COURSE · PART 1 · MODULE 1 · PAGE 3

Remission, Recovery, and What Improvement Can Mean

> **"FND symptoms may recur or worsen regardless of what a person knows, tries, or has achieved. Symptom severity must never be used to judge effort, acceptance of the diagnosis, treatment participation, or personal progress."**

Course principle

This is a short introduction. Later modules will discuss treatment, rehabilitation, setbacks and long-term management in much more detail. Here, we only need enough information to understand what people may mean when they talk about getting better.


For the Person With FND
For Family, Friends, and Other Supporters
For Clinicians and the Care Team
Research and Sources —

For the Person With FND

One of the big questions, once, perhaps the shock of diagnosis fades, is “Can this go away?” Maybe instead of ‘go away’ words like remission, cure, or recovery might replace them. If we are talking about a cure, meaning, the disease functional neurological disorder is no longer present nor will ever come back, then as far as anyone currently knows, no. There is no cure. However, people do experience recovery or remission. Because the two words can be used to mean the same thing, let’s give them definitions that this course will use.

For this course, ‘remission’ refers to all or some of a person’s symptoms disappearing for a time. Some have experienced remission for years - the likeliness often depending on a few factors especially what symptoms were disrupting their lives. [1][2][5][6]

Recovery has a few meanings. For instance, I might say, ‘After a functional seizure I need a few days of recovery.’ In that sense, recovery means bringing myself into a more stable state, where my symptoms are less triggered and that my energy or ability to cope returns. [2][3]

Recovery does not have to mean that every symptom has disappeared.

Four equally meaningful outcomes show fewer symptoms, safer days, more participation and better quality of life.

Illustration: improvement can take more than one form. A person may value different outcomes at different times.

A key thing to take away in this section is that FND symptoms can grow worse or go away for a time. [1][2][5] A return of symptoms does not mean failure; it’s just the progress of the disease.

Questions

If one part of your health or daily life improved, which change would matter most to you?

What would recovery mean to you if some symptoms remained?

What can you safely try at home?

Choose one small sign of improvement that would matter in your life. It might be a symptom change, but it could also be recovering more quickly after an episode, preparing part of a meal, enjoying time with someone, asking for help more clearly, or doing an activity with less fear. Write down one sentence if it’s useful. [3]

Crosswords


For the Person With FND
For Family, Friends, and Other Supporters
For Clinicians and the Care Team
Research and Sources —

For Family, Friends, and Other Supporters

Thank you for supporting someone’s recovery process. It’s important for both you and the sufferer to have a clear goal in mind with steps along the way of what recovery looks like. When a person has many symptoms at once, what recovery looks like can range from adapting to their most disabling symptom to just getting stable after the trauma of diagnosis. [2][3]

What is important to many sufferers of FND is holding some independence, comfort, feeling safe, and keeping or gaining relationships. [2][3] In fact, making life safer and more accessible may do a lot to lower the intensity of their symptoms. It’s also important to help them access mobility equipment.

When functional neurological disorder was less understood, it was felt that providing mobility aids could *“prevent the return of normal movement”. Recently, the guidance is that mobility aids are “reasonable and appropriate” when they improve safety, independence, and access to the community.

Figure 1

If symptoms return or don’t respond to a treatment, help the person notice what they have learned and what still works. Recovery may include becoming better prepared for difficult periods, adapting, and it can’t be about preventing every symptom. [2][3]


For the Person With FND
For Family, Friends, and Other Supporters
For Clinicians and the Care Team
Research and Sources —

For Clinicians and the Care Team

You are an essential part of recovery. The question is, what does recovery look like for your patient? Let’s define key terms. Symptom Remission. Some or all of the patient’s symptoms are absent for a period of time.

Symptom Improvement. This refers to symptoms becoming less frequent, severe or prolonged.

Functional Improvement. The person can do more, participate more or be more independent despite continuing symptoms.

Personal Recovery. Rather than be about their symptoms, recovery speaks more to their quality of life; their personal confidence, their relationships and purpose or identity and safety.

Recovery after an episode. This is the shorter process (hours to days, sometimes longer) of returning to the person’s usual level after flare of symptoms or a functional seizure. [2][3]

Although many of these outcomes overlap, they are not interchangeable. Research supports making the patient’s experience central while also considering symptoms, daily activities, mental health and quality of life. [3]

A useful prognosis conversation sounds like:

“Improvement is possible, but we can’t predict exactly how much, how quickly, or how permanently you’ll improve. Some people experience complete or long-lasting remission. Others improve partly, fluctuate, or continue to need substantial support.” And at a later time, perhaps, “Let’s decide what improvement would look like for you and review it together.” [1][5][6]

This avoids two damaging extremes:

  • “You will recover if you accept the diagnosis and work hard.”
  • “You have had this too long, so nothing will help.”

[5][6]

A psychologist reviewing my case in behalf of an insurer wrote, “The longer conversion symptoms are present, the worse the prognosis” Later, a neuropsychiatrist assigned to assess how FND had affected me wrote, “Functional barriers …, in combination with poor prognosis owing to the duration of symptoms (and) history of trauma.

— (Lived experience)

Clinicians should explain the intent of a particular referral. On this site, there is a reference guide on treatments for specific symptoms, our reference page contains a complete index of techniques. These can help to determine which treatment may be best. [7]

Recovery is not one binary verdict. The clinician’s responsibility is to define outcomes with the patient, communicate uncertainty honestly, match care to what matters, and continue helping even when symptoms persist.


