Overall it has been fine and I have no regrets so far. I am no longer diabetic, my mobility has improved, and despite the first few weeks being rough due to lack of fluids, constipation, and a possible wound infection, which many ops suffer from, I feel a lot better than I did before.
Yes, eating out has been a steep learning curve, managing fluids and food 30 minutes apart is fine at home but not so good if you are in a pub, but they are things you learn to live with.
For me, having it done gives me hope that I can walk again (even if with sticks) much further than a few yards without pain, and enjoy things that others take for granted.
Watching my body shrink and buying new clothes has been particularly pleasurable.
From visit to GP in Jan 15 to surgery in Sept 16, it was a bit of a journey, as appointments were spaced apart a lot, and I was one the waiting list for 7 months instead of the NHS up to 18 weeks because it was also a cancer centre and they took priority. Other than that, my only complaint really has been the lack of psychological support available afterwards as I live out of area to the hospital, so different CCG, and I have had to fight to get it.
Do read others stories on here, particularly some of the long termers who have lived with it a lot longer than me. I get dietitian support for two years.