ME/CFS & Post-Exertional Illness
We measure and address the systems responsible for regulating blood flow to the brain — the variable most ME/CFS care never looks at.
If any of these sound familiar, you're in the right place.

In study after study, ME/CFS patients show impaired cerebral blood flow when upright — neurovascular dysregulation that standard testing never measures and most clinicians never look for. That's where we start. Not as a theory, but as something we can measure on day one and build a treatment protocol around.
More than 9 in 10 people with ME/CFS have never been diagnosed. Why? Because most doctors were never given a useful framework to properly evaluate ME/CFS. The medical system is built to only rule out obvious disease — so patients with something as complex as ME/CFS are left with no real explanation.
Before booking your visit, schedule a free phone consultation with a Keiser Clinic physician. They'll listen to your story, answer your questions, and tell you plainly whether coming in makes sense for your situation.
Schedule a Free ConsultationWhat to expect
Our diagnostic workup brings cutting-edge methods from leading neurovascular and autonomic research — including real-time cerebral blood flow measurement that most ME/CFS experts still don't have in routine practice. We do — and we use them with every patient. We also work with ME/CFS patients every day. Every test is paced and structured to stay within your metabolic window — so you leave with answers, not a crash.

The brain is the most oxygen-sensitive organ in the body — and in ME/CFS, it's often the one being starved. We measure blood flow to the brain in real time using transcranial Doppler ultrasound, giving us a live picture of whether your brain is getting what it needs to function — something no standard test ever looks at.

CO₂ is one of the brain's primary signals for controlling blood vessel dilation. When CO₂ levels drop — which research shows happens consistently in ME/CFS — blood vessels constrict at exactly the moment the brain needs more supply, not less. We measure this directly, because it's one of the most treatable variables in the picture.

In ME/CFS, thinking feels like exertion — because for your brain, it is. We measure what happens to cerebral blood flow when we ask you to do cognitive work, because the crash that follows mental effort follows the same neurovascular logic as physical exertion. Understanding that distinction shapes how we approach your treatment.

We assess the visual and vestibular systems using video-oculography (VOG) and pupil response testing. If these systems are misfiring, they can keep your autonomic nervous system stuck in overdrive.

We use deep breathing, Valsalva, and postural stress to measure how your autonomic system responds and recovers under challenge. Then we layer in cognitive, cervical, and visual demands, because many patients only break down under combined load. What looks manageable at rest often becomes obvious when the system is pushed.

Some of the most important findings still come from an experienced doctor examining you directly. We assess reflexes, eye tracking, cervical motion, and coordination to catch the neurological patterns that may not show up on a screen.
A Note From Our Team
Several of our doctors have been patients or caregivers themselves. They know what it feels like to be dismissed and sent home with no answers. When you become a patient here, you have a care team of doctors who understand where you've been — and what it actually takes to get better.
Your rehabilitation is not a program that existed before you walked in the door. Nothing is prescribed before we know exactly where the failure is and what's driving it. Instead of pacing & pain management being your only options, we prescribe an individualized neurological treatment — dose-specific to your needs, within your energy envelope.
Whether your primary driver is autonomic dysregulation, neurovascular dysfunction, vestibular failure, or a combination — we strip away the labels and identify the mechanism that's failing in you specifically, so that we can treat the actual problem rather than the presentation of it.
The mitochondria are the factory. But if blood flow to the brain is impaired, there's nothing to run through them — no oxygen, no glucose, no output. You can take every supplement on the market and it won't matter if the delivery system is broken. The mitochondria aren't failing because they're damaged. They're failing because they're not being fed. That's a cerebral perfusion problem, and that's where we start.
Therapies begin by being applied to you — passive stimulation targeting the specific neurological systems that are failing — so your brain gains capacity before it's asked to perform. As those systems strengthen, therapies progress to active participation, then to independent function. That's how we expand your energy envelope without triggering harmful crashes. And throughout, we use capnography to monitor CO₂ in real time — giving us an objective early warning signal before your body crosses into PEM, so we can stop before the crash occurs, not after.
Virtual follow-up is included in your visit. Your protocols go home with you. We check in, answer questions, and make sure you stay consistent with what's working — until you no longer need us.
Most patients who come to us carry more than one of these diagnoses. These pages exist because that is often how people find us, not because we treat each diagnosis on a separate track. Our testing measures what your brain and nervous system are actually doing. The label you arrive with does not change that.
"Pacing as treatment has a ceiling. We work above it — in the brain."
Some of what you may be prescribed during your visit

