United Brachial Plexus Network

Hi all. It's been quite a while since I have been on any forums as life has just gone on for my now almost 18yo son Paul. I have just noticed that Paul has developed a facial twitch which seems to be getting worse on his affected side (ROBPI C5/6/7 affected). It affects his mouth/cheek mainly. I ask...

<t>Hi Kath and all.<br/> <br/> I haven't been here for a while. I quite often "Lurk". I couldn't believe it when I came across this post.<br/> <br/> I'm currently seeking further treatment/advice for my 9yo son who has been complaining of electric shocks for the past 18mths ~ 2yrs which come out of ...