This morning was our phone consult with our new Dr in Sydney. It went pretty well, I suppose. Nothing I wasn't expecting.

He was very lovely

very understanding of our situation

and very sorry to force a 6 month wait on us.

so where do we go from here?

So what does this mean for me now?

Dr P told me of another patient who had a recurring disjunction problem. She had a trisomy 18 baby, a trisomy 13 baby, a trisomy 21 baby and two miscarriages.

I simply cannot face something like that. Because of my own personal belief that all life is sacred, I could never terminate a pregnancy. Not only that, but I personally am friends with 3 adults whose parents would have been offered a medical termination. I personally cannot imagine the world without them. I also am friends with someone whose baby faced a 0.01% chance of survival – she chose to continue the pregnancy and her child is still here (please do note that I am not against abortion. I am pro-choice. But my own personal belief is that it’s not an option for me).

So I have decided that Caden will be the last of my biological children.

In one sense I am lucky, in that biology has never meant a great deal to me. My mother's biological family disowned us when she divorced my father (still the best move she ever made) and she created her own family. Her best friend became like her sister, her best friends mother is the only grandma I have ever known and I love her dearly.

I can but assume most of my astute readers have picked up on the fact that I am also a lesbian, and my partner had no biological link to Caden. She unequivocably is his mother. She said the second she saw him any worries she had over whether he would feel like hers disappeared. The second she saw him, she knew he was hers, no questions asked.

So knowing that I will not give birth to another biological child, while there is some feeling of loss, does not leave us without options. Dr P suggested PGD - which is a technique used during IVF, where they allow an embryo to grow to blastocyst stage and then extract a few cells to test for chromosomal abnormalities. However, it is only 80-90% effective, and they still recommend all the screening tests to be sure. Add to that the fact that it is a new technology, and there are no long term studies on how it might affect the child’s development. Plus hey, we have another option.

The final option, the one that makes the most sense to both of us, is to do IVF with Kim as my egg donor. The act of carrying the baby and giving birth to it will give me a connection just as great as a biological link. Kim will also have that link through biology. We have spoken to both our families, who were not 100% receptive to the idea of us haing children in the first place, and they are all on board with this plan. My mother (herself an IVF veteran) said to me “look at it this way. If you were in a heterosexual relationship, and there was male factor infertility and you had to use a sperm donor, only one of you would have a biological link. Or if there was this problem with you, and you needed an egg donor, only one of you would have a link. This is no different!”

Uhh, I didn’t actually need reassurance, I love the idea of carrying my partner’s child, but thanks!

So now we start with the probably very long process of counseling, medical tests and eventually IVF. So there is at least a light at the end of this very, very long tunnel.