Sunstone Health

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Sunstone Health Our mission is to end the 7-year Diagnostic Odyssey with data precision and fierce advocacy. The system isn't delivering. We are. The system is broken.

Because "be patient" isn't a treatment plan. Families with genetic diseases deserve answers, not a 7-year loop of uncertainty. We’re Sunstone Health, and we’re here to break the Diagnostic Odyssey. We use data precision to find the answers the system misses, turning years of waiting into 12 weeks of clarity. We’re the fix. We believe every family deserves a champion. At Sunstone Health, we’re fighting to end the chaos of the healthcare system by providing the genetic answers families need in weeks, not years. If you’re tired of fighting the status quo alone, you’ve come to the right place. Stop the chaos. Start the healing.

In most of healthcare, your own information isn't really yours. It sits in a system you can't access, owned by someone e...
10/15/2026

In most of healthcare, your own information isn't really yours. It sits in a system you can't access, owned by someone else, requiring a new sample every time a new question comes up. Your genome works differently. It's yours to keep.

Ownership matters more than it sounds. When the data belongs to you, it stops being a thing you have to re-buy and re-collect every time medicine moves forward.

Here's what "yours to keep" actually means in practice:

→ One sequence, so no repeat blood draws or cheek swabs down the line
→ The information belongs to you, not locked away in a system you can't reach
→ Future questions get answered from data you already have on hand
→ No starting over each time a new therapy or test becomes relevant

Think about what that spares a family. No dragging a scared child back for another draw. No waiting weeks for a new sample to process. The data is already there, ready to answer the next question the moment it matters.

𝗬𝗼𝘂𝗿 𝗴𝗲𝗻𝗼𝗺𝗲. 𝗬𝗼𝘂𝗿 𝗱𝗮𝘁𝗮. 𝗬𝗼𝘂𝗿𝘀 𝘁𝗼 𝗸𝗲𝗲𝗽.

Your genetic information is the most personal data you have. It should belong to you, work for you over time, and never require you to start from scratch to get an answer.

Sequence once. Keep it for good.

10/14/2026

This is the biggest epilepsy event anywhere. Every top neurologist and epileptologist wants to present. The talks are technically brilliant. Families watch from the front. Doctors crowd the back row to hear what their peers have to say.

The doctors volunteering at the Let's Talk Genetics booth are asking for longer shifts.

A neurologist talked to me this morning. She's assigned a one-hour slot at the booth. She asked: can I extend that? Because she knows families will be waiting in line and she wants to make sure every single person gets their questions answered. Not rushed through. Actually answered.

That's rare. Doctors like that are heroes.

There aren't enough of them out there. But the ones who exist—the ones who would trade prestigious speaking slots for more time with families—those are the people Sunstone Health brings to Epilepsy Awareness Day.

→ Epileptologists extending shifts voluntarily.

→ Neurologists prioritizing family conversations over conference prestige.

→ Clinical teams committed to answering questions, not checking boxes.

→ Real expertise combined with genuine care.

This is why the Let's Talk Genetics booth matters. It's not a booth. It's access to some of the most committed neurologists in the country, all of them there because they want families to get real answers.

Those doctors are changing lives. Sunstone Health is making sure families find them.

Come see Sunstone Health at the Epilepsy Awareness & Education EXPO, presented by Sofie's Journey - November 16–17, 2026 in Anaheim, CA.

The average family searches 7 years for a diagnosis. We've cut that to about 12 weeks. Seven years versus three months i...
10/13/2026

The average family searches 7 years for a diagnosis. We've cut that to about 12 weeks. Seven years versus three months is the difference between a childhood spent in waiting rooms and one spent being a kid.

The diagnostic odyssey isn't just slow. It's a loop that drains families emotionally and financially while the clock keeps running on a child's development.

Look at what those seven years actually cost a family:

→ Years of ER visits, referrals, and repeat tests that often find nothing
→ One family drove three hours for a twelve-minute exam that came back empty
→ Misaligned incentives, because when everyone bills for their own piece, no one owns the fastest answer
→ The loop spins, expensive and exhausting, while the real diagnosis waits

The system isn't broken by accident. It's fragmented by design, with each specialist billing for a slice and no one accountable for the whole journey. The patient pays for that fragmentation in time, money, and hope.

𝗘𝗮𝗿𝗹𝘆 𝗮𝗻𝘀𝘄𝗲𝗿𝘀 𝗰𝘂𝘁 𝗰𝗼𝘀𝘁 𝗮𝗻𝗱 𝗴𝗶𝘃𝗲 𝗰𝗵𝗶𝗹𝗱𝗵𝗼𝗼𝗱 𝗯𝗮𝗰𝗸.

