Saturday, June 19, 2021

Well Done

A tiny memorial of Nancy on a beach stone at her favorite place, the beach at the end of our road.

Nancy Lou Severn, 58 of Oostburg, passed away early Saturday morning, June 19, 2021 at her home, surrounded by her family.

Nancy was born to Glenn and Jean (Schnell) Steinbrecher on January 26, 1963. She graduated from Oshkosh West High School in 1981.

Nancy was united in marriage to Kenneth Severn on June 4, 1983 in Oshkosh.

She was employed as a special education teachers’ aide at Plymouth and Cedar Grove-Belgium School districts.

Nancy enjoyed the Lake Michigan beach, paddle boarding, hiking, biking, but most importantly, investing in people and relationships, and living out her faith in Christ Jesus.

Nancy is survived by her husband of 38 years, Kenneth; children, Andrew, Timothy and Matthew (Malorie) Severn, and Sarah (Ross) Fale; grandchildren Desmond, August and Isla; parents, Glenn and Jean Steinbrecher; siblings, Deb, Susan, Brian, and Lauri; parents-in-law Doris and Robert Lowell; sister-in-law, Ruth; nieces, nephews, other relatives, and friends.

She was preceded in death by her sister Judy in November, 2020 and father-in-law William Severn.

Private family services will take place at a later date.

The Wenig Funeral Home – Oostburg is serving the Severn family. For more information or to leave online condolences, please visit Wenig Funeral Home .


- Nancy Severn's Legacy of Love - 
Ken, Matt, Andrew, Tim
Malorie, Nancy, Sarah (missing Ross Fale)
Desmond, Isla, August






To the prettiest, most gracious woman I ever met:
It was a privilege and a blessing to be your husband.
Thank you for sharing your life with me. I miss you dearly.

Thursday, June 10, 2021

Journey Home

Nancy and I have been working on a draft for several weeks, but now things have changed, so I'll share what has been happening since April 21.

On May 6, we had a new MRI done and a consult with our oncologist. It was a bit discouraging hearing the cancer had shown some growth since the last MRI. We were advised to consider starting treatment with the drug Avastin as a "quality of life" measure, being aware that the drug does nothing for treating or inhibiting the cancer's growth. The more we read about the drug, the more we thought of the need to trust God and not limit Him. It just seemed out of character to put poison in Nancy's body to "improve quality of life", when that phrase can have different meanings to different people.

It is our belief, based on the facts clearly laid out in the Bible, quality of life begins with our relationship with Jesus and His work on the cross, His death, His resurrection, and the resulting restoration of relationship we can have with our Heavenly Father. Paul, with all the things he suffered, makes this abundantly clear. Solomon and Job talk about this, and David beautifully articulates many life thoughts and illustrations of this. My favorite and a most concise statement of this is found in Romans 8:28 where it says, "all things work together for the good, for those who love God and are called according to His purpose." Understanding this is foundational. Quality of life is having our Heavenly Father embrace us with His love and mercy as we trust in Him through all life's circumstances.

Some of April and the entire month of May was a time of waiting. Every week, Nancy's blood labs returned with flags indicating acute issues prohibiting her from continuing with round three of the monthly chemotherapy treatments. As we waited, Nancy continued to decline in function with left side proprioception, reading, speech, and general cognitive work. Why was this happening? What was God doing in all of this?

Then on Monday, May 31, Memorial Day, I took Nancy to the ER at Froedtert, thinking she may have had a minor stroke. A new CT scan was taken and no stroke was indicated, but after I saw the scan, I realized Nancy was in trouble. 

On June 2, we got a call from our oncologist who said after a review of the CT, the doctors feel there is no need to continue any chemotherapy or other treatments, and no follow-up MRI will be done. The evidence in the CT is sufficient to see there has been substantial change in the growth of the cancer, and there are no options left to consider. At this point, we were directed to seek palliative care and hospice.

The doctors found the following. 

She continues to decline clinically, despite chemotherapy and supportive measures to treat her GBM and left sided weakness/neglect.

Marked vasogenic edema on right parietal with likely disease recurrent at center with significant mass effect and MLS.

CT showed increased size of GBM, increased vasogenic edema, and new midline shift (right to left) of 9mm concerning for herniation.

The right frontoparietal GBM mass appears to have increased in size by at least 4mm since the study performed 4 weeks prior, now measuring 3.4cm.

 
Thursday, June 3, Sarah and Nancy near the beach. The two most beautiful women in the world!


On Friday, June 4, our 38th wedding anniversary, Nancy and I went out to breakfast with two of our dear friends, Michael and Carolyn. After breakfast, we met with two Sharon S. Richardson Hospice representatives at our home. After some paperwork, we planned to meet with a hospice nurse the following Monday at our home. We intended to stop at our local funeral home to gather some  information, but we were both too exhausted to go. Just the kinds of things most people do on their 38th wedding anniversary, right?

