Not really sure what I want from this post, but I am so tired, anxious, devastated and have cried so much over my recent diagnosis of stage 4 endometriosis at the age of 33.
I feel so helpless as NHS waiting lists are so long, it feels so unfair that they have dropped this news on me and expect me to wait so long for a follow up appointment. I know I am one of the lucky ones in that I don't suffer with the excruciating and horrific pain that I keep reading about from other people. (I have a heavy flow for the first two days of my cycle, sometimes painful and sometimes I get brain fog, but it is not every period so it is manageable). But going from being fine to one month later, being told that I have a severe chronic condition which will affect my fertility has been really hard for me to process.
The first sign I had anything wrong was when my stomach bloated up one month ago and I was in severe pain. I ended up going to the hospital where I was put on IV antibiotics and a two week course of oral antibiotics. The stomach pain and bloating is completely gone and I have had a normal period since that episode, but they wanted to do an MRI scan on me as a follow up which revealed endometriomas on both ovaries, thickened uterosacral ligaments, endo in my pouch of douglas and suspected blood in my fallopian tubes. I am so terrified as one consultant very casually told me that he would remove both fallopian tubes if he sees they are damaged. He then threw in that IVF was an option for me, like it is a guarantee.
I don't know how to cope with this. I really wish this was not happening to me and finding it so hard to live normally now, I am completely consumed by it.