Guest guest Posted February 10, 2000 Report Share Posted February 10, 2000 Hello to one and all I guess I am a " lurker " too, as I only post when I have questions. Does anyone know of any specialists, or good places to go, in Texas? I lost my son at 9 weeks old last year, and it was only recently that we received a non-specific mito diagnosis (No one did a muscle biopsy, but he had high lactic levels and abnormal pyruvate levels). Now we are expecting another child in August, and trying to LEARN as much as possible, even though we hope this child does not have mito. All of you on this list have been so helpful, allowing me to learn from your experiences. I need all the help I can get--the doctor and I both seem to be learning as we go. That seems like a common experience with mito Thanks L W __________________________________________________ Quote Link to comment Share on other sites More sharing options...
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