Tracking my efforts to beat Myalgic Encephalomyelitis (ME), aka CFIDS, aka CFS

Tracking my efforts to beat Myalgic Encephalomyelitis (ME), aka CFIDS, aka CFS

Tuesday, December 11, 2012

An advent calendar, CFS style



6 comments:

  1. clever! how have you been doing?

    i'm hopeful...been over-doing so having pain...
    resting in Him...our sure Hope and the Hope of the world.

    ReplyDelete
    Replies
    1. I've been so-so, thank you for asking. Not quite as well as October and November, because I too have been over-doing it a little, but not as bad as pre-October.

      We have to both remember to take it easy as we heal I guess, right? Hope you pull out of your pain cycle soon.

      Take care

      Delete
  2. Thank you. Yes, I told a friend after my first visit with Dr. C that my priority for the 2 years is to do all I can, given this new treatment, to get as well as possible. i already need her to remind me of that! With 7 grandkids, and feeling so much better some days...I am my own worst enemy sometimes!

    I pray you are able to enjoy your family, especially during this Christmas season...and for wisdom in your activities.

    cris

    ReplyDelete
    Replies
    1. 7 grandkids....that will keep you active alright! I know what you mean about being own worst enemy sometimes.

      And thank you for the kind words. I wish you and your family the same this Holiday season.

      Delete
  3. ha ha - love it! Perfect - mine would be my Imunovir blister packs.

    Sue

    Live with CFS

    ReplyDelete
    Replies
    1. Ha! Too bad we don't get Christmas at the end. Just another pack. lol.

      Delete