In just about a month, it will be three years since one very scary week in the hospital and my subsequent diagnosis (and relatively happy ending) with Addison’s disease. I’ve learned a whole lot about the disease, biology and how best to handle my own personal situation, but the biggest learning has been about how to continue to exercise safely.
I’m an active person. One of those strange breeds of human that truly enjoys sweating, exercising and pushing the limits of my heart rate monitor. It’s one of the things that makes me happiest. I believe it makes me a better person to be around. It’s also one of the things that was most threatened with the diagnosis.
Three years on, I’ve learned a few best practices about how to exercise with Addison’s in a way that doesn’t put myself at further risk. In fact, exercising and continuing to workout is something that can help with many of the symptoms of the disease (bone density, chronic fatigue, irritability), as long as you do it safely.
Just drink plenty of water and you’ll be fine. Right? Not exactly. Anyone that has run in the heat and ran face first into “the wall” can tell you that sometimes figuring out what enough means can be complicated. With summer training comes the heat and humidity, two of Mother Natures tougher foes for endurance athletes.
If you don’t have access to a coach or a lab, how do you figure out how best to hydrate so you don’t end up crawling along the sidewalk?
There are a couple simple rules of thumb that should keep you safe and running.
After all the partying this past weekend, Cecilia came down with a cold that kept her out of school the past two days. She was back at it today, but I started feeling crappy yesterday afternoon.
Michelle and I have very different reactions to feeling a cold coming on. She will try to bull her way through it. I basically go the opposite way. At the mere tickling of symptoms, an errant sneeze, I throw all the switches and do my best to head off any cold before it can get started.