Crohn's Disease in America 2016


The Crohn’s Disease in America 2016 online survey was conducted to gather insights from over 2,000 individuals currently diagnosed with Crohn’s Disease. The primary goal of this research was to better understand the symptoms, treatment, and life impact experienced by those individuals. A survey specific to those with ulcerative colitis was also conducted and will be presented at a later date.


99.8% of respondents currently lived in the US, spanning across the various regions of the country


96% of respondents had health insurance or Medicare/ Medicaid, with group coverage being most common


42% had family members who also had been diagnosed with an inflammatory bowel disease and 45% had family members who had an auto-immune disease other than IBD



Respondents experienced an average of 5 symptoms before receiving a diagnosis


Finding a good HCP was also no easy task – most respondents saw 2-3 healthcare providers while seeking a Crohn’s diagnosis


However, respondents endured an average of 5 different diagnostic tests before receiving a diagnosis


The number and variety of potential symptoms was another desired topic. Only 2% of respondents felt they knew everything at the time of their diagnosis



At the time of the survey, respondents were experiencing an average of 7 symptoms. Bloating and abdominal cramps/pain were the two most common.


For those who experience fatigue, over 65% said they fight it daily


Of the ¾ who had experienced a remission at some point, most (75%) experienced remission for less than 3 years


Malnourishment and anemia were also experienced by over a third of individuals respectively


75% experience at least 4 flares a year, often even more


Half the respondents cited greasy/fried foods as a trigger and another half reported raw fruits and vegetables as a trigger. This further emphasizes how difficult it is to identify a universal “Crohn’s diet


For the 5% not seeing an HCP, the primary barrier was a lack of financial resources and/or insurance


Doctors’ lack of empathy, understanding and communication were the primary reported reasons for dissatisfaction


Most respondents saw their HCP every 3-4 months to discuss their Crohn’s.


Additionally, most had little difficulty finding an HCP with whom they felt comfortable


Not only do individuals feel they play a role in their treatment, most reported that they actively seek information about the latest Crohn’s medication developments


Most of the respondents had been on their treatment plan for less than 3 years


The potential side effects were a primary barrier for those not using biologics, but of those who had used them, 60% had been prescribed more than one


Bowel resection was the most common surgery endured by individuals


Respondents felt that their relationships with partners, children and family were affected by Crohn’s to a lesser degree


In descriptive terms, individuals felt Crohn’s was annoying, unpredictable, debilitating and frustrating



Once again, on average, individuals felt that Crohn’s had a minimal impact on their ability to maintain relationships. This especially speaks to the strength of those diagnosed with this disease

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