This is interesting... does this have some sort of effect with epiderals? Mine didn't quite "take" for some reason... DS got the EDS from somewhere and I always looked towards my DH for this stuff since he quite clearly passed on the dysgraphia! But I noticed I have a lot of the symptoms (and my mom's fingers I found out pop in and out of her joints so maybe it runs from her?). But, while I have a lot of the symptoms and some of my joints are/seem hypermobile they do not literally pop and click out and in like my son's do... I do have mild scholiosis (and one shoulder higher than the other)
