Hi all, after 5 years of symptoms and 2 years of tests I’ve been told I’m depressed and stress is causing the symptoms. I don’t feel depressed or stressed so is this just an easy way out for the neurologist if he can’t think of anything else?
Sorry for what you have been told, can’t really offer any advice but it’s so frustrating.
If you feel this is wrong go back to your doctor
Thanks, I will go back to my gp. The neurologist said its not Ms because I could feel his fingers touching my arms and legs. I didn’t realise ms took away all sensation in the limbs.
Seems strange to me but I’m far from an expert!
That’s what I thought. Oh well, back to square one again!