For the Person With FND
For Family, Friends, and Other Supporters
For Clinicians and the Care Team
Research and Sources —

Research and Sources

Three focused quotations

  • “Reported symptom outcome was highly variable.” [1]
  • “recovery often follows a pattern of symptom remission and exacerbation.” [2]
  • “all believed that the patient’s subjective experience should be central.” [3]

Citation table

Citation Figure Full citation
[1] — Gelauff J, Stone J, Edwards M, Carson A. The prognosis of functional (psychogenic) motor symptoms: a systematic review. Journal of Neurology, Neurosurgery & Psychiatry. 2014;85(2):220–226. FND-CIT-0007. https://doi.org/10.1136/jnnp-2013-305321
[2] Figure 1 Nicholson C, Edwards MJ, Carson AJ, et al. Occupational therapy consensus recommendations for functional neurological disorder. Journal of Neurology, Neurosurgery & Psychiatry. 2020;91(10):1037–1045. FND-CIT-0011. https://doi.org/10.1136/jnnp-2019-322281
[3] — Rutten S, Bradley-Westguard A, Nicholson TR, et al. Outcome measurement in functional neurological disorder: a qualitative study on the views of patients, caregivers and healthcare professionals. Journal of Neurology. 2025;272:189. FND-CIT-0012. https://doi.org/10.1007/s00415-025-12912-9
[4] Figure 1 Nielsen G, Stone J, Matthews A, et al. Physiotherapy for functional motor disorders: a consensus recommendation. Journal of Neurology, Neurosurgery & Psychiatry. 2015;86(10):1113–1119. FND-CIT-0028. https://doi.org/10.1136/jnnp-2014-309255
[5] — Sekine ER, Kanaan RA, McMillan J, Oxford S, Iles RA. Biopsychosocial prognostic indicators in Functional Neurological Disorder: a systematic review. Journal of Psychosomatic Research. 2025;195:112201. FND-CIT-0017. https://doi.org/10.1016/j.jpsychores.2025.112201
[6] — Thomas ST, Thomas ET, Schembri E, Lehn AC, Palmer DDG. Treatment outcomes in functional neurological disorder: a systematic review and meta-analysis exploring the influence of symptom chronicity. BMJ Neurology Open. 2025;7:e001150. FND-CIT-0051. https://doi.org/10.1136/bmjno-2025-001150
[7] — Dworetzky BA, Baslet G. Functional neurological disorder: Practical management. Neurotherapeutics. 2025;22(4):e00612. FND-CIT-0013. https://doi.org/10.1016/j.neurot.2025.e00612

This page is a brief introduction. Detailed discussion of rehabilitation, pacing, psychological treatment, setbacks and progress belongs in the later course modules.

Author accuracy review — suggested wording not yet applied These notes are for the author and reviewers. They identify wording that may overstate the evidence, blur an important distinction, or be misunderstood. The suggested replacements are written in the course's direct, plain-language tone. They have not been inserted into the lesson. ### 1. Remission and what research can predict **Accuracy warning:** The current wording may imply that symptom type can reliably predict one person's chance of remission. References [1], [2], [5], and [6] show that outcomes vary, but they do not support a dependable individual prediction from symptom type alone. **Suggested wording:** > For this course, remission means that some or all of a person's symptoms disappear for a time. Some people experience remission lasting months or years. Outcomes vary widely, and current research cannot reliably predict one person's course from symptom type alone. ### 2. Recurrence is not “progress of the disease” **Accuracy warning:** Describing recurrent symptoms as the progress of the disease may wrongly suggest that FND is necessarily progressive. A change in symptoms also says nothing about the person's effort, knowledge, acceptance, treatment participation, or progress in life. **Suggested wording:** > FND symptoms can become worse, improve, disappear for a time, or return. A return of symptoms does not show that the disease is progressing. It also tells us nothing about what the person knows, tried, accepted, or achieved. ### 3. Accessibility does not need to lower symptom intensity to matter **Accuracy warning:** The current wording may overstate accessibility as a way to reduce symptoms. Safety, accessibility, and support have value whether symptoms change or not. They can reduce harm and make life more manageable without placing responsibility for symptom control on the person. **Suggested wording:** > What is important to many sufferers of FND is keeping some independence, comfort, safety, and relationships. Making life safer and more accessible is worthwhile whether or not symptoms change. It can reduce injury, exhaustion, isolation, and the amount of help a person needs. ### 4. Definitions for clinicians **Accuracy warning:** The current definitions of symptom improvement and recovery after an episode need clearer grammar and a firmer separation. Symptom improvement describes a change in symptoms. Recovery after an episode describes returning to the person's usual level after a flare or functional seizure. **Suggested wording:** > **Symptom improvement.** This means that one or more symptoms become less frequent, less severe, or shorter. > > **Recovery after an episode.** This is the shorter process—hours to days, sometimes longer—of returning to the person's usual level after a flare of symptoms or a functional seizure. ### 5. What the reference guide can decide **Accuracy warning:** The reference guide can organize treatment options, evidence limits, and safety notes. It cannot determine which treatment is best for an individual. That requires discussion of the person's symptoms, needs, preferences, access, other conditions, and goals. **Suggested wording:** > Clinicians should explain what a referral is meant to help with. Our reference guide lists approaches organized by symptom, together with their evidence limits and safety notes. It can help a patient and clinician identify options to discuss, but it cannot determine which treatment is best for one person. ### 6. Quotations from insurer reports **Accuracy warning:** “In behalf” should be “on behalf.” More importantly, language presented inside quotation marks must match the original report exactly. The second quotation is currently incomplete and its ellipsis and added wording are unclear. **Suggested wording:** > A psychologist reviewing my case on behalf of an insurer wrote: “The longer conversion symptoms are present, the worse the prognosis.” > > Later, a neuropsychiatrist assigned to assess how FND had affected me wrote: “[exact wording from the report].” Before replacing the second quotation, copy it exactly from the report. Use an ellipsis for omitted words and square brackets only when a word has been changed or added for clarity.