Yes, I am feeling this way more often than not. The fatigue and ensuing brain fog are the most disabling parts of autoimmune for me. I can muscle through pain butvit is very hard to function when you feel like the plug on the drain has been pulled and you are sitting on empty.
Hugs and prayers to everyone on here. Reading your stories let's me know I am not alone, as I do not personally know anyone else that has AS. Here is some of my story.
I am only 44 and have been battling the fibro since my early 20s and was diagnosed with the AS when I was 29. I am about to go in for my third back surgery and having a fusion.
The brain fog is awful, I can't think straight and have a hard time articulating what I want to say. I can look at someone and call them the wrong name even though I have known them for years. I lose stuff all the time.
My body feels broken, bruised, beaten and wrapped in barbed wire all the time. And the worst thing of all is people look at me and have no idea that I am constantly in pain from head to toe, I dont "look" sick.
I even had to edit this, as I put in the wrong words. Ugh.
Hi Angel, the brain fog and misuse of words i presume comes from the fatigue, which is brought on by inflammation and the body working to get rid of it. The humira is not the cause in fact hopefully it will get better once it reduces the inflammation.
I found out i have iron deficiency anemia so that wouldnt help but ive started taking iron and B12 this works tremendously! Its night and day with B12.
Please hang on,I do understand what you're going through!!!
So bad so I thought I must have had a stroke.The Lord has a perpus for you.Be a worriar .You Have helped others.
I completely thought I was alone in this!!! I'm amazed at how many other people are going through this too. I started mixing up the words right after my neck surgery. It gets so frustrating..my kids made fun of me not realizing how much it bothered me. And there are days when all I can do is lay down on the couch and try to watch TV..