If you or someone you love is living with primary mitochondrial disease, you already know how lonely the road can be. Years of specialists. Tests that come back inconclusive. A diagnosis that finally has a name, but no clear map for what to actually do, day to day, to feel even a little steadier.
I’ve spent my career reading the body as a single energy system, the same machinery that mitochondrial disease disrupts. I can’t change your genetics, and I would never claim to. But I’ve seen how much room there often is to support the parts of your metabolism that nutrition, movement, rest, and careful monitoring can still reach. Sometimes that’s the difference between running on empty and having a little margin back.
My daughter has primary mitochondrial disease. I’ve sat in the waiting rooms, watched the specialists come and go, and seen up close where even good medicine runs out of answers. The tests that find nothing. The appointments that end with “let’s wait and see.” The long stretches where you’re left to manage the day-to-day on your own, with no one looking at the whole picture.
That experience changed how I work. It’s also why, every month, I set aside one full spot, with the same assessment and the same hands-on coaching my paying clients receive, for one person with confirmed primary mitochondrial disease. No cost, and no catch. It’s a small way of giving another family the kind of careful attention I wish we’d had sooner.
The pro-bono spot is for you if you have a confirmed diagnosis of primary mitochondrial disease (genetic or biochemically confirmed) and you’re looking for support alongside the care of your medical team, not instead of it.
Not sure whether yours is primary, or still working toward a diagnosis? Add your name anyway, and Chris, our co-founder, will help you figure out where you stand.
To be clear about what this is: it’s coaching and education focused on your metabolic capacity, meaning your nutrition, movement, and daily rhythms. It is not a treatment or a cure for mitochondrial disease, and it does not replace your neurologist, geneticist, or metabolic specialist. Think of it as another careful set of eyes on the parts of your health that everyday habits can still move.
The person who gets it receives a full three-month engagement, the same one my paying clients get. Nothing is scaled back because it’s free.
Andrew Reid I’ve spent my entire career on both sides of the same problem: caring for patients and clients directly, and teaching the science of metabolic health to the clinicians who treat them. Mitochondrial function sits at the center of everything I teach, because it sits at the center of how the body makes and spends energy.
I see every client personally, which is exactly why I can only offer one pro-bono spot a month. It keeps the assessment thorough and the coaching genuinely personal.
Physician AssistantUC Davis · MS, Personalized NutritionUniversity of Connecticut · DieteticsCal State LA
Leave your details below and Chris will reach out to learn a bit about your situation, confirm the pro-bono spot is the right fit (including a look at your diagnosis), and walk you through how the process works and where you stand in line. There’s nothing to prepare right now.
Chris will call or email within one business day. Keep an eye on your phone and inbox, and he’ll take it from there.
This is a coaching and education program. It is intended for informational and educational purposes and is not medical advice, diagnosis, or treatment, and it does not replace care from your physician or qualified healthcare provider. Mitochondrial disease requires ongoing care from qualified medical specialists; this coaching is intended to complement that care, not replace it. Always seek the advice of your physician or qualified healthcare provider with any questions about a medical condition. Individual results vary.