Our Partners

Allergy & Asthma Network is a national patient education and advocacy nonprofit dedicated to ending needless death and suffering due to asthma, allergies and related conditions through outreach, education, advocacy and research.

Bright by Text: Kids don’t come with instructions—that’s why Bright by Text sends free, timely tips delivered by text message with information timed to your child’s due date or birthdate. To sign up for messages in English or Spanish, simply text BRIGHT to 274448.

CreakyJoints, part of the nonprofit Global Healthy Living Foundation, was founded in 1999 as an online support community for people living arthritis. Since then CreakyJoints has grown to a community of over 90,000 by providing meaningful support, education, innovative advocacy and global research projects.

The Foundation of the National Lipid Association (NLA) is a patient-focused nonprofit organization dedicated to improving the welfare of patients and families affected by cholesterol and triglyceride problems. Their values are education, awareness, and advocacy.

MyHealthTeams creates free social networks for chronic condition communities. People diagnosed with a chronic health condition can get perspective from other informed patient-peers as well as medically reviewed resources that help them manage their health. See the current and growing list of social networks that MyHealthTeams has created here. These web and mobile apps are only for those diagnosed with a condition (and not healthcare providers).

The National CMV Foundation is a non-profit organization dedicated to promoting awareness, providing access to resources and sharing prevention information to eliminate congenital CMV.

The National Multiple Sclerosis Society believes people affected by MS can live their best lives as we stop MS in its tracks, restore what has been lost and end MS forever. The Society helps people affected by MS by funding cutting-edge research, driving change through advocacy, facilitating professional education, and providing programs and services that help people with MS and their families move their lives forward.

National Organization on Fetal Alcohol Syndrome (NOFAS) works to prevent prenatal exposure to alcohol, drugs, and other substances known to harm fetal development by raising awareness and supporting women before and during their pregnancy, and supports individuals, families, and communities living with Fetal Alcohol Spectrum Disorders (FASDs) and other preventable intellectual/developmental disabilities.  Our vision is a world where all children are born free of exposure to alcohol, drugs, and other substances known to harm fetal development.

Patient Education Genius gives clinicians one access point for the world’s best evidence-based patient education resources. Combining an ever-expanding library of over 50,000 titles with simple digital delivery tools and never-before-documented insight into clinician and patient behavior, the Patient Education Genius is designed to facilitate shared decision-making at the point of care.

PatientsLikeMe is a free, online patient network where people can connect with others who have the same condition, and track and share their own experiences. When members share information on PatientsLikeMe, they generate data about the real-world nature of disease that helps industry partners develop more effective products, services and care.

The Pediatric Environmental Health Specialty Units (PEHSUs) are a source of medical information and advice on environmental conditions that influence reproductive and children’s health. PEHSUs are academically based, typically at university medical centers, and are located across the United States and Canada.

Preventive Cardiovascular Nurses Association (PCNA) is the leading nursing organization dedicated to preventing cardiovascular disease (CVD) through assessing risk, facilitating lifestyle changes, and guiding individuals to achieve treatment goals. This is accomplished through the integration of public and professional education and advocacy. The current state of healthcare demands that nurses play a leading role in identifying and implementing cardiovascular risk reduction strategies. PCNA is committed to educating and supporting nurses so that they may successfully rise to this challenge.

The Society for Birth Defects Research and Prevention (BDRP) was established in 1960 as the Teratology Society. Today, this international multidisciplinary scientific society consists of approximately 700 members specializing in a variety of laboratory and clinical disciplines, including developmental and reproductive biology and toxicology, epidemiology, cell and molecular biology, nutrition, genetics, maternal-fetal medicine, pediatrics, obstetrics, medical genetics, and pregnancy risk counseling.

The Society for Maternal-Fetal Medicine (SMFM) is a non-profit, membership organization based in Washington, DC. With more than 3,500 physicians, scientists and women’s health professionals around the world, the Society supports the clinical practice of maternal-fetal medicine by providing education, promoting research and engaging in advocacy to optimize the health of high-risk pregnant women and their babies. SMFM hosts an annual scientific meeting in which new ideas and research related to high-risk pregnancies are unveiled and discussed.

The Spondylitis Association of America (SAA) is the leading US nonprofit organization 100% dedicated to improving the lives of people living with all forms of spondyloarthritis. Visit us for trusted and physician vetted information on spondyloarthritis, for support resources and programs, and to connect with others living with these conditions.

The Mighty publishes real stories by real people facing real challenges. Having a chronic illness while pregnant doesn’t have to be isolating – that’s why The Mighty exists. Check out their stories about chronic illness, pregnancy, and mental illness.