Invisible Illness: Searching for a Cure

2 responses to “Invisible Illness: Searching for a Cure”

1. playingthehandiwasdealt | March 16, 2013 at 2:00 am |

   Hi Dr. Diana,

   I’ve seen your videos on YouTube! What a small world! I love your personality, even if I’m not the typical EDS patient you discuss. I didn’t know your last name, so had no idea–just saw Ehlers-Danlos in the categories and presto! Nice to know you and your husband. I just found you both as the other post I commented on (about scleral lenses) was reblogged on a site I follow (keratoconusGB–but I’m in the SW of the US). FYI, I was misdiagnosed with fibro for 12 yrs. I fought for a new Dx to no avail until I got KC at 37 and did my research. I have EDS, Type II and a bit of vascular overlap, but negative for VEDS. Can you believe they just kept calling me a fibromyalgic? I blog on KC and EDS as one led to the other. That’s me–all acronyms!

   Take care and best of luck with your EDS and videos (and on and on),
   Alisa 🙂

   • RAD | March 16, 2013 at 1:51 pm |

     Thank You for the kind words. If you are looking for more information on Chronic Illness check you can find it at Dr. Diana’s website, http://www.Prettyill.com