Hi everyone. Looking for some friendly advice from someone or people who have been in the same or similar position, it's quite long winded so please bear with me!
My whole life since starting puberty I have always suffered with problems in my lady region. I always knew I was different to my friends as no one used to have the same pain or periods like I did. Fast forward to my late teens and early 20's turns out I had Polycystic Ovaries, I thought, it's fine and minor and don't want children yet so not an issue for me! A couple of years went by and I was suffering with horrendous pain down there, I had numerous scans on the NHS, internal and normal, each scan said yes you have a cyst there but nothing big enough to worry about, cutting a long story short I ended up going private through a scheme at work as I couldn't even bend down or cross my legs! Turns out I had a 16 cm cyst which was taking over my left ovary and left tube, after coming around from Laperoscopy, they said that most of my left ovary was taken away but won't prevent any infertility issues etc, great for me, pain free, all checked over, nothing to worry about eh? A couple of years later, I met the man I wanted to share my life with and have children. After nearly a year of trying and using ovulation sticks we went to my GP and we were instantly referred to our local fertility clinic. I had a 3D scan and it turns out, I have a unicronate uterus (Half a womb) meaning the right side of my tube was not attached to anything and my left side had severe scarring meaning they think my left tube isn't working at all. They also suspected Endometriosis which runs in my family so that wasn't a shock. I was obviously devastated and I had to have another Laparoscopy and Hysteroscopy to have this confirmed, had my left tube tested and my worst fears were realised when I woke up. I'd had to have my left tube removed, I had half a womb, no working left ovary, cysts on my right ovary and endometriosis, literally nothing worked. After recovery they said given the circumstances we could start IVF straight away, we were over the moon that we were given this opportunity.
We went through the long process, as we had to wait longer due to numerous cysts coming and going, and with only one working ovary we managed to fertilise 4 eggs! I'll never forget how happy we were that day given the circumstances. Unfortunately after a few days 2 died and one became abnormal which left us with one left. They proceeded with the Embryo transfer and I actually became pregnant! However, I started to bleed a couple of days later and our worst fears were realised, we were having a miscarriage. They said once my body was recovered and I'd had a couple of periods, that we could proceed again, but due to our area, we were only entitled to one funded round and had to fund the rest. I'm sure there are 100's of people that can sympathise with that situation, we got in touch with our local MP and she backed us all the way, and asked us to write a letter to our CCG and we can attempt part funding but it might not work. We are still waiting to hear back, the letter was only submitted a few weeks ago, but after we'd suffered the miscarriage we felt like we were fobbed off and that was it, no after care was given.
This was back in March, I called up last week to try and get in for a scan because I've been experiencing discomfort, they admitted that I should have been asked to go back for a baseline scan, however they won't see me at all now because I have to be an active patient going through IVF?! But they're the ones that should have given me a scan in the first place and I feel like I'm just being completely fobbed off, they were great throughout the whole process, but now I just feel like a number again and like I'm no use to anyone? I have good and bad days but hearing the slight bit of bad news literally sends my head into such a sad state. I am 26 so I appreciate people think oh your still young however... I went to my GP the other day about this stuff as we feel stuck on where to go now, and although he was great his words were "Time is what you need, but time is not what you have"
I appreciate the honesty, but what am I supposed to do? I wanted to ask you all how your experiences have been going private compared to NHS? We have looked into lots of different private clinics but it's like I'm scared that we're going to spend money to potentially not have the same care and treatment. The clinic said they would change the dosage of treatment that I was on before as they think if they up my dose I'll hopefully get more eggs! But I'm scared this wont be put in place if we went elsewhere?
Thank you for any advise, tips and opinions in advance!