About a year and a half ago my nephrologist diagnoised me with LPHS and everytime I go to the dr any doctors office visit and tell them I have this LPHS I get crazy looks from not only the doctors but also the nurses. When I did my own research on the diagnosis it seemed to fit all my symptoms and I also lived in central ohio (columbus) most of my life, but I am still puzzeled and want to make sure it is the correct diagnosis, and I am not just getting pushed to the side. If you have any similar stories or could help in any way or just have any ideas PLEASE let me knowReply Follow This Thread Stop Following This Thread Flag this Discussion
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