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Thread: Thoughts on Sjogren's

  1. #1
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    Default Thoughts on Sjogren's

    Everyone,
    This is a great article about living with Sjogren's and other AI diseases:
    http://www2.timesdispatch.com/lifest...74/#fbcomments

    The author used to post here on WHL, but she hasn't been here in a while. Many of us deal with Sjogren's and have Lupus and other AI diseases overlapping.
    Kelly did a great job of writing about how we all feel.
    Enjoy!
    Hugs,
    Marla

  2. The Following 2 Users Say Thank You to magistramarla For This Useful Post:

    Nonna (11-07-2011), ritzbit (11-06-2011)

  3. #2
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    Default

    Thanks for that Marla,she did do a good job.For me i have plurisy a few times and on my second chest infection in a few weeks.Pleurisy hurts allot when i breath and breathless when i talk too much or walk.Srjogrens isnt a pleasant thing to have at all.Thats on top of difficulty swallowing dry eyes constant dry mouth,zero energy and basically feeling poo!
    How are you Marla?
    Love
    Amanda.xxxx
    I am still here,just been on new meds so unable to function like i used to.I will pop back,just know im thinking of you all and hoping you are keeping on keeping on.xxxxxxx

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