How Many Of You Deal With Fibromyalgia Memory Loss? How Do You Deal With It Personally? How Has It Affected YOUR LIFE? | MyFibroTeam

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How Many Of You Deal With Fibromyalgia Memory Loss? How Do You Deal With It Personally? How Has It Affected YOUR LIFE?
A MyFibroTeam Member asked a question 💭
posted February 2
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A MyFibroTeam Member

Mine is getting worse. I sometimes don't even remember words we use daily, like furnitures, foods etc. I have to explain what the articles look like in order to got understood.

I have to apply for a job but it's taken my confidence completely.
My last job interview I couldn't even name the projects I've worked on.

I also type everything important on my phone which is exhausting and energy taking.

But this is our weird life, what could we do but acceptance :)

posted February 2
A MyFibroTeam Member

I always marvel how the medical profession use the "fibro fog" euphemism for what feels like intermittent dementia. We probably all get it with different severity and duration. It didn't seem to get much of any attention at all until long Covid came along with it's similar symptoms and larger numbers of people affected. It's devastating of course, especially because there is realization of what is happening to us, and I'm not sure that is always the case with true dementia. Now, mine begins and ends, but I wonder if one day, if it just won't
end. 💜

posted February 2 (edited)
A MyFibroTeam Member

I have journals. One for meds to document what and when I took them, one for important things, one for symptom tracking.....

posted February 21
A MyFibroTeam Member

I get that quiet a bit and affects my life when I do let people know that I forget sometime they get cross and don't believe me I have a diary I write things down in

posted February 18
A MyFibroTeam Member

Important things hand write them down .I find that typing tends to give me more fibro fog.

posted February 11

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