I am looking for some advice in regards to my rising RF factor. I have many signs and symptoms of lupus but all my basic blood work is borderline, the only obvious flag To my pcp was anemia. I see a specialist in less than a month. I cannot wait for this. However am wondering if over the years this has started my rf has gone from 4 to 8 to 10 and if anyone has had a similar experience? Should in specifically bring this up to the doctor?
Secondly- just hoping for any advise on some good questions to ask him.
I have joint pain, neuropathy, tingling ins feet hands, serious fatigue, dry Sandy eyes at times, shortness of breath, fevers, constipation, diahrreaha, among many other symptoms I have written down for him. These all seem to happen together worse at once or in cycles. My hands, feet and nose- always cold and my joint pain is regular especially in my wrists where I had developed avascualr necrosis in the lunate bones.
Thank you for any advise or response. I'm new here so if I'm post in the wrong place please remove! Sorry!