Scleroderma: Morphea vs. Systemic Diagnosis
in Health ·
Just checking in here since 🙂
isn't around.
I was diagnosed with morphea about eight months ago.
What’s everyone else’s experience been like—did you get your diagnosis at a major hospital in a city like Chicago, or somewhere else entirely? Also, how often are you all running ANA and ANF blood panels to monitor for any systemic progression?
Let's swap some stories. 🙂
isn't around.
I was diagnosed with morphea about eight months ago.
What’s everyone else’s experience been like—did you get your diagnosis at a major hospital in a city like Chicago, or somewhere else entirely? Also, how often are you all running ANA and ANF blood panels to monitor for any systemic progression?
Let's swap some stories. 🙂