In a dream the other night I realized that, for some weird reason, we’ve left Loren at a hospital for six months. In my dream I stood still, shocked. I frowned and tried remembering why and when we would have decided to do such a stupid stupid thing. I thought how much I’ve been missing him and how much he must be missing us too. Then realization – and a great deal of joy – dawned. I started dressing hurriedly. I was going to go and fetch him. Immediately.
Even though he is clearly here in my subconscious, the physical reminders of him are becoming less and less. On my mother’s advice I’ve not packed his clothes away, but kept them for Magnus to wear. In some instances I cannot remember which of the little suits and boots and hats belonged to which baby first. Magnus is now starting to grow into Loren’s biggest clothes. Yes, Magnus at almost six months is bigger (definitely heavier, if not taller) than his seventeen-month-old brother was. Soon I will not even have the slight sting of remembering how Loren looked in this vest or that hat. It is only the clothes he died in that I’ve kept separate in a bag. And I’ve taken them out and examined them, pressed them against my face time and again, but there is nothing left. Not even his smell.
Our hurt is becoming private. Often I could see the pity in people’s faces as they watched me with Loren. Now – with real reason to be pitied – I pass unnoticed in crowds. When people ask, “Do you have two kids?” I nod more often than not. I can sense Dirk wanting to contradict me, but then holding back. Explaining is becoming too hard and too emotionally draining. In my heart, I always will have three kids even though the world can only see two. Besides, I’m becoming tired of the better-this-way-brigade. I always experience it as a direct blow to the solar plexus even though I’ve come to expect it. I patiently explain why I can never agree with them, but people don’t get it. They will never get it.
I feel the need to bring Loren into conversations with family and friends – sometimes just because. Sometimes they keep quiet – uncomfortably- and sometimes I can sense that they are trying to humour me by reacting with too much enthuisiasm. Either way, I don’t feel better afterwards. I read this and it made me cry in recognition. Because that is exactly what I would do.
Later, putting away the leftovers from dinner, I paused to look at the photo again. There was the smiling girl we knew, and the tree like any other. But then I looked again, more closely, noticing the large angel ornament just over her right shoulder. Was that a coincidence? But, no, when I looked over her left shoulder I could make out one of those picture ornaments, and,inside, a photo of her big brother, now forever younger than she.
I knew then that the photo, so like the many others taken this season, was not exactly like all the rest. This child had not fidgeted in front of the tree like my girls did, wandering more or less aimlessly in and out of the camera’s viewfinder, laughing and pretending to take luxurious sniffs of the tree’s artificial needles (mmmmm, fresh!). No, her mom had placed her just so in front of the tree, being careful to make sure that both her children were captured in the photo, even as her daughter posed in the usual, expected way, with a radiant smile on her face.
Loren is as much a part of me as my own head. Not a moment goes by when I’m not keenly aware of his existence – somewhere. It is a different awareness than with my other two children, but there nonetheless. I can’t go and fetch him physically, but in a symbolic way I can. Maybe my dream has been a way of telling me that I need to talk less and do more.
I know that Loren in life has made a difference in the lives of people. I know that his memory means something. Thank you for pointing that out. I am deeply grateful for that. There are other ways in which Loren’s life could remain a blessing. Even though it felt like we were often short of time, energy, money and courage I now realize that we somehow always had enough to keep going. We could afford to do ABR – which I still believe in. Many other parents are not as blessed as we were. In some small way I want to help.
There is, of course, Loren’s savings – paid out to us as part of his estate. Being in South African rands it would hardly be enough to make much of a difference. But if it is managed properly, it may grow to become enough to help other children afford therapy. Maybe ABR? I’m not sure. It will require some thinking. But I will let you know.
For the moment I will reserve this blog for Loren and grieving and the subjects of Cerebral Palsy and disability awareness. That was its original purpose and I would like it to remain so. Later I may open another blog. Who knows?
Ummm, watch this space?

