DECLINING AN EDUCATION

Declining an Education

Most of us have been on both sides of this moment: someone mentions they've been dealing with a bad hip, or recovering from a procedure, or in the midst of a serious illness and suddenly the air changes. The person sharing it worries they sound like they're complaining. The person hearing it isn't sure whether to express concern, offer help, or just move on. Both end up feeling awkward, and the conversation retreats to safer ground.

That awkwardness is understandable. It is also costing us something.

When a neighbor is managing a serious illness, or a significant loss of function, or a long recovery, they are living through something many of us have faced or  haven't faced yet. They are making decisions daily that the rest of us aren’t making right now. They are learning things  about the medical system, about their own body, about what actually helps and what doesn't, about how to keep going when keeping going is hard that we will almost certainly need to know someday. Their caregiver is learning a different and equally demanding set of things alongside them. They are not being courageous. That makes them seem exceptional.  They know they are not.  They are doing what needs to be done, and in doing it they are learning things the rest of us may one day need to know. 

That knowledge doesn't announce itself. It sits quietly in people we already know, in conversations we keep steering away from because we're not sure what to say, or because we're afraid the subject is too heavy, or because we don't want to remind them of something painful. What we don't quite realize is that most of the time we're not reminding them of anything. It is already with them, every day. What we're actually doing when we change the subject is declining an education.

We should say plainly what we all know but don't always say out loud: most of us will not get through this stage of life without facing something serious. Which means we are not talking about those neighbors over there. We are talking about all of us, and about whether we want to arrive at our own hard moments having paid attention to the people who got there first.

Illness doesn't end someone's importance to the people around them. In most cases it deepens it. The person dealing with a serious diagnosis is still exactly who they were before.  They have the same history, same judgment, same sense of humor and now they know something more. The caregiver beside them knows something more too. Asking about it, making it part of matter-of-fact conversation, treating what they've learned as the ordinary and valuable information it is, that's paying attention to people who have something to tell us.

And the exchange runs in both directions. How we see each other, whether we recognize someone as a full person rather than as a diagnosis has a direct effect on how they come through it, physically and emotionally. People who are allowed to remain fully themselves in the eyes of those around them do better and most of us have seen it in ourselves and in people we've known. Staying in the conversation isn't only good for us. It matters in ways that are observably true.

None of this asks anyone to take on more than they can carry, or to have the right words ready, or to fix anything. It asks only that we not look away. The people in this community who are living through something difficult are not a situation to be managed carefully from a distance. They are, if we let them be, some of the most useful neighbors we have.

 

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