Mike’s Story

Site created on July 19, 2018

The original story from 2017: Mike Westberg was diagnosed with leukemia in 2017. He has endured chemotherapy every three weeks to keep his CMML in check, which can only help until it no longer helps. As a family we were told this from the start: The only option was on-going frequent chemo, which wouldn't work endlessly. The only true cure would be a bone marrow (or stem cell) transplant, which a doctor would have to be convinced is the best route, which isn't that common for 70 year old guys. So, unless a doctor would agree to do a transplant, and  only if a marrow match was found, our dad wasn't getting the best news and we were all so sad. 


But then. In the spring of 2018 it was discovered that Mike's sister Sandi is a perfect bone marrow match. This was fan-freaking-tastic news, but still Mike's doctor needed to agree to give this risky procedure a try. You see, the recovery road for most people is very difficult and not always worth the risks, especially in the "golden years."   


Long story short, Mike's doctor said yes, and we said HALLELUJAH. The doctor said yes because of the rare perfect match in Sandi (there was only a 20% chance of that) which helps a whole lot with the process, and because Mike is in such excellent health for being nearly 70. His doc considers his body's organs and functions to be more of that of a 55 year old. (Thanks, metabolism! Thanks Westberg genes! Other than that cancer stuff, you're pretty great!) 


And so the journey has begun. Mike and Sandi's stem cell transplant journey will begin on August 4th, and he will be in Rochester for at least three months. We (Mike and his wife Linda of nearly 50 years, daughters Shelly & Heather (ages unknown) and grandkids, Zachary, Maxwell, Miles, Asher and Elsie) appreciate your thoughts and prayers as we walk the precarious transplant journey together. We are learning to be less in control than we have ever been. We are scared and hopeful at once, and ready to face what may come. We are so grateful for all of our friends and family, and for Sandi especially, as she sacrifices her time and DNA to give life back to the loving, supportive and hilarious husband, son, father, grandpa, friend, cousin, uncle and father-in-law we love so dearly. We feel your thoughts and prayers and appreciate you all so much. 


(A lot has happened since this intro, so please read the latest updates for the most recent news.) 

Newest Update

Journal entry by Heather King

To those of you that only get updates through Caring Bridge, I apologize. (This is daughter Heather.) I update a lot on Facebook, Instagram, and now with writing on Substack and forget to update here. But I remembered today. :) 

Our time as a family on hospice has been beautiful. Or "brutiful" (brutal and beautiful) as writer Glennon Doyle likes to say. There are so many ups and downs, and we are constantly learning how to ride those out. 

For several months, dad stayed about the same. He didn't lose more weight, he was walking well for a guy in his situation, and he didn't have a lot of pain. That has changed in the last month or so. His Graft Versus Host Disease has been working on his legs, skin, lungs, and most likely other places we don't know about yet. Dad is short of breath a lot, and his muscles seem to have decided to only weaken now. It's getting quite difficult to walk, but he's still plugging along. There have been days when we thought we were very close to him being bed-bound, but he rallies and keeps going despite the pain and stiffening from the disease ruling his legs. 

I have been his main caregiver, with some other caregivers coming in for respite. Shelly has had a lot of life changes and recently moved to Florida. That move ended up not sitting well with her as she ached to be here with dad. She has made trips back to New London and stayed for about a week at a time and is now coming back to stay at dad's house indefinitely. The band is back together and we all have more peace because of that. She will head back to Florida, Dave, and Jarvis the dog in time. 

We are so blessed to be able to spend this time together. We are grateful for every moment with dad, enjoying his quick wit, hugs, and everything about caring for him. He is patient in his suffering. He shares a lot of stories from his life and continues to love as well as he always has. We are so grateful for him. The loss that is coming will be very difficult for us, and at the same time, we really want dad at peace and free of this horrible disease. Please send your love and prayers dad's way. And if you have a moment, send him a message (he can still see his Facebook messages) or note in the mail. He is cheered by every kindness. 

204 Pine St SW 
New London MN 56273

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