Skallagrim, a YouTuber with 1.63 million subscribers, made a video about his experience with ME/CFS. He does videos about HEMA (historical European martial arts aka mostly swordfighting). My fiancée watches his videos and previously bought boots from him. I want to watch the video with her. If I do, I'll let you know my thoughts here. The comments on his video is mostly of other people with ME/CFS sharing their experience. It's nice to see, but also sad to be reminded of how many people have our disease. Hell, a year and a half ago, I didn't even know what it was. Now I feel like I see it everywhere. The power of recognition and awareness (but also covid increasing the numbers of course).