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Our Immediate Goal: Help 15 Families suffering with Multiple Sclerosis (MS)
This fundraiser will directly support 15 families with MS, providing them with:
- A full lifestyle intake including symptomology and past test analysis
- A letter to their family doctor or MS specialist introducing the theory and asking to partner on the requisition of blood tests and iron-sensitive MRIs
- Interpretation of the test results and letter to specialists with full differential diagnosis aligned to the Iron Trap
- Access to coaching and customized healing protocols with qualified practitioners
- Targeted supplements and healing products
- Symptom tracking and data collection
- Scientific documentation to publish our findings in a peer-reviewed journal
These are not generic interventions, each person's biochemistry will be carefully analyzed and supported through a health protocol based on the Iron Trap theory which is designed to reduce inflammation, support detoxification, halt demyelination, and bring development back to the brain and spinal cord.
NOTE: We are already helping our first family, 14 spots left! ❤️
Why This Matters
People with MS are suffering not only with MS, but a range of related comorbid conditions that are related to the Iron Trap including heart, liver, kidneys, and more. This is more than a fundraiser; it’s an act of hope where we aim to:
- Test and document key iron metabolism markers
- Apply interventions across light, nutrition, detox, and neuro-integration
- Track symptomology alongside physiological improvements
- Publish outcomes in a transparent, peer-reviewed format for the world to see, making the results available for millions worldwide
NOTE: We are not funded by pharmaceutical companies, and we are not profiting from the sale of products or supplements.
How You Can Help
Your support will allow us to:
- Build a large scale data collection mechanism along with data analysis
- Cover lab testing and analysis for 15 families
- Supply families with the therapeutic tools they need
- Support the small but committed team behind this mission
- Compile, interpret, and publish the findings in a professional journal for peer review
Honoring Vimala Sait
This mission is now carried forward in the name of a woman whose life embodied everything we stand for.
Vimala Sait was a lifelong champion for vulnerable families with medically complex disabilities in Canada. Her most notable work was with SafeHaven in Toronto, where her warmth, precision, patience, and fierce compassion shaped countless lives.
Vimala passed away on September 25, 2023, at Mount Sinai Hospital after a brave battle with ovarian cancer. Her early departure devastated those who loved her, but also galvanized us to ensure her spirit of service would live on.
In her honor, we created The Vimala Foundation, a not-for-profit initiative committed to restoring coherence and hope to the families most in need through well-researched, scientific interventions based on the Iron Trap.
Her husband, Ameen Sait, now serves as a Director of the Vimala Foundation and sits on our Board of Directors. He is also an active member of our fundraising team, standing beside us to continue the legacy of care and healing that defined Vimala’s life.
About Us
As a published author and independent researcher I believe I’ve stumbled upon the root cause of a number of neurological disorders which we call the The Iron Trap.
This proposes that environmental stressors like toxic exposures, artificial light, poor nutrition, estrogen loss, and chronic inflammation suppress a key enzyme called heme oxygenase-1 (HO-1). When this protective system collapses, iron becomes trapped inside cells, leading to mitochondrial failure, glutathione depletion, neuroinflammation, and cell death known as ferroptosis. Using the best AI tools available, we have performed advanced statistical modelling which has revealed that The Iron Trap Hypothesis explains every major clinical and biological observation of MS better than any other theory.
The Iron Trap is, by a statistically overwhelming margin, the most likely explanation for MS currently available.
Not only that, our first client's blood tests and MRIs have confirmed our predictions and is currently working with us to reverse her more severe symptoms (including vision loss).
We are a federally incorporated not-for-profit (751423567RC0001). All funds will be deposited into the Vimala Foundation account and used with full transparency and accountability to advance this mission and help these families heal. Whether you're a parent, practitioner, philanthropist, or simply someone who believes we owe it to the next generation to do better, we invite you to stand with us.
Thank you for believing in what's possible.
David K. Millar
Director, The Vimala Foundation
Author, Free the Iron Slaves: The Key to Unlocking Neurodiversity
Disclaimer: The Vimala Foundation does not offer medical advice, treatment, or diagnosis, and is not a healthcare provider. Content is for educational and research purposes only. None of our methods or statements have been evaluated by Health Canada, the FDA, or any regulatory authority. Always seek the guidance of qualified medical professionals before making healthcare decisions.
Organizer
David Millar
Organizer