by Susannah Fox, Associate Director, Digital Strategy, Pew Internet & American Life Project
Summary of Findings
The internet gives patients and caregivers access not only to information, but also to each other.
Many Americans turn to friends and family for support and advice when they have a health problem. This report shows how people’s networks are expanding to include online peers, particularly in the crucible of rare disease. Health professionals remain the central source of information for most Americans, but “peer-to-peer healthcare” is a significant supplement.
This report is based in part on a national telephone survey of 3,001 adults that provides an estimate of how widespread this activity is in the U.S. All numerical data included in the report are based on the telephone survey. The other part of the analysis is based on an online survey of 2,156 members of the National Organization for Rare Disorders (NORD) who wrote short essays about their use of the internet in caring for themselves or for their loved ones.
One-in-five internet users have gone online to find others like them.
Eighteen percent of internet users say they have gone online to find others who might have health concerns similar to theirs.
The most striking finding of the national survey is the extent of peer-to-peer help among people living with chronic conditions. One-in-four internet users living with high blood pressure, diabetes, heart conditions, lung conditions, cancer or some other chronic ailment (23%) say they have gone online to find others with similar health concerns. By contrast, 15% of internet users who report no chronic conditions have sought such help online.
Other groups who are likely to look online for people who share their same health concerns include: internet users who are caring for a loved one, internet users who experienced a medical crisis in the past year and internet users who have experienced a significant change in their physical health, such as weight loss or gain, pregnancy or quitting smoking.
Some of the most notable interactions involve people who meet online for the first time. There were numerous examples of these powerful long-distance connections in our online survey of patients and caregivers who take part in rare-disease communities. One adult living with a rare condition described how she connected with another patient online, bonded, and then enriched the friendship with in-person encounters: “The first time I met another patient, face to face, I sobbed. I was overjoyed and began to communicate with them on a regular basis and my network grew.”
In the moment of need, most people turn to a health professional for information, care, or support.
When asked about the last time they had a health issue, 71% of adults in the U.S. say they received information, care or support from a health professional. Fifty-five percent of adults say they turned to friends and family. Twenty-one percent of adults say they turned to others who have the same health condition.
The majority of health care conversations happen offline: Just 5% of adults say they received online information, care or support from a health professional, 13% say they had online contact with friends and family, and 5% say they interacted online with fellow patients.
In our online survey, patients and caregivers were asked the same question about the last time they had a health issue. The people living with a rare disease who responded to the survey far outpaced all other groups, including those living with chronic conditions, in tapping the wisdom of their peer network. More than half of rare-disease respondents say they turned to family and friends. Another majority say they turned to others who have the same health condition.
A mother of a small child with a rare condition wrote about the lifeline she has found online: “When a disease is so rare and there are no folks in your town, and few in your state who are going through what you are going through, you need a support group that encompasses people from all over the world. Getting to know people through the disorder has been an amazing experience and has created incredibly wonderful friendships and ties.”
People turn to different sources for different kinds of information.
In the national survey, adults were asked which group is more helpful when they need certain types of information or support: health professionals such as doctors and nurses or peers such as fellow patients, friends, and family. A relatively clear pattern of responses emerged: When the issue involved technical issues related to a health issue, professionals held sway. When the issue involved more personal issues of how to cope with a health issue or get quick relief, then non-professionals were preferred by most patients.
Many people find the internet to be a valuable tool, whether they are using it to search for a quick answer or gain a deeper understanding of a new treatment option or prescription. As one respondent in the online survey commented, “When time is of the essence, search on the internet is the only way to time travel.” The internet is also, as this study shows, a way to tap into our instincts to gather together, help other people, and be helped ourselves.
Read the full report at pewresearch.org/pewresearch-org/internet.
