Early detection of Alzheimer’s disease offers clear benefits, yet many people struggle to acknowledge signs of dementia. A sizable share of individuals noticing concerning changes—roughly one third—choose to keep those observations private from family members and clinicians, and only about 15% feel ready to discuss the issue without delay. This finding comes from a British charity focused on dementia support, Alzheimer’s Society, which has published survey results through area organizations and regional partners. The data highlight a real gap between recognizing potential symptoms and seeking professional input, a gap that can hinder timely care and access to essential services.
The survey reached 1,137 adults under the age of 85 who either live with dementia or provide care for someone living with the condition. It confirms that a significant portion delays action, with one in three choosing to hide symptoms for at least a month and nearly a quarter waiting more than six months from the first signs before consulting a health professional. These delays matter because dementia is a progressive disease, and early medical engagement can help families plan, access treatments where appropriate, and participate in clinical trials that may slow progression or improve quality of life for a period of time. These patterns were documented by Alzheimer’s Society in collaboration with partner organizations and researchers, underscoring the lived reality behind the statistics.
The most common reason cited for postponing a diagnosis is fear about how others will interpret the signs—63% of respondents in the broader dataset expressed concern that symptoms would be mistaken for normal aging. A substantial portion also worried about how a diagnosis would change their treatment conversations and daily interactions, fearing that they or their loved ones would be treated as if they were younger or less capable. This stigma can create a moral panic that makes people retreat from professional help, even when early action could yield important planning opportunities. The outcome of delaying a formal evaluation is not simply a personal inconvenience; it can slow access to supportive services, assistive devices, cognitive rehabilitation options, and social support networks that help families navigate the condition more effectively. These insights come from Alzheimer’s Society’s public health research and are echoed by clinicians who observe the real-world consequences of late presentations and the additional stress borne by caregivers who bear witness to avoidable delays.