Experiences with

Functional neurological disorder (FND)

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I was recently diagnosed with Functional Neurological Disorder after a 10-year-long search for a diagnosis to figure out what was wrong with me. I am still learning a lot about this. I had no idea that my issues were even neurological.

my 15 year old is being diagnosed with Functional neurological disorder FND for short, she has been collapsing with non epileptic seizures. Does anyone know of any medical papers/ studies/ test that surgest a link between B12 and FND?

Functional Neurological Disorder: Neuropsychological and psychological management in children and adults (November 2024) DOI: doi.org/10.53841/bpsrep.2024.rep181 (not yet registered) Hopefully this link will work: https://explore.bps.org.uk/content/report-guideline/bpsrep.2024.rep181 The Pre-Paces

It can be used to study brain function in functional neurological disorder (FND). For more details see link below https://doi.org/10.1016/j.nicl.2024.103625 Why is BOLD signal variability important?

I was just diagnosed with functional neurological disorder about 4 weeks ago.

I have B12 deficiency that causes severe neurological problems - functional movement disorder and sulphite allergy. I use B12 to control asthma - especially as I'm allergic to sulphites in inhalers and nebulisers. I can't have steroids as they make my functional neurological disorder worse.

How many of us have been told that it's all due to being depressed or anxious or to being a hypochondriac, to having FND (functional neurological disorder), MUPS (Medically Unexplained Symptoms) etc..... I'm not a health professionals so please correct my explanations if needed.

I have recently been diagnosed with FND functional neurological disorder. And Charles Bonnette syndrome this is all taking Francis in my life now as I’m having, episodes two or three every day now and I’m fairly exhausted with it all.

I'm Angie and have been battling with weird physical symptoms for 3 1/2 years to Finally get a Functional Neurological Disorder/Functional Movement Disorder diagnosis.

Apologises if posted somewhere before, but it was the date of this article and the recommended Care Model that caught my eye, I was searching for "rule in" signs for FND to post. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8633865/ Hopefully now the medical professional are beginning to see the light

(Functional Neurological Disorder) I'm waiting for the next saga in my life to unfold. ( Sorry I sound so gloom and doom guys) It's just exploding in my mind/thoughts all the time.

So after reading some heart breaking posts, I thought I would find some success stories: https://www.refinery29.com/en-gb/functional-neurological-disorder-recovery-experience Luckily they managed to get the intensive six week therapy which I think should be offered to all newly diagnosed sufferers, so

The bit that caught my attention: Full resolution of FND symptoms occurs in 63%–95% of children if diagnosis and treatment are promptly delivered using a multidisciplinary, biopsychosocial, stepped-care approach. Despite this need, pediatric FND services are scarce worldwide. The link to the article

A tweet from a Specialist, Zach London: Saw another patient with sensory neuronopathy who had been misdiagnosed with functional neurological disorder.

Neurologist finally confirms diagnosis of Functional Neurological Disorder (FND) with paroxysmal non-epileptic events. Being referred for CBT . Anyone had same diagnosis ? Any useful information on how to manage condition whilst waiting for CBT appt would be appreciated. TIA

hello, I'm just wondering if anyone has taken NAD injections before or during IVF? Any stories or thoughts please do share. I’m deciding if I should take it during my next round. Any advice is appreciated.

I have had this nearly all my life due to stresses and traumas throughout my childhood. At present I am just recovering from my 4th breakdown at the end of 2024. Still going through immense stresses and anxiety issues with lots more too follow up. My stress levels are rising constantly and I am now

Hi everyoneI've been taking mirtazapine for a year. Unfortunately, the side effect is weight gain, so I'm thinking about stopping it. Has anyone stopped taking it? What are the withdrawal effects and how long do they last?