I just scheduled my first PCP visit on new health insurance! It's a meet and greet. The doctor, she is Family practice, graduated in 1978 from Michigan University. I'm in MD but the receptionist I spoke with disclosed to me that she is the same age as me and she has been seeing this doctor since she was 16. She told me the first visit she ever had with her, the doctor went an hour over her appointment, sat with her and didn't allow her to walk out of the office until every little last thing that was concerning her was addressed or at least a game plan was created. She told me that she is the most gentle thorough doctor she has ever known.
I was sold. So, I'm excited about it. I'm going to take your advice around here and see a Gastro right away. There are other things going on that are personal so I think you are on to something. And it all just started over the last several months since these lesions were found so I don't understand it. I'm happy that I'm going to get treated finally. I'm also going to take my hospital records from both hospitals over to John Hopkins and have them study my case as well.
I'm not excited about waiting 3 months to have another MRI but I understand this isn't easy for the doctors either. They want to be absolutely sure that their thoughts of "early onset of MS" are correct before starting me on a course of treatment. I get it and know that I'm blessed to have this happen so quickly.
What do I bring to my appointment for PCP? Do I bring my journal of symptoms? I logged symptoms for over a month and then I stopped for a month because I was really overwhelmed and frustrated. I just started up again a few days ago at my husband's request.
What sort of questions do I ask my PCP?
Thanks for reading and for any advice you give to me
I was sold. So, I'm excited about it. I'm going to take your advice around here and see a Gastro right away. There are other things going on that are personal so I think you are on to something. And it all just started over the last several months since these lesions were found so I don't understand it. I'm happy that I'm going to get treated finally. I'm also going to take my hospital records from both hospitals over to John Hopkins and have them study my case as well.
I'm not excited about waiting 3 months to have another MRI but I understand this isn't easy for the doctors either. They want to be absolutely sure that their thoughts of "early onset of MS" are correct before starting me on a course of treatment. I get it and know that I'm blessed to have this happen so quickly.
What do I bring to my appointment for PCP? Do I bring my journal of symptoms? I logged symptoms for over a month and then I stopped for a month because I was really overwhelmed and frustrated. I just started up again a few days ago at my husband's request.
What sort of questions do I ask my PCP?
Thanks for reading and for any advice you give to me
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