I have chosen to write this blog post around the blanks. With this I mean things that I cannot answer or know anything about because I do not know anything about my donor. These are small things that have played a part in my life.

I have chosen to write this post about what I call the blank spots. The blank spots are for me the things that I can’t answer or know anything about, because of my status as a donor child. These are small things that has played a part in my life. The blank spots are situations I my life that i think only happens to donor children. 

Who do I really look like?

The blank Fields-my family

It is no secret that I was very concerned about these thoughts when I was younger. I think everyone remembers that they have been compared with their parents. People have commented on who you look like and who you certainly don’t look like.
Naturally, this mean a lot to me.
A phrase like “God you look like your mother” also made me think about how my donor looked. What traits I had clearly from him and which were just mine.
Who looks like who is often smalltalk, but can have great significance. I know it meant something for me. I spent a lot of time thinking about how my donor looked. Whether I had his nose or eye color or height?
For me it was a wonder, not grief. We as a family has always talked openly about these things, so I just felt that I was a little cool with my mysterious traits.

Genetics – What do I have with me?

Genetic is one of the places where I think the donor can cause many unanswered questions.  For a period I have worked in a genetic department, and I have always had both knowledge and interest in genetics in general.
As a donor child I have 50% genetics which is unknown.
We got very much aware of this Just a few years ago. Here we found out that I was lactose intolerant. It is an inheritance you must have from both the mother and father to become lactose intolerant.
And just as far as these hereditary qualities are concerned, I have been confronted on several occasions with the lack of knowledge of the donors genetics.
At the doctors I’m often asked for diseases of family in different occasions. Again here the blank spots made me unavailable to give the full answer.

But is it so bad?

I could not find any other than these 2 points in my life where I really felt that I was a donor child meant that I lacked answers. Therefore, I can only conclude that it hasn’t been a major loss for me so far.
Who knows maybe it can change it. But right now I live in happy ignorance and find myself well with it in my life right now.

I am very happy to hear your thoughts and experiences. Please write in the comment box below the post!

Hugs Emma

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