On Sunday, June 6, after tucking Nancy into bed, things took a significant turn for the worse. Since then, Nancy requires 24 hour care. Monday at noon, the hospice RN started Nancy on morphine to control the headache from the intracranial pressure. 

On Monday evening, a hospital bed was delivered. I put the bed in the living room so we can all be together, and Nancy can have a great view into the woods and watch the sun set to the west. 

Tuesday morning Nancy said to me in the most innocent voice, "I guess we get to spend one more day together." Since Tuesday evening, Nancy can no longer swallow, so she can no longer eat or drink. She cannot talk or move around on her own. She is now readying for her journey home to be with her Lord and Savior, Jesus and her Heavenly Father. 

Wednesday, June 9 was a day filled with family and friends supporting Nancy and family.

Things are much different now, and changing rapidly.


Tuesday, June 1 with Tyler & Amanda visited with their beautiful new daughter.
We have a special place in our hearts for this family!

Wednesday, June 2 my Mom and Dad visited. We had "juice burgers" from Leon's and spent some time at the beach.

Wednesday, June 2 Nancy can't walk down to the water anymore, so I carried her.
I think her face says it all!

Friday, June 4, our 38th wedding anniversary, we had breakfast with our dear friends Michael and Carolyn.
Now 38 years married to this amazing woman so full of grace!
Friday afternoon, we met with Sharon S. Richardson Hospice and set an appointment to meet the RN on Monday.

Saturday, June 5 the Ryan Baumann family felt lead to stop by while we were at the beach with our kids and grand kids. What a blessing!

Sunday June 6 the three of us went to Christopher Farm gardens for a SCCCF event.
We had a great day, but it seemed like Nancy knew something was wrong.
I knelt down to take this picture and tell her I loved her. She said, "Mmm, I know you do.".


Monday, June 7th Nancy is very happy to be in her new hospital bed in the living room

Nancy and "Pops" sharing their love for each other with hand squeezes

Nancy and her "Mum" looking forward to meeting up again soon

June 10, Pastor John praying with us

Recent Photos

















Wednesday, June 9, 2021

Accepting What Is

Nancy mentioned to me some time ago that she started a draft for a blog post. We never found time to work on it together, but I stumbled across it today. These are her thoughts, with very little editing on my part. I trust that her words will touch those who need to hear them.

Nancy's Thoughts

There is only one thing harder than accepting what is; living in denial of what is. Acceptance is a lot of work, daily facing the reality of what is, feeling the pain, and staying connected to who I am and who God created me to be.

As I struggle to accept what is happening to me, I look in the mirror and reality strikes me hard. I wonder is that really me dying of cancer? How can that person be me? How can this be happening to me? I look in my children’s faces and realize that they are going to lose their mother, and my husband is going to lose his wife, and this is how my life is going to end. But it helps to know that Ken and the kids can - and will - take care of each other. 

Gratitude always lets fresh air in the room. My whole life I have dreaded the thought of when I would lose my mom. I am so blessed that she and my dad are alive at ages 90 and 89. My loving and faithful parents have watched over their 6 children, always available to encourage us and cheer us on to live, love, and grow. I wish I could continue doing this for my children. 

Before all of this, I readily accepted the many good times and blessings my family and I have had over the past 58 years. But looking back, It seems my prayers of gratitude were slightly obligatory and somehow only half-hearted, lacking the deeper sense of appreciation from the vantage point of today. Often when I think I am accepting the reality of my diagnosis, the gravity of my future smacks me as I grieve new awareness of my losses.



This past January, it was time to face the fact that I will never drive a car again, so we sold my car. In early May, Not long after, I realized that I will never ride a bike again, and so we considered selling them. Thankfully, our awesome neighbors were already interested in them and so they bought them. Now we see Jason and Janelle riding past our house with happy faces and their dog Callie running along beside them. I thought Ken and I would be riding these bikes for years to come, into our old age with bad knees and all.

June 3, the day the doctor called and recommended we stop the cancer treatment, our son Andrew wrote a poem that put many of our feelings to words.

Between

The clock ticks loudly now, and much too fast.
Her moments slip away so soon, it hurts.
Nothing seems to last.

We linger, too, and unbearably so.
Eons pass, her time expands and contracts
Around our sorrow.

Here we wait, hardly breathing, suspended 
Between the past we loved and a future
We can’t comprehend.

I often feel like I will wake up from this and find it was just a bad dream. But I want to accept this part of my journey knowing that God is good, and that I can trust in His sovereignty.  God cares for me, and He loves me, and He loves and cares for my family. I can be still and know that He is God.

