One of the many fun aspects of MCS is how much your body betrays you.You try to go do normal things, things you could do before, things that everybody else still does, and your body freaks out. You try different treatments and therapies and you make progress and then your body suffers a significant setback … Continue reading
Each year it gets harder to imagine what I would be like if I had never developed MCS. But I know this one thing- I would still want to live where I can easily be outside year round. By easily, I mean without a lot of extra layers, gear, or people in my way. My … Continue reading
I am so tired of food and health problems. And I know when other people ask what I’ve been up to, how I’ve been, etc, it’s mostly those subjects that I talk about since that is what I do with a large part of my time. I have no training, interest or skill in medicine … Continue reading
