Posts - Functional Neurological Disorder - FND Hope | HealthUnlocked

Functional Neurological Disorder - FND Hope

5,638 members • 2,941 posts

All posts for May 2023

Hello

I see that a few of you have experienced cluster goosebumps. I am getting them on my one arm with tingling sensation, does anybody know what it is please ? ☺️

I see that a few of you have experienced cluster goosebumps. I am getting them o...

Chocs2020

•11 months ago

2 Replies

Interesting discussion about the prevalence of FND and the validity of the Hoover's sign going on ...

... here: https://virology.ws/.../trial-by-error-questions-about.../

210272

•11 months ago

7 Replies

Support

Hi, I have recently been diagnosed with FND and I'm finding this diagnosis very overwhelming. My GP is very good, specialists etc are good but I just need...

Hi, I have recently been diagnosed with FND and I'm finding this diagnosis very ...

Pip_louise

•11 months ago

11 Replies

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functional myoclonus

Hi I am looking for anyone who has functional myoclonus, I was recently diagnosed as a consequence of a car accident I suffer from weakness in one hand and...

Hi I am looking for anyone who has functional myoclonus, I was recently diagno...

L5XXY

•11 months ago

12 Replies

Rosa Burden Centre

Hello everyone! My neuro consultant has recently referred me to the Rosa Burden Centre in Bristol and I wondered if anyone has any experience of going there...

Hello everyone! My neuro consultant has recently referred me to the Rosa Burden ...

BeeYou22

•1 year ago

17 Replies

supplements??!

Has anyone had any success with nutritional supplements?

wlpg

•1 year ago

1 Reply

Been awhile and now possible new symptoms

hi all, it’s been awhile. I had a bad year with symptoms then things seemed to ease, still got odd bouts of stuff but not as consistent as when it all kicked...

hi all, it’s been awhile. I had a bad year with symptoms then things seemed to ...

Sjbuck

•1 year ago

1 Reply

Medication you found helpful

Hello I'm interested in anyone who has found any benifit from medication for FND if so what was it ?

Hello I'm interested in anyone who has found any benifit from medication for FND...

ToesKnees

•1 year ago

14 Replies

Neurodivergent? Disabled?

Has anyone been told that their FND has now put them under the umbrellas of neurodiversity and/or disability?

Has anyone been told that their FND has now put them under the umbrellas of neur...

Obrien8175

•1 year ago

9 Replies

My First Post - Mostly Myoclonus

I told my story in my profile. I'm 65. I'm from California. My mom had MS. She spent years trying to get a diagnosis. I have been struggling with "Essential...

I told my story in my profile. I'm 65. I'm from California. My mom had MS. She s...

RubyRena

•1 year ago

6 Replies

If you're in the UK please consider signing this petition from The Neurological Alliance before midnight tonight.

https://tinyurl.com/BackThe1in6 #FND2023 I signed for everyone with migraine, Mal de Debarquement Syndrome and other rare neurological conditions (there are...

https://tinyurl.com/BackThe1in6 #FND2023 I signed for everyone with migraine, M...

210272

•1 year ago

1 Reply

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Posts - Functional Neurological Disorder - FND Hope | HealthUnlocked

Functional Neurological Disorder - FND Hope

All posts for May 2023

Hello

Interesting discussion about the prevalence of FND and the validity of the Hoover's sign going on ...

Support

functional myoclonus

Rosa Burden Centre

supplements??!

Been awhile and now possible new symptoms

Medication you found helpful

Neurodivergent? Disabled?

My First Post - Mostly Myoclonus

If you're in the UK please consider signing this petition from The Neurological Alliance before midnight tonight.

Search posts

Pinned Posts

Latest poll

Are you FND aware? Do you wish others were? How are you most likely to engage in advocacy for FND:

Topics

Archive