So How Are You Doing?

“So, how are you doing?”  Even though this question has been asked multiple times, I still don’t know what to say.

Our first meeting to discuss Veronica’s diagnosis was with Dr. Adams at the University of Minnesota.  While Dr. Adams talked about what they found in the MRI with us, the resident who was with Dr. Adams pulled up the MRI images on a screen behind her.  In that moment I recognized this is something real and monumental.  I felt very small and unprepared, but I knew I would do anything to help Veronica.

At first when people asked me the question of “How are you doing?” my thoughts went right to the little guy that on the Axiom in the movie Wall-E.  The whole situation seemed epic and on its own trajectory, while I just needed to be around to help remove “foreign contaminants.”

I soon realized that this was completely wrong.  This isn’t just about Veronica, it is about all of us supporting her.  When we started to tell people about the diagnosis we were met with an outpouring of compassion and offers to help from almost everyone that we shared with.  Even people I consider casual acquaintances have offered time and resources.  I need to allow everyone around us to do their part.  This makes me feel like Veronica, the kids and I can get through to the other side of this not unscathed, but well cared for.  So how am I?  I feel well.  I feel at peace knowing that so many people are prepared to help in any way they can.

Approved!

I spoke with Kris at UCSD a little while ago.  She shared that the surgical coordinator spoke with my insurance company yesterday and it’s official, surgery is a go for 1/23. The exact time may change from what I was told several weeks ago, but only by a few hours.  I will know the definite time when I have my pre-op meeting with the surgeons on 1/22.

Jake asked me how I feel now that I have this news.  Honestly, I think I’ve reached the point in the process where I’ve accepted what is in front of me and I’m ready.  I know there are still many unknowns (e.g. How will I handle anesthesia? Will they be able to remove the entire tumor? What will the impact on my facial nerve be?  How quickly will I regain my balance? How will the adjustment to SSD go?) but I will face each one as I’ve faced my initial diagnosis and I know I’ll get through them.  I’m not anticipating any of it will be easy, but I know I’m not alone.  I have the love and support of my husband and kids and so many others who have stepped forward to walk through this alongside me.

Now my focus can shift to prepping things for the Shecklets and my in-laws for the two weeks we’ll be gone.

T minus 2 weeks.