When the worries and fears of the next checkup, or just of life as it is these days, threaten to overtake me, I have a new weapon. I dream myself away. To after the doctor’s appointment, when she’ll have given me the news that I’m doing fantastically, that the results are better than they had dared to hope for. To a holiday in the sun, playing with the kids. The more real the worry, the more real I make the dream.
Yesterday it was time for the half time checkup I’ve been dreading and hoping for for months now. The checkup itself was done quickly and more or less painlessly (they just insert a needle and at one point give you contrast fluid through that), just lying down and then you get moved back and forth through a huge machine with a round hole. The day before that was the blood sample which will tell me if my all-time high of 112 was a fluke, or if my body really is producing blood on its own again (which would mean the cancer cells in my bone marrow are fewer), and tomorrow its time for another mammogram. And for all I’m willing my body to have done well, there really isn’t anything more to do but wait for the results.
So, I start dreaming away, to a holiday in the sun with my family. My lovely friend Heidi started a fund-raising when I got diagnosed, to send me away on a dream holiday. The fund-raising went through the roof, and it means I will get to take the kids on their first holiday in years. I’ve some red tape to get through first, like getting OK to going on holiday while I’m still on sick-leave (Sweden has loads of rules on stuff like that), but my oncologist cleared me for travelling, just to go somewhere “safe and practical” as she phrased it.
So now I’m looking at holidays - the kind of chartered ones with preferably all-inclusive and pools and beach just around the corner. The kind I never would have looked at before having kids, and that always seemed too expensive or over-the-top once I did. This summer, I think, in the end turned out to be a good one for the kids. Thanks to the car we could go to fun places we didn’t really go to before, and all of us, Ilir, my brother and my dad, made an effort to take them out as much as possible, so that they could go swimming, or go to the really fun park across town. But we couldn’t go away, at that point. Everything about the diagnose was still so new, so raw, so dangerous. The year before that I had time off in the summer, but no money to take them anywhere, and the year before that I worked all summer, so they’ve really waited long enough for this. We all need this, I think. For one week, just to get away from it all, the morning stress and the homework that needs to be done and the constant, constant worrying…
Now, when I start to worry about the result and what it will show and I realise that it’s just one of those improductive worries, I start to think about our holiday instead. I know we will have an amazing time once we get there, and for that I’m so very, very grateful. But even before that, just now, it’s doing me a world of good to just have this to dream away to, as a counteract to those worries that will just lead me nowhere. I just start dreaming away to a place where I’m lying by the pool sipping goldfish-bowl-sized drinks and watching the kids splash around in the water. This trip will be another thing that I hope they can remember for the rest of their lives, something we did together as a family.
I’m so, so grateful to everyone who helped the fundraising become such a success. Thank you so much, for caring, sharing, contributing. And a massive thank you to Heidi, who as always knows how to make stuff happen!
The image above is borrowed from fritidsresor.