Forum Replies Created

  • AGASimpson

    Member
    December 7, 2023 at 1:51 pm in reply to: Thymoma Surgery

    My son was only 13 when he was diagnosed with MG. His thymus looked fine. The doctors at Stanford Children’s Health did not push for the surgery. They told me that it would be plan B, and they want first to see how he reacts to prednisone and mestinon treatment. My son went into remission after about a year. Three years later, he manages with occasional mestinon every few days if he is very active. We never did the surgery.

    It looks like the decision about the surgery depends on the individual situation.

  • AGASimpson

    Member
    February 11, 2023 at 3:55 pm in reply to: Funding for MG Research and Care

    Another element that I truly believe needs to be addressed: according to our doctors at Stanford Children’s health, no research tracks kids with MG after they become adults.

    Two years after his first crisis, my son is now off the prednisone and in remission. During our last visit, the doctor told us that a large percentage of kids go into remission, but they do not know precisely because there is a lack of data after they leave pediatric neurology.

    How is that even possible with current technology? We should be able to fix that and start tracking it now to help the future generation.

  • AGASimpson

    Member
    February 11, 2023 at 3:46 pm in reply to: Funding for MG Research and Care

    I wish there had been more research on diet and MG. My son’s medication did start working until we took out dairy from his diet. Was it a correlation? We don’t think so. My teenager can feel the difference in his performance when he stops paying attention to his diet and exercise ( that is through for all of us, isn’t it), but his doctors are never interested in our holistic approach. They will never even ask about his diet or supplements, and when we volunteer the information, they never mark that in their record.

    Someone has to prove that, like with many aspects of our self-care, we first change the things we can and then let the medication work and perform to its optimal capability. ( just a note here, I believe in Western Medicine, and I’m grateful for the doctors and nurses that helped my son during the MG crises, but I don’t like that we are trying to fix stuff with medications only, not recognizing that many behaviors need to follow to optimize the process).