Skip to main content

Life-changing genomic care when it matters most.

Life-changing genomic care when it matters most.

Designed for healthy newborns and young children, our screening service identifies childhood-onset genetic conditions using state-of-the-art genomic sequencing and supported with guided care. We help you uncover and act on invaluable health information, early.

Our screening service is currently on backorder, but don’t miss your chance to be first in line! Join our waitlist to secure early access as soon as it’s available.

Join Our Waitlist

Designed for healthy newborns and young children, our screening service identifies childhood-onset genetic conditions using state-of-the-art genomic sequencing and supported with guided care. We help you uncover and act on invaluable health information, early.

Our screening service is currently on backorder, but don’t miss your chance to be first in line! Join our waitlist to secure early access as soon as it’s available.

Join Our Waitlist

HOW IT WORKS

Identify. Understand. Act.

Infographic of a sample collection tube.
Infographic of a strand of DNA.
Inforgraphic of two hands clasped together in the shape of a heart.
Swab

We mail you a gentle, cheek swab collection kit. You activate the kit online. Once activated, our physicians will review and authorize your order.

Screen

Once received at the lab, we'll sequence your child's genome and analyze it for 400+ actionable, childhood-onset, genetic conditions.

Support

Results are delivered online, shared with your pediatrician, and supported by virtual consults from our genetic counselors.

HOW IT WORKS

Identify.
Understand.
Act.

Infographic of a sample collection tube.
Swab

We mail you a gentle, cheek swab collection kit. You activate the kit online. Once activated, our physicians will review and authorize your order.

Infographic of a strand of DNA.
Screen

Once received at the lab, we'll sequence your child's genome and analyze it for 400+ actionable, childhood-onset genetic conditions.

Inforgraphic of two hands clasped together in the shape of a heart.
Support

Results are delivered online, shared with your pediatrician, and supported by virtual consults from our genetic counselors.

WHAT’S INCLUDED?

We’re at your side, from insight to action.

Unlimited access to genetic counseling anytime, before and after testing

Virtual consultation with your child’s pediatrician to review results with your consent

Care navigation to direct you to the right specialist for follow-up care

When needed, help in facilitating appointments on your behalf

Secure storage of your child’s genome for timely access for any future needs

Detailed results reports provided online for download and easily shared with your pediatrician.

WHAT’S INCLUDED?

We’re at your side, from insight to action.

Unlimited access to genetic counseling anytime, before and after testing

Virtual consultation with your child’s pediatrician to review results with your consent

Care navigation to direct you to the right specialist for follow-up care

When needed, help in facilitating appointments on your behalf

Secure storage of your child’s genome for timely access for any future needs

Detailed results reports provided online for download and easily shared with your pediatrician.

WHAT PARENTS ARE SAYING

“It was honestly incredible how timely the information was. It was just like all these positive forces in the universe coming together.”

SHAYE W. — FIRST-TIME MOM

WHAT PARENTS ARE SAYING

“It was honestly incredible how timely the information was. It was just like all these positive forces in the universe coming together.”

SHAYE W. — FIRST-TIME MOM

Frequently asked questions

Will insurance cover the cost of Nurture’s service?

No. Insurance doesn’t typically cover whole genome sequencing for healthy newborns; however, Nurture’s service may be HSA or FSA eligible. Please check with your plan’s administrator to confirm.

What is included with my purchase?

Nurture’s service includes whole genome sequencing to screen for 400+ actionable, childhood-onset conditions, plus genetic counseling to help you understand your results. Early Access Members get additional Premium services in the first year. They include:

  • Access to genetic counseling throughout the journey, pre- and post-test
  • Care navigation to direct you to the right specialist for follow-up care
  • When needed, help in facilitating appointments on your behalf
  • A consult with your child’s pediatrician to discuss screening results
  • Information about clinical trials your child may be eligible for
  • Secure storage of your child’s genome for timely access for any future needs

Who can order the Nurture service?

The parent or legal guardian of the child to be screened can order from Nurture’s website. No doctor visit is necessary. After an order is placed, Nurture will send the order to an independent physician to verify eligibility and approve it. Once approved, a DNA collection kit will ship to the address provided.

When can I expect to receive the sample collection kit?

You can expect to receive the collection kit within two weeks of purchasing Nurture’s service.

How long will it take to receive the results?

You can expect to receive results about 4 to 6 weeks after your child’s collection is received at the lab.

What is Nurture's refund policy?

If you have placed your order, but have not submitted a sample, you are eligible for a 100% refund for one year starting from the date of purchase. Once you have submitted a sample, you are no longer eligible for any refund. In all cases, Nurture cannot accept returned/unused kits. If you do not wish to continue with the test, we ask that you dispose of the kit.

Frequently asked questions

Will insurance cover the cost of Nurture’s service?

No. Insurance doesn’t typically cover whole genome sequencing for healthy newborns; however, Nurture’s service may be HSA or FSA eligible. Please check with your plan’s administrator to confirm.

What is included with my purchase?

Nurture’s service includes whole genome sequencing to screen for 400+ actionable, childhood-onset conditions, plus genetic counseling to help you understand your results. Early Access Members get additional Premium services in the first year. They include:

  • Access to genetic counseling throughout the journey, pre- and post-test
  • Care navigation to direct you to the right specialist for follow-up care
  • When needed, help in facilitating appointments on your behalf
  • A consult with your child’s pediatrician to discuss screening results
  • Information about clinical trials your child may be eligible for
  • Secure storage of your child’s genome for timely access for any future needs

Who can order the Nurture service?

The parent or legal guardian of the child to be screened can order from Nurture’s website. No doctor visit is necessary. After an order is placed, Nurture will send the order to an independent physician to verify eligibility and approve it. Once approved, a DNA collection kit will ship to the address provided.

When can I expect to receive the sample collection kit?

You can expect to receive the collection kit within two weeks of purchasing Nurture’s service.

How long will it take to receive the results?

You can expect to receive results about 4 to 6 weeks after your child’s collection is received at the lab.

What is Nurture's refund policy?

If you have placed your order, but have not submitted a sample, you are eligible for a 100% refund for one year starting from the date of purchase. Once you have submitted a sample, you are no longer eligible for any refund. In all cases, Nurture cannot accept returned/unused kits. If you do not wish to continue with the test, we ask that you dispose of the kit.

Read More

Safe and secure.

Your child’s genomic data is stored by our partner Broad Clinical Labs of Harvard & MIT.

Broad has a 30-year track record of handling sensitive patient data.

Broad has completed sequencing on half a million genome samples and counting.

The systems they use to host genomic data meet the highest security standards.

Broad Clinical Labs is CLIA/CAP-accredited laboratory.

Safe and secure

Your child’s genomic data is stored by our partner Broad Clinical Labs of Harvard & MIT.

Broad has a 30-year track record of handling sensitive patient data.

Broad has completed sequencing on half a million genome samples and counting.

The systems they use to host genomic data meet the highest security standards.

Broad Clinical Labs is CLIA/CAP-accredited laboratory.

Nurture is available now in
California, Illinois, New Jersey, Texas, and Florida
with more states coming soon.

Notify Me

Nurture is available now in California, Illinois, New Jersey, Texas, and Florida, with more states coming soon.

Notify Me

Prepare today for a healthier tomorrow
with Nurture by your side.

Join Our Waitlist

Prepare today for a healthier tomorrow with Nurture by your side.

Join Our Waitlist
Close Menu