I know exactly how you feel - in fact I think you have analysed your own fears very well. Having written it down here you might be able to take the next step which would be to ring the surgeon's office (we have a specialist nurse who fields calls like that). After my first surgery I went to the GP a couple of times to no avail because they don't have the experience to deal with the after effects of surgeries like ours. That leaves us with having to get hold of the surgeon or his/her team. My eldest son has great rationales for that. "They're there to help us, Mum. They get paid a lot for what they do so never feel guilty about asking for help etc."

I don't know what the earache could be except that you will be having a lot of nerve regeneration going on. If it's sore enough to make you want to reach for the strong stuff then that's another justification for getting in touch with your doctors.

And what nonsense about being intrusive on this site! People love to help. It seems a waste to go through all this and not share the things we've learnt.

Regards from a fellow worry wart and self-effacer:)


1996, ovarian cancer surgery + cisplatin and taxol.
September, 2007, SCC of left lateral tongue. Excision.
October, 2009 recurrence in scar tissue, T1NOMO. Free flap surgery from left wrist - neck dissection. 63 year old New Zealander. No chemo, no RT.
February, 2014. New primary in left buccal mucosa. Marginal mandibulectomy, neck dissection, right arm free forearm flap. T1N0M0 but third occurrence and some areas of concern: RT started 8 April and finished 19 May.