I am freaking out waiting for Professor Hughes to review my medical report for an appointment. I have had such a bad time from other drs., being ignored, being told they wish they had time to figure out what was wrong with me, or just throwing the MS dx on me even though I don't have a lot of the symptoms. I am so afraid he won't see me. It's crazy for me to think that because I have had a PE in 1978, 3 miscarriages between 16-20 weeks, 2 pos. IgG in 1994, MS like symptoms, headaches, grape rash, my inr is .9, and seronegative blood test now. I feel like that because the neurologist told me anticardiolipin antibody went away, since I haven't had a recent blood clot & the test is neg. I didn't know what to send the clinic so I sent the neurologist exam, blood test results, & a report from my husband who is a dr. Should I be worried that he won't give me an appointment? The neurologist report says she is not sure what is going on because the lesion is small & to anterior for MS. I just don't know we're to go if Prof. Hughes doesn't see me. I hope I am worrying for nothing. It has been 3 days & I haven't heard from them. I feel desperate. Did anyone else feel like me? How long does it take before they get back to you?
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