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0 posts 5 comments 0 discussions 07 Jun 2026
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Replied to ANTIBIOTICS CURED ME OF FND ! · 02 Jun 2026

This is common behavior for a person who can't accept their FND diagnosis. It doesn't even make sense. I'll break it down using research not beliefs driven by the widespread online misinformation of Lyme disease.

The UK has a high false positive rate of Lyme. 77% of patients referred for possible LD never had it. https://academic.oup.com/qjmed/article-abstract/105/6/537/1560675?redirectedFrom=fulltext&login=false

A UK study on Lyme neuroborreliosi found the time from tick bite to symptoms was days to 1 year (not 10+ years!) and the most common symptom was unilateral facial nerve palsy. Central nervous system manifestations were uncommon. Of the symptoms reported, almost none of them reflect this author's symptoms. https://www.sciencedirect.com/science/article/pii/S2590170220300042

It is wrong to claim the LymeScience website is misinformation. They back up everything with good research. They even have a page showing the international scientific consensus that "chronic Lyme disease" does not exist. https://lymescience.org/scientific-consensus/

They also post many of the disciplinary actions taken against all of the predatory chronic Lyme grifters who abuse and harm so many vulnerable patients. https://lymescience.org/category/rogues-gallery/

The author is wrong to claim that you cannot get treatment if you have a negative test. NICE clearly states: " We want this guideline to make a difference to people with Lyme disease by making sure: people are treated for it without waiting for tests if they have the rash that shows a bite from an infected tick". It does not make sense why they did not receive treatment with the classic bulls-eye rash. No doctor would deny starting treatment, especially when it is known testing can be negative in acute phase. https://www.nice.org.uk/guidance/ng95/informationforpublic

NICE also does not recommend tests like DualDur. Many guidelines advise against dark field microscopy due to high false positive rates. The DualDur makes it sound like a valid and reliable test but it does not seem to be validated by external organizations.

She had an extensive work up including lumbar puncture which would have very likely identified Lyme neuroborreliosi.

Using treatment to inform the diagnosis is highly problematic and considered bad medicine. This is especially true when there is so much evidence against this person having Lyme disease.

Unfortunately the author is not alone in clinging to a well known pseudo-diagnosis. Hundreds of scientific organizations across the world are all in consensus that chronic Lyme disease does not exist. It is a highly predatory pseudoscientific field.

Given all of information against the author's beliefs, the author having an extensive workup and neurological evaluation, and the fact that the author even states their symptoms "could have been taken from the neurosymptoms.org list", the most probable answer is that they did have FND.


In summary, we suggest that conversion disorder be renamed "functional neurological disorder" and that the requirement for the exclusion of feigning and identification of associated psychological factors be relegated to the accompanying text Jon Stone American Journal of Psychiatry 2010

Fascinating documentary, got me thinking. How Jon Stone helps functionally blind patients to see again; “When I help people get their seizures under control, see them walk again, or sometimes even help blind patients see again, it feels pretty amazing.” (Quote from the BMJ, 2023;381: p889, ‘fighting the FND stigma: the consultant neurologist’). I don’t doubt it, it must be an incredible feeling. It’s just those FND faith healing parallels. Here’s a paper on Functional vision loss, a subtype of FND, aimed at ophthalmologists. One of the authors is Professor Jon Stone, world leading authority on FND. https://www.nature.com/articles/s41433-024-03126-w Drop Box 2, describes a ‘vignette’ of a 16-year-old male, with complex regional pain syndrome, found to have functional vision issues, without evidence of structural abnormality on OCT, MRI, etc. Funny how he suffered blurry vision and dizziness when put on Pregablin. I’m no expert by any means, but could it be the medication? Visual disturbances, and dizziness are listed as a common side effect of pregabalin. Can’t believe any doctor is that myopic! Which leaves me wondering, what else are the authors not disclosing here? Doesn’t seem too convincing a sales pitch for ophthalmologists, but what would I know? Also, weirdly the patient’s gender appears to change mid-sentence!? Maybe this was in the interest of gender equality, as we know FND disproportionately affects females! Or, are females just more open to suggestion? Parallels with Faith Healer tactics are disturbing; 1. The use of hypnotherapy (suggestion therapy) in both cases 2. In response to patient scepticism emotional leverage (using close family members) to achieve the desired outcome; believing the diagnosis. 3. Explanation for headache, as “challenging the block in the brain”. I’d only believe it if it were backed up by firm scientific evidence. Otherwise, it’s just pure mysticism to me. Maybe there’s a demon in there. And here’s the Faith healer blurb, quote; “There is consensus that patient’s confidence in the diagnosis of FND and motivation to engage with rehabilitation therapy is essential for successful treatment. Conversely, if a patient rejects the diagnosis, perhaps because it’s poorly explained, or because information is hard to access or understand, rehabilitation often fails. A successful explanation about FND to a patient is therefore a vital first step to allow successful treatment. In some cases, a well communicated diagnostic explanation can be, in of itself, therapeutic.” If rehab therapy doesn’t work, it’s the patient’s fault! It really is all just too confusing. I find it’s not how well FND’s explained, it’s the fundamental concept that makes me shudder. And graded light therapy for photophobia? WTF! “The use of sunglasses is therefore reasonable to the patient and has short term benefits, although in the longer term makes things worse. We recommend starting by explaining that the brain is sensitive, but the more you wear sunglasses the more sensitive it becomes. Management involves graded sensitisation to light which may involve a structured plan to have reductions in opacity of sunglasses or spend longer and longer without sunglasses. This kind of graded exposure is generically familiar territory for clinical psychology, for example in relation to insect or flying phobia, but they may need support to understand that this approach can also work for photophobia. A clinical psychologist may be helpful but is not always essential to help people wean themselves off sunglasses in our experience.” Echoes here for discredited GET therapy for ME patients.

Replied to Who am I? Why am I doing this? · 10 May 2026
Is it from the c19 vax ?

Sadly, sometimes the symptoms of misdiagnosed FND are so severe that the patient lacks cognitive capacity to mount a meaningful challenge.

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