Comments on: Invisible Illness: Searching for a Cure http://theeyedocblog.com/2012/11/09/invisible-illness-searching-for-a-cure/ A resource for patients. What you want to know about your eyes and forgot to ask. Sat, 27 Apr 2013 05:54:02 +0000 hourly 1 http://wordpress.com/ By: RAD http://theeyedocblog.com/2012/11/09/invisible-illness-searching-for-a-cure/#comment-3032 Sat, 16 Mar 2013 18:51:43 +0000 http://theeyedocblog.com/?p=1400#comment-3032 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

]]> By: playingthehandiwasdealt http://theeyedocblog.com/2012/11/09/invisible-illness-searching-for-a-cure/#comment-3030 Sat, 16 Mar 2013 07:00:52 +0000 http://theeyedocblog.com/?p=1400#comment-3030 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 :-)

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