Skip to main content

On Writing

 Writing is a funny thing. It is truly an art - being able to describe how you feel in a way that is not only accurate but interesting and with style. I don't feel quite equip often - like my words aren't exactly what I want them to be but I try not to let that stop me from writing. I tend to have thoughts fly through my head that make me think "I should write about that." Sometimes the thought leaves my brain and I move on with life. Other times the thought sticks in there. It almost pings around in my brain, going from the forefront of my thoughts then back into my subconcience and then pings back out to the foreground again as if it isn't leaving my brain because I need to chew on it for longer. And often I chew on it by writing about it. I am not a 'sit peacefully and ponder in silence' person. My thumbs like to twiddle, my knee likes to bounce, and I oft can't sit still if there is unfinished chores in my immediate surroundings. 

My best thoughts frequently occur when I drive myself somewhere alone - when I am forced to sit and do only one mindless task alone (with a radio of course.) In the same way writing forces me to sit, with fingers moving, and just think. I would describe my writing as raw, simple, and pointing to truth and maybe even too much of a "word vomit" theme is strung throughout these blog posts. But it is an outlet to say it simply. An outlet for me to lean into my heart and sit in it - to reflect, to ask God to work, to ask God to change my heart. Sometimes I don't share it. Sometimes it feels right to share. Often, I walk away feeling a little lighter. Feeling like I put those thoughts on paper and it helped me through them and I can move onward. 

There are many blog posts I could write - about Jack, about pregnancy with a CHD diagnosis, about our hospital stay, about grief and loss, about living in Africa, about dietitian stuff. But often those are big broad topics that feel intimidating, not the mundane day to day that is pressing on my heart and mind. Thinking about biting off a big topic like any that I just listed feels like a research project that the teacher said has to be at least 20 pages (and let me tell you that in my BS at JMU, I never wrote anything longer than 10.) 

I don't know why I am sharing this - maybe to say this: whatever it is that lets you just feel, that gives you the space to sit and reflect and let God work on you, do that thing. It is important. It is part of your story. It is shaping you. 

Comments

Popular posts from this blog

Day 1 - July 12th

    I have desired to write about Jack and our child rearing experiences in general for a while and I frequently push it off and it just simply isn't a "right now" priority. Starting today, on what would have been Jack's 2nd Birthday, I am going to write daily (or try to) for the next 35 days in remembrance of the 35 days he lived on this earth. It will likely be unedited, imperfect, and intentionally raw - partially for the sake of time (I work, do school and we have a toddler in foster care ok?!) and partially because that is the theme of our story, imperfection (made perfect through Christ).  Today, I want to talk about birth. More specifically, medically complex birth. I get asked often if I had to have a mandatory c-section - thankfully no I did not. But I also did not expect to go into labor at 35 weeks and 5 days either and I am certain that is the worse option here. We came home from a week at the lake with Ike's family and as we are getting into bed Ike s

Day 2 - The NICU

 The NICU is a place you are extremely grateful for but you also dread its existence. You are so thankful that your fragile baby has around the clock expert care but you also hate that your baby has to be there without you. And then when you are there you feel awkward - you’re the mother but his caretaker is the nurse - you have to ask permission or for help to hold the baby (so many lines/drains so it’s not easy to pick them up). It’s also just heartbreaking to see the other babies that have been there for weeks or even months. Jack’s isolette/crib/bed was next to a baby born at 24 weeks (on April 8 actually) and it was July 12… he was still tiny with a young mom who we witnessed have hard conversations about her capacity to care for such a tiny fragile baby. The baby on the other side was born via c section because his organs were on the outside of his belly (omphalocele) and he cried and cried and cried. (We actually had a mom bring a baby with this same diagnosis to our house in Ug

Day 6 - ECMO

After all that surgery talk, this seems like an appropriate time to talk about ECMO.  ECMO stands for extracorporal membrane oxygenation - basically an exterior heart and lungs. Only a few hospitals in Virginia have trained teams and adequate machines to run ECMO. We learned a lot about it because there had to be someone in Jacks room 24 hours a day to monitor/run the machine. Like for bathroom breaks or lunch breaks - they had another trained ECMO person come and sit in the room while they took a break. We met almost every ECMO worker (a few didn’t do peds) and we talked with them a ton. They were present for many hard conversations with doctors, surgeons, nurses, chaplains, etc. They did things like get us lunch when the free lunch carts rolled by, bring us honey from home, update us on medical rounds that we missed. They felt like a second family. We wrote down almost all the nurses and ECMO techs Jack had - we wrote down 15 names for ECMO and I know we missed a few (like the night