Twelve months of living in an IVF bubble
The strongest women become the strongest mothers before their children are even conceived.
— Anon.
I have always wanted to be a mother. I was going to be married with 2 kids by the time I was 30. But as it happens, I passed 30 with no kids and no husband. I met Johnny at the age of 34, we clicked instantly and on our first date I told him I wanted nothing more than to be a mum. I was ok if this scared him off, but he stuck around. 6 months later we were living together, we were married 4 years later on the 4th October 2018. He is the love of my life, my strength and my comfort. He was most definitely worth the wait.
Our fertility journey started about 2 years before we got married, I went off the pill which I had been on most of my adult life. My cycle was regular, nothing indicated we would have fertility issues. I went to the GP and was referred to do ovulation tracking, everything seemed fine but still we didn’t fall pregnant. It wasn’t until Johnny went and got checked out that we realised that things weren’t going to be as easy for us as it is for most people. He had low count and poor mobility and he was told the only way we would conceive was through IVF. We were gutted but we also felt excited because we had an answer and there was hope that perhaps IVF would help us in having our baby.
We went to an open day and heard a specialist do a presentation on the whole IVF process. The next day we booked in to see her. We did all the tests required, I came back with everything normal, Johnny as we had already known had low count and poor mobility, but it also turned out he has poor morphology and high DNA fragmentation. On top of this he also came back as having a Robertsonian Translocation of chromosomes 13 & 15. Now this all sounded scary to us, but our specialist assured us that if we were to go ahead with treatment it would mean that we would do ICSI and PGD testing to ensure we have the best embryos to transfer. We then met with the genetic councillor and scientist to help understand the process and statistics.
We started treatment January 2019. In our first cycle we collected 9 eggs, 7 fertilised, by day 3 we had 2 and by day 5 we were only left with 1 embryo. Unfortunately, this embryo couldn’t be biopsied, so we made the decision to transfer it untested. Knowing the chances of this embryo being successful we had prepared ourselves for it not to work. When I did a home test at day 8, we were completely shocked to see that second pink line come up. It had worked…first go! We were ecstatic however this was to be short lived as by the time it came around to my blood test HCG was low, second test confirmed it was a chemical pregnancy. We were gutted, we had no other embryos and were back to square one but ready to try again.
Our second cycle started March 2019, this time we had 8 eggs, 7 fertilised and there were 7 still growing by day 3. We booked in for a transfer on day 5 just in case we ended up in the same situation as our previous cycle. We were so excited as this was better results than the first time but again our hearts were shattered when we arrived and were told that only 2 had survived, 1 of those was able to be biopsied the other we took the chance again and transferred a fresh untested embryo. This time we came back as negative, as upset as we were, we also knew that this was a high possibility and we still had that one in the freezer. Our PGD tested embryo results came 3 weeks later as a perfect embryo to transfer. As it was our only embryo, we decided to do another full stimulated cycle and see if we can collect any more.
Our third cycle started is May 2019, to increase our chances we decided to change things up a little. Johnny had his sperm collected through TESE surgical procedure hoping for a better sample. This cycle we had 12 eggs collected, 9 fertilised and again only 1 embryo by day 5. This was suitable for biopsy and sent off for testing. We waited the 3 weeks and when the results came in for this one, we were stunned when told it was genetically unknown. The sample they had taken didn’t have enough genetic material to know what was going on.
We were now were left with 2 frozen embryos. 1 genetically fine the other unknown.
In July 2019 we transferred our genetically viable embryo which was our best chance so far at falling pregnant and taking home our baby. The two-week wait was an anxious one, on day 8 I did a home test and were ecstatic to see that second pink line come up again. But we were still cautious knowing from experience that it doesn’t always end up with a baby. A few days later after blood tests we were devastated to find out that yet again we had another chemical pregnancy. This result hit us hard. We knew we were making embryos, why weren’t they sticking?
We met up with our specialist to discuss our next steps, she suggested I go in for some exploratory surgery. I was booked into hospital in August 2019 for a Laparoscopy, hysteroscopy, D&C and dye studies. The aim was to check for endometriosis, biopsy my uterus and check my tubes were ok. To our surprise they found I had stage 3 Endometriosis. I had no symptoms, no out of the ordinary pains, no bloating or anything else that would suggest I had endo. As shocked as we were, we were also excited, maybe this is the reason we haven’t been successful and why the embryos are not sticking.
Cycle 4 started September 2019. We were so hopeful, 8 eggs collected, 6 fertilised, 6 still going at say 3 so we booked in for a transfer on day 5. We had 3 still going strong, 2 were looking good for biopsy and 1 we decided to transfer untested. Again, we had hope, but the transferred embryo came back as a negative. The two we had tested looked perfect; this was the best outcome we could have had. Two chances for a baby. We waited the 3 weeks for our 2 perfect looking embryos PGD test results to come in. This was the most anxious wait of all. We still had that one little genetically unknown embryo in the freezer and were hoping to add two more to that. The results finally came in whilst I was at work, it was the worst news of all, the news I had feared the most. Both our embryos had chromosome abnormalities unrelated to the translocation that Johnny has and if transferred would not go on to be a healthy baby. What a kick in the guts this news was, so much it took the breath out of me, I cried more than I had cried this whole journey. I called Johnny and broke the news to him we both swore and got angry and sad but not for long. He reminded me we still have one more chance. That one genetically unknown embryo. Could that be our miracle baby?
Our first year of marriage has been consumed with IVF. In a weird way this journey has brought us closer. We have concluded that nothing is in our control, we can only take it all one day at a time. Focus on ourselves, our jobs and our relationship. We trust in our medical team, and we understand that everyone’s journey is different so comparing what we are going through to another couple doesn’t do us any good.
We don’t have our happy ending yet, and we also know the journey isn’t over either.
November 2019 will see us transfer our last embryo. Will this year finish with a happy ending? We must stay positive and take it one day at a time. But whatever happens, we will work through it together.