A Simple Timeline

A Simple Timeline...

March 9, 2014- Admitted to St E with minor symptoms (on eve of move from house to condo*)
March 10- Guillain-Barre diagnosis and progression to full paralysis and intubation
March 12- Transfer to University Hospital NSICU
March 12-26- NSICU at UC
March 26-27- Brief stay at LTAC- Drake Hospital at Christ
March 27- Emergency surgery for bleeding trach, transfer to SICU
March 28-April 14- SICU at Christ (pneumonia and PE treatment)
April 14-19- MICU at Christ
April 19th- Transferred back to Drake Hospital (at Christ) ROOM 3083 (Easter weekend)
July 31- First time outside in 21 weeks
August 25- First meal in 5 1/2 months
October 16- 67th birthday at Drake
October 31- MICU at Christ for treatment of pneumonia and MRSA infection
November 17th- Return to Drake Hospital (at Christ)
Thanksgiving-Christmas-47th Anniversary- New Year 2015
January 17th- Hematoma (dealt with for about a month following)
March 19- 2 weeks off the ventilator! Trach capped for first time ;)
April 4&5- Baptism service and Easter
April 20- "So long" party with Drake staff
April 23- Move to Providence Pavilion rehab center in Covington, KY
May 26- June 10th- St E hospital (trach out, MRSA treatment)
June 10th- moved to Gateway Rehab in Florence, KY (feeding tube removed)
July 2nd- moved to Rosedale Green in Latonia, KY
August 8th- first time sitting in the seat of a car in 17 months
Oct 16th- 68th birthday party at Rosedale
November 26th- Thanksgiving with family+ at the Rickerts
*November 27th- first time in condo since purchase*
January, 2016- began using a motorized wheelchair controlled by head
July 10- move to HealthSouth rehab to prepare for move to assisted living
July 28, 2016- moved to Elmcroft Assisted Living in Florence, KY. After 871 long nights apart finally sharing a roof with wife again!!
August 2018- moved out of Elmceoft. Steve to Emerald Trace. Nancy to the condo.

Tuesday, March 24, 2015

Blog post from Becky

We finally got a chance to go back down and visit Mom and Dad last weekend. It had been too long. Alex and the kids helped Mom at the condo, preparing for spring  - which has finally come - and I got in some quality time with Dad.

It is so wonderful how much Dad has improved recently. I cannot help but sit and stare at him when I am visiting. I wonder what he's thinking, I reflect on our past together, and I ... just stare. I watched him as he slept, talking a bit in his sleep, and wonder what he is dreaming. Is he having another dream about Heaven? Is he dreaming of times spent with Tim and me as kids? Is he dreaming of trains? Dreaming of Mom?

As I was leaving, he told me how proud he was of me and how I am raising my kids, how I am doing in school, etc. I tried not to, but I cried. It is SO GOOD to hear my dad's voice again and especially to hear such loving words. He apologized for not being more "entertaining" while I was visiting, but I told him I enjoyed my time with him immensely. It was as if we were just sitting at home, relaxing and watching TV - doing our own thing. It's what we do. And I love it.

Thank you for continuing to pray for our family. It means so very much.

- Becky ;)

Monday, March 23, 2015

The Frontporch in our thunderstorm

We have often referenced this GBS journey as feeling like we are in a boat rowing against a storm. This sermon from our college friend, Shawn Spradling, helps flesh out that image even better. (Reposted with permission) Thank you for straining against the oars with us.


Click here to listen The Water Walker 3/22/15



Friday, March 20, 2015

New Accomplishments! (Blog update from Nancy)

As we head past the first year of this illness, we have some new accomplishments of Steve to celebrate!

He has achieved almost two weeks without the ventilator, just receiving oxygen through his trach.  Today, they “capped” the trach and he now wears a nasal cannula to receive oxygen and he receives just a little higher percentage than what we all breathe! He has worked up to four hours a day with this new process.



Steve is also enjoying more choices in his diet, due to passing a swallow test a couple of weeks ago.  He is on the middle level diet, allowing soft pieces of food. No steak yet! Because of his increased oral feedings he will now only be on the feeding tube at night! He thoroughly relished a milkshake brought in by his former boss, Mitch☺

So, as Steve reaches these milestones, it is time to start researching places for him to move for continuing his recovery. A daunting task, representing the real progress we’ve all been praying to see!  Longtime blog readers will remember when we were praying to hear a word and for him to be able to swallow.

