It was important to me to have my DNA tested now so it was “banked” and might be a source of future studies for my health. Today, I read an article that poses the question, “Is Fibromyalgia A Mitochondrial Disorder?“. I maintain that I have had fibromyalgia all of my life. I may not have always known it, but I felt the effects when I was very young and they have never ever gone away.
While I understand the reasoning behind the FDA limiting the health results of those of us who have taken the 23andMe DNA tests (my brother has also taken the tests to fully round out our DNA profiles) but it infuriates me a bit that I may have a medical breakthrough in my reach, but not in my grasp. I won’t go into the money and lawsuits part of it all, but suffice it to say that’s probably what drives the reasoning behind it.
I invite any of my genealogy/DNA savvy friends to weigh in and leave their thoughts.