The All of Us Research Program is a historic effort to gather data from one million or more people living in the United States to accelerate research and improve health. It is seeking one million or more people from across the U.S. to help speed up medical research. Our website uses cookies, as almost all websites do, to help provide you with the best experience we can. You will not get direct medical benefit from taking part in the All of Us Research Program. Our plan is that the All of Us Research Program will last for at least 10 years. If people know in advance that they are at higher risk for one of these health conditions, there are steps they can take to help prevent it or identify it early on. At the end of that consent, tell us if you want to get your DNA results. Our website uses cookies, as almost all websites do, to help provide you with the best experience we can. Stay up-to-date with latest program updates, events, and more with our bi-monthly eNewsletters. The Genetic Information Nondiscriminatory Act of 2008 (GINA) is a federal law that protects you from. Also, we will let researchers check the results of past studies.

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Even without your name, there is a chance someone could figure out who you are. The All of Us Research Program is a research effort, so we cannot provide any health care.

We plan to check your DNA for a variety of information.

You might get some results pretty quickly but have to wait longer for others. A sample is blood, urine (pee), saliva (spit), or other material from your body. Research Program will not share your DNA results with your employer.

Taking part in the All of Us Research Program may have risks that we don’t know about yet. PwC refers to the PwC network and/or one or more of its member firms, each of which is a separate legal entity. If you have more questions, you can ask us. Please remember that All of Us Is a research program. We will create a database on the All of Us Research Program website. A Henry Ford Health System hand surgeon discusses why carpal tunnel syndrome can get on your nerve — and what to do about it. Yes, you can share your All of Us Research Program information with anyone you choose. Because there are different ways to check for different types of DNA results, you can expect to get multiple messages over time. We may send you emails about the All of Us Research Program. We will offer regular updates about the All of Us Research Program. We may ask for your Social Security number to help match your information to other information, but you do not have to give it to us. We will use this information for health research. Playstation Account Link. We also have Certificates of Confidentiality from the U.S. government. Gmail blocks 99.9% of dangerous emails before they reach you. Also, the Patient Protection and Affordable Care Act says health insurers cannot use your health information to decide whether to cover you. As long as you are not planning to move to another country soon, you are welcome to sign up. Since we plan to check your DNA in a variety of ways, you could possibly get some DNA results fairly quickly but then wait years to get other DNA results. It is up to each researcher to decide what they study. You can say yes or no. Biomarkers are signals your body gives off. If I am already enrolled in another study, can I still join the, If I am already enrolled in another study, why should I join the. You can set the app to use only Wi-Fi to avoid this. We believe the chance of this is very small, but it is not zero. Simply hit tabswipe right to accept and you're done. If you choose, you will be able to share your All of Us information with your health care provider. Only researchers approved by the All of Us Research Program will be allowed to see data from individual participants. It takes into account factors like where you live, what you do, and your family health history. We take your privacy seriously. The American College of Medical Genetics and Genomics maintains a list of genes that are associated with the risk of certain serious health conditions. ranks Henry Ford Health System #2 in annual ranking of top hospitals & health systems for diversity and #4 nationally for supplier diversity, On Saturday, Oct. 3, the Detroit chapter of, Facial Plastic and Reconstructive Surgery, Hyperthermic Intraperitoneal Chemotherapy (HIPEC), ask you to share different kinds of information, Henry Ford Medical Center - Detroit Northwest, Henry Ford Medical Center - New Center One, Free Bikes 4 Kidz used bike donation program back with COVID-19 safe plan to connect kids with fun, freedom and physical activity, All of Us Research Program Continues Enrollment, Henry Ford's accomplishments, commitment to diversity recognized again in national rankings, All of Us Enrollment Coming to Your Neighborhood, 5 Ways Acupuncture Can Enhance Athletic Performance, What To Know Before Taking A Probiotic Supplement. Probiotic supplements are a huge category in health and wellness, and many people are self-prescribing them. Since we plan to check your DNA in a variety of ways, you could possibly get some DNA results fairly quickly but then wait years to get other DNA results. If you are already in another study, you may want to talk with your health care team before joining the All of Us Research Program. A link to this web page has been copied to your clipboard. You also may learn about your own health. The All of Us Research Hub will store health data from a diverse cohort of one million or more participants in the All of Us Research Program.. You can call the All of Us Research Program Support Center at (844) 842-2855. To find out if you are protected by these kinds of laws, contact the attorney general for your state or territory.