As we mark a year fighting this disease, we want to share with you a picture that represents what each of you means to us. The image came to me of a blanket, woven from brightly colored ribbons.  Each ribbon represents a person or persons who have come around us and provided prayer, visits, cards, yard work, moving an entire houseful of contents, putting those contents into a new house, yardwork, meals, help with water pipe burst and repairs, installing dishwasher, fixing dryer, building storage shelves, fixing cars and/or taking them to garages, care for Charlie (dog), haircuts (thank you, Lisa, our hairdresser!), creating the blog (dear Flora), fixing computer issues and setting up Steve’s access to  the internet, overseeing the Helping Hands calendar for visits (thank you, Kristy) AND the constant vigilance and care of the teams of medical personnel at Drake LTAC at Christ.



Whenever we have felt alone, fearful, or weary, we have wrapped up in this blanket.  We believe that God prompted each act of compassion, empathy, kindness, skill and generosity in those who became our blanket. These scriptures say it best:

 Isaiah 65:24 “Before they call, I will answer and while they are still speaking, I will hear.”

 James 1:17 “Every good and perfect gift is from above, coming down from the Father of heavenly lights, who does not change like shifting shadows.”

Thank you all so very much for being with us in this.

Steve and Nancy

Monday, March 9, 2015

365 Days of GBS... (Blog update from Tim)


One year ago today I was visiting my parents on the eve of their big move from their house of 20 years to their condo. More than just a change of address, this move signified their transition to mutual retirement. Their months of down-sizing and their well-stocked camper, "Cubbie," testified to the fancy-free spirit with which they were approaching this next chapter of their lives. 

Unfortunately, this chapter would be preceded by another, unforeseen and unwelcome chapter. That night, at around 3:00 in the morning, I awoke to my mom knocking on the guest room door and found her and my dad in the hallway. Dad was struggling to keep his balance and Mom explained that his eyes had locked cross-eyed and his arm had lost sensation. We quickly drove to the hospital for what we feared was a stroke. Over the next few hours, we watched helplessly as Dad continued to lose the use of his arms, then his legs, then the rest of his body until only a slight twitch of his eyebrow remained. With Dad now on a ventilator and completely paralyzed, but still able to hear and feel everything around him, our family too felt paralyzed as we stood there, confused and horrified by what we were witnessing. Up to that point, most of us had never even heard of Guillain-Barre Syndrome (GBS), the diagnosis doctors determined as to what was happening to Dad. Since then, we have become reluctant experts on this inexplicable and torturous medical condition. 

It is hard to believe this blog now represents a year of this unwelcome chapter. Flora has so diligently captured the challenges, questions, fears, and celebrations that our family has experienced – and continues to experience – as Dad makes his way forward through his recovery. And while Dad IS recovering, he is still functionally paralyzed and has now lain in a bed for 1 entire year of his life. As I write these words, and try to reflect on this past year, I find myself pausing… getting stuck… simply unable to find the words to describe this journey and do it justice. There is no summary for something so overwhelming. 

I was able to spend this past weekend with Mom and Dad. Saturday night Mom and I went to dinner and reflected together. I said to her, “I feel like I should say something like ‘Happy Anniversary,’ but obviously that’s not right.” Congratulations? No. Still, something Herculean has been accomplished here. Despite the ups and downs of the past year, and multiple near-death encounters, Dad is still here. And for Mom, her steadfast presence by his side has not faltered, despite her own fears and exhaustion.

Mom said to me, “It is an accomplishment. But I wouldn't feel comfortable taking the credit. It really has only been by God’s strength and the help of our family and friends. I have truly learned what it means to walk by faith, being grateful for each day as it comes. All I can say that I've done is just show up, each day, and try to be present for what is right now.” 

I cannot express how incredibly proud I am of my mom. Her commitment and strength inspires me. The love she and my father share continues to be a blessing that pours down throughout our family. 

Dad is doing noticeably better. His voice is stronger. While still paralyzed, he continues to regain movement a little bit at a time. When I left on Sunday afternoon, he had been off the ventilator and on the trach collar for nearly 3 days straight! In fact, he now considers the ventilator to be an uncomfortable interference to his breathing! Considering where he has been this past year, this truly is something to celebrate. 

