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After their treatment they blog about it, stating how wonderful they really feel and how great the doctors are, but these blogs appear to stop after three months and are managed by the treating company. I have spoken to a parent of a patient treated for optic nerve hypoplasia sounds untreatable doesnt it (and it is), but not to stem cell treatment businesses in Asia. Her son worsened post treatment and developed unequal limb growth, but her initial positive blog remains. Even a legal threat couldnt budge the post, but they did offer a refund, but no remarkable cure for the continued unfettered growth of the stem cells still circulating within the childs bone marrow. Suspicious?
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