Jordan Rausch Idaho Genetic Counselor

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Jordan Rausch Idaho Genetic Counselor Board-Certified Genetic Counselor in Idaho

I want to help you feel empowered by your genetics.

09/03/2026

I just want the best for you! Which is why I offer a free 10 minute discovery call to see if genetic counseling is right for you and what type of package would be most beneficial for you and your health.

28/02/2026

Rare disease = fewer than 200,000 people in the U.S.
But 1 in 10 of us are living with one.

I’m one of the 1 in 10. I have systemic mastocytosis. For years, my symptoms didn’t quite fit in a neat box, but they have a name and I can use that to make personalized choices about my lifestyle and health.

Awareness leads to earlier diagnosis.
Earlier diagnosis leads to better care.
Better care changes lives.

If you’re part of the rare disease community, I see you.
Drop your diagnosis below if you’re comfortable sharing.

27/02/2026

When you look at symptoms one by one, they seem random.
When you look at them together, they tell a very specific story.

The Clues:
-Fainting spells
-Rapid heartbeat episodes, even at rest
-Blurred vision before getting dizzy or passing out
- A mother with multiple miscarriages
- A brother diagnosed with seizures
- A cousin who was a strong swimmer and p drowned unexpectedly

Fainting during exercise, stress, or sudden emotion isn’t always “just dehydration.” In Long QT Syndrome, the heart’s electrical reset runs too long, which can trigger dangerous rhythms and briefly cut off blood flow to the brain. Rapid heartbeats at rest point to ion channels misfiring, not poor conditioning. Blurred vision before passing out can be the warning sign of an arrhythmic episode. A history of miscarriages, a sibling labeled with “seizures,” or a cousin who drowned, especially while swimming, can all fit the pattern of KCNQ1-related Long QT.

KCNQ1 affects the heart’s electrical timing. When that reset phase runs too long, it can trigger dangerous rhythms, especially with exercise, stress, or swimming.

KCNQ1 is one of the most common genes linked to Long QT. Genetic testing can confirm the diagnosis and guide family screening.

But a negative test does not always rule it out. Some clinically diagnosed Long QT cases have no identifiable variant yet. ECG findings and family history still matter.

26/02/2026

Hot take for Rare Disease Month 2026:

You don’t need more random health information.
You need context.

If you’ve ever:
-Been told your labs are “normal” but you feel off
-Tried multiple medications before one finally worked
-Seen specialist after specialist who never zoomed out
-Wondered if your symptoms are connected

You are exactly who I created this page for.

Genetics is not just for pregnancy.
It’s not just for rare conditions.
It’s a tool for connecting patterns, understanding risk, and personalizing care.

I’m a genetic counselor who helps proactive adults stop guessing and start understanding their biology.

If you’re into root-cause thinking, prevention, and personalized health plans follow along.

We’re doing healthcare differently here.





24/02/2026

POV: your friend orders a triple espresso at 8pm and sleeps like a toddler… and you’re still vibrating from your 10am latte

It’s not “just anxiety.”
It’s not “just tolerance.”
It might be your genetics.

A 2024 study in the Journal of Translational Medicine looked at how we metabolize caffeine, and one of the biggest players is the CYP1A2 gene. This gene helps your liver break down about 95% of the caffeine you drink.

✨ Rapid metabolizers clear caffeine quickly. It barely has time to tap your brain on the shoulder.
✨ Slow metabolizers hold onto caffeine for hours, which can increase risk for high blood pressure or heart concerns if intake is high.

When you know how your body actually processes things like caffeine, medications, and other exposures, you can make choices that support your long term health instead of working against it.

I help proactive adults use their genetic information to build personalized, preventative health plans.

If you’re ready to see what your DNA actually says about you, follow along or connect with me at empowergeneticshealth.com

19/02/2026

Why wait for a bad side effect to find out a medication isn’t right for you? 💊
Trial and error is for science experiments, not your body.
Pharmacogenomics (PGx) allows us to see exactly how your unique enzymes metabolize drugs, from heart meds to mental health support.
At Empower Genetics, we believe proactive testing should be the standard, not the exception. Get your clinical-grade PGx panel today and stop guessing with your health.
Visit empowergeneticshealth.com to start.

Most of our healthcare system is designed to react once you’re already sick. But if you’re healthy today, your goal shou...
18/02/2026

Most of our healthcare system is designed to react once you’re already sick. But if you’re healthy today, your goal shouldn’t be “waiting for symptoms”, it should be prevention.
I offer a suite of genetic consultations at Empower Genetics for patients who want the blueprint to their own bodies. From identifying hereditary cancer risks to optimizing your nutrition, we look at the root cause of your long-term wellness.
What we screen for:
✅ Hereditary Cancer & Heart Risk
✅ Medication Compatibility (PGx)
✅ Personalized Nutrition & Metabolism
✅ Family Planning (Carrier Screening)

You don’t need to wait for a “red flag” to get answers. Take control of your biological future today.

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