Before we could rely on our bodies. But now it is difficult to predict what we will be possible tomorrow, next week or next month.
Time shifts. Goals feel more distant.
The roles and achievements around which we have built our lives and identities may begin to feel as if they belong to someone else entirely.
We can never know for certain if the science of medicine applies to us
In reality, all of medicine involves uncertainty. Tests give false positives and false negatives, and there are always a significant number of people for whom standard treatments are not the right fit.
Even as treatments become more personalised, each body and situation remains unique, and complete certainty about what is happening now—or what will happen in the future—is rarely possible.
While this is true across medicine, functional symptoms have a particular uncertainty profile. In functional disorders, the tools and knowledge structures of medical science often fall profoundly short. There may be no blood test, scan, or biomarker that definitively explains what is happening in the body.
Sharing Uncertainty
Clear diagnoses and definitive test results function not only as medical tools but also as social ones, allowing everyone—patients, professionals, families—to agree on what is happening. This shared understanding itself can bring relief.
With functional somatic symptoms, reaching this shared understanding can be difficult.
Different professionals may offer different explanations or advice. Without clear test results, it can be hard to align understanding not only within healthcare settings but also with family, friends, and employers. The uncertainty can feel like a burden you are carrying alone.
Uncertainty within established knowledge frameworks
When trying to understand any illness, we need to engage in a process of gathering the best available information and trying out approaches that seem most likely to help.
This process always involves uncertainty, regardless of diagnosis.
However functional symptoms may feel particularly difficult to pin down, perhaps in part because they challenge our usual ways of understanding illness.
One of these frameworks that shapes medical thinking is the mind–body divide. For example, we tend to understand depression as a mental illness. If someone becomes depressed after major life stress, we readily accept this explanation. We don’t need a scan or blood test to validate their suffering. We see the evidence of depression in their suffering and behaviour, and we respond with compassion and support.
Our frameworks for understanding physical illness bring a different set of assumptions. We expect to find a localised problem in the body that explains the symptom. These assumptions are often based on model conditions such as infections or cancer, where a clear biological cause can be identified.
Functional symptoms do not fit comfortably into either category. They are neither clearly “mental” nor fit with the assumptions we make about “physical” illnesses. In falling between these frameworks, functional symptoms challenge the language we have available to talk and think about ourselves.
Related to this, functional symptoms are often invisible in how healthcare is organised, and how research is designed and funded.
A rational, pragmatic approach to understanding symptoms
Despite the absence of clear biomarkers, we are not without ways of understanding functional symptoms.
When we look beyond narrow frameworks and draw on a wider range of evidence and experience, we see that there is helpful knowledge to draw on.
At the same time, it is important to remember that knowledge gained in one context—whether through experimental research or the experiences of others—may not map neatly onto our own situation. We always need to be prepared to test our theories out through practice, and be prepared to keep an open mind.