I think most people who have lost a child would tell you, that in those first days, one of the most painful things is that unrelenting march forward of the days. Each dawn after each sleepless or drugged oblivious night taking you one day further from the last day you heard your child laugh, looked into their eyes, watched their breath rise and fall while they slept (until it didn’t), held their warm body.
Perhaps it’s different for those with other children, but after a while I took comfort in the idea that each day was also one day closer to being with my daughter again, that each day could be endured on the basis that at the end of it, there was one less to slog through before I could look into her eyes again, hear that little chuckle. Each new wrinkle and each gray hair a sign that we would be together all the sooner. All I had to do was put one foot in front of the other and keep going. Continue reading
This is an ordinary story, one that happens across the world in many different ways, but nonetheless one worth recounting.
Tonight I’ll be attending the 10th Anniversary dinner of the group of women I first met at an ante-natal class in January 2006. It’s taken us a couple of months to get it organised around school starting, kids weekend activities, commitments with work and partners. But it’s no small thing to have been regularly meeting for ten years, it’s worth celebrating. Continue reading
It’s that time of the year where every day I think about what we were doing three years ago today, in the days leading up to Zoe’s relapse and the last few weeks we had with her before she died. I think about it in vague terms because I didn’t keep a diary, just posted a couple of random blog entries and I have never gone back and looked at my facebook posts from that time.
But earlier this year I unthinkingly activated facebook memories. Now I am getting daily reminders of what I was thinking and doing on this day last year, the year before, and the year before that. Continue reading
It still haunts me to know that being bullied was a feature of the last few months of my daughter’s life, that in the beginning it wasn’t handled very well and that I failed her in this.
Early in her second year at school, around the time she turned 6, Zoe told me that some older girls were seeking her out every day at lunchtime to tease her, particularly about the way she spoke. Zoe had some speech issues relating to nerve damage either from her cancer or the radiation treatment. She had undergone surgery to her palette before the school year started and along with speech therapy, this was greatly improving the situation, but it was enough to single her out as a victim in the eyes of these girls (I want to say bullies, but that label seems to make them less human than they really are).
I took her in to school early one morning to catch her teacher before others started arriving and explained to the teacher what had been happening. Her teacher’s first response was “Well, I hate to tell you Zoe, but some people just aren’t very nice.” She went on to say that the next time it happened, Zoe should find the teacher on duty and point out who the girls were. While I was a little shocked at the comment, I felt there was a plan of action. And as a busy working solo mum, I didn’t want to rock the boat and be “one of those” parents. I assumed the school had it’s way of dealing with these things.