Still relatively young, Milo was dealing with a few health problems – sleep apnea, type 2 diabetes and high cholesterol – that taken together concerned him. Already a father of three boys, Milo’s wife was pregnant with a boy. Suddenly Milo’s long-term health became that much more important. “I wanted to be there for my sons,” he said. Milo saw that he was at increased risk for diabetes, which is something he already knew he had, but it was when he looked at his carrier status report that he learned something new. “When I drilled down it was kind of surprising – I found not just one (variant) but two that put me at higher risk for hemochromatosis,” Milo said. As he read more about the disease and how it can impact the body if untreated, Milo became concerned. “I was worried that if I had it, it could exacerbate some of the other conditions I already had,” he said. So he printed out a copy of his 23andMe results and took them with him the next time he saw his doctor. “None of the doctors had ever heard of (23andMe) so not surprisingly they were pretty skeptical,” Milo said. Hemochromatosis is typically hard to diagnose until it gets to more acute stages. But Milo explained that he carried two genetic variants that put him at a higher risk for the disease. Because of his existing conditions, Milo said he didn’t want to wait for symptoms to appear. He had additional blood tests done and one showed significantly elevated serum ferritin levels, essentially an indication of how much iron is stored in his organs. “My (doctor) said, ‘this is something we’re going to want to look at,’” Milo said. After working with other doctors and having a liver biopsy, Milo learned that he indeed had hemochromatosis. “I had significant iron overload in my liver,” he said. His liver was under stress and had internal scarring, but the condition was found early enough that there were specific treatments he could undergo to manage it. “I can do other things like change my diet and lifestyle to improve my health and I’m working on that,” he said. “I think 23andMe may have saved my life or at least prolonged it and I want to let others know that.”
Read more 23andMe customer stories here. If you have one of your own that you want to share email firstname.lastname@example.org.
Editor’s note: Pending an FDA decision, 23andMe no longer offers new customers access to health reports referred to in this post. Customers who purchased prior to November 22, 2013 will still be able to see their health reports, but those who purchased after that time will not. Those customers will have access to ancestry information as well as access to their uninterpreted raw data.