Before leaving, I asked Dad what thoughts he’d like to share for the blog. Mom was there too, and we both listened as he thoughtfully shared these reflections of this past year: 

“Well, I know more about how many alligators are on TV.” (This said after hours of History Channel reruns of Swamp People. A good sign that Dad’s dry sense of humor is still intact.)

“It’s still obvious I've got a long way to go, but I’m doing ok. I can really feel the prayers of all the people thinking of me. I really appreciate that. I am healing, although very slowly. Still, it is very comforting to know everyone is praying for me. 

I really appreciate the way family and friends have come by to visit me. It really helps break the monotony… but also gives me opportunity to hear the Word of God. Thank you especially to Rick Thomas for reading the Scriptures to me.

The staff here has been good. I’m thankful for the nurses, surgeons, and RT’s who have been caring for me – I wish I could name them all, but I’m afraid I will forget someone. Dr. Krause has been like a mother to me, always checking in to make sure I’m comfortable. 

Thank you to Flora for putting this blog together and keeping all of my friends and family up to date on my story. 

My grandkids have been most attentive. I have colorful cards and pictures hanging all over my room.

I couldn't have done this without Nancy. She has been the light of my existence. I am so lost without her. 



Then Dad’s thoughts turned to the future: 

I think about the things I can do when I get better. What will I be able to do? The things I CAN do give me strength. But I also remember that I've pledged my life to Christ to do whatever he calls me to do. So I believe he will only call me to things that I’ll be able to do. But still, I've committed the rest of my life to doing his work. This is the reason I want to be re-baptized. I want to mark this time in my life. 

When I first got this, I had a dream. I was brought to some kind of meeting where there were two doors: one leading to heaven and one leading to hell. Standing there was an angel. As I stood before the doors, I told the angel I wasn't ready. That I needed more time to be sure Nancy was taken care of.  Then after Nancy’s heart episode, she told me she was taken care of. I had the dream again and this time I said I still wasn't ready. The angel seemed to understand. I haven’t dreamed of that meeting since, and at first I worried that I had missed my chance. But now I believe it is because I still have work to do in this life. 

After a few moments of quiet, Mom said she probably should get going since she was headed to someplace she didn't know how to get to. Dad looked at the clock and said, “You still have 5 more minutes to hold my hand before you have to go.” So she did.

After that, I walked Mom to the elevators. We hugged and I said, “Let’s not give this thing another year. This year, let’s be done with it.” 

She agreed and said, “It’s hard not to feel like we've been robbed this year.” 

“We have been robbed,” I said. “We've had a year stolen from us. But thankfully, we haven’t been robbed of what’s most important.”

Returning to the room, I told this to Dad. To my surprise, he replied, “I don’t feel like I've been robbed. I feel like I've been drawn closer to the things that are most important to me.”

On Saturday, I noticed Dad had a bunch of lilies sitting in the window that had yet to open. On Sunday, at one point during Dad’s reflections, Mom drew our attention to the windowsill and said, “Oh look! Your lilies bloomed.” 

A good sign for the year to come… 


Thursday, March 5, 2015

Tears of Joy

Very encouraging news to send along this week! Steve has regained the ground he lost during the hematoma setback of January into February.

He is off of most of the pain medicine and is much more alert and conversational. Visits with him are so much easier.

It has been determined by pulmonologists that he has the use of his diaphragm now and the breathing results he achieves are with the correct muscles, instead of secondary muscles which is all he had to use before. Yesterday, the pulmonologist said that he had “beat the odds” referring to his opinion of almost a year ago that Steve probably would not come off the vent.  He also praised Steve as a “fighter!” While he is still using the ventilator, his current goal is to be off it and on the Trach collar (just provides oxygen) 18 hours a day. They will raise it up as the daily numbers dictate. He has steadily climbed from 12 hours off the vent to 18 in the last week.

Yesterday, Steve got to get Hoyer-lifted into the wheelchair (last done in September) and we went rolling around the halls of the unit, carrying oxygen behind. It was so good for him to escape the room and the constant beeps of equipment.

Many thanks to friends who, over the past week, kept me able to visit the hospital by fixing our cars, loaning a car to me, and giving me rides. I also got to take that trip to refresh with family in Ft. Wayne. Thanks to those who visited Steve during those days.

Thank you all for prayers and other thoughtful help!

Nancy and Steve