All posts by Katya Gordon

About Katya Gordon

Katya Goodenough Gordon lives in Two Harbors, Minnesota, just a block from the north shore of Lake Superior. She has lived in this picturesque setting since 2008 when she and her family completed their first yearlong voyage living aboard a sailboat. Aside from home, marriage, and family, she is an author and reporter, a radio show host, a climate activist, and an active member of the United Church of Two Harbors. Born and bred in Bryn Athyn, PA, she is increasingly aware of and grateful for the ideas instilled in her childhood from Swedenborg's Writings, and always looking for ways to spread these life-giving truths in her community and beyond.

Connective Tissue – An Important Function For the Body and the World

Recently I wrote here about how I experienced a “Kingdom of uses” this past summer. Reflections on the kingdom of uses continues to evolve for me. 

In my late 20s, I worked for a program called “Amicus, Inc.” which served offenders and ex-offenders in the criminal justice system, offering them practical services and relationship and harm-healing. The goal was to fill in the often-gaping gaps of support and meaningful accountability for people who have numerous needs coming out of prison, and who are often tasked with re-building themselves into useful citizens by themselves with few resources or family help. I absolutely loved the work, and part of what I loved was working for my boss, the director of Amicus, whose name was Louise. Louise and Amicus were deeply intertwined over her decades of leadership there. Her vision and spirit were recognized and appreciated not only by offenders and their families but by judges, volunteers, mentors, law enforcement and probation officials, church leaders, and community members. I simultaneously worked for her and watched her: what is her magic? Why is it such a privilege to work for her? How is that those on the bottom (offenders) and those on the top (judges) seem to not only respect but love her? 

I came to see, or rather sense, a basic humility in which she walked. Subconsciously, she positioned herself below or behind others. Her job was to serve me, to empower me to do my very best. Because my job was a new one, and we were exploring together how to best accomplish it (restore or kindle necessary relationships for serious and chronic teenage girl offenders in Minnesota), she leaned heavily on my instincts, morals, and social skills. I became braver, more skilled, and more honest with her behind me. I learned to open my heart to parents who had terribly abused their children and then, the next day, to wealthy donors. 

Over time, I came to see Louise, in the “grand person referred to in the Wrigings,” as connective tissue. Her mind was always on the conversations that could lead to a good end. She not only saw the best in people—she strategized on how to bring that best out. Should she bring together the St. Paul police department with the head of public schools? Who in each department would be the best person to address the issues? What issues could best be addressed there? Her network of colleagues, partners, and well-wishers in even as large an area as the Twin Cities (population 2+ million) was so extensive that it was hard to go anywhere with her without being engaged by a “friend” somewhere. (Amicus, which also inspired the name of our sailboat, means “friend” in Latin). 

One of the lasting lessons she taught me was the importance of creating or finding a safe, respectful space for open-hearted, clear thinking conversation. As we grew in our Restorative Justice work (victim/offender/community dialogue), it seemed that the biggest barrier to success was simply “readiness.” One has to be “ready,” and waiting for or encouraging readiness (and believe me, patience is NOT my strong suit) was an area of continual challenge and growth.

Fast forward a quarter century. The need for safe, respectful places to share, brainstorm, challenge, and support, has never been greater. Currently, my work in media (I am a radio show host for a local radio station and a reporter for a local paper) brings to the forefront the constant question: who needs to talk to whom to bring about a good outcome? I am coming to see this as a network of uses. How can this person best serve his/her use? What are his/her skills to be tapped? 

Some of the most rewarding work I have done in the last twenty years was simply in having the conversation that needs to be had. On the radio, the question becomes “How can a public conversation better the situation?” Once there was a scare at the Two Harbors high school in the form of a social-media-driven rumor about a gun in the school. It began in the evening and by 5:00 a.m. the principal felt it would be impossible to open school as usual. So school opening was postponed, then canceled. Students arriving were told to go home. To say the rumor mill was flying is an understatement. Parents on Facebook were the worst of all; accusations and rumors became enshrined in comments with nothing but fear or malice behind them.

The investigation continued throughout the day and by the end of the day, the administration was able to say with full confidence that there was no danger and never had been and school would resume the next day. That was not enough for most parents or students and the rumor mill, including a frightening vitriol against the perceived offender, continued unabated on social media.

I contacted the principal, whom I had interviewed many times before, inviting him to share what he could on the radio the next morning. And he did—he laid out exactly what had happened, the actions they took, the results, and the plan. Word had gotten out about this interview, and everyone was listening. After that, the social media craze simply fizzled out. There was nothing left to say. With direct communication in real time, the issue had passed.

All of which is to say, it’s far more difficult to maintain our foreboding or fearful fantasies of each other when the connective tissue is in place. The connective tissue not only holds things together, but ensures that they can function. 

From the Swedenborg Foundation website:

The spiritual lesson of the Universal Human, then, is that we, like the various parts of our own body, should find ways to provide a useful function in human society. At the same time, we can appreciate the many and diverse ways in which other people are playing their role in helping us. When everyone works together in harmony, moved by divine love and guided by divine wisdom, there is an image of God—the Maximus Homo, or Universal Human.

