Sequence MD

Sequence MD SequenceMD provides medical genetics services within community health systems to adults and families with rare conditions, unique, or unmet medical needs

Understanding your genetics changes everything. SequenceMD evaluation and counseling services turn that knowledge into a...
03/06/2026

Understanding your genetics changes everything. SequenceMD evaluation and counseling services turn that knowledge into action — with early diagnosis, proactive health management and precision care across a full range of specialties:

• Hereditary Cancer Risks
• Cardiogenetics
• Disease Risk
• Ehlers-Danlos Syndrome (EDS)
• Family Planning
• Intellectual & Developmental Disabilities (IDD)
• Nephrogenetics
• Neurogenetics
• Pediatric Genetics

Learn more at sequencemd.com

-DanlosSyndrome

Every year on Rare Disease Day (that's today!), we’re reminded that behind every rare condition is a person still search...
02/28/2026

Every year on Rare Disease Day (that's today!), we’re reminded that behind every rare condition is a person still searching for answers. For so many families, the road to a diagnosis is long ... years of appointments, second opinions and hearing “we’re not sure.” It can mean knowing something isn’t right — but not having the language or validation to explain or deal with it. That’s why this day matters. And that’s why we stand up.

Standing up for the undiagnosed is about more than awareness. It’s about listening when patients speak up. It’s about encouraging loved ones to keep asking questions. It’s about advocating for testing, expertise and deeper answers when “wait and see” just isn’t enough.

At SequenceMD, we work alongside patients, families and providers to help uncover those answers through comprehensive genetic evaluations and personalized support. Because getting a diagnosis can change everything — it can open doors to targeted care, connect families to resources and finally replace uncertainty with understanding. Learn about moving past misdiagnosis here: https://sequencemd.com/moving-past-misdiagnosis-the-value-of-a-genetic-evaluation/

If you’re still searching, don’t give up. Your story matters. Your questions matter. And you deserve answers.
This Rare Disease Day, let’s stand up — together — for the undiagnosed.

The zebra is the symbol of rare disease patients. Traditionally, doctors are taught when they “hear hoofbeats,” expect a...
02/27/2026

The zebra is the symbol of rare disease patients. Traditionally, doctors are taught when they “hear hoofbeats,” expect a horse, not a zebra. But in the rare disease community, one in 10 Americans is a zebra. And Rare Disease Day (Feb. 28) is all about shining a spotlight on them.

At SequenceMD, we’re committed to finding and supporting the zebras. Through comprehensive genetic evaluations and counseling, we help families gain diagnostic clarity, uncover answers and improve outcomes. Read more about pediatric genetics here: https://sequencemd.com/pediatric-genetics/

This Rare Disease Day on February 28, stand with the rare disease community. Whether you’re a patient, parent or provide...
02/26/2026

This Rare Disease Day on February 28, stand with the rare disease community. Whether you’re a patient, parent or provider, advocating for genetic answers can lead to better care and stronger support networks.

At SequenceMD, we help families pursue diagnosis clarity through comprehensive genetic evaluations and personalized counseling. Because when you have answers, you can make informed decisions, access the right specialists and plan for the future with confidence. Your voice matters. And so do answers. Read about the four areas where genetics matters most in primary care: https://sequencemd.com/4-areas-where-genetics-matters-most-in-primary-care/

A diagnosis can change everything — care plans, ongoing monitoring, family planning decisions, and access to the right s...
02/25/2026

A diagnosis can change everything — care plans, ongoing monitoring, family planning decisions, and access to the right specialists and support networks. Rare Disease Day (February 28) is a global initiative to raise awareness and generate support for everyone who’s on a rare medical journey.

At SequenceMD, we believe clarity is powerful. Through comprehensive genetic evaluations and personalized counseling, we help patients and families understand what a diagnosis means — and what to do next. From testing to long-term care coordination, our team walks with you every step of the way. Because the right answers don’t just explain the past ... they help shape a stronger, more informed future. Learn more about ”Moving Past Misdiagnosis: The Value of a Genetic Evaluation” at https://sequencemd.com/moving-past-misdiagnosis-the-value-of-a-genetic-evaluation/.

Rare Disease Day (Feb. 28) is about more than awareness — it’s about action. According to the National Organization for ...
02/24/2026

Rare Disease Day (Feb. 28) is about more than awareness — it’s about action. According to the National Organization for Rare Disorders, there are more than 10,000 known rare diseases, yet fewer than 5% have an approved treatment. And on average, it can take five or more years to receive a diagnosis. That’s a long time to live without answers.
Learn more: https://rarediseases.org/understanding-rare-disease/rare-disease-facts-and-statistics/

If you or a family member has unexplained or unresolved health issues, a genetic evaluation may help connect the dots and open doors to more targeted care, resources and support. At SequenceMD, we help families move from uncertainty to diagnosis clarity through comprehensive testing and expert genetic counseling. Read our article, “From Diagnosis to Treatment: 7 Benefits of Genetic Testing for Adults,” to see how genetic insights can reduce the financial and medical burden of undiagnosed disease, and help guide safer, more effective care:
https://sequencemd.com/from-diagnosis-to-treatment-7-benefits-of-genetic-testing-for-adults/

For many families, the hardest part of a rare disease journey is the not knowing. At SequenceMD, we help uncover genetic...
02/23/2026

For many families, the hardest part of a rare disease journey is the not knowing. At SequenceMD, we help uncover genetic answers — bringing clarity to prognosis, management and next steps, so uncertainty can become understanding.

