“Wait… What was I doing here?” Between 20% and 60% of lupus warriors battle lupus brain fog.
If you are battling lupus and find yourself feeling confused, fatigued, or forgetful you are not alone. Perhaps up to half of all Lupus Warriors experience a unique feeling of mental fogginess. These symptoms are collectively known as “cognitive dysfunction.” They can be very frustrating and may cause challenges in work and relationships.
It is import to identify if you or a loved one are experiencing lupus brain fog so you can know what to expect and create a plan to cope with the issue.
I was just telling my husband I feel like I’m in a fog some times
I try to put things back in there regular place immediately after using them because if I don’t frequently I never find it or don’t find it until I no longer need it or have replaced it.
I find myself unable to call the word I’m looking for to describe something. It can be something simple and in a conversation I will forget several common words that I would normally just automatically call to memory on any other given day.
This is me, I forget my dogs names, street names, random words during a conversation. Its embarrassing
Feel very alone with my brain fog,;
I was diagnosed an undiagnosed
Now have breathing problems seeing a second cardiologist Friday, fatigued a lot just need to ignore the fatigue and go outside Sometimes. Today I feel wiped out, but will try as not moving my body is not good at all.
Brain fog; misunderstood by others
I’ll try one more time if I get a duplicate comet comet message it must be my brain fog!
I feel like I’m going crazy sometimes. I forget a words meaning, forget who people are, forget what I’m supposed to be doing. I feel so sorry for my family…
I know exactly how you feel! For years I thought I was going crazy.
Before I was diagnosed with Lupus, I had a family doctor that loved to prescribe Prednisone for any time I’d go see him. I recall telling him that I loved the Prednisone because it always cleared my thinking. I have felt like I’ve been in a fog for years.
Then after being diagnosed with Lupus, I began to realize the insidious nature of what it was doing to me.
But lately, it’s been getting worse, not better. I’ve been taking my medications, but I’m definitely going to have to talk to my doctor. It’s scary because this is beginning to affect my work.