My Friend in a Wheel Chair
I’ll start with the present and work backwards, I started chemo therapy this last Friday, April 5. I’m scheduled for two or three cycles (two or three months) with a review afterwards for possibly doing a stem cell transplant. Because I have multiple organ involvement, heart involvement being the most serious, my case is riskier than normal. I have an amazing oncologist who is also the Stem Cell Director at Good Samaritan Hospital in Portland. Along with the staff at Compass Oncology in Portland, I couldn’t be in be in better hands.
Three weeks ago I was sitting in the lobby of the Compass Oncology Clinic. I was there for a blood draw and meeting with Dr. Segal. Waiting for my name to be called, I watched as a man was wheeled in for his weekly chemo treatment. He was agitated. He didn’t want to be here. He wanted to go home. Nobody wants to be here, but if you have to receive treatment somewhere, this is the place to be.
His caregiver took him up the elevator where the treatments are administered. And, then he received the bad news. He wouldn’t be going home; he was to be transported to the hospital. It appeared he was too fragile after the fall he took which landed him in the wheel chair. Reminded me of my fall back in January. The hospital is last place most of us want to be, but that’s where he was headed.
Two weeks ago Monday I went to see my primary physician to be checked out for flu like symptoms- the typical ones- fever, cough, aches, headaches, etc. The lab test to confirm came back negative. To be safe, I was put on Tamiflu anyway which after a couple of doses I stopped taking. My amyloid infested gastro system reacted negatively immediately. I had to make a choice.
By Saturday, beyond a cough, my other symptoms were gone. Jenny and I went to the Woodburn Tulip Festival with my son, his with wife, and our grandkids. We had wonderful time. However, in the wee hours of Sunday morning my cough had returned and I had trouble breathing. Off I went to ER that morning for x-rays to see about the possibility of pneumonia. The chest x-rays came back tentatively negative. In other words, they weren’t conclusive. The doctor I met with recommended I complete a five-day anti-biotic regiment to be safe given my compromised- immune system. I didn’t follow through on this either knowing I would start my chemo regiment the following day.
So what am I saying? I suppose for me, it comes down to making the best decisions I can based on the advice of the experts I trust along with weekly blood draw numbers. While I’m online researching regularly, I resist basing my decisions a weekend’s worth of surfing when the experts I’m employing have spent years in school and in practice honing their skills. Still, as my wife Jenny says, sometimes you just have to simply take into account how you are feeling and your instincts- sometimes regardless of what the numbers are saying.
As I left the treatment room yesterday, who do I run into but the guy in the wheel chair of a few weeks ago. This time he wasn’t in the wheel chair. We struck up a conversation. He was being treated for Multiple Myeloma. He had broken several ribs with some complications, the result of the fall he took. Now he was healing and no longer need the extra oversight provided by the hospital. I’m likely to see him again now that I’m getting weekly treatments. I think of him as a new acquaintance, even a friend.
This week I was reading, pondering, and praying Psalm 6 and Psalm 34, in particular verse 18 which says:
The Lord is near to the brokenhearted and saves the crushed in spirit.
And in Psalm 6:2-3 which reads:
Be gracious to me, O Lord, for I am languishing; heal me, O Lord, for my bones are troubled.
My soul also is greatly troubled. But you, O Lord—how long?
And in verse 9:
The Lord has heard my plea; the Lord accepts my prayer.
I’m counting on God’s being near me, his graciousness, his hearing my plea and accepting my prayer, all on the basis of his steadfast love as it says in verse 4. This being the case, the pressure’s off me to perform in any way to get God to do stuff on my behalf other than simply ask and plead. I like it this way and am finding comfort in these words. Please be in prayer for me too that I will tolerate this next round of chemo and that I will reach an even deeper remission.
Thanks for reading!
Curt Bumcrot, MRE
Post cards announcing group testing opportunities around the state were sent out last week. Be sure to sign up soon to reserve the day and testing time that you desire for your children. Also, we recommend using one of our popular practice tests available in one of two formats- available as an instant download or mailed hard copy. To order, go to our practice tests page.
Curt ,I love the fact that you continue to minister to others , where God has placed you. You are a missionary in an familiar territory and a blessing to others .
Thanks, Donna, for reading what I write. Sometimes I feel like what I’ve written is a bit of a ramble. Getting it down on paper though helps me get some perspective, not that I understand any better what’s going on in my life or necessarily what God is doing, although there are hints. The people I’ve met are remarkable, each in their own way- a combination of strength, weakness, and vulnerability. The encouragement I’ve received is a back and forth exchange as together we resist this awful disease, Your prayers and the prayers of others are making a continual difference in my life.
Curt, so beautiful, so inspirational, so YOU. Love you brother.
I love you too, Michael. Thanks for you and Kim being there for Jenny and me.
You’re one strong dude, Cuz. Praying for you every night. Will update our prayer chain. My best to Jenny and family.
Thank you, Susan. I know you and Roger prayer regularly for me as do so many others.
You can ramble all you want my friend, if that helps you get your thoughts and feelings out. I appreciate it that you want to share this journey with us. It helps us know specifically the things that we can pray for you. It sounds like you are back on a routine and that horrible spell is in the past. I hope that I am reading that right. It is great that you can meet others and take the time to get to know their stories too. Thank you for keeping us updated so that we can continue to celebrate with you even the small steps. Much love sent to you and your clan!
I’m hoping there won’t be a repeat of the past- being wheel chair and walker dependent with no driving privileges. My oncologist at Mayo said the success or lack of success of the first 6 to 12 months of treatment will be a predictor of long term outcomes. the heart is the chief concern. I am hopeful the next 3 months will go well, especially having a new oncologist. Please keep praying!
Continuing in prayer. Love you so much and appreciate the updates and openness. Our Lord must love you greatly to trust you with so much. Blessings…
Yes, please keep praying!
Thanks for the update Curt and the flag on FB that you posted one here. I am happy to hear you are back on schedule with treatments as last time we chatted, you were too weak and in the wheelchair. We will continue to lift you and Jenny to the Lord as you journey through uncharted waters.
What encourages me is having a new “guide” (oncologist) who is knowledgeable about Amyloidosis and whose reputation is remarkable in the profession and with the patients he serves. Thank you for praying.
Curt, you are an inspiration to everyone. My kids loved to go to the testing every year because of you. You are definitely in our prayers and in our hearts. I will pray for you to get well soon.