This Saturday, February 28, is Rare Disease Day. According to the National Organization for Rare Disorders, 1 in 10 Americans is living with a rare disease — and more than 300 million people are affected worldwide. Too often, individuals and families are left feeling isolated and without answers. Rare Disease Day is a global movement to raise awareness and build support for everyone navigating a rare diagnosis. Learn more: https://rarediseases.org/rare-disease-day/

Wondering if genetics could provide answers for you or your family? Read our article, “10 Red Flags You May Have a Genetic Disease,” to see if testing and counseling may help: https://tinyurl.com/3ayh6tec

Rare Disease Day (Feb. 28) shines a light on the 300+ million people worldwide living with a rare disease. Advocacy star...
02/22/2026

Rare Disease Day (Feb. 28) shines a light on the 300+ million people worldwide living with a rare disease. Advocacy starts with awareness — and access to diagnosis.

At SequenceMD, we assist families as they pursue comprehensive genetic testing and personalized support. Because navigating genetics can feel overwhelming, our genetic counselors break down complex results, explain what they mean for you or your child, and help you move forward with confidence.
Understanding leads to answers. And answers change everything.

Learn more by reading our article, “Genetic Counseling: 7 Ways Our Genetic Counselors Help Patients”: https://sequencemd.com/7-ways-our-genetic-counselors-help-patients/

Learn more about Rare Disease Day here: https://rarediseases.org/rare-disease-day/

A new diagnosis. A long wait for answers. Or an adult who’s never been tested.At SequenceMD, we serve three key groups i...
02/21/2026

A new diagnosis. A long wait for answers. Or an adult who’s never been tested.

At SequenceMD, we serve three key groups impacted by genetic neurodevelopmental disorders (NDDs): newly diagnosed children and young adults, kids facing 6–18 month waits for genetic testing, and adults with IDD who’ve never received a genetic evaluation.

With faster access to comprehensive testing (aligned with 2025 AAP recommendations), coordinated specialist care and lifelong management support, our team helps families move from uncertainty to actionable answers.

See how genetic insights today can shape care for generations to come. Read more here: https://sequencemd.com/genetic-neurodevelopmental-disorders-3-patient-groups-we-serve/


Ever wonder why a medication works wonders for one person — but not for another? The answer may be in your genes.Pharmac...
01/12/2026

Ever wonder why a medication works wonders for one person — but not for another? The answer may be in your genes.

Pharmacogenomic (PGx) testing looks at how your DNA affects the way your body processes medications. Instead of trial-and-error prescribing, PGx helps providers choose safer, more effective medications and dosages ... based on you.

With PGx testing, your care team can:
• Reduce side effects and adverse reactions
• Avoid medications unlikely to work for you
• Find the right dose faster
• Personalize treatment across mental health, cardiology, pain management and more

At SequenceMD, we offer clinically validated PGx testing with expert interpretation and clear, actionable results — so you and your providers can make confident, informed decisions. TO LEARN MORE, READ OUR LATEST BLOG: https://sequencemd.com/can-your-genes-help-you-find-the-right-medication/

And if you’re ready to take the guesswork out of medication management, contact SequenceMD to learn more about personalized medicine through pharmacogenomics.

Say hello to Lucy Holt, our newest genetic counselor at SequenceMD! Lucy joins us with a background in oncology and hema...
12/12/2025

Say hello to Lucy Holt, our newest genetic counselor at SequenceMD!

Lucy joins us with a background in oncology and hematology genetics, gene-therapy research, education and psychiatric patient care. She’s passionate about guiding patients through hereditary cancer risk assessments and rare disease evaluations — and helping those on long diagnostic journeys finally get the answers they deserve.

Originally from the Bay Area and with degrees from UW–Madison and the Keck Graduate Institute, Lucy brings both expertise and heart to every patient interaction.

To see her complete bio — and learn more about the entire SequenceMD team — go to the About Us section of our website: https://sequencemd.com/about-us/.

Genetic testing is reshaping kidney care. It can pinpoint the cause of unexplained kidney disease, identify risks early ...
12/08/2025

Genetic testing is reshaping kidney care. It can pinpoint the cause of unexplained kidney disease, identify risks early and guide more personalized treatment based on your unique genetic makeup. It also helps connect patients to targeted clinical trials and supports informed family planning and testing for relatives who may be at risk.

Explore the full blog to see how genetic insights are improving diagnosis, treatment and long-term kidney health: https://sequencemd.com/unraveling-the-genetic-puzzle-of-kidney-disease/


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1601 E 19th Avenue STE 6450
Denver, CO
80218

Telephone

+13038327109

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