hi all, just found this site!
Starting to research what happens if I have to retire from work on medical grounds due to severe unrelenting pain which at this time can not be identified although there is consideration that it may be pudendal neuralgia(PD). This along with fibromyalgia and functional neurological disorder (FND). The PD started last November with severe nerve pain in a previously operated on left leg which radiated into my cervix, this pain has been increasing more and more - morphine and buprenorphine patches still not addressing it. Waiting for another pain clinic appointment next month.
Meanwhile been off work for 6 months now and about to go on to half pay (long term NHS service). However job is community based travelling up to 100 miles a day - guess what - due to high level of various drugs it is not safe for me to drive so am very concerned I will not be able to return to work.
So my questions are around medical retirement and/or any extra pay I can get on top of half pay. I will struggle to live on half pay (as do many people) but want to do the right thing going forward.
Lots of advice already been read but if anyone has any ideas it would be great to hear.