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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Thyroid health remains essential during menopause. Optimal labs should show FT3 around 4.0 and FT4 near 1.5, and testing through Direct Labs makes it easy to track. Supporting with supplements like Thyromin can help, but only if guided by accurate lab results.
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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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We go beyond ordinary genetic testing and nutrient plans. Our approach is unmatched:
✅ Precision Genetic Testing – We dive deep to uncover the root of your health need
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
TMG (trimethylglycine) can sometimes lower homocysteine—but only if it’s not caused by genetics. When homocysteine is high from genetic SNPs, TMG won’t fix it, and restrictive “low-methionine diets” are both harmful and outdated. The real s
TMG (trimethylglycine) can sometimes lower homocysteine—but only if it’s not caused by genetics. When homocysteine is high from genetic SNPs, TMG won’t fix it, and restrictive “low-methionine diets” are both harmful and outdated. The real solution lies in addressing deficiencies and genetics directly.
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Your body’s ability to detox depends on one critical pathway—turning homocysteine into glutathione. But for millions with MTHFR or other genetic SNPs, this process is broken, leaving them vulnerable to toxins, inflammation, and cytokine sto
🧬 After 15+ years deep in genetics, Dr. Purser sees two root causes over and over again: 1️⃣ Inflammation 2️⃣ Gut & liver dysfunction. Almost every chronic issue—including fibromyalgia, fatigue, and brain fog—ties back to 17 homocysteine SNPs or PEMT mutations. That’s why he built treatment guides, books, and the CMA + Redox + genetic testing combo. If you’ve been told “everything looks normal” but still feel awful, this is where to look next.
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