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Other causes of carnitine deficiency besides mutations in the SLC22A5 gene are classified as secondary carnitine deficiency and include other hereditary metabolic diseases (e.g., fatty acid oxidation defects), medication (valproic acid, cyclosporine, and pivampicillin), malnutrition, hemodialysis and renal tubular dysfunction (Fanconi nephropathy), and prematurity (lower placentary transfer)

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provides powerful antioxidant protection to brain tissues promotes the proper regulation of cell membrane excitability and cellular osmolarity improves cerebral glucose utilization and energy production supports phospholipid synthesis for enhanced cognition enhances acetylcholine and neurotransmitter synthesis Please note : The new Neuro Optimizer packaging has a child-safe cap, which may cause the jars to become dented because they have been vacuum-sealed

Heres what helped me shift that thinking: Eat with smaller utensils or bowls