Tim’s Story

Site created on February 18, 2019

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.


On Monday February 11th around 5pm Tim went to the urgent care in Brooklyn Center due to a long term cough, shortness of breath, and chest pains. A chest x-ray was done at the urgent care clinic and the results showed "fuzzy white dots" everywhere on his lungs. With his increased need for oxygen supply and the results of his x-ray the decision was made to send him to the University of Minnesota Hospital via ambulance. Upon arrival to the emergency room they performed a CT scan which confirmed that there were mass amounts of "white fuzzy dots" everywhere. The ER doctor informed us that these are very unusual findings and rare to see so Tim was admitted upstairs to the hospital for further investigation.

On Thursday February 14th he was scheduled for a low risk procedure called a bronchoscopy and a biopsy. Their first attempt was a fail due to Tim requiring an excessive amount of oxygen. A few hours later they presented us with the option to do the bronchoscopy with a breathing tube to help with the oxygen need. At 3:00pm Tim agreed to do the procedure as it would give him some answers as to why he has been experiencing a heavy cough and chest pains for over 6 months. The procedure only took about 45 minutes, however after the procedure was done Tim was in critical need for oxygen and the decision was made to keep him on the breathing tube (ventilator) to help provide him with the most oxygen needed.  

On Saturday February 16th (Tim's Birthday) around 4:00pm the doctor's informed family that Tim was declining and he was declining at a fast rate. They started him on a steroid IV drip to help with the inflammation  of his lungs. Family was all together at the time and provided several prayers to him and asked for healing hands. 




On Sunday February 17th early morning around 3:00am the decision was made to put Tim on paralytics which ultimately paralyzes his whole body allowing his body to rest and focus on healing his lungs.




On Monday February 18th the doctors presented to the family that a diagnosis has still yet to be made and the option to do exploratory surgery is needed in the future to retrieve another biopsy to give the doctors a different view to inspect why his lungs are failing him. In Tim's current condition it was decided that he is not stable enough to perform this surgery and they will reassess him later on as time goes on.




We have set up a GoFundMe page to help the family with medical bills and having to miss work as well as having multiple other expenses. I have attached a link that will direct you to the page to help support Tim in a very crucial time in his and his families life.


Www.gofundme.com/go-pher-murph


**Please do not donate money on this site as it will go to the caringbridge and not to the family.  

Newest Update

Journal entry by Kaylynn Murphy

On Thursday, May 9th the family received the autopsy of Tim Murphy. 

Written on this autopsy was a very detailed explanation of each individual organ. As the family continued to read the autopsy we learned the diagnosis and finally got an answer. 

Tim passed away from a cancer called "Invasive mucinous adenocarcinoma."  To break that down, it's a cancer that spreads to the healthy tissues in the glands of the lungs that produces mucous secretions. We also learned that this cancer became metastasis and spread to his esophagus. In layman terms, Tim had lung cancer and throat cancer. Followed by kidney failure and ultimately becoming brain dead. (Encephalopathy) The brain damage was due to the multiple organ failures and means he had failure to make any brain functions due to it. 

I wanted to rewrite a paragraph from the autopsy report on here that really gave me some understanding of this cancer. 
It states:
"Lung cancer is the leading cancer in terms of mortality across the world. Although adenocarcinoma is a common type of lung cancer, mucinous adenocarcinoma is the rarest subtype. Cytology is usually inconspicuous or absent due to which a definitive diagnosis via biopsy is frequently challenging" 

So what that says to me is that, Tim was diagnosed with THE rarest form of lung cancer. So rare that a diagnosis is challenging to come across and tissue samples, blood work, and imaging would have not found the answer. 

I did a bit of research on this cancer, granted that not much is out there, but I found that chemotherapies have proven to be unsuccessful with this cancer. I've also found that the longest documented case of this cancer says that someone lived the longest with it for only 5 years. The survival rate is very low. 

Family believes that Tim was living with this cancer for at least a year. However, we have not confirmed that and plan to do so. If you have questions, feel free to ask. I'm always around, and I love talking about my dad. It's actually all I want to talk about. If I miss a call/text it's usually because I'm taking a break from it. Or needing some time to myself. Thank you again for everyone's love and support. Let's keep Tim Murphy alive with our memories and kind words. Rest in Paradise. We love you!
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