Case Studies

JANE* ~ No more miserable medications at the hospital.

By age 19, Jane was in and out of the hospital 30+ times. Ever since she was a baby she’d suffered from severe GI symptoms, low blood sugar, and a racing heart. Our technology identified the enzyme malfunction that was causing her symptoms. Then, in collaboration with her physician, Jane was able to implement a simple dietary intervention and finally found relief, ending her lifelong diagnostic odyssey.

DAN* ~ Celiac disease in hiding.

At 53, after years of GI symptoms, indigestion, bloating, and diarrhea, Dan’s clinician diagnosed him with irritable bowel syndrome, with no relief in sight. Our technology found a sub-type of celiac disease based on Dan’s unique molecular signature. In collaboration with his physician, his symptoms were relieved with targeted dietary interventions and with nutritional supplements.

MARY* ~ Diabetes complications are the worst.

At 64, Mary dreamed of traveling again. Unfortunately, she developed severe diabetic ulcers over the past few years due to her long-standing obesity and diabetes. Her symptoms severely limited her travel plans and social interactions. Our technology found the underlying mechanism of her diabetes. Mary’s ulcers completely resolved within a few months, as her physicians implemented a clinical plan based on our findings. She is planning an international trip with her girlfriends this fall.

JACK* ~ Conserving cognition.

Jack is a high-functioning executive interested in healthy living and longevity. However, when tested with our technology, an Alzheimer’s disease gene was uncovered, along with molecular signatures indicating the presence of amyloid protein deposition in Jack's brain. In response to this finding, a top-notch multi-disciplinary team was assembled with his physicians, with the goal of conserving his cognition and to monitor clinical trials in the field that he may benefit from. By taking action today, Jack is able to plan for a brighter future.

JENNIFER* ~ Breast cancer scare … not so fast.

At age 53, Jane underwent routine mammography. She has an increased risk for breast cancer based on her family history, including her mother. She underwent a series of breast ultrasounds and MRI exams with ambiguous results. Her physicians gave her confusing and contradictory recommendations, ultimately recommending bilateral mastectomy. However, testing with our technology gave Jennifer the clarity she needed. No causal gene mutation or any molecular signatures for breast cancer were found, and Jennifer avoided bilateral mastectomy. She has continued to have benign tests ever since.

MAX* ~ Cardiovascular disease ... maybe?

After 20 years of routine cardiovascular preventive care, Max was starting to decline. A lifelong cyclist, he was struggling on rides, almost to the point of stopping his beloved hobby. Our technology identified a genetic mutation for his cardiovascular disease. In collaboration with his physician, a team was assembled to address and reverse the damaging effects. Max is back on his bike, enjoying his 40–60-mile rides yet again.

*Names and faces have been changed to protect confidentiality.