Yep that's right,and the head contains the brain.Hallelujah to the proof that parts of the brain are showing changes in F.N.D patients.Mmm now let me see what could possibly do that,Gadolinium from M.R.I, Mercury from Amalgam fillings have you any others to add to the list.Yes i have been diagnosed with F.N.D and accepted it BUT decided to do my own research to find out the why,cos we all know there has to be one.Our bodies are amazing well fed rested and nourished they should last for many years without problems.Unless a traumatic injury occurs or born with an abnormality why then do we suffer from disease or illness.Toxins and heavy metals, vaccines, air food and water pollutants Pharmaceuticals personal body products,make up etc etc.No wonder my body is stressed then on top of all that childhood abuse rape trauma after trauma.Work stress family stress financial stress,sheesh it amazes me that i still walk this earth.So now to heal, do whatever it takes to be rid of all chemicals healthy eating de-stressing with meditation counseling, reduce the toxic overload.Anyone else on hear resonate with what i have written i would love to hear your thoughts.I am not responsible for what happened to my body but i am responsible to fix it. Namaste 
Nicola.
ITS ALL IN YOUR HEAD: Yep that's right... - Functional Neurol...
ITS ALL IN YOUR HEAD
Totally agree same experiences totally relate best wishes claire
What the hell are you supposed to do !!!
What do you mean ???
Its totally not in your head i think that personally they use our abuse and depression past experiences in our life that happen to many of us in all different ways as an excuse towards our fnd diagnosis personally thats my opinion but that's how I felt when I got diagnosed by my specialist they looked more in to my past and over medical history and problems that I suffer with I suffer with many more medical problems. Then the findings of my mri results and spinal result and medical problems rather then the symptoms and struggle worries and most of all .I felt like I wasn't listened to at all by my specialist... .we all struggle on a daily basis with fnd they also looked for ms in me but the lesions didn't fit the typical pattern as the doctor said ...I do have alot of lesions on the brain and lesions attacking the corpus callosum part of the brain does anyone else have these lesions when diiagnosed with fnd this would be good to know from anyone ??? As my normal gp dosent think this is typical with some one with fnd they then referred me to speacialist who did all usual checks they find this in me but all normally with other test except walking gait ect . I have more bad days that good lately I try to stay positive and strong for my family I simply got discharge and sent home with a website I am now seeing another speacialist which I have had to push for has well has my gps as things are getting worse.i wish u well u and I am more then happy to talk with you about fnd struggles and maybe past experiences if you find this may help you so that you do not feel alone maybe this may help as I am always happy to help share experiences and the struggles and symptoms we all experiences I hope this helps x
Best wishes claire
Thank mate so much appreciated but that is what the doctor said last episode!
What do you mean??? that is What the last doctor said
I’m done but in a good way
Severe leg vibrating 
My daughter has FND and CFS is there any doctor's out there who really no what doing ?
All Of Me
Who are we
