I have been noticing my fingers are changing. I talked to my rhemy, who was not concerned. I, of course, would like to know everything there is. Before being diagnosed, I had some issues with my knees. I went to the Muscle, Bone and Joint center and he just gave me braces for my knees. Now, I'm wondering if I have the worse of this disease or is it a figment of my imagination. I always get the rarest of everything, which includes the rarest of animals. I'll shed some light, I have a hermaphrodite dog, another who is blind and a screaming pig. So, I would not be surprised having mutilans. I was just diagnosed in October so I am looking at everything and when I see changes, I always bring them up. I'm actually thinking I should go back to the Muscle, Bone and Joint center or talk to my primary to get some solid answers. I hate not knowing and would rather not sit and wait before things happen, at least I can just expect the worse.
Does everyone's hands/feet start to deform with this or is it just with mutilans? I hope someone can help or enlighten me.
Thanks