‘Sometimes you will never know the value of a moment until it becomes a memory’ (Dr Seuss).
Tonight I lay in bed singing my little boys to sleep – dear love them I haven’t got a note in my head but they love it. This is nothing new, I do it nearly every night. But tonight as I lay there croaking my heart out, I was reminded of how Mark and I would have lay in our mum’s bed some nights as she sang ‘Big Empty Bed’, a song Mark always wanted her to sing. With the exception of the song lyrics I remember much about those nights… the warmth of mummy’s bed, the feeling of comfort, the ‘not a care in the world’ feeling that only a child can experience. Those nights seem like just a blink ago and somehow here we are 30 years later. It got me thinking about how precious time is, and of course the thought of time always brings me to the dreaded reality of how limited my time is with Luke.
In just a blink those ‘lying in mummys bed nights’ were over, I became a teenager, I lost my brother, I turned into an adult and I became a mum. And that makes me ponder all the blinks that I will take as Luke grows up.
My Luke just loves being active, I would need eyes on the back of my head. But what if I blink and he can no longer run outside with his little brother? This thought makes me want to wake him right now, take him outside and run around with him until he falls asleep on the grass.
What if I blink and he can no longer lift those little arms to catch a ball, or wave at his granny or lift an ice cream cone to his mouth or hug me? What if I blink and the only thing he can do with his upper body is push a light touch button that sits right next to him?
What if I blink and his lungs can no longer work on their own and even a regular cough becomes a deadly enemy?
These things I can handle. I would carry Luke bare foot to the ends of the earth and back if he said that’s how it ought to be – yeah he is spoiled – so what? No physical disability will ever stop me from making my little boy feel happy and valued and capable of achieving anything he wanted. My love for Luke and his love for life will help us to conquer anything this wreckless, unforgiving disease can throw at him. We will throw it back even harder.
But I know Duchenne too well. It has haunted us for years. We have looked it in the eye so many times and have never even come close to defeating it, we haven’t even managed to wound it. Without a miracle Duchenne will take my son. It will leave Coen without a brother and will leave an unfillable void in so many lives.
My most fearful thought every day is what if I blink and that little heart that I have nourished, so full of love can no longer sustain life in his little body? What if I blink and I’m standing at his graveside? How do I move on from that blink?… I couldn’t!!
I know that I should live in the present and not let worries of the future interrupt my life. But these fears, to me, are acceptance, or at least my version of it. I accept that Luke has Duchenne, it took me a while but I got there. I accept that he will become severely disabled. I accept that his body will give up piece by piece. I accept that I will have difficult questions to answer from both Luke and his brother. I accept that Duchenne is not going away. I even accept that a cure will not be found in Luke’s life time (we’re aiming for a treatment not a cure – something to transform DMD to a chronic condition instead of a fatal one). But I cannot accept that Duchenne has some God forsaken right to my son’s life. It is his life and I will do whatever it takes to make sure that he is in control of that life not Duchenne. The fight will be long and hard but I am in no mood for giving up.
So from me Duchenne… Do One!!!!!!!!!!!!
2 thoughts on “What if I Blink?”
Wow what an amazing story, I am new to duchannes muscular dystrophy and my sons Dusty and Ty are 3 and 1 both have it. It’s been a year and a half sence Dusty was diagnosed and Ty seven months. Thank you for your story and I hope to someday connect with you in person. I want to meet more mom’s with boys with Duchannes and know what I feel is normal. Gail
Hi Gail, I am sorry to hear that both your boys have Duchenne, that must be really tough. I think these boys are just the happiest in the world, always smiling 🙂. If you want to connect with other families there are a couple of Facebook groups I would recommend. I’m not sure where you are from but if you are in the UK the group Duchenne Parents zone UK and Ireland is really good. I also really like the group Duchenne Under Ten, parents from anywhere can join and it’s good for those with younger children especially newly diagnosed families who may not want to face some of the issues the older kids have yet. MAD, Mothers Against Duchenne is pretty good too. I feel that meeting and chatting to other families is a great help, even if it’s just meeting socially or at Duchenne events, it’s good to know there are others who know exactly how you feel. I wish you and your family all the best and thank you for reading my blog xx