
Originally Posted by
freakyschizogirl
Hey all, just a mini update and a bit of good news for me...My funding has been approved by the primary care trust and i can finally start my Rituximab infusions! No date booked as yet but very soon, hopefully, and could be withing the next 2 weeks if i'm lucky!
On a side note, i just wondered if anyone else suffers with Neuralgia in the face? mine is always across my forehead. I've been on Amitriptyline for a few years now which numbs the pain, every now and then i slip and forget to take it and end up with pain which feels like a headache but wont go away no matter how many drugs i take, like tonight.
I've read a few bits online about Neuralgia and it seems some forms of neuralgia can be treated with certain proceedures etc...thinking i should ask Addenbrookes to look into this for me. As i just accepted Neuralgia as a diagnosis and didnt really think about the cause or long term relief.
Anyways...thanks for reading. x