Retrains the balance system when dizziness, motion sensitivity, visual instability, or autonomic symptoms are being worsened by vestibular dysfunction.

Targets the visual control systems that stabilize gaze and helps the brain build a more accurate map of the body in space. This can reduce neurostrain, disorientation, overload, and instability under cognitive and sensory load.

Uses targeted stimulation, including tools like the Neuro20 suit, to improve sensory input from the body and give the nervous system better information to regulate from.

Addresses mechanical strain and poor sensory signaling coming from the neck and upper cervical region, where instability can interfere with brainstem function, and autonomic regulation.

Rebuilds cleaner movement patterns so activity becomes more tolerable and less likely to trigger compensation, overload, or crash responses.

Challenges the brain's ability to regulate under mental load, helping improve function when symptoms flare with thinking, multitasking, or divided attention.

Uses carefully dosed activity to improve tolerance and function without relying on generic exercise protocols like CHOP or GET that ignore cerebral blood flow, autonomic limitations, and issues related to fatigue.

Uses red light and laser therapy to support tissue recovery, reduce irritation, and complement neurological rehabilitation in areas that need targeted stimulation.

We use the non-invasive Magnetolith in patients with ligament laxity, including hEDS, to treat tendons and joints that may be contributing to instability in joints or the upper cervical spine.
| Category | Conventional Care | The Keiser Clinic |
|---|---|---|
| Framing | ME/CFS is a syndrome — manage symptoms, pace carefully, stay within your energy envelope | A measurable neurovascular mechanism underneath the symptoms — one we can test for and build treatment around. |
| The Crash | Post-exertional malaise — avoid triggers, rest after exertion | A measurable neurovascular event. We use real-time CO₂ monitoring to catch it before it happens — and dose activity to build capacity, not trigger collapse. |
| Testing | Bloodwork and MRI return normal. No further workup ordered. | Real-time cerebral blood flow, CO₂ reactivity, vestibular and autonomic reflex testing — measuring what actually fails. |
| Treatment | CBT, graded exercise therapy, pacing advice, antidepressants | Individualized neurological protocols built from your data — not a generic ME/CFS program. |
| Progress | Patient self-report of energy and symptoms | Objective retesting throughout your stay — if the data doesn't change, the protocol does. |
| Comorbidities | POTS, MCAS, and small fiber neuropathy often missed or treated separately | Screened for and treated as part of the same clinical picture — they frequently share the same underlying mechanism. |
| Doctor Access | 15–45 minute visits spaced months apart | Multiple hours a day with a full clinical team — with direct follow-up after you leave. |
We intentionally see a small number of patients each week. When you're here, you have a full clinical team — not a rotating roster of one-off appointments. Our waiting area has movie theater reclining chairs to make your breaks comfortable.
Most patients stay two to three weeks. Some stay longer. But when you arrive, the only thing you commit to upfront is that first day of diagnostic testing. What comes after is your decision.
We don't run a copy-and-paste ME/CFS rehabilitation program. We become your care team and design a protocol specific to you.
Schedule a Free ConsultationWant to hear directly from patients who've been through this?
Read POTS & dysautonomia recovery stories →A Keiser Clinic physician will listen to your story, answer your questions, and tell you plainly whether coming in makes sense for your situation. No pressure. No false hopes.
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