I thought this was a place where we could go to talk and share our thoughts and feelings. I was just reading a responce to one of the discussion post and OMG some of you on here are just plain mean. I've been on here for oh I think 2 yrs now and I have never heard such mean spirited comments. I have Fibro. You know what I have not been tested for MS, or alot of other things that cuz the same symptoms. If someone wants to share their story with us, AMEN!! That is what we are here for. We get enough judgement out in the world from ppl we know face to face we should not have it on here, our place of refuge. If we don't like some things some one posted well why can't we just not post a comment and go on with our lives. And for a certain someone I am jjh1825, MY name is Jackie.
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I would love some guidance from anyone who has ideas to help my fibro pain. To outline my history, my nerve pain actually started after I was diagnosed with endometriosis in my early 20s. I had lower abdominal pain along with chronic joint pain for over 10 years. In 2015 I had a hysterectomy and no longer have abdominal pain which is amazing!! But I still have super bad chronic joint pain. ...
good morning and don't be deceived. Terror in this case was raelized the power went out so we slept through the alarm. The trash guys arriving woke us. On one hand, yay, sleep. On the other, utter terror as Hubby realized he's meant to be at work about 15 minutes after he wakes up. Whoops. And today? He haas to work in the office. WHich is 30 minutes away (not many miles, but town traffic,...