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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.

10/22/2026

Many families avoid genetic testing because they’re afraid of a verdict: a diagnosis with no cure, a sentence they can’t change. But a genetic answer was never meant to be a verdict. It’s a map.

The fear is understandable. “What if we find something and there’s nothing we can do?” But that framing misses what an answer actually gives a family, even when no cure exists yet.

A map changes the journey in ways a verdict never could:

→ It ends the exhausting search, replacing uncertainty with a direction
→ It guides better care today, shaping decisions even without a single “fix”
→ It connects families to the right specialists and communities for their condition
→ It opens doors to trials and therapies that could emerge tomorrow

Knowing where you are, even on hard terrain, beats being lost. A clear answer lets a family stop wandering, plan proactively, and position for whatever research brings next. That’s power, not a sentence.

𝗚𝗲𝗻𝗲𝘁𝗶𝗰 𝗮𝗻𝘀𝘄𝗲𝗿𝘀 𝗮𝗿𝗲 𝗮 𝗺𝗮𝗽, 𝗻𝗼𝘁 𝗮 𝘃𝗲𝗿𝗱𝗶𝗰𝘁.

An answer with no cure today still tells you which way to walk, who to walk with, and what to watch for on the horizon. Uncertainty offers none of that. A map, even an imperfect one, always beats the fog.

The answer doesn’t close the story. It helps you write the next chapter.

10/21/2026

Walk into Mass General with a genetic report from another provider. Even a reputable one. Even the same company Boston Children's uses.

Their response: "Do you have insurance? We'll run our own genetics. We're not taking outside reports."

Translation: they want to get paid. They want control.

For families planning to attend Epilepsy Awareness Day:

→ Get genetic testing at the expo for free.

→ Meet with top neurologists immediately.

→ Get expert interpretation of results you already have.

→ No waiting for institutional approval.

→ No insurance requirements.

→ No gatekeeping.

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

10/20/2026

To truly keep up with new medical research, a doctor would need 140+ hours a week. There are only 168 hours in a week, total. The expectation we quietly place on physicians was never physically possible.

We imagine the ideal doctor as someone who has read everything and remembers it all. That picture was always a myth, and it’s getting further from reality as research volume explodes.

The honest math reframes the whole problem:

→ 140+ hours a week just to stay current, which no human has to give
→ New studies published faster than anyone can read, let alone retain
→ A single physician expected to know every condition across every specialty
→ The real failure isn’t the doctor; it’s asking one person to be superhuman

So the fix was never “find a doctor who knows everything.” That person doesn’t exist. The fix is changing what we expect one human to carry, and building a system that brings the right knowledge to them exactly when a case needs it.

𝗡𝗼 𝗱𝗼𝗰𝘁𝗼𝗿 𝗰𝗮𝗻 𝗿𝗲𝗮𝗱 𝗶𝘁 𝗮𝗹𝗹. 𝗦𝗼 𝘄𝗲 𝗯𝗿𝗶𝗻𝗴 𝘁𝗵𝗲 𝗸𝗻𝗼𝘄𝗹𝗲𝗱𝗴𝗲 𝘁𝗼 𝘁𝗵𝗲𝗺.

Instead of demanding the impossible from physicians, we deliver the relevant expertise straight to the doctor who already knows your family. They stay the trusted guide. We make sure they’re never working from incomplete information.

10/19/2026

The genetics component is exploding. Doctors are saying "this is so needed." The response has been overwhelming. Next year, you're going to need an entire day dedicated just to genetics at Epilepsy Awareness Day.

That's not hype. That's the reality of what's happening.

More genetic conditions are being discovered every single day. More testing is available. More families are demanding answers instead of accepting diagnosis without understanding the underlying cause. The genetic piece of Sunstone Health's offering has unlocked something the epilepsy community didn't even know it was missing.

Here's what's driving the excitement:

→ Top neurologists volunteering extended time at the genetics booth instead of their assigned slots.

→ Families getting answers they couldn't access through traditional channels.

→ Doctors discovering new genetic insights through screening.

→ Real-time genetic expertise instead of months-long waits.

→ Actionable information families can use immediately.

The fact that it needs its own dedicated day next year isn't a problem to solve. It's proof that Sunstone Health is addressing a genuine gap in how epilepsy care actually works.

Genetic testing. Expert interpretation. Family empowerment. All happening simultaneously at an expo, not scattered across months of appointments and referrals.

This is healthcare access working the way it should.

Sunstone Health built the infrastructure. Now the field is responding.

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

10/16/2026

Genetics research is turning assumptions about autism upside down.

The goal isn't to prove autism is genetic. The goal is to identify underlying causes that can be treated to reduce symptoms.

Here's an example: three siblings from the same parents. Same household. Same vaccines. Same variables across the board. One child has autism and is non-verbal. Two are neurotypical.

If autism were inherited genetically, why would only one sibling have it when all three share identical genetics and environment?

De novo mutations. Random genetic changes that happen in one individual, not passed down from parents.

Sunstone Health's approach uses whole genome sequencing to identify those de novo mutations and understand what underlying conditions might be treatable. Not to label or categorize. To intervene.

→ Identify the actual genetic mutation causing symptoms.

→ Understand what's treatable within that genetic profile.

→ Reduce symptoms through targeted intervention.

→ Give families actionable information, not just diagnosis.

Sunstone Health sequences the genome to find what's actually fixable.

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

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.

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.

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.

Address

10 Derne Street
Boston, MA
02114

Opening Hours

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

Website

http://sunstonehealth.com/

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