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I believe you, at no moment I have told you you were wrong on all the post I have made, I think I am not the only one on the DIHALS section who simply ask questions. I have definitely understood the concept now, you can be sure of this. You can close the thread and delete my previous posts if it...

Okay, However, I know perfectly what a terminal disease is because I am Leukemia free and even if it is only a cancer, it is something serious but it belongs to the past now a long time ago. Now, there is a problem in front of me and I truly hope I will find the solution, anyway I stop to...

Thanks very much Wendy for your support, I am in a waiting room, a nutshell where it is extremely difficult to find the clue. I really appreciate all the support and answers the members gave me, it is a big help, believe me. I think you point the main problem between me and the doctors : I...

Nikki J, Yes, I meant TMS or triple stimulation transmagnetic which came back normal. I am in agony these days with my legs, again I don't want to diagnose myself but every test came back negative, except emg and my personnal knowledge of my body : I can't do normal tasks anymore. I am...

Tillie, Thanks for your care. I apologize for my numerous posts, but I can't trust my neuros who told me before there was nothing, now they say bfs, tomorrow maybe something else? I have to see the best als center in my country next month and I hope they can find a clue because I can't live...

Hi everyone I come back on the DIHALS because my symptoms are becoming worse day after day. I had to tell you about my TST, (very painful test by the way), which came back normal. Since 1 month now, I am suffering from constant twitchings (plus bodywide twitchings since 8 months) in boths...

Thanks Nikki J, I am trying to made up my mind, to live, to be in state of mind of "wait and see". This neuro I met was fine for the first time of my life (she was not french, maybe the reason). As you told me, it is transcranial Magnetic stimulation, she wants to test me to definetely put...

Hi, I wanted to post on my previous thread but it was closed. I had an another emg (5th) since the onset of my problems and it is the first time that I could ask questions and the first time that problems have been detected. The neuro who worked in a french als center before noticed...

I precise that I have noticed atrophy in my foot and my I would like to know what are the denervation potential. Is it related to twitchings of something else?

Yes, you are right. I would like to definitively fix those pains. Thanks a lot