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Follow-up involves scheduling your next visit based on the protocol, tracking weight, measurements, and subjective energy over several weeks, and adjusting frequency or dose if side effects or a lack of benefit emerge

Primary carnitine deficiency (PCD) is a rare autosomal recessive disorder of fatty acid oxidation caused by deficiency of plasma membrane carnitine transport resulting from impairment in the plasma membrane OCTN2 carnitine transporter

All medications come from licensed 503A compounding pharmacies, and treatments are HSA/FSA eligible with no insurance requirement

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