30-Day Open-Label Observational Findings
Participant-Reported Changes in Symptom Frequency, Severity, and Daily Well-Being
Research Methodology & Data Transparency
We measured how quickly participants experienced symptom relief, tracking reported reductions in symptom frequency, intensity, or both throughout the 30-day observational study. Percentages reflect the proportion of participants who reported improvement by each time point.
Summary of Reported Findings
Selected participant reports
Reported Daily Usage by Symptom Group
Selected participant-reported daily usage patterns during the observation period.
Data reflects selected participant-reported daily usage patterns during the 30-day open-label observational period, including individuals reporting PVCs, PACs, tachycardia, AFib, and blood pressure concerns. Each dose represents 1 mL of Colloidal Magnesium.
Progress Beyond 30 Days
Experience the Difference in Every Drop

