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View Full Version : Thoughts on Sjogren's



magistramarla
11-06-2011, 09:04 PM
Everyone,
This is a great article about living with Sjogren's and other AI diseases:
http://www2.timesdispatch.com/lifestyles/2011/nov/06/tdflair01-in-my-shoes-no-match-for-sjogrens-syndro-ar-1430674/#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

Angel Oliver
11-07-2011, 01:10 PM
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