We compress diagnostic time from about 7 years to about 12 weeks, with roughly 60% average cost reduction per case. And for employers, it's pay-for-results: no upfront cost, no per-employee-per-month fees. One early diagnosis pays for itself many times over.

See what one diagnosis can actually save, in dollars and in years.

10/12/2026

Sunstone Health is doing something we normally never do at Epilepsy Awareness Day: accepting families who already had genetic testing done elsewhere.

Don't have your results stuck in a folder gathering dust. Bring them to the expo.

Here's what's happening:

→ Full trio genetic testing for families getting tested on-site. Deep variants. Real analysis.

→ Expert neurologists and clinical teams reviewing existing genetic tests from other providers.

→ Real pre-workup consultation so families understand what their existing results actually mean.

→ Constructive conversation turning information into action.

Most families get genetic test results and have no idea what they mean. The doctor who ordered it moved on. The lab shipped results. Families are left interpreting complex genetics alone.

Sunstone Health is changing that. Bring your existing tests. Meet with neurologists. Get expert interpretation. Understand the implications. Get guidance on what to do next.

This removes the barrier between having genetic information and understanding genetic information. Between getting tested and getting answers.

Sign up at Sunstone Health or the app. Bring your genetic test results. Meet with our clinical team at the Let's Talk Genetics booth.

You don't need new testing if you already have results sitting unused. You need expert interpretation of what you already have.

That's what Sunstone is providing.

After years of searching, most families don't just feel tired. They feel alone. Appointment after appointment, they carr...
10/09/2026

After years of searching, most families don't just feel tired. They feel alone. Appointment after appointment, they carry the weight of being their child's advocate, researcher, and case manager all at once, usually with no one truly in their corner.

That isolation is its own kind of exhaustion. The medical system can feel like a series of closed doors, each one handing you back to yourself with no answer and no next step.

This is the part we take seriously, maybe most of all:

→ You are not a case number; you are a family we're walking beside
→ The years of fighting you've already done are seen, not dismissed
→ You don't carry the search alone anymore; the burden becomes shared
→ Someone is finally in your corner, as committed to the answer as you are

For families this deep into the journey, hope can feel risky. You've had it raised and dropped too many times. But being genuinely on someone's team, not selling them something, means standing with them whether the road is short or long.

𝗬𝗼𝘂 𝗮𝗿𝗲 𝗼𝗻 𝗼𝘂𝗿 𝘁𝗲𝗮𝗺. 𝗪𝗲 𝗮𝗿𝗲 𝗼𝗻 𝘆𝗼𝘂𝗿𝘀.

To every parent still searching after years of fighting: the work you've done to get here matters, and you don't have to do the rest of it alone. We're here, and we're with you.

Whatever the road ahead looks like, you won't walk it by yourself.

10/08/2026

Phillip Pearl. Chief of Harvard Med School's pediatric epilepsy program. One-year waiting list for clinic appointments.

Asked how much time he could spend at the genetics booth: "Am I limited to one hour each day or can I spend most of my time there?"

His hospital CFO will be furious when he finds out what's happening. Pearl has a one-year clinic wait. He's offering free expertise at the expo. Patients from that wait list will show up. They'll get answers immediately instead of waiting twelve months. The clinic waiting list collapses.

But Pearl doesn't care about the CFO's problem. He cares about families getting genetic testing and expert guidance they can't access otherwise.

Jim Wheless, another top neurologist: "I don't know how much time I'm gonna spend at my booth. I think I'm gonna spend a lot of time at the genetics exhibit. Tell my manager to text me if they need me. Otherwise I'm camping out at the genetics booth."

These aren't administrators optimizing schedules. These are the best neurologists in the country deciding that helping families at the expo matters more than their institutional commitments.

That's Sunstone Health's value: it makes top experts choose to help directly instead of filtering access through gatekeeping institutions.

Top doctors. No barriers. Families getting real answers.

That changes outcomes.

10/07/2026

Sunstone Health is opening 25 genetic test trios preemptively at the expo. Not a waitlist. Not a lottery. First come first serve.

Last year, we swabbed on site. Families got tests. This year we're going deeper: bringing dozens of doctors to the expo to provide real-time counseling, feedback, and expertise.

Families are signing up now. Applications are being reviewed. But here's what matters: this is access most families have never had.

Genetic testing requires expertise. Most families either can't access it or face months of waiting and coordination. Sunstone Health is collapsing that barrier by putting doctors and testing infrastructure on-site simultaneously.

→ Immediate genetic testing without months of waiting.

