Dysautonomia program waitlist

Have you heard about our dysautonomia program?

Do you often hear that 'everything is fine', or that the symptoms are 'all in the head'?

Yet, deep down in your cells, you know that something is profoundly wrong physically and that you need help.

No one knows your body like you do. Until late-stage dysautonomia, your blood work can appear perfectly normal.

Your doctor may even be pleased with your seemingly excellent results, as dysautonomia primarily affects the nervous system, not the blood.

Many of our clients spend months, even years, trying to ascertain a diagnosis.

Many of our clients receive a misdiagnosis, or no diagnosis at all.

Do You Ever Experience Any of the Following?

Neuropathy

Numbness

or tingling

Issues with circulation

Intense brain

fog

Chronic pain

or fatigue

Insomnia

Random spikes in your heart rate

Inconsistent

blood pressure

Low energy

Chest Pain

Shortness

of breath

Histamine issues

Poor sleep or intense dreams

What we find often is that our clients are being treated for symptoms individually.

It is important to note how much the medical community misunderstands how this condition, but also how understandable it truly is. It can take the medical community up to 70 years to establish a treatment protocol for a condition, and this condition was only properly diagnosed in 1990.

So right now, even with a proper diagnosis of long-Covid, POTS or dysautonomia the available treatments don't restore one back to full ability.

It is not enough to simply increase your salt, rest, wear compression stockings or build up a conditioning exercise. We need to look at the body as a whole.