What is EDS?

I received a comment on my “Open letter” that asked some questions about my condition. So without Google to help, I am going to answer the questions from my perspective.

1. How does one contract the disease? Well it is genetic thing, a cool ass┬ámutation like an X-man, that will make EDS‘rs the perfect space explorers. So no worries, it isn’t contagious.
2. What is the disease? It is a genetic defect that affects the connective tissues. Now that is not all, there are 3 types of EDS (Erhlers Danlos Syndrome). I have the hyper mobility/ vascular type that is 2 types blended. In my case the disease manifests as severe joint pain and major fatigue.
3. This is actually a summation.
I get very tired easily, mornings are the worst time of day. As far as treatment, well there is no cure. I rely on pain medication and warm soaks in a bath or hot tub. For myself, I have been advised to stay away from any high impact exercise. I try to get to the Y and use the exercises I learned in pool therapy. When I go out, I have a great pair of leg braces that keep me upright and able to go to events I might be covering. I also have a great support system at home, that is the best thing for anyone with EDS.

If you have anymore questions, feel free to ask.