I read another blog this morning from an inspirational lady called Wendy Keller which talks a bit about feeling lost and recovery – this
motivated me to get a blog that has been running around my head for the last 24 hours out of my head! One of her comments ‘it’s always darkest before the dawn’ really rang true with me – I know far too many people purely because of the tragedies that have become part of our lives and I know from my own personal experience that sometimes we have to hit a real rock-bottom dark low before we find the strength to enable us to start to recover.
Yesterday was another milestone which seems appropriate to mention – Mark and I met with Gregor’s pathologist… feels kinda odd even writing that. It was a strange kind of meeting, not one anyone would choose to go to but one I think its important to talk about openly as this somehow may help other families going through similar stuff.
The idea of a post-mortem, particularly that of your child is such a taboo discussion, so difficult to even contemplate as it means having some thoughts about what is involved with a PM and definitely not one any parent would like to even begin to think about! As I have said before we wanted to donate Gregor’s organs for transplantation but were unable to do so. I had wanted to meet this pathologist the week I found out about the change in Gregor’s cause of death when we received the final post mortem results but was put off by our paediatrician who told me to channel any questions we had (and there were many) via him. I do slightly regret not listening to my gut instinct that was telling me it was important to meet her but at the time I went with the flow as I was in such heightened emotional turmoil and just didn’t have the energy to turn the tide. And with the benefit of hindsight I may not have been able to cope with yesterday’s conversation 2-3 years ago so maybe it was for the best at that time.
Last year whilst working with the SCDT I realised that some families DO meet their child’s pathologist and that the pathologists are usually very willing to sit with parents and try to help with explanations/information in any way which could be useful. So a full year later we set up the meeting. I’m really glad we had the meeting, absolutely no regrets and I think quite a few positive outcomes came from this meeting. The purpose of me sharing this is so other’s know this is a possibility and that these guys are real people who care and who have in most cases been one of the last people to have contact with your loved one.
My question is this – should it take a charity to organise something such as this or should it be an option (as I fully appreciate this would not be helpful to everyone) readily available at whatever time is most appropriate for each family? Could be after 6 months, one year or ten years but if it could somehow be helpful then surely it should be possible?








