What it is, honestly

TPE devices are FDA-cleared, and TPE is an established treatment for specific medical conditions. Its use for longevity or healthy aging is off-label and investigational. We do not promise outcomes.

How it works

• Candidacy consultation with a physician
• Pre-treatment labs
• Session of about 2–4 hours
• Recovery and post-treatment labs
• Results review and next-step discussion

Inquire.

Risks can include low blood pressure, bleeding, infection, allergic reaction and electrolyte changes. Informed consent is required; registry or IRB participation is under consideration.

The candidacy flow

Step	What happens
1. Candidacy consult (60 min)	History, goals, contraindications, and a frank discussion of the evidence and its limits.
2. Pre-labs	CBC, coagulation, protein/albumin, calcium, lipids, inflammation and IgG levels.
3. Session (2–4 h)	Apheresis-trained nurse, physician available on site, continuous monitoring, private suite.
4. Recovery and post-labs	Observation for citrate-related symptoms, low blood pressure and access issues.
5. Review	Cadence decided with your physician. No outcome is promised.

Who may not be a candidate

People with certain bleeding or clotting disorders, unstable heart conditions, poor vein access, active infection or pregnancy, among others. Your physician decides.

Is plasma exchange FDA-approved for longevity?

No. Devices are FDA-cleared and TPE is used for specific conditions; longevity use is off-label and investigational.

Is it safe?

It has known risks and is performed with monitoring and informed consent.

Is it part of a study?

We are considering an IRB-approved registry or protocol, on counsel's advice.

Your next chapter starts with a conversation.

Come for the data. Stay for how you feel.

---

Educational content, not medical advice. Services follow physician evaluation, results vary, and some services are not FDA-approved for the uses described.