Hi there! This is a very interesting video. Thank you. Has anybody here with FND experienced stiffness on their lower back that make their legs very week? Thank you in advance ❤

Thanks Tom, I am only on the beginning of my Journey, And yes, I have found that many doors have shut on me, that is probably one of my biggest things that upsets me the most. I was told by the hospital that my GP would take over my case. Unfortunately, he had never heard of FND. I have a really good Physio, Krystle and with her help I have got a team together to help me along my path to recovery. I like what you said in your video, the biggest thing I have got out of it is "Never give up." Cheers.

Is project brain computer interface , in problem the health or war cognitive ?

THANK YOU FOR the excellent talk. A sufferer of a painful,few years I I Do wish to raise awareness (fellow musician ) clinging on to Faith Hope & Love )

Thank you for this video..i think we should talk more about nutrition and food corelation with this disorder, because it is huge. All the Best

I am in Melbourne too and developed my FND symptoms a few weeks after my 1st and only mandated AZ jab. Two years and several doctors later I was diagnosed a few months ago. Doing lots of physio and exercise as recommended but cannot see any consistent improvement as yet. Hope this neurological condition is also not something that can be triggered by the AZ vaccine like many others eg. Guillean-barre and transverse myelitis.

My FND symptoms began a few weeks after my first and only AZ covid vax. I feel very strongly that there might be a connection but this is not an answer I am ever going to get from the doctors seeing how protected these jabs are. Thank you for a very informative video.

Thank you so much for your important work on behalf of humans globally. Medical Gaslighting in particular of female/female presenting patients is systemic and needs to be addressed at the highest levels. Your research addresses this and SO much more. Thank you for representing women/female presenting people worldwide 🌸

It's people like Tom Plender who give me hope for a brighter future for those of us living with FND. Thank you always for all that you do.

Thank you for sharing your story. My FND diagnosis has been a strange journey, it’s always good to know we aren’t alone ❤

Thank you, learned a lot through this video 😊

Thank you, Tom. I appreciate all you are doing 🙏

Brilliant Tom Plender, thankyou for speaking out for FND patients and for women

😑 'Promo sm'

I have FND and I’m from Melbourne! Good to see more content on FND, it is very much needed for this misunderstood condition. Thank you

So grateful to her for sharing her story!

I love that purple butterfly.

I have a sister who has Myasthenia Gravis.

very nice video reminding us to care others.

I have been dealing with HIV for the past 5 years until i got review on KZbin about #drabiolahome and I got Dr Abiola herbal medicine last month, now I am free from HIV #drabiola 🥰..

I have been dealing with HIV for the past 5 years until i got review on KZbin about #drabiolahome and I got Dr Abiola herbal medicine last month, now I am free from HIV #drabiola 🥰..

please, wig please

I hate sophia

Held a conversation better than slot of human. Seriously that should tell us about ourselves.

That interviewer is stupid as hell asking all sorts of dumbass leftist questions. “Hey Sophia what gender do you identify as?” “will you kill somebody if they misgender you?” What the fuck are you talking about bitch? It’s a robot not a dumb “feminist” it’s not alive & doesn’t have a gender it’s a machine.

C'est pas encore ça !

Mesmerized research for me .

It's recommended guys 🙂🙏

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I certainly endorse this new perspective.

Uniting different professions, different sciences has never been easy. WBP has demonstrated great talent supported by an extremely committed human group. Keep in that way

Excellent initiative, many successes to all its members. Your work is necessary