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Introducing No Other Life’s Podcast

by Rick Seaholm

2023, It’s been a tough one for me and many of those whom I hold dear. Early this year I began to explore composing as a tool for coping. You’ve heard some of that music here. But I found I still had much more to say and am now launching a project called No Other Life, in which I will dig deeply and honestly into some pretty heavy topics over the course of a season. With this autumnal equinox I invite you to share with me as we develop the tools to help others as well all process our own “New Beginnings”.

At the time that I started the project, it was my full intention to let the project breathe a bit, to see how people responded and in what ways and places. I am thrilled at how popular it got and the ways in which it inspired people. Season 2 is slated to begin airing with the vernal equinox, March 2024.

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Appearance on Articulate OX Podcast

by Rick Seaholm

Early this year, when I released “Snowrise”, I was approached by a high school friend I hadn’t spoken to in well over twenty-five years. I had followed his work early in social media days and thus knew him primarily as an excellent visual artist. He told me that he was starting a new podcast series for 2023 and was soliciting guests. He called it a podcast about artists and their inspiration. I was sold but at that point in time I was dealing very heavily with the health scares in my family that would eventually make their way onto my first album release. Fortunately, my buddy allowed me to table the appearance until Bluewing was released and that was a large part of the conversation, but we also went into Parkinson’s, The Simpsons, our shared love of hip-hop, and thus a new exciting partnership would develop between us.

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Another Town

by Rick Seaholm

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Bluewing.

by Rick Seaholm

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A Mirror, Dimly

by Rick Seaholm

This post is the working copy of a sermon I gave at Edwards Church, UCC in Framingham, MA on August 20, 2017. The live version deviates a bit, in that I was not reading from these notes. (PDF)

sermon road side sign“For as in one body we have many members, and not all the members have the same function, so we, who are many, are one body in Christ, and individually we are members one of another.” (Romans 12:4-5, NRSV)

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Being There

by Rick Seaholm

It’s been well-stated that I can suffer from a distracted mind. I focus on “what’s next” and how quickly I can get through the current activity or task. Sometimes that is to my great advantage. I’ve been heralded by every supervisor I’ve ever had for being the “most efficient” employee each has ever seen. And I don’t doubt that’s true. At work, one of my greatest strengths is being able to live with an existing system for a certain period of time, before I instinctively determine what is essential, and what can be altered. Soon enough I have a new workflow which may reduce production time (and headaches) several-fold. Then, I get to enjoy the task of seeing what else can be crammed into a work day that previously had seemed like it had too few hours.

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My New Battle

by Rick Seaholm
Facebook post from July 11, 2020

Last year I was diagnosed with Young Onset Parkinson’s Disease. I had been to a variety of specialists, peddling a variety of symptoms, for a few years prior, and not one of them had a clue because no one is looking for PD in a forty year old. But I persisted, certain it was all related. I’m grateful for my neurologists who finally connected the dots and have led my team ever since. I never stop reading and learning about my condition, and, armed with a list of symptoms which will serve as my bingo card as this develops, I realize this has been quietly with me a very long time.

So, this morning as I was inexplicably drawn to Facebook Memories for the first time in ages, I saw that I am at a milestone day here. 10 years since a mysterious nerve discomfort was noticed and aggravated by a weekend of casual video gaming. I am now quite familiar with that arm nerve discomfort. For a while I would announce his arrival to my wife. “Pedey’s about,” I would say. But he’s since moved in permanently with us and she simply knows. I can’t imagine the emotional, helpless toll that must take on her everyday.

I didn’t ever post my diagnosis here until now. It’s never been a secret amongst people I see in real life, and some relationships have grown stronger with those who are willing to talk. I have been fed up with FB for the same reasons as all of you, and typing is a lot harder for me now. But this Memories post inspired me to plug away at this for an hour. I possibly will begin to include my PD reflections with the others I usually think worthy of posting, not for pity (as the original post jokingly requested), but because transparency is my watchword. So far, we’ve done a good job of facing this with humor and gratitude. My wife is my biggest supporter as anyone who knows her would expect. She ribs me just the right amount and I laugh the hardest of all. It’s given me a chance to cherish all the activities that I can still do, and has authorized me to slow down and enjoy those that are legitimate forms of physical and neurological therapy (origami, piano, woodworking, yard work, gardening, among them), all while observing (but not judging, as my yoga instructors say) those activities which are only going to become more challenging. It’s really weird to think that this is as good as it will get for me, by true definition of “degenerative”, but I am doing all I can to slow its progression and foundations are raising money for scientists to perform research.

In all that’s wrong with the world right now, you’ve got to try to stay hopeful or you’ll lose your mind. Right? That’s what we’re supposed to be doing these days? Right?

The sun’s out. The birds are chirping. And I’m loved. That’s where I’ll place focus today.

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