eight years

Feb 20, 2020 by

Today is the 8-year anniversary of my initial hip injury. For the first time, I don’t have a celebration planned. In past years, we have had dinner parties, breakfasts, walks, and bike rides, but I’m not up to it this year. I’m fighting some immense emotional battles and with the loss of our babies last week, I don’t really want to talk to anyone, much less celebrate with a party, but I am definitely still remembering that day. How could I forget the day that changed our lives forever?

I remember running around the greenbelt on the 17th and how good it felt. It was the first run I was able to successfully manage my breathing and actually enjoy instead of feeling like I was in some sort of torture machine of my own making. I remember the back handsprings I did that day in the gym, a whole string of them across the mat. I remember feeling like Keziah and I were going to have an epic year of training and participating in triathlons, laughing and growing and accomplishing hard things.

That all changed on our run on the 20th. A searing pain started in my hip joint that brought tears to my eyes. My steps became shorter and slower as I struggled to breathe through the pain. I was determined to finish my training schedule for that day and tried to limp-jog while physically pulling my leg forward with my hands. It did nothing for the pain and I slowed to a walk. Keziah told me I didn’t need to keep trying, she would run on her own and that I should go sit down. Refusing to give in, I kept trying to continue, but finally the pain was so great, it was all I could do to hobble over to our Suburban. With tears frozen to my cheeks and pain coursing through my body, I tried to talk myself out of thinking something was really wrong.

But something was really wrong. It took us weeks to find out that I had torn my labrum in my right hip socket. That injury started a cascade of many other injuries and damage to my nervous system. For about six years, I lived in a variety of braces, splints, and wheelchairs. The nervous system damage progressed to sympathetic nervous system responses which look and feel like seizures, but are not brain-mediated. In 2015, after months of my nervous system shutting down more and more and being unable to digest food, I was given a miraculous gift of treatments with Dr. Calzada in Tijuana, Mexico. Since then, I have gone seventeen times and received stem cell treatments along with chelation, magnet therapy, radionics. These treatments saved my life. I don’t know if I would have actually died or not, but they have definitely given me back the functioning of my body. I can now walk and ride my special forward-crank bike and kayak and hike and drive and so much more that I never knew I would be able to do again.

And so today, my heart is grateful. So, so grateful for the many friends and family members who have taken care of me time and time again when I was unable to take care of myself during seizures or injuries. I’m so grateful for the nurturing our family has received, especially the love and support our children have been given as they had to adjust their lives to having a mama regularly pass out, shake uncontrollably in front of their eyes, and spend much of her time in bed. I’m so grateful for the life my friends have helped me to live by including me in their activities even when it wasn’t convenient to haul me around. I’m so grateful for the amazing treatments I have been blessed with that have strengthened my ligaments and calmed my nervous system.

I’m so grateful for Richard. He has taken care of me for the past eight years with so much patience and tenderness. Not a single time has he been frustrated with me for getting injured again or passing out or causing our family great inconvenience. He has willingly served and loved and filled me with hope and laughter again and again. He has sacrificed much, working 60-80 hours a week to provide for our family and then coming home exhausted and willing to keep working here to make up for all the things I couldn’t do. His heart and hands are always ready for one more conversation, one more act of service, one more challenging situation.

And now he needs us. In one short week he is having brain surgery to remove a vestibular schwannoma. We have no idea how surgery will turn out. It is quite possible he will never be able to work in his current profession again. Our lives are about to change dramatically. At times that feels absolutely overwhelming, but most of the time, we are filled with peace. We know we are in God’s tender hands. We know we are not alone. We know we have an army of people who love us. We know we have each other and that we can weather fierce storms together.

So we are sailing forward, with courage, hope, and faith, not in an outcome that everything will be okay, but in confidence that God is with us, that our covenants are eternal, and that somehow, someway, we will come out the other side.

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i never saw this coming

Feb 10, 2020 by

Oh my goodness, how to even start here again. I need to, because I want to remember these days forever and I want our children to have a record of this time of our lives. So much has happened since I last posted in May of 2019.

We had a glorious summer of adventure, camping and kayaking together as a family. I felt and functioned the best I have in nine years and we played as hard as we possibly could. Then September came and I completely fell apart emotionally. For seven weeks I barely functioned as I dealt with the death of our dear nephew, Kyler, mountains of survivor’s guilt, and deep personal pain.

In December we discovered we were miraculously pregnant. And on January 8, Richard was diagnosed with a brain tumor.

The last four weeks have been a blur. We are surviving and holding on to faith and hope and love and each other. But the days roll on, one after another, and I can barely keep up. The first four weeks were busy, all day, every day, with phone calls and doctor’s appointments. The last few days, since his surgery to remove it has finally been scheduled, have been much needed balms for my soul. The fight for surgery with our preferred neurosurgery team and insurance to cover it was intense and now that that fight is over, I feel like I can finally breathe again.

This journey needs documented and I’m going to give it my best effort, which at this point my best is sorely lacking, but I am going to really try.

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