Polymyositis & Dermatomyositis Support Group
Polymyositis (PM) is a type of chronic inflammation of the muscles (inflammatory myopathy) related to dermatomyositis and inclusion body myositis. The inflammation is predominantly of the endomysium in polymyositis, whereas dermatomyositis is characterized by primarily perimysial inflammation.
I do feel like my accomplishments are one fourth of what I used to be able to get done in a day physically. Mentally, I am so DIRT SLOW when it comes to thinking, doing paperwork, or accomplishing tasks at my standards of acceptable level.
Today, my muscles in my arms are weak and filled with tremors. My legs are weak too. I do have some nausea present today that was thankfully not there yesterday.
I do think that everyone on this site deals with the same issues that you describe in your post. I do normally have an aversion to activity because of the on - off feelings of well then bad that alternate.
I would like to get a part - time job, but I do have concerns about the ability to be reliable. On a normal day, I need to lay down a couple times due to feeling bad. On days when I feel seriously bad, I need to lay down a lot. The seriously bad days are totally unscheduled and unpredictable.
I do not socialize much due to concerns that I can not commit to an event.
I do have similar feelings about the crappola through my veins. I have liver disease. If the liver disease becomes bilary cirrhosis then I would have literal crappola in the veins. HA! We shall see what the future holds!
I do not get depressed about my situation since I think that is a waste of time. I do use my time to try and study the bible more. Just thank The Lord for the testing opportunity, get back on the saddle and think about those scriptures. It takes a strong faith/trust in what you claim to share His happiness. Stay filled with The Spirit, I John 1:9 and be encouraged with The Word Proverbs 3:13. That is success.
I also try to find new things to include in my diet to help feel better physically too. When I really drag, I will juice and that helps.
You are not alone!
We seem to be expected to suffer our pain along with everything else regrding this illness alone and if we do come up with an answer to why or how, well so be it. No one seems to know anything regarding this illness or what we are suppose to do in treating it, but us. Now that I am no longer working, I guess I can do more research, but at this point I am too tired to even research anything, but maybe I will again sooner or later. Right now I am trying to control what I can and make plans for the future when I am not longer on STD. It seems that now I am getting calls and letters regarding my STD from my insurance company regarding possible repayment when I have just started to get any type of payment from them and my brain tends to shut down after a few hours in the morning so I can only focus on a few times at at time and the pain is one that I no longer want to focus on. I guess that I have accepted it as a given for now. In fact I just woke up a couple of hours ago after taking more pain medication. I am sorry that you are going thru this, but once you have found your way around it and come to terms with what works best for you, you will be able to function with it your way. No proofing for me.