Young-onset colorectal cancer patients and caregivers should have their voices heard and stories told. The Never Too Young Survey Report amplifies the experiences of this often-overlooked group.
The latest report (2020), divided into patient and caregiver editions, details the unmet needs of the young-onset colorectal cancer community.
The survey report details dozens of findings from more than 1,000 patients and caregivers. These are just a few.
of patient survey respondents were initially misdiagnosed, 43% with hemorrhoids alone or in combination with other conditions.
patients, ages 19-39, were more likely to report that a doctor dismissed their concerns.
of patients saw three or more doctors before receiving a diagnosis of colorectal cancer.
of young patients were told about fertility preservation, while 37% of women and 16% of men reported treatment-related infertility or sterilization.
of patients were working full-time at the time of diagnosis, and 28% of those patients were no longer working.
of stage III and 61% of stage IV (metastatic) patients did not have any discussion of clinical trials before starting treatment.
of patients reported concerns about their mental health, and 64% said they required help for depression.
of patients expressed a fear of recurrence, which is when the cancer comes back.
of patients reported having at least three symptoms of colorectal cancer before being diagnosed.
In 2016, the Colorectal Cancer Alliance initiated a pioneering survey on young-onset colorectal cancer. This effort aimed to comprehend the distinct challenges and unmet needs faced by patients under the age of 50. The 2018 iteration of the survey was the first to include caregivers, a section that saw substantial expansion in the survey reports published in 2020.
Alliance research and other evidence highlight a troubling trend: Younger patients are often diagnosed with advanced disease, necessitating aggressive treatment. This situation contrasts with diagnoses made post-50. Despite the increase in young-onset cases, limited studies address the effects on patients’ and survivors’ quality of life (QoL) and their specific unmet needs.
By analyzing aggregated, self-reported results, the Alliance aspires to enlighten both the young-onset colorectal cancer community and healthcare providers about prevailing trends and gaps in the care of affected patients, survivors, and caregivers.
Majority of Americans say they don’t have time for colorectal cancer screening, prioritizing household chores instead of health.
The meetings are part of a broader government advocacy initiative by the Alliance to address the growing prevalence of CRC and improve patient care, advance research, and break down regulatory barriers that limit access to life-saving treatments.
A common method for educating a new administration about an organization’s cause — and sharing how the president can improve the situation for the American people — is through a document called a transition memo.