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Thank you Nikki, I cant see trying to switch doctors again just to start all over. I am hoping for the best for all of us.

Thank you all for you responses, I guess I will have to wait and see what comes of next follow up's. I would imagine that since every ones symptoms are different it will not mater to try to compare to narrow down whats going on. I feel so lost and my family is suffering with me. I pray for all...

I figured a way to get the info in here from word this is my last visit has my EMG info and what was tested and I still have my first one that I will copy over after you see this most recent. I dont understand most of it only what she explains to me but I feel short on questions to my neuro...

There are 10 pages to my EMG study from the first one is there a way I can post it here as a pdf or something and cut out my personal info? My second EMG was given by my neuromuscular and i have no reading but a summary of what she tested I can copy the info and post it that way Dusty

I still at this moment do not know for sure if it is PMA or something that is a mimic of MND seems this is my third neuromuscular I have seen and she will not yet say what I have for sure. She has performed a battery of blood work that all shows nothing and EMG and NCS to see if any change has...

I was wondering if someone can help me with some questions here on PMA my first EMG suggests that spectrum of lower motor neuron only. I did have a second EMG that shows no changes in since prior 6 months ago. I am now at 16 months with no real diagnosis. I cant seem to find much info on...

Ok thank you Nikki J

I see no new posts here, I had some questions about PMA for myself if anyone can direct me around to the proper section to post. Thank you