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 did have another thought, however. Have you been checked for thyroid problems? I believe some thyroid issues can cause swallowing and voice problems, which could be cyclical. You might want to check with your doctor. Best wishes to you.
I have occasional swallowing difficulties. I have an even bigger issue with GERD at night. I will try to sleep and acid comes right up my esophagus. I would rather drink water to keep it down than take too many omeprazoles.
I am post menopausal (yes, lucky me!). Your doctor could answer the question about hormones affecting YOUR symptoms. Hormones can make anyone feel bad. I also suggest looking on the internet to see if there are any articles or current studies on hormones and DM. I am not aware of hormones exacerbating the actual disease of DM. You do raise an interesting topic. I am interested in hearing if hormones have caused a direct problem with DM in anyone here.
Thank you for your post!
Yup, everyone has suspected my thyroid all along, but it's ALWAYS stone cold normal!
The hormone thing is just a pain, as It really really gets to me,, as does heat! When it's hot out I feel like an elephant is sitting on my chest- I can barely breathe and my hips and shoulders are mush! Does heat affect yall?
Heat affects me tremendously. My shoulders feel liquified almost, my heart starts pounding, my breathing becomes shallow and fast, and I have exacerbated sternocostal pain. It almost feels like I have pleurisy. It's just a burning, nagging pain in my chest.
Did any of you have a normal emg, but were diagnosed with muscle biopsy?? I have normal emgs- but I have obvious muscle wasting.. they all say it's something autoimmune.. (my ANA is always elevated).. The dr's haven't done a muscle biopsy, (I see neuro and rheumy), they don't think it's necessary, but I say they have done everything else, why not that?
momcoach
It is a little bit more than noticeable to me but I asked others they claim they don't see any change in my speech patterns. But I feel them I hear them and I know they are there; I have both PM DM.