Anyone ever get this rash?
I develop this rash quite frequently. It seems as if I have it more often than I don't have it. It's usually on my elbows and sometime my hands and knuckles. For forever, I assumed it was a ringworm 'outbreak' becuase there are usually several clusters of them. But now that I've started paying closer attention to them, they are much patchier and swollen and VERY unnattractive LOL! They never respond to normal ringworm treatment. I usually won't waste thre trip to the PCP and I let them resolve on their own.
But, since my recent diagnosis of Lupus/System Sclerosis or Scleroderma.. Or possibly even MCTD, I don't know if I should make an appt. with the doc or not. I have an appt. around the 2nd week of March, can I wait? The rheumy is supposed to be calling me to make an appt., not sure sure when that will be.
Anyways, take a quick look. Anyone recognize this? Ever had it? It's not too itchy, if it is, it's usually the ones of my hands, but it is painful to touch. I have a bad habit of supporting myself on my elbows and I DEF. cannot do this now with these little boogers.
"Rule number one is, don't sweat the small stuff. Rule number two is, it's all small stuff."
Dx: Potential Lupus, Diffuse Systemic Sclerosis, Mixed Connective Tissue Disease
Rx: Prednisone 5mg 1x daily, Lyrica 75mg 2x daily, Omeprazole 200mg 1x daily, Xanax .5mg prn