I've had annual colposcopies since abnormal smear 5 years ago. Only ever CIN1 and went yesterday expecting the same or that it had started to improve. Instead dr took one look and said "Oh we're going to need to treat that. Can we do it today?" I was quite shocked that it has progressed so much that it was really obvious treatment is needed rather than having to wait for smear and biopsy results first :(
In the end he decided best to wait as I had DD (10 weeks) with me and was going to collect DS from nursery so he didn't want me to be fretting about her while being treated, or wobbly and in pain after while in sole charge of them.
He took a biopsy so they know for definite how severe it is and will get me back in the new year, likely for LLETZ rather than anything else, when DH can be there to look after me and the children
Feeling a bit wobbly - have 2.8yo and 10 week old and had lots of morbid thoughts during night feeds last night even thought I know this is a long long way from being cancer. Need to get practical which is my usual way of dealing with things! So in that spirit, can you let me know what LLETZ was like - physical and emotional side of treatment and then any issues you had after?
Just looking for general info, support, stories etc.
Thanks!!