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Hi, I have recently been diagnosed with Scleroderma by a scleroderma specialist. She is re-running all the blood work (initially run by local rheumatologist) to confirm whether it's limited or diffuse. Looking back now, it seems I've had symptoms over the last 2 years but only recently started progressing. I developed Raynauds in October and immediately started getting sores on my fingers that wouldn't heal, which finally sent me to my primary care physician. I want to ask about other symptoms I've been having to find out if this is something any of you may be experien