I was just diagonosed this week with systemic Scleroderma and my Rhemotologist
Suggested I come back every 3 months and we will begin the journey of keeping an eye on the symptoms and body changes. I am feeling like I should set up an appointment to meet with a doctor at a hospital that specializes in this research. Am I thinking right? I am considering applying for an appt. At John Hopkins in Maryland. My symptoms are stiff hands, pursed mouth/lip area and very fatigued. I would also love to meet a support group in the southwest Florida area (Naples) area. Thank you in advance for your help.