 

    I certainly hope ginger stays on our list of good things.  I love it in every possible form.  You can even get chocolate-covered candied ginger.  Yummy!

  • shed
    shed Member Posts: 27
    edited August 2008

    thanks for all the replies.  I juice ginger in the morning with carrot, beetroot, garlic and celery.  i also snack on "snacking ginger'.  I too would hate to give it up.

  • althea
    althea Member Posts: 1,595
    edited August 2008
    I haven't heard that either, and I've been reading a lot this year about nutrition.  shed, I juice also and like to add a slice of ginger.  I've been juicing lemon, orange, apple, carrot, celery and cucumber with a slice of ginger.  It's my all time fave so far, but when I get friends to sample it, they grimace.  Gotta say, just thinking about your combo makes me grimace.  lol  ginger in juice is really great though.  We agree there. 

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