John’s Story

Site created on September 26, 2018

Welcome to our CaringBridge website. We are using it to keep family and friends updated in one place. We appreciate your support and words of hope and encouragement. Thank you for visiting.

John was first diagnosed with Idiopathic Pulmonary Fibrosis in January 2013. This means scarring of the lungs with cause unknown and no known cure. Scarring continues and ultimately reduces the volume and transfer of oxygen. Post diagnosis John continued to pursue the things he enjoys such as travel, playing guitar, daily trips to Caribou, etc. John was prescribed Ofev in January 2017 - which was designed to slow the progression. During the summer of 2018, his lung function was reduced enough that he was struggling to do small things without oxygen. At his last check-up, the doctor asked if John would like to be placed on the lung transplant list. The answer was "Yes" and as of September 10, he was on the official list. 

John and Melinda received a phone call late on Tuesday, September 25 that a lung was available and a "good match". They were prepared, packed up their bags and headed to the University of Minnesota Medical Center. John received one healthy lung on Thursday, September 26. One lung requires a less invasive surgery and with reduced recovery time and discomfort. He will be in the hospital for a couple weeks, with additional weeks spent near the hospital following discharge. John will require 24/7 care for many months to come and the first year post transplant will be critical.  

Newest Update

Journal entry by Melinda Goetsch

Hell everyone,

By now many of you have seen John's Facebook postings or received emails from him.  He was released from the hospital in the afternoon on October 3rd.  He came to our apartment happy but exhausted.  People typically stay in the hospital 14 to 16 days if all goes well.  John was out on day 7.  He has lots of meds but only 4x/day so not too bad.  Some may be eliminated; others may change but he will be on many for the duration of his life.  He is still fatigues easily.  The docs say he is doing great but we have no reference point.  We were told that it takes about a year to recover.

 We had a clinic visit the day after release and rehab started the following day with a six minute walk.  The idea is that he will gradually be able to cover more ground during his six minute walk.  We have clinic 2 mornings each week and rehab 2 other mornings each week.  We are usually done by noon or 1:00.  The labs start at 7 or 7:30 so it's great that our apartment is just across the street from the clinic.  We are required to be within 30 minutes of the hospital in case something happens.  That was part of the agreement for the transplant.
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