RPV + CareCrowd

You’ve been figuring this out alone.
Now you don’t have to.

Reserve My Membership

Early Enrollment limited to 500 members

Life interrupted
Diagnosis delay
Wait time

You’re not complex.
The system is just designed to make you feel that way.

These aren’t edge cases. This is the standard experience for people navigating rare disease. And it’s not a flaw in individual doctors; it’s a structural gap that no one has been built to fill.

Until appointments, there is no physician in your corner. We built CareCrowd to close that gap  with a physician advocate who is present in the space between your care visits, consistently.

A doctor as your advocate.
In your corner, consistently.
Starting at $49/month.

$69/mo

per month, cancel anytime

  • Physician-matched advocacy
  • Appointment preparation sessions
  • Guided 1-on-1 monthly sessions
  • Secure HIPAA-compliant communication
  • Early member pricing locked
$49/mo

billed annually – save nearly $400 your first year

RPV Members: use code ‘RPV25‘ for an additional 25% off for a limited time.

  • Everything in monthly, plus:
  • An additional 25% off exclusively for RPV members
  • Priority matching queue
  • Founding member status, permanently

CareCrowd is a direct-pay, physician-led service. Not covered by insurance currently. We are building the evidence base for future coverage.

Common questions

Right now, this is not a fully built-out app experience.

What it is… is real physician presence.

You’ll be matched with a physician advocate and able to communicate through text, voice, and video.

So instead of waiting for the next appointment… you have someone to reach in those in-between moments—when things actually come up.

That’s correct. We’re in an early pilot phase, which means you’re getting access to the experience now while we continue building the technology around it.

The presence is real. The physicians are real. The experience is real.

The platform is what we’re building to support and scale it.

Most communication in this phase is asynchronous, primarily through text.

That means you can reach out in real time—when something actually comes up.

To support relationship-building, voice and video check-ins are available; And depending on your plan, frequency of check-ins vary.

This is designed to fit into real life—not just scheduled appointments.

CareCrowd is not a messaging platform. It’s physician presence in the gaps between visits. Physicians who are strictly focused on advocacy, not treatment. They do not replace your treating physicians.

This is about having a doctor help you think through decisions, interpret what’s happening, and guide you—outside of system constraints.

If you already have that level of physician access and support, you may not need this.

But for many people… that presence doesn’t exist.

In the early pilot phase, matching is done manually and intentionally.

We consider factors like your condition, your situation, communication preferences, and overall fit.

As we build out the platform, this process will become more sophisticated— leveraging technology and AI to match based on deeper inputs like condition language, preferences, and interaction style.

When you feel stuck. When something changes. When you get new information you don’t understand. When you’re trying to decide what to do next.

This is not for emergencies or clinical requests. We do not diagnose, prescribe or treat.

It’s for clarity, guidance, and interpretation—where most real decisions happen.

And just as important—it’s not only for when something is wrong.

This is also about building a relationship with your physician advocate… so when something does happen, you’re not starting from scratch.

Don’t be surprised if your physician advocate reaches out just to check in or say hello. That connection is part of the care.

We hear that—and this is meant to do the opposite.

CareCrowd is not something you manage. It’s someone who helps you manage everything you’re already navigating.

It reduces the mental load—it doesn’t add to it.

That’s a fair question. Insurance pays for visits. It doesn’t support what happens in between.

CareCrowd provides continuous physician presence—time, judgment, and guidance outside of appointments.

That’s the gap we’re filling.

Physician advocates don’t need to be experts in your specific rare disease to support you well.

What they bring is clinical thinking, judgment, the ability to navigate complexity and their network.

And just like we do in real life—when something falls outside our specialty—we don’t stop.

We reach out. We tap into our network. We consult colleagues. We bring in the right perspectives.

The same way you would call a doctor in your family or friend group and say, ‘Can you help me think through this?’ That’s exactly what this is.

You’re not getting one physician in isolation— you’re getting a physician who knows how to access insight, clarify what matters, and help you move forward with confidence.

That’s completely valid. This isn’t replacing your care—it’s supporting you around it.

For many people, the real question becomes:  what is the cost of navigating this alone?

This is about having support in the moments where it matters most.

Advocacy organizations provide community, education, and shared experiences.

CareCrowd brings a physician into your personal decision-making process.

It’s the difference between having information… and having someone help you apply it to your life.

This is not temporary. You’re joining during an early pilot phase, but the goal is to build something lasting.

Your experience helps shape how CareCrowd grows and evolves.

Yes. Your information is not shared without your consent. 

CareCrowd is designed to support you—not to use your data. You remain in control.

No. This is not diagnosis or treatment.

This is physician-led advocacy—helping you understand, interpret, and navigate your care. We don’t replace your doctors.  We support you alongside them.

No. We are very intentional about this. We do not override or replace your care team.

We help you understand their recommendations, prepare for visits, and navigate decisions between them.

That’s okay. This is not about constant use—it’s about having someone there when you need them.

Some weeks you may not reach out at all. Other times, you might need more support.

It’s there when it matters. And even in the quieter moments, this is about building a relationship with your physician advocate— so when something does come up, you’re not starting from scratch.

You may even hear from your physician advocate just to check in. That’s part of what presence looks like.


That’s exactly where this model is most valuable. Rare and complex conditions often don’t follow clear paths. This is where clinical thinking, pattern recognition, and physician networks become critical.

You don’t have to figure that out alone.

This is not transactional—it’s a relationship. Think of it like having a doctor in the family.

After you register, it takes up to 2 business days to be matched with a physician advocate.

From there, you can typically schedule your first video meet-and-greet within 48 hours, based on availability.

Ongoing communication is primarily asynchronous (text), with responses within 24 hours.

During this early pilot phase, scheduled video or voice conversations are typically monthly—and if members want more time with their physician advocate, that’s valuable feedback as we continue to build.

Over time, the relationship grows—so when something comes up, you’re not starting from scratch.

That’s actually the closest comparison. This is like having a doctor in your inner circle—
someone you can reach out to, think things through with, and trust.

Because healthcare has been built around visits—not what happens between them.

And while physicians have always shown up in those in-between moments… it’s been informal.For family. For friends.For people in their inner circle. Unstructured. Ungoverned. Not scalable.  Not sustainable.

CareCrowd is the first time that kind of presence has been intentionally designed— to exist for everyone, not just those with access to a doctor in their life.