No-cost genetic testing & counseling for primary ciliary dyskinesia (PCD)

Free genetic testing and genetic counseling for eligible patients who complete a profile with Probably Genetic.

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Testing Partners

Patient survey

We’re conducting a survey to understand more about the Von Willebrand disease community and to enable access to more resources and information for those that are interested. Your email address is required to receive the £10 gift card. Your email address will be used to share information about Von Willebrand disease and resources only, you can opt out at any time. Individuals should have proof of diagnosis to share.

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100,000+

Patients

Over 100,000 patients already use the Probably Genetic platform.

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50+

Patient Advocacy Partners

We're partnered with over 50 patient advocacy groups to help connect patients with support & community.

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More about testing

How Does Testing for PCD Work?

If approved for a no-cost genetic testing program, you'll receive a clinical-grade test kit delivered right to your door, offering both convenience and accuracy. Simply provide a saliva or cheek swab sample; our advanced technology will handle the rest, revealing valuable genetic insights. The testing offered is whole exome sequencing, and it will not only test for the gene associated with PCD. It’s our goal to do our best to uncover an answer for your symptoms by providing broad and comprehensive testing.

Physician-ordered, with a free genetic counseling appointment to go over results
CLIA-Certified & CAP-accredited lab
HIPAA-compliant to protect your data

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Check Eligibility

No-cost genetic testing & counseling for primary ciliary dyskinesia (PCD)

Just a Few Easy Steps...

To be eligible for free genetic counseling and testing, patients must be experiencing PCD-like symptoms. Additionally, patients must be in the United States.

Complete the assessment

Complete our health and diagnostic assessment to build your personalized profile. We’ll gather brief details about your current and past diagnoses, family history, and essential personal information to offer counseling and testing.

Confirm eligibility status

Once you have completed your assessment and profile, you will be notified of your eligibility status. You will be notified of your eligibility status via email but you can also view in your profile.

Testing right to your door

If you are approved for testing, we will send a sample collection kit right to your door. If you are placed on our waitlist, we will notify you if you are approved for future testing and/or resources. We are regularly expanding our programs.

‍About PCD

Understanding PCD

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check eligibility

Ready to check eligibility?

Choose where you would like to start with the health & symptom assessment.

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We will ask the necessary information to determine eligibility for our free genetic testing or patient resource programs.

Share a diagnosis

Start by providing detailed information about current diagnoses.

Share a hereditary risk

Start by providing detailed information about hereditary risks and family history.

Share unexplained symptoms

Start by sharing symptoms that have not been explained by current medical diagnoses.

I don't know where to start

If you're not sure where to start, we can give you guidance to get started with the assessment.

Testimonials

What patients say about us

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After I received my results from Probably Genetic, my doctor suddenly began running all sorts of tests/asking all kinds of questions, things I had told him but he never heard. So THANK YOU. I can't thank your company, your testing enough. It led to breakthroughs and actions from my doctors that would have never happened without you.

Kellie E.

September 19, 2024

We've been searching for answers for over a decade and I'd almost given up. I'm so grateful that Probably Genetic has taken it upon themselves to make this kind of potentially life-altering testing accessible to families like mine.

Rob

September 19, 2024

interviews

Hear from patients like you

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https://www.youtube.com/watch?v=Wxb890ioFEg

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About us

Find out more about us

robably Genetic is changing the lives of patients living with severe, complex diseases. Our technology discovers undiagnosed patients online, analyzes their disease state using machine learning and at-home testing, and connects patients to relevant resources. In doing so, we help patients access diagnoses, clinical trials, and treatments as early as possible. Our data platform is used by drug developers and patient advocacy groups to develop and launch treatments for these patients.

Founded in 2018. Probably Genetic has been helping patients and their families access no-cost genetic testing, counseling, and patient resources since 2018.
Patient-first. Probably Genetic launched the first patient-initiated (patients apply for testing themselves), no-cost testing program in the United States.
Patient-centric privacy. Probably Genetic does not sell or share any of your personally identifiable information to outside third-parties.

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100 000+ patients have created a profile with Probably Genetic

This is the number of patients who used our platform due to unexpected symptoms and incorrect or incomplete diagnoses.

start your profile