Personal stories, practical reflections and honest notes about living with Functional Neurological Disorder. New guides now cover sleep, symptom hangovers, heat and seizure thresholds, driving rules, sensory overload, neurodivergence, hypermobility, hormone tracking, emergency symptoms, PIP, work adjustments, pacing, relationships and diagnosis.
Having Functional Neurological Disorder does not automatically stop you getting travel insurance. The important part is to answer the insurer’s medical questions accurately, make sure FND-related problems are not silently excluded, and keep written proof of what the policy will cover.
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If FND means you need help with personal care or someone nearby for safety, you may be able to claim a pension-age disability benefit. The diagnosis is not the deciding factor: the form needs to show what help or supervision you reasonably need, how often and whether that need happens by day, at night or both.
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Can stress worsen FND symptoms? Learn why symptoms may flare, how to spot patterns, and gentle, practical ways to support yourself safely with care, too.
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Understanding FND causes: why symptoms are real, why there is rarely one explanation, and how to make sense of diagnosis, triggers and next steps today.
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We wanted to create a dependable new way to fund FND support without asking people to make an extra donation every time. The answer began with something millions of us already do: choosing gifts for people we care about.
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A jury summons can feel daunting when FND affects movement, awareness, speech, concentration, fatigue or recovery. This guide explains how to reply, what help to ask about and when a different date or excusal may be the more realistic request.
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FND memory problems can be frightening and disruptive. Learn why they happen, practical ways to cope, and when to seek medical advice and support locally.
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FND pain management: practical, compassionate ways to track pain, protect your energy and prepare for NHS appointments as symptoms change day to day.
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Why FND care still depends on where you live in the UK. National pathways exist, but many ICBs and health boards have not funded them. Explore the live map and what to do next.
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FND can make an exam harder to access without changing what you know. The useful question is not “Does this diagnosis get extra time?” but “What barrier happens in exams, and which arrangement lets this student show their knowledge fairly?”
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If you regularly help someone with FND, you may be doing the work of an unpaid carer even if neither of you uses that word. Carer's Allowance is not awarded because of the diagnosis itself: the deciding rules are the care you provide, the disability benefit the person receives and your own circumstances.
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It is a fair and hopeful question. Stem cells are often talked about as a repair kit for the body, so it makes sense to ask whether they could fix FND too. The short answer is no — and the reason why is actually one of the more hopeful things about FND.
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A major meeting in Wales brought together patients, families, neurologists, researchers and patient organisations to examine new population research on functional seizures — and what needs to change in the care pathway. The medical detail was dense, so FND Connect has produced a free plain-English report anyone can open and understand.
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If FND makes studying harder or more expensive, you may be able to get Disabled Students' Allowance. The useful evidence is not simply the diagnosis: it is how your symptoms create barriers to learning, travel, communication and completing your course.
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This week FND Connect issued grants for two wheelchairs — practical mobility support for real people living with Functional Neurological Disorder. That is your kindness in action.
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Pain is common alongside Functional Neurological Disorder, and it can be every bit as real and disabling as weakness, tremor or seizures. But that does not mean every new pain should be labelled “just FND”.
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When symptoms change, closeness can change too. That does not mean connection has to disappear.
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Broken words, sudden stutters, total silence or fluent, unrepeatable "ancient languages from the land before time". Why FND episode speech happens, why it's not faking, and why so many of us sound weirdly alike.
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FND mobility can change from one day, or even one hour, to the next. This is a practical, judgement-free guide to using a wheelchair or walking stick part-time, choosing the right aid, and handling the comments that come with fluctuating ability.
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Functional Neurological Disorder is hard for adults and clinicians to understand. For a child, it can be even more confusing. Parents are left trying to learn the condition, steady their own fear and help their child feel safe at the same time.
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Hope matters. But when recovery is presented as an expectation rather than a possibility, people whose FND symptoms persist can be left feeling blamed, judged or as though they have failed treatment.
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FND does not only change bodies and routines. It can change who calls, who keeps inviting you, who believes you and which friendships are able to adapt when life becomes unpredictable.
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Dental care can be particularly daunting when managing FND symptoms. Bright lights, loud drills, and vibrations can act as significant triggers. A practical guide to navigating dental appointments, fostering better communication, and advocating for reasonable adjustments for a safer and more comfortable experience.
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Flying with Functional Neurological Disorder is not a simple yes or no. The useful question is whether your current symptom pattern, pressure sensitivity, airport load and recovery plan make this journey manageable today.
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FND can make you doubt your own reality. Not because the symptoms are fake, but because fluctuating symptoms, normal tests, stigma and disbelief can teach you to question yourself before anyone else gets the chance.
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When you have Functional Neurological Disorder, parenting can become a sensory and emotional balancing act. You can love your children deeply and still need distance from the noise, arguments and intensity that teenagers sometimes bring.
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A good day with Functional Neurological Disorder can still be a carefully managed day. It can mean planning, pacing, masking, aids, recovery time and a cost that other people do not see.
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Poor sleep can reduce the spare capacity your nervous system has to stay regulated. Here is how to plan the next day with FND.
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One busy day can create a delayed FND flare. Learn how recovery debt works and how to plan activity without feeding boom-and-bust cycles.
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Heat is not just uncomfortable for many people with FND. SeizeControl evidence shows that rising environmental temperature can lower the nervous-system threshold for functional seizures, tics, tremor and overload, making forward planning essential when the forecast climbs.
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FND symptoms vary hugely, so UK driving rules are not applied by the diagnosis label alone. They are applied by the symptom, the risk, the licence group and whether you can drive safely today.
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Why autism, ADHD, hEDS, HSD, sensory overload and functional neurological symptoms keep coming up in the same conversations - and how to make the overlap useful without over-claiming it.
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A practical guide to deciding when symptoms fit a familiar FND flare and when they need urgent medical help because they are new, sudden, severe or different.
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A practical guide to noticing patterns around periods, perimenopause, menopause and functional seizures without turning every symptom into a hormone explanation.
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What to ask for, what your employer should consider, how sick leave works, and where to get help when FND starts affecting your job.
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A practical guide to PIP, Adult Disability Payment, benefits checks, Blue Badge, Motability and mobility support when Functional Neurological Disorder affects everyday life.
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The emotional reality of being a partner, not just a caregiver.
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A practical guide to finding your pacing sweet spot: doing what matters while protecting energy for later.
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