Stage 1 of my ME/CFS research completed and in a short summary I have experienced; daily improvement of brain fog lifting, 4 kilos of pure FAT loss and improved energy levels. The statistical analysis is kept in a separate diary which one day i hope might help or support millions of others who have lived with ME/CFS.
However...My sleep has become unrestful... And my myalgia has worsened. Could it be the toxin release? I have made many changes to my diet and the myalgia IS located at every lymphatic junction. The strained sleepless nights? Maybe the change of diet is not exhausting my bodies immune system..
Stage 2 of my research begun today...
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