My son has suffered three times in the past from balanitis xerotica obliterans - an infection at the end of his willy - he is now 8. The first time was when he was about 3, then about 5 and then once more recently. I took him to the emergency doctor on a Saturday in November as I could see his willy looked a bit inflamed when he was in the bath. The doctor said it was a bacterial infection and gave us some medicine. After two weeks it hadn't cleared up (the doctor said it would take 2 weeks to clear) so took him to my own GP. She said the infection wasn't bacterial but fungal so gave us some different cream. Again, it didn't clear up. By now it was nearing Christmas so could not take son until between Christmas and New Year. My doctor said that she didn't want to keep on giving us cream for it but would take a swab and then get back to me. I phoned early in the new year and she said the swab came back clear but she would refer him to the hospital (I didn't really realise why).
Had the appointment on 12 February and the doctor said it was balanitic xerotica obliterans and the only way to clear it was a circumcision.
I AM DEVASTATED. Why, you might ask (and I ask myself the same question).
My Ex-DH was circumcised at age 9 because of the same reason but after reading about the circumcision operation and what it involved I really do not want to put him through this (although it has been medically suggested). I want his willy to be intact, don't want him going through the pain and then having a "different" looking willy.
I know his dad had it done but I can see how it affected him with our sex life (sorry to be so blunt). He was never very confident in bed and I always put it down to the fact that he was circumcised and didn't feel comfortable about it (he is now 39 by the way). Although this might only be my perception of why he was not confident - he has now got a new girlfriend and I am sure he is more confident in bed with her than he was with me.
How can I ask for a second opinion on my son having to have this operation or what other routes could we go?
Any advice gratefully received.
It sounds strange, but I cried in bed that night after we found out about the operation. It just seems to be one thing on top of the other - my mum is in a psychiatric ward, my youngest daughter has sotos syndrome and global developmental delay, am trying my hardest to work and look after 3 children.
This message may come across as being selfish as why am I so upset about my son having to have this done, after all, it is happening to him and not to me - but I don't want to put him through an unncessary operation unless that is the only option.