So angry ye

Hi
Yesterday i had an emg tests for weakness to my limbs the outcome shocked me and made me question all thats been going on with my ppms diagnosis. I have had physios saying that inactivity has caused my problems how wrong they were. No ammount of moving will restore my muscle function without treatment. I have lost all faith in my nhs neurologist because signs and symptoms were over looked. Not everything is down to ms and having ms does not mean you are immune to other conditions. Thank goodness there are some informed medical professionals out there who are not sheep but think ouside the box.
I guess this post is my rant at the system and the ms label which does not prevent me from other conditions. Now if im my symptoms ard down i will reply prove it and not just go with the flow.

My advice is follow your gut instinct and go with a neuro it ligist you are comf⁷ortable woth and trust to do the right thing. Take some control and sack off people who generise and dissmiss your concerns.
Take care everyone
Christinesterday

I can only empathise - this link probably won’t help but it mighthttps://gavingiovannoni.substack.com/p/medical-gaslighting#details