Skip to main content

Bucket List Part Two

“If you had a year to live, what would you do?”


People ask each other this question over lunch or sitting on the couch at home watching TV.

More often than not people’s lists include travel, adventures, skydiving, seeing the Grand Canyon, or any number of things.
There was even a movie where two older men were dying and traveled around the world.

For Mathew, the reality was, what can you do in 11 months when half of that time was spent in the hospital, often times too sick to read or write because this was the reality of stage 4 soft tissue Sarcoma.

The other half of the time, at home, immune compromised, all the time in pain. Each day provided maybe three hours of energy and concentration.

Add in doctor visits and outpatient procedures and anything beyond that was a bonus. A few times we stopped on our way home from appointments and Mathew bought a book or a new game or we stopped for lunch.

Fortunately, two of the things on Mathew’s bucket list was passive on his part; his brothers birthday and the birth of his nephew.

Something I admired about Mathew was that his bucket list involved goals he had pursued for years. He practiced guitar several hours a day and worked on his music even when he could barely function in life, pre-diagnosis. This is one of the qualities I remember when I think about Mathew’s life. He lived it as if he knew his time was limited.

Comments

Popular posts from this blog

Replace the 3 Lumen Pic Line with a Port

Mathew's 3 Lumen Pic Line was replaced with a Power P.A.C. Both Mathew and I were given Medical I.D. cards to carry at all times. I have mentioned before that texting from the DRC is almost impossible. The staff told me it used to be the X-ray department so the walls are leaded. Again, the phone tree would have helped so much. I texted the following information to my niece, my sister and Mathew’s Dad and Stepmom. And probably Joseph and Carlos. I know that could have been reduced to two texts, three at the most. At the time  I didn’t know about group messaging as my phone was an old Android. Texts Between me and Diane Hi. We are at the hospital early because Mat is in a lot of pain.  We think the bill stent may have moved. Sent 3-31-14 Because he was NPO for other  procedure they should be able to fix today. Sent 3-31-14 In the DRC sending texts is almost impossible so if you don’t hear from me for a while don’t worry. If ...

Why is it Called Confections for Cats?

I want to take a moment and talk about why Project Mathew is called Confections for Cats. The main reason is that it was going to be the title of his first album. He had sketched up some artwork. We were working on it in Photoshop. Here is an early permutation of the artwork. Mathew's life, his story is mainly about music, his music, and his journey through cancer. When he created his Facebook page, he named it Confections for Cats and I continued with that name. I have been thinking about a logo, a way to incorporate cats, Sarcoma and his music. I like to brainstorm. So, I was thinking about the word confections. When Mathew first told me that title, this was before his diagnosis, I recall thinking about how he practiced his guitar into the night and early morning and that his cats have been his constant audience. Sweets, confections for his cats, and his music as delicious morsels for our ears. I looked up the word confections and yes, a confection is a sweet. Bu...

The Rollercoaster of Chemotherapy Fewer Highs and More Lows

TEXTS BETWEEN ME AND ARPIE Mat sees Dr. Reed Thursday at 9 and then at 1 he goes to have biliary stent changed to a larger gauge. We had to reattach a bag this morning. Sent May 12                                                                  I have Dr's appointment myself Thursday                                                                  will call after and see if you are still                                                                  with Dr. Reed.   ...