Rheumatoid Arthritis Support Group
Rheumatoid arthritis is a chronic, inflammatory, multisystem, autoimmune disorder. It is a disabling and painful condition which can lead to substantial loss of mobility due to pain and joint destruction. The disease is also systemic in that it often also affects many extra-articular tissues throughout the body including the skin, blood vessels, heart, lungs, and...
Maybe it is worse when the meds and aging are combined. In that case, not much chance for me LOL. I have a calendar on the wall and a diary in my handbag and make sure both are the same. I also keep a small book in my handbag to jot things down, such as Things to do today, Bills to pay, Questions for various doctors etc etc etc.
I also think it is like the fuzziness and fog. Sometimes what I actually say is not what went from my brain, almost like it is not processing correctly. I might add, it drives my husband crazy.
Do remember, though, Suzi that between the lady mentioning it and now, you've been travelling and done many things that have taken precedence.
Don't let it bug you. Just smile and blame the "evil meds" you have to take for RA.
Love
Angel
Conversations only kinda remember most of the time, I write down anything I think I might need to remember. I have started a diary of sorts, to keep track of my life, so I remember why I did this or that, or even that I did it.
But I also tell everyone that my memory is shot, and blame it on Fibro. People are more willing to believe that memory issues are a result of fibro than people are to believe my arthritis makes my memory bad. And it boils down to the same thing, I try to make my memories and thoughts recall-able by writing them down
So , no help, I guess, but no, you're not the only one! My memory was never sterling, but it's not getting any better!
In all seriousness, my memory is shot. I live in a constant fog!! I blame the RA, the RA meds, and my med I take for trigeminal neuralgia.
I don't think any one of us is alone in this fog...but my headlights sure are getting dim!!!!
Matthew
Best wishes
Roni
I play a lot of puzzle games and read. On days I'm not feeling well or have the Mtx, I watch really bad TV and notice my brain feels like mush. On those days, I find myself just sitting in lala land. I snap out of it by the second day. But I write stuff down on a calendar. And have reminder apps on my phone too. On Mtx days, I don't plan anything or the day after. I find on those days, I even feel overwhelmed if I'm given to much information. Mtx is baaaaaaad!
Lin
I guess it is in comparison to being on a 6-lane interstate at rush hour with everyone speeding along at 80 mph and I feel like I am on a tricycle pedaling as fast as I can, my legs are worn out, and I'm about to get run over!
I have been in college for the past 4 1/2 years (went back at 43 and have one more year to finish) and I know that just since being diagnosed 1 1/2 years ago my memory and concentration capacity has been greatly diminished due to pain meds and RA drugs!!
Sometimes I, too, feel like I want to just yell "slow down people and just give me a little more time to process this information!" :)