This blog began as a quiet, anonymous space to work through the emotions of the biggest decisions of our lives — pursuing donor egg IVF in Thailand to build our family. It served as a space to make sense of trying to conceive, travelling abroad for treatment, and finally becoming parents. Now, years later, our story continues — not just in written form, but through The Donor Eggs Journey Podcast. We remain anonymous, out of love and respect for our children.
Sunday, November 4, 2012
Pop's Boy
Tuesday, September 4, 2012
Amidst Grief, Cautious Optimism....
Sunday, September 2, 2012
Shocked
Tuesday, February 21, 2012
The Hard Truth....
I am still struggling to write posts but I am hoping that I will get back into the rhythm of things soon. My Dad is not going well. He was in the hospital for a couple of weeks having radiation treatment for the cancer that has come back where the lung was that they removed and on his adrenal gland. He chose this treatment because it was supposed to have minimal side effects but I don’t think that he has been eating properly for more than a couple of weeks due to the nausea. He came home on Friday and had a fall and Mum was afraid (because he was not eating or drinking) that he was dehydrated. She had to take the exceedingly hard decision to see if he could go back to the hospital. A hard decision for Mum because Dad doesn’t like being there and he takes it out on her. She has had to make so many hard decisions – I feel very sad for her, they had always wanted to be spending their retirement going on trips and having coffee everywhere around Melbourne (they loved going for coffee – loved it!!).
On top of the cancer is the fact that he has the hydrocephalus (fluid on the brain) and this has caused his short term memory to be irreparably damaged. In the past years he has changed significantly from the person that he used to be but right now – there is good and bad in what the hydrocephalus has done to him. It seems to have affected his pain centre so that he doesn’t seem to be in as much pain as you would expect in this situation, which is good. He has also had some humiliating things happen to him (accidents and such) that he doesn’t remember which is also good. The worst of the hydrocephalus is that we just don’t know what he understands about the situation because one day he seems to be accepting of what is happening and the next day he will be wondering when the treatment will fix him. We are all having trouble accepting that we have limited time with him but I also have things that I want to say to him. The problem is – I don’t want to freak him out if he is not remembering why he is in the hospital and having treatment but I also don’t want to regret not saying the things to him that I want to say. The other hard part is that I could say everything I want to say to him and he won’t remember it the next day.
I’m gonna say it here and then hope that I will get a chance to tell him.
I want to thank him for being a great Dad. I want to thank him for taking me to the footy with him every week when I was a kid – it has created amazing memories and has also enabled me to relate to him at all times. I want to let him know that the times that he told me that he was proud of me, I hold precious in my heart. I want to thank him for teaching me how to laugh at myself. I want to hug him for him taking JBB into his heart so completely – they have a beautiful relationship, it makes me so happy to see them together. I want to thank him for the single minded drive that he has given me – he was the most motivated person that I have ever known - unfortunately the hydrocephalus has taken it from him now but was so fit (he ran 9 marathons), it was amazing. I want to thank him for giving me so many belly laughs throughout my life, he knows how to tell a story and honestly, he’s had an aptitude for getting into ridiculous situations. I want to tell him how great it was that he worked in the garage out the back because he was always there when we got home from school. He (and mum of course) gave us an amazing childhood filled with family, holidays away together and lots and lots of fun – whenever we are all together, we reminisce!! I want to thank him for everything that he taught me – to drive, to work hard, to excel. Mainly I just want to tell him that I don’t want him to go, that I will miss him, that I love him.
The thought that he will most likely not even meet any more children that we have makes me want to sit in the corner and sob my heart out. I hope desperately that he will be around for the birth of my sister’s first baby in June, it will hurt my heart if he misses it. I know that these things are all selfish, I also know that he is suffering and that his life has become a complete struggle. Despite the fact that he is rarely the Dad that I grew up with, the hydrocephalus has taken him bit by bit away from us, I can’t contemplate him not being there at all. I am very sad for all of us.
Sunday, January 22, 2012
Good News, Bad News
Tuesday, January 17, 2012
On Hold....
In addition, JBB has his tests tomorrow to check that there has been no damage to his heart – we will not know the results until Monday and I am hoping against hope that he is cleared of damage to his heart but will just have to deal with it if the news is not good. He has been very good and active, so I am hoping that it means that he will be cleared but it is hard to know what is going to happen. But we are waiting.
I am trying very hard to not worry until I have something concrete to worry about but I do find it very difficult – especially when they are both important things. Add these to the waiting that I have done over the past 4 years with IVF and I feel like my life has become and interminable purgatory of waiting. You would think that after all of this time, I would have gotten better at it but it is very wearing.
My Mum tells me all the time how hard it is with Dad being sick (I honestly think that in the last 5 years, he’s had around 15 operations and a gazillion appointments) because she can’t make any plans – I absolutely know what she means cos we have been in the same place. We usually only book a holiday at the last minute because who knows if a cycle is going to happen and we have to be going to Thailand? Our Christmas holiday was cancelled, so that I could go to Thailand for the cycle and my sister asked me the other day if we were going to go next year – of course my answer is ‘who knows?’.
I feel like our life is mostly, waiting for the results of Dad’s operations and tests and waiting, preparing for or recovering from IVF cycles. We had a blissful (though not without a hell of a lot of worry) 8 months where we were waiting for JBB to be born and then another 5 months where he pretty much occupied my every thought but then it was back to work to get enough money for another cycle and the waiting began again. Now we have to wait to see what Dad’s treatment is going to be, wait to see what JBB’s results are going to be and then 6 months of waiting and preparing for another cycle.
I need some strategies to handle a life perpetually on hold – anyone got any ideas?
Thursday, April 28, 2011
Struggling
Sunday, April 17, 2011
Massive amounts of information....
Sunday, April 10, 2011
I'm devastated..
Tuesday, May 11, 2010
My Dad
Starting the Blog Again
So, we are almost ready to start the relaunch of the blog and the Donor Eggs Journey podcast. We have talked about it a lot. The boys are ...
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So, we are almost ready to start the relaunch of the blog and the Donor Eggs Journey podcast. We have talked about it a lot. The boys are ...
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I got the call from my GP today and the results are in - I am most definitely pregnant and the HCG level of 1,185 - holy moly, I had roughly...