In God’s economy, He doesn't let an ounce of our pain go to waste.  Our tears are not futile. They have a purpose. God knows each of His children intimately, and every tear we shed has meaning to Him. He remembers our sorrow as if He kept each tear in a bottle. In the end, He will share His joy with us when 

He will wipe every tear from their eyes.
There will be no more death, or mourning, or crying, or pain,
for the old order of things has passed away.

He knows. This has always brought me comfort. For the many people who suffer and might think that no one knows or cares, He knows. He cares. God is a tender-hearted Father, a God who feels with us and weeps with us. His promises are a source of comfort to us. 

The Lord said, “I have indeed seen the misery of my people in Egypt. I have heard them crying out because of their slave drivers, and I am concerned about their suffering."  --  Exodus 3:7

When Jesus saw her weeping, and the Jews who had come with her also weeping, he was deeply moved in his spirit and greatly troubled. And he said, “Where have you laid him?” They said to him, “Lord, come and see.” Jesus wept.  --  John 11:33-35

May 6, 2021

After my brain surgery, we had our first follow-up appointment at Froedtert’s Hope Clinic for cancer patients. It seemed to take forever to make our way down the many halls to get checked in. As we were walking, I was thinking of how many people there were in the halls and waiting rooms we passed by, all with cancer. I felt pretty sad and in denial that I was now part of this group. 

Over the weeks and months of doctor appointments, I was able to pick out the people that were probably there for the first time; they still walk with the most normal function. Then there were the others, those being pushed in wheelchairs by worn-out caretakers looking so exhausted, waiting for even just a little relief to come. Oh, how I did not want to be in these waiting rooms. How I did not want to be the one in the wheelchair, and I didn't want Ken to be the vacant-eyed spouse pushing my wheelchair.

At the Jan and Feb appointments, we checked in and then took the opportunity of walking around the hallways for exercise during the 20-minute wait since it was nice and warm inside. Those days are over now. Here I was feeling good having fewer deficits and enjoying the ability to walk around and get some miles in.  I wonder what the other people in the waiting rooms thought of me knowing that this was a very temporary stage, knowing I would soon be like them, in a wheelchair within weeks.


May 6, we find the necessary transition to a wheelchair emotionally difficult yet somehow welcome

Well, this last week I couldn't walk the distance to the Hope Clinic, so Ken got a wheelchair from the front desk. I felt a deep sadness rising in the core of my body and soon I was sobbing in the elevator.

So how am I doing? I am losing my left side rapidly. I can no longer do my own self-care, I can't walk unassisted, and I can't use the stairs. I feel like the expiration date on my body might be getting close. While I love life, I think the time to stop trying to preserve this body will soon come to an end. After all, I have terminal brain cancer. It's going to take my life.

I have peace about the surgery, radiation and chemotherapy treatments I have done so far, but I don't want to spend my last three months fighting cancer or battling the side effects of chemo.  I want to make the most of each day, enjoying the beautiful place we live, and having coffee or tea on the porch with anyone that stops by with fresh baked homemade cookies! Or if you want to make dinner, we can eat, play a game of cards, and talk about what God is doing in our lives. 

Trust in the LORD with all your heart,
and do not lean on your own understanding.
In all your ways acknowledge him,
and he will make straight your paths. --  Proverbs 3:5-6.

So teach us to number our days,
that we may apply our hearts unto wisdom.  --  Psalm 90:12

Now that I am seeing how few days I have left, such that I am numbering them in months and weeks, I am hoping I'm not forgetting anything. Whenever I start to worry, I think about how nice it would be to have a checklist to go down and check things off.  Kind of like when we pack for camping and double-check the list to be sure we packed salt and pepper and matches. Then I remember that I only need to live in this moment and just do the best I can. I certainly don't want to waste today crying about tomorrow!

Naked I came from my mother’s womb, and naked I will depart.
The Lord gave and the Lord has taken away;
may the name of the Lord be praised.  --  Job 1:21

For God so loved the world that he gave his one and only Son,
that whoever believes in him shall not perish but have eternal life.  --  John 3:16

God loves you and me and wants us to have eternal abundant life.

There is only one thing harder than accepting what is; living in denial of what is.

Note

There is so much sadness and so much to grieve in this process, but Ken and I are doing our best to make every day count. Please please let us know if there is something you would like to talk to us about.


Recent Photos


Matt and Mom sharing a moment together

The Brian and Rebecca Kirk family came from Pennsylvania to visit and say goodbye to "Aunt Nancy"

Matt, Tim and I went to the beach without Nancy for the first time.
It's amazing how much relationships add to life, even at the beach.