The Mighty Logo

Please Think Before Asking Personal Health Questions at Holiday Gatherings

The most helpful emails in health
Browse our free newsletters

As I do every year around this time, I will be writing about body autonomy. It’s that time of year. Lights, chocolates, eggnog, shopping and topics that are no one else’s business.

The reason I get so riled up about this is that for the entire rest of the year, people with epilepsy and other health conditions work to empower ourselves. We embrace things that make us happy. We struggle through trauma, we endure circumstances that are challenging, we face the odds. We build new lives for ourselves. We create and enter environments that give us peace and joy. We might even support others! Often part of our lives is helping others when they are down or they need a friendly voice or companionship.

Other relevant stories:
Can Flashing Lights Cause Seizures Without Epilepsy
Can Students with Epilepsy Participate in Sports
Can Epilepsy Cause Memory Loss

Then December comes around and all of a sudden it’s very personal questions from people we only see once a year. It’s sitting next to someone you don’t know and having them ask you about your life story. Then, although they may not be neurologists (I have yet to run into a neurologist at a holiday party), they provide advice from a show they watched, from their second-cousin-twice-removed, from seeing someone have a seizure in elementary school.

A couple of years ago, I was informed I should be grateful that people care so much about me and what is happening with my health. First off, I hate the word “grateful,” so that was a bad start to that conversation. Second, there are different ways to show concern or interest without being condescending. Third, there are so many other things happening in the world, I don’t think that the only conversation directed at me should be about why I shouldn’t choose pharmaceuticals or whether I am worried about living alone.

I was also informed that because I run a blog about epilepsy and do public speaking about epilepsy, I should not be surprised when people talk to me about it. So please note, I am not just talking about epilepsy or health conditions or myself right now. I am not personally averse to talking about my epilepsy. I do it all the time. But not everybody is as comfortable with discussing their health condition or other sensitive personal matters. Yes, I will talk about my epilepsy, but even I have topics I don’t want to discuss.

How do we know which topics are which? Before starting a conversation, let’s use our brains for one second. Just think. How will this be received? Maybe the intention is a genuine concern and interest in someone’s health, relationships, career. I imagine that a fair amount of times it is. But if the response is less than enthusiastic, be open to changing the subject.

I like to think that people like building relationships with others. I like having solid conversations with people I know or with people I have just met. There are a million topics to choose from that avoid making anyone uncomfortable. If I start a conversation with an open-ended question, like “How are things?” the person can answer with any topic they choose. Have they started a new job? They can say. Have they gotten divorced? They can mention it. Have they invented time travel? They can talk about that. The important thing is the decision falls on that person. If I start with, “So, are you and your significant other still at that job where you were working on the space-time continuum?” and the answer is “No, we broke up, I got fired, and the time travel device exploded and failed,” maybe they don’t want to talk about that at a party. Stick with “What’s new?” Open-ended questions.

Every person has the right to talk about things or not. It’s not a matter of being polite and making polite conversation. Our bodies are our bodies. Our brains are our brains. The decisions we make in our lives are ours. We do not have to justify why we have made those decisions or explain ourselves. We are not a community project open for discussion. Just enjoy the eggnog and be excited about Disney+.

This story originally appeared on Tremors of My World.

Originally published: December 9, 2020
Want more of The Mighty?
You can find even more stories on our Home page. There, you’ll also find thoughts and questions by our community.
Take Me Home