Our FibroFog moments!
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Latest Activity: on Wednesday
Started by Carol Davidson. Last reply by Jackie Foster Dec 1, 2010. 1 Reply 0 Likes
I want to thank you for writing the fibrofog article and symptoms. I showed it to my family and emailed it to my friends because it is such a hard thing to explain. It along with all the spasms and…Continue
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Comment by MikefromsouthNZ on April 9, 2012 at 7:54pm Hi Guys.. I haven't been here for some time now but I want to share my advice about fog.. The worse my fog got the more I became withdrawn and isolated from all friends and even family. The secret I found was to forget about the fog no matter how bad it was, and focus more on the abilities I'm still able to do well.. Somehow by pure accident my fog started to go.. It still sneaks up on me but I now don't let it worry me as we all have a bad day now and then.. I feel the more comfortable and confident I believe in myself, the better my friends and even new colleagues accept me, fog and all..
Have as much brain time-out when you need but try not to worry of when the fog will attack again, just to see if what I've said can help you ? It isn't rock solid proof nor a scientific fact but it helped me, so it may also help you too..
Take care - Mike
Comment by Suzanne Gergel on April 9, 2012 at 3:08pm Fog is a big one for me . It started long ago with forgetting , now it's i open my mouth to speak , be in mid sentence and the next word is gone . Or it's words deleted from my brain that I no longer can spell . I frequently sound like a fool when talking lol not fun
Comment by Joanie on October 28, 2011 at 6:21pm
Comment by Chris on August 3, 2011 at 10:55am Happy Aussie,
I know what you mean about feeling like you have Alzheimer's. My fog is really bad right now and that isn't a good thing considering my new school year starts in about 2 weeks. I am a teacher! That makes it hard to remember my schedule, my students' names, and meetings. I even forgot about using this message board until someone sent one in the other day and it sparked my memory. I hope I can keep up with it now.
Hearing about you all is uplifting. I got diagnosed 3 months ago after 28 years of pain. I'm going through an increasing amount of fibro fog where I can't remember most things like names, directions, places, where I've been, school dates etc....It's very hard and my family are quite worried about me - feel like I've got alzheimers and not fibro!
I also had to go into hospital to be "snowed" - enforced into a coma every night for a few days as my insomina was so bad I got 1-2 hours sleep a night for a few years and couldn't carry on. WIth the right combination of sleeping tablets it seems to have re-booted the system thank God!
I never lose hope of a cure or at least better medication to help us, but support plays a huge part.
Take care
Comment by kmccann on August 2, 2011 at 11:35am
Comment by Chris on August 2, 2011 at 9:53am
Comment by Diana Parker on August 2, 2011 at 9:01am
Comment by MikefromsouthNZ on August 1, 2011 at 6:29pm oopppps, can see my fog is bad today, "Just as your booties" need to rest to function well, so too do our brains but even more so with having fibro and fog....
Should read - "Just as your body" need to rest to function well, so too do our brains but even more so with having fibro and fog....
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