Guest guest Posted February 16, 2005 Report Share Posted February 16, 2005 The researcher's name was Dr. Linnane. He was the keynote speaker at the UMDF conference last August. My son is the first mitochondrial patient he knows of trying magnesium orotate. I believe his research was on muscle fatigue, but I am not sure. He felt from the good results he was seeing that mitochondrial patients might benefit as well. He hesitated to share the info at the conference, but thought it was so promising he had to share it. I hesitated to share Craig's progress for awhile, as well, for fear of getting people's hopes up. But it's been 7 months, and I have to tell as many as possible now. I know it may not help everyone, but I anything is worth a try when you are out of ways to stop the progress of this disease. Craig's doctor is Dr. Bruce Cohen in Cleveland. Since I talked directly to Dr. Linnane at the conference about the safety and dosages I did not confer with Dr. Cohen. I called to report the results to him initially, but it was still too early to count our chickens at that point. I need to give him a call again. Please let me know how it goes for you with magnesium orotate. You can email me directly with any questions or comments. God bless! Quote Link to comment Share on other sites More sharing options...
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