Brad’s Story

Site created on March 3, 2018

Brad was admitted to Methodist Hospital in Des Moines on Thursday, March 1 after a week of being sick. He was first diagnosed with RSV on Feb 24 and sent home with an inhaler, and then was diagnosed with pneumonia yesterday morning in the ER. He is currently being treated with oxygen, fluids and antibiotics. During the first few hours in the ER yesterday, we came to learn that Brad's white blood count was very low. And after 36+ hours of treatment, his white blood count has remained the same. We met with a hematologist/oncologist this afternoon who strongly recommended doing a bone marrow biopsy to determine why his white blood count was so low. Unfortunately, because Brad was still coughing so much, he was unable to have it done today. It is now scheduled for Monday morning. Late this evening we met with an infectious disease doctor who talked us through what to expect on Monday and in the upcoming week and answered many of our questions. He was a believer and that was a great comfort to us. We are scared and apprehensive, but not shaken.

I am asking for prayer for several things. First, please pray that God would miraculously increase Brad's white blood count in the next 24-48 hours. Normal numbers are between 4-10. Brad's is at 0.7. His body is unable to fight off the pneumonia, so he's being monitored closely and his vitals are checked often.

Please also pray for protection for Brad. He is very, very susceptible to infection. Right now he isn't allowed any visitors except for me, and that is only as long as I stay healthy.

Please pray for preparation for our family for whatever medical journey the Lord has for us. He is sovereign. He is good. We can trust Him with this.

Please pray for the biopsy on Monday. That Brad would be able to lay completely still for the duration of the procedure without coughing. Also pray for quick and accurate results. It could be up to 3-5 days until we receive a full pathology report.

Please pray for our kids. They miss Brad so much and aren't able to see him. Long hospital stays are completely foreign to them. Please pray that they would put their hope in God.

And finally please pray for me. Through many of our years of ministry together, God has used me to love and care for others. It is very hard for me to be on this side.

We are holding fast to Christ, the only solid rock we have.

"Because he holds fast to me in love, I will deliver him; I will protect him, because he knows my name. When he calls to me, I will answer him; I will be with him in trouble; i will rescue him and honor him. With long life I will satisfy him and show him my salvation." Psalm 91:14-16

Newest Update

Journal entry by Jenny Aust

"So we do not lose heart. Though our outer self is wasting away, our inner self is being renewed day by day. For this light momentary affliction is preparing for us an eternal weight of glory beyond all comparison, as we look not to the things that are seen but to the things that are unseen. For the things that are seen are transient, but the things that are unseen are eternal." 2 Corinthians 4:16-18

Brad had a good appointment today with his oncologist. We continue to be very grateful for the care Brad is receiving at Mayo Clinic. We felt heard and understood and had many of our questions and concerns answered.

We first discussed his most recent labs, which showed a slight increase in his WBC from 2.3 last month to 2.7 and a slight decrease in his neutrophils from 1.15 to 1.06. His monocytes and lymphocytes (2 other subsets of the WBC) continue to be low as well. But the rest of his labs were normal. Then Dr. Parikh walked through the additional tests that were done on Brad's bone marrow in December. (It was A LOT of tests.) Even though we already knew those extra tests came back normal, it was good to get more specifics on what they were looking for.  And after hearing about all the chromosomal abnormalities,  pathogenic mutations, and other types of leukemia they tested for, we were that much more thankful that they were all normal! We also looked in detail at his blood panels since he was first hospitalized March 1, 2018 up until now. Unfortunately, because Brad never had a complete blood panel before he was diagnosed with hairy cell AND we didn't do a repeat bone marrow biopsy after his chemotherapy in 2018, we don't have a complete picture. 

So the plan going forward is for Brad to have labs every other month. If his numbers continue to decline, we may need to begin some sort of treatment. The average time between hairy cell relapses is about 8 years, and next month will be 6 years since his diagnosis. 

We did ask about how restrictive Brad needs to continue to be with regards to masking and spending time with large groups of people. Since his numbers are relatively stable, and he has had ZERO signs of infection....really since his diagnosis...we can back off on some of them. We are so thankful for a bit of relief! So Brad will continue to eat well and exercise, and I will watch him like a hawk for any concerning symptoms.  

While we had hoped his numbers would have been higher, we are resting in the fact that God knows when doctors don't and that our hope is in God and not in modern medicine. Though I am tempted to live my days in fear and worry...watching and waiting for Brad to get sick, I hope, instead, to live my days like Elisabeth Elliot:

“Waiting on God requires the willingness to bear uncertainty, to carry within oneself the unanswered question, lifting the heart to God about it whenever it intrudes upon one's thoughts.”

May we all lift our hearts to God when worry and uncertainty fill our minds. 

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