Over the last hour, I’ve been watching an amazing sunset. We have a wall of windows and a sliding glass door that leads out onto a huge balcony. The sunsets in California are out of this world. As the sunset progressed, a huge cloud sat right above the mountains and the ocean, creating some magnificent colors and shadows. Purples, pinks and grays are about to completely be hidden as the sun is almost gone and night sets in.
As I watched the sunset, I texted my grandmother (yes, my grandmother!) to ask about my grandfather who just had major surgery and had just come home a few days ago. I knew I should call and have a more in depth conversation with her, but I don’t have it in me. I realized that I had gone dark, like the setting sun.
By going dark, I mean that I hadn’t been in communication as much with my family or friends like I typically am. When I don’t text back or they get my voicemail for a few days, it gives them the message that I’m likely sick. I don’t mean to do it, but at that point I’m just trying to survive. If they get concerned they will typically text my boyfriend to make sure I’m still alive.
When I just texted my grandmother, I asked about grandpa but also let her know that I’ve had a few rough days. During this transition time for him, I want to be at home in WV to help. Since I can’t be, I should be checking in with my family more often than I have since he got home. I’ve gone dark. My text let her know that I’m thinking of them, but need some space. I think it’s just a pattern we’ve all adjusted to over the years.
It’s probably harder on the person I’ve neglected than on me. I feel guilty, but I add it to the “To Do” list and I’ll get back to them soon. I’m lucky they are all so understanding and supportive.
The sun is completely gone now. From my vantage point, all I see are lights littered along the hillside. There are patches of complete darkness. That’s where you’ll find me for the next few days until I can break this cycle: I’m in the dark.
The American Migraine Foundation (AMF) has launched a new campaign called Move Against Migraine. This initiative aims to spread awareness that migraine is a disabling neurological disease. Their website says the program aims to empower individuals living with migraine to advocate for themselves, to find the support and treatment they need. Below is the Content…
I’m sitting at the original muscle beach in Santa Monica by the pier. In the middle of the swinging rings, balance beams, ropes and slack lines, there is a large patch of astroturf dedicated to yoga. At times there can be 50 or more people crowding the space- all wanting to practice, learn or support…
You may have seen me post about the Invisible Project, but I don’t think I’ve taken the time to explain it. It’s a magazine that highlights the lives of those LIVING with chronic pain and tells their stories, emphasizing pictures from their personal archives. The main purpose is to make the invisible more visible. The…