→ Real-time expert counseling from dozens of doctors.

→ Families get answers, not referrals.

→ Access that typically requires insurance approval or significant cost.

This is what breaking access barriers actually looks like. Not talking about it. Doing it. Twenty-five tests. Dozens of doctors. On-site. Live.

If you have a child with unexplained symptoms. If genetic testing has been denied or delayed. If you need answers without months of coordination.

Apply now. First come first serve.

Sunstone Health is making genetic expertise accessible.

Staying current on medical research would take a doctor 140+ hours a week. That's more hours than exist in a workweek, s...
10/06/2026

Staying current on medical research would take a doctor 140+ hours a week. That's more hours than exist in a workweek, spent only on reading. Then the same doctor gets about 11 minutes with you. The math was never going to work.

When a diagnosis stalls, families often blame the doctor. Usually that's the wrong target. Even a brilliant, dedicated physician is working inside constraints no amount of talent can overcome.

Look at what they're actually up against:

→ 140+ hours a week to truly keep up with new research, which no human has
→ An 11-minute average visit, rarely enough to dig into a condition outside their specialty
→ A rushed, misaligned system that holds back doctors who are in it for the right reasons
→ The impossible expectation that one person knows everything about everything

The problem isn't effort or intent. It's structural. We ask one human to hold an ocean of knowledge and then give them minutes to apply it. So the answer isn't a better doctor. It's a better-supported one.

𝗜𝘁'𝘀 𝘁𝗵𝗲 𝘀𝘆𝘀𝘁𝗲𝗺, 𝗻𝗼𝘁 𝘁𝗵𝗲 𝗱𝗼𝗰𝘁𝗼𝗿.

That's why we bring the specialists to them. Sunstone acts as a force multiplier, delivering precision expertise to the doctor who already knows your family, so your care never stalls waiting for one person to have every answer.

Your doctor, backed by a team. That's how care keeps moving.

Two children can share the same autism diagnosis and need almost nothing in common. One is nonverbal and sensory-sensiti...
10/01/2026

Two children can share the same autism diagnosis and need almost nothing in common. One is nonverbal and sensory-sensitive. The other is chatty and struggles with transitions. Same word on the chart, entirely different child.

A diagnosis is a starting point, not a description. It names a category, but it can't tell you who your child actually is, what they need, or what will help them thrive.

That's the gap families keep running into:

→ A single label gets applied to an enormous range of real, individual kids
→ Generic support built for "the diagnosis" often misses the specific child in front of you
→ What helps one child can do nothing, or worse, for another with the same label
→ The whole picture, not the category, is what actually guides the right care

When care is built around the label instead of the child, families get plans that look right on paper and fall flat at home. The word was never the point. The individual behind it is.

𝗦𝗮𝗺𝗲 𝗹𝗮𝗯𝗲𝗹, 𝘃𝗲𝗿𝘆 𝗱𝗶𝗳𝗳𝗲𝗿𝗲𝗻𝘁 𝗸𝗶𝗱𝘀.

We help families see the whole, individual picture, the full profile of their specific child, so support fits the person and not just the paperwork. Because your child was never a category.

Understand the child, not just the diagnosis.

09/30/2026

My father-in-law is that guy. Falls through a floor. Walks out. Has a b**r. Doesn't get sick. Bounces back from everything. That's genetics. Some people are built to be resilient.

But resilience isn't destiny. It's a spectrum.

A kid who grows up in the inner city with certain genetic predisposition might have been perfectly healthy in the countryside. That same kid in the countryside where PFAS contaminates water might struggle instead. A child genetically predisposed to autoimmune response might thrive with one set of environmental pressures but collapse under another.

Now environmental pressures on kids today are unprecedented. PFAS in drinking water. Air quality variations by neighborhood. Processed food availability. Stress levels. Infection exposure. Our bodies evolved for a different world than the one kids inherit now.

Some kids' genetics handle this modern environment fine. Others' don't. It's not about being weaker. It's about genetic predisposition meeting environmental reality.

At Sunstone Health, we understand this intersection. We identify genetic vulnerabilities not as destiny but as important information. A kid genetically predisposed to autoinflammatory response needs different environmental protections than a kid whose genetics are naturally resilient.

Know the genetics. Understand the environment. Modify what you can control.

Your child's outcome isn't predetermined. But understanding their specific genetic predisposition lets you stack the odds in their favor.

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10 Derne Street
Boston, MA
02114

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Monday 9am - 5pm
Tuesday 9am - 5pm
Wednesday 9am - 5pm
Thursday 9am - 5pm
Friday 9am - 5pm

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