Winter driving is simply a “test-run” to teach us how to get through the tough stuff in life!
Winter driving is simply a “test-run” to teach us how to get through the tough stuff in life!
The phone finally rang – two days, three hours and fifty-seven minutes later than it should have. I was a shredded pile of emotions from the waiting. She took an infinitely long breath, cleared her throat, and dealt the blow: It is as we feared – lymphangioleiomyomatosis. I know what you’re thinking: that’s not a word, it sounds like a kindergartener made it up. It’s most definitely a word and it’s definitely no joke. While initially I was relieved that it wasn’t the “C” word – the one disease we’ve all learned to respect – now I’ve come to wish it were. I remember learning in nursing school that cancer should really be viewed as a curable disease. Many times people with cancer receive successful treatment and are cured and we need to stop thinking of that diagnosis as the kiss of death.
Not so with lymphangioleiomyomatosis (or LAM, its kinder acronym). It is not curable. In fact, “they” – those great minds of the medical elite – make no concessions about that. “They” don’t even know how you get it or how to treat it. Paul and I have been to multiple physicians and even drove across the state to the University of Michigan and talked to the most special specialist who specializes in LAM. I have also now read from nearly hundreds of websites – six weeks since I first heard there was an evil in the world called LAM. Six weeks since “they” first suspected I have it.
I am 47 years old. I basically feel healthy and strong, but for years I have wondered if I was more short of breath than I should have been. Although I can walk for miles, I couldn’t really carry on a conversation while walking, and try as I might, I was simply unable to run for lack of air. I blamed it on being 20 lbs overweight and vowed that someday, when I finally got in shape, I’d run a marathon. I was also more tired than I wanted to be – but I blamed that on four kids, multiple moves overseas, middle age, and an affliction that makes me unable to say “no”. And, apparently, I cough. It doesn’t bother me any, but I’m finding out my loved ones have noticed it (a lot) and find it rather annoying. But I would have sworn to you I’m not sick – just, well, a little bit not quite right. But now “they” have assured me those are all symptoms of a disease which initially lets you appear healthier than you are. I guess LAM has started to take over my lungs and moved toward my kidneys. And slowly, I will find it harder and harder to breathe until I simply cannot. “They” say this takes, on average, ten years.
Where does one even begin to process that? Before we even started telling family and friends – or our own kids for that matter – I was thrust, unwillingly but entirely necessarily, into a mind-numbing exercise of trying to make sense of all that is life, and all that is death, and how to fully live in every gifted breath. I hope, and believe, that as my plus or minus ten years progress, I will discover more about the meaning of life and that I can exit this reality with more peace than I have today. Because today I’m still a bit of a mess.
One day, or maybe it was night (they’re all a blur lately), while being swallowed both in self-pity and a sea of snotty Kleenex, I decided someone with a terminal illness should probably make a bucket list. Ten years is not near enough time to do all the things you thought you had 40 years in which to do them. My list included many things one would expect to see on a typical bucket list: see “Wicked” on Broadway, visit Machu Pichu, walk the great Wall of China, run a marathon, see Coldplay in concert, hike the Himalaya’s, learn to speak Spanish, sky dive, etc.
But before I even got to #9, I had a revelation. I realized that if I really only had 10 years left, I better first figure out the pointto this life and then waste no time trying to get there. I don’t really have time for pointless activities – unless of course they were done with people I loved – but then, that would be the point. The more I thought that through, the more I was convinced I couldn’t (wouldn’t) make a bucket list full of typical things one does before one dies. Because, I reasoned, those typical entries were all deposits made into “ME”. Places I wanted to go, wonders I wanted to see, things I wanted to do – all of which, are all for ME. With only 10 years left, why would I only make deposits into ME? When I die, those deposits all die with me. The only legacy one can possibly leave behind that makes any sense at all is a deposit into OTHERS. What I really must do for the last 10 years is pour whatever energy I have left in me into other people. In my less selfish moments, when I’m not grieving over the fact that I will be robbed of maybe 20 or 30 years on this planet, I have concluded I must spend my years sharing the love that I believe can only be found in Christ Jesus my Savior. I want to live like Him – just extravagantly loving others and pouring myself out for them.
So, this is my better bucket list: