Guest guest Posted March 6, 2004 Report Share Posted March 6, 2004 Sunflower I dont' know if this has been addressed because I'm so behind on my mail, but SOMEWHERE I read several years ago when I was diagnosed that when you stand with pressure on your feet little spheroids pop out under the skin on the inside side of your foot. They are called pieozenic(not sure about spelling) papules and are related to EDS and other connective tissue diseases. It didn't say that it was only classical type. I remember having these for years- even as a child. I never said anything to anyone because I thought it was normal. With me when I start hurting real bad in a certain area unrelated to my OA I can feel those lumps under my skin. They are real numerous in my hip and thigh area and rib cage and ankles. I had a young lady that I worked with last year start complaining of overall pain everwhere and fatigue. She described the same kind of symptoms as me. Being the nurse that I am- I started trying to diagnose her. I noticed that in some pictures that she had of herself in shorts that her body makeup and skin looked alot like mine. She was very doublejointed. I asked her to take her shoes off and she had those papules on her feet. That's what alerted me because I remember reading it very early on in my info obtaining phase. She went to a rheumatologist and he diagnosed her as Hypermobility Syndrome. It was a start. I gave her info to read and websites to go to and suggested she not r/o eds even though that may be what he meant(who knows- Dr.s are so misinformed). She was only in her very early 20's and though it was heartbreaking to know what she had to endure in her future, I am so glad that she has been told about EDS now instead of 10 years from now Vicki Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 6, 2004 Report Share Posted March 6, 2004 I have these on my ankles. I also learned about them early on in my investigation of EDS. I never said anything about them, cause I thought they were normal. I have the hypermobile type. My daughter also has these little bumps. There is a picture of them on the ceda site on the pictures page. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 6, 2004 Report Share Posted March 6, 2004 I have these on my ankles. I also learned about them early on in my investigation of EDS. I never said anything about them, cause I thought they were normal. I have the hypermobile type. My daughter also has these little bumps. There is a picture of them on the ceda site on the pictures page. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 6, 2004 Report Share Posted March 6, 2004 I have these on my ankles. I also learned about them early on in my investigation of EDS. I never said anything about them, cause I thought they were normal. I have the hypermobile type. My daughter also has these little bumps. There is a picture of them on the ceda site on the pictures page. Quote Link to comment Share on other sites More sharing options...
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