“A Kingdom of Uses”— What Does That Look Like?

“A Kingdom of uses.” Sometimes a phrase I  have known since childhood takes on new meaning with a new state in MY life. This happened to me this summer, a season full of unexpected developments—a long-awaited sailing trip in Greenland, an epic 6-day journey home, my mom’s death, a stent for my husband’s heart, a re-injured head for a niece, and a family reunion at memorial service time. It may seem like an unlikely time to discuss use, but now that fall is here and life is settling down, I notice things that I did not see before, that seem to live out this idea of a “kingdom of uses.”

I did not start out the summer thinking much about the kingdom of uses. First, there was a long-planned adventure. My husband Mark and I joined another couple to sail in Greenland together, a rare opportunity. As it turned out, this trip was dampened almost from the start with the realization that my mom was failing, maybe this time finally.  By the time we got far enough north to take ferries and flights back south, it was clear that we might not get back in time to say good-bye. While Mark and I were flying over the fjords of Greenland, he in the pilot cockpit in a most unusual turn of events (another side story), the most beautiful flight imaginable, my mom made that transition to the spiritual world.

Continue reading “A Kingdom of Uses”— What Does That Look Like?

A Trip to Unimaginable Places in the Mind

Editor’s Note: We are republishing Katya’s article because of a glitch that prevented comments on the original post. Sorry for the confusion!

Some of you may know that our family is going through a journey together, along a road that has taken us all to places unanticipated and even unimagined. My mom has shown signs of dementia for years, who knows how many? Slowly and often imperceptibly growing, often without change or attention for months, and then a leap forward with a telling comment, or outburst, or uncharacteristic action, that leaves us with more questions than before.

After a stint in the hospital due to a UTI (which is a brain virus for seniors) and C-Diff, a dreaded infection that stems from antibiotics, my mom, who is rarely, if ever, sick or injured, returned home with a body much recovered after years of neglect, and a brain that had developed much further into dementia. It seemed that she was dying, which she daily requested that we orchestrate, and which provided the only end in sight that looked possible or feasible. But slowly it became apparent that her body was still recovering from illness, and her mind was not going to recover beyond a certain point. And thus we quickly pivoted to move her into assisted living (which she had often mentioned in the past, certain she belonged there) which, once there, she alternately appreciated and hated. That was over six months ago.

I am currently reading a book called “Travelers to Unimaginable Lands” which analyzes not just the disease of Alzheimers but the relationship of patient with the caregiver. Reading this has given voice to some of my most difficult questions and feelings. Caregivers, being human, cannot help but be drawn into the reality of someone with dementia, unless and until they come to the clear conclusion that the person is not really “there” anymore, in which case all motivation for loving them and caring for them becomes a moot point. So of course we search for the person, we rejoice when we see him/her, and we encourage actions, thoughts and feelings which we find desirable or healthy. The closer we are to the person with dementia, the harder it is to simply have a dispassionate compassion, which is the most sustainable mental perspective of a caregiver who must withstand daily, minute changes in everything from mood to purposeful action, including those that feel very close to being the “real” person!

Continue reading A Trip to Unimaginable Places in the Mind

A Trip to Unimaginable Places in The Mind

Some of you may know that our family is going through a journey together, along a road that has taken us all to places unanticipated and even unimagined. My mom has shown signs of dementia for years, who knows how many? Slowly and often imperceptibly growing, often without change or attention for months, and then a leap forward with a telling comment, or outburst, or uncharacteristic action, that leaves us with more questions than before.

After a stint in the hospital due to a UTI (which is a brain virus for seniors) and C-Diff, a dreaded infection that stems from antibiotics, my mom, who is rarely, if ever, sick or injured, returned home with a body much recovered after years of neglect, and a brain that had developed much further into dementia. It seemed that she was dying, which she daily requested that we orchestrate, and which provided the only end in sight that looked possible or feasible. But slowly it became apparent that her body was still recovering from illness, and her mind was not going to recover beyond a certain point. And thus we quickly pivoted to move her into assisted living (which she had often mentioned in the past, certain she belonged there) which, once there, she alternately appreciated and hated. That was over six months ago.

I am currently reading a book called “Travelers to Unimaginable Lands” which analyzes not just the disease of Alzheimers but the relationship of patient with the caregiver. Reading this has given voice to some of my most difficult questions and feelings. Caregivers, being human, cannot help but be drawn into the reality of someone with dementia, unless and until they come to the clear conclusion that the person is not really “there” anymore, in which case all motivation for loving them and caring for them becomes a moot point. So of course we search for the person, we rejoice when we see him/her, and we encourage actions, thoughts and feelings which we find desirable or healthy. The closer we are to the person with dementia, the harder it is to simply have a dispassionate compassion, which is the most sustainable mental perspective of a caregiver who must withstand daily, minute changes in everything from mood to purposeful action, including those that feel very close to being the “real” person!

Continue reading A Trip to Unimaginable Places in The Mind