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Officially diagnosed with FND about 6 months ago. I can't thank you enough for making this film! I cried tears of HOPE🙏

I just came across your video and I resonate with your story. 7 months ago, I began to have a pulling sensation in my neck and face. This was late May but the next month my world came crashing down when I began to experience seizures, tremors, severe pain, and a mental disconnect from the world around me. October 11, 2024, was the day that changed my life. I had been seeing a neurologist since the beginning of the journey, but this was the day that I finally after months I got an official diagnosis. My doctor diagnosed me with Functional Neurological Disorder. Though my wife and I were happy to have a diagnosis we had so many questions. Many days I look back on my life before FND and it's hard to understand that 7 months ago I was normal working an excellent job, providing for my family, and had so many things I wanted to