Enjoy this interview between Dr. Purser and Dr. Gabe Roberts on the topic of the MTHFR genetic errors! Contact us at (801) 796-7667 or info@danpursermd.com for help. Check back often for the newest updates!
Explore the relationship of vitamin deficiency and neuropathy, a painful and disabling condition. Learn how a SpectraCell Comprehensive Nutritional Panel can help reveal intracellular deficiencies. Explore the relationship of how genetic diseases, such as MTHFR, relate to neuropathy. Discover how Methyl B12 (Methylcobalamin) may treat neuropathy. Contact us at (801) 796-7667 or info@danpursermd.com for help. Check back often for the newest updates!
Dr. Purser explains the diagnosis and treatment of MTHFR (methylenteterahydrofolate reductase enzyme deficiency disease). Learn the genetic component of this illness (such as C677T or A1298C) and how it affects the body's inability of methylation to convert carbohydrates into ATP (Adenosine Triphosphate). Discover how the complex enzyme pathways of the Krebs cycle and citric acid cycle convert carbohydrate molecules into ATP molecules in the mitochondria. Explore the relationship of MTHFR to vitamin and hormone deficiencies while understanding how vitamin supplements can replace key missing (u
Dr. Purser explains symptoms of Metallothionein dysfunctions and how metal toxicity can cause fibromyalgia. Learn how high serum copper levels cause painful inflammation in muscles, nerves, and joints. Explore the genetic components associated with fibromyalgia. Discover key nutritional supplements that help reduce symptoms of fibromyalgia. Contact us at (801) 796-7667 or info@danpursermd.com for help. Check back often for the newest updates!
Discover how a common genetic variant in the PEMT gene can block your body’s ability to make phosphatidylcholine — leading to chronic pancreatitis, even if you’ve never touched alcohol.
Yes—your genetics can directly cause vitamin deficiencies. Certain SNPs lower your body’s ability to process or make key nutrients, like MTHFR reducing folate use, PEMT lowering phosphatidylcholine production for gut and liver health, and SOD decreasing antioxidant defenses against free radicals. These deficiencies drive inflammation, fatigue, and chronic illness, but with the right genetic and intracellular testing, you can target them and supplement with the exact forms your body needs
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When Justace first had CMA testing done, Dr. Purser told him he was malnourished—even though he was a young athlete eating constantly. The results showed real deficiencies that explained why he struggled to gain and maintain weight. After following Dr. Purser’s protocol, he not only put on healthy weight more easily but no longer had to force himself to eat as much. He now encourages others, especially younger people, to get tested early to avoid genetic breakdowns later in life.
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One of the most powerful success stories at Purser Wellness came from a young patient who went from having 3–5 seizures a week to none for three months after completing CMA and genetic testing. In another case, a woman with almost no measur
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One of the most powerful success stories at Purser Wellness came from a young patient who went from having 3–5 seizures a week to none for three months after completing CMA and genetic testing. In another case, a woman with almost no measurable niacin in her system saw her seizures stop within two weeks once her deficiency was corrected. These aren’t “cures” in the traditional sense—just treating obvious nutritional deficiencies revealed by precise testing—but the results can be life-changing.
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CMA testing shows the vitamin deficiencies happening inside your cells, while genetic testing reveals why they’re happening in the first place. Patients often find their symptoms match exactly what the CMA shows, and when paired with genetic results, the root causes become clear. In most cases, it’s the genetic errors that drive the deficiencies—not the other way around—making the combination of both tests powerful for finding lasting solutions. DanPurserMD.com for all testing options or reach to my office!
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Glutathione is called the “master antioxidant” because it protects every cell in your body from oxidative damage, supports detox, and reduces inflammation. People with high homocysteine or MTHFR gene variants often can’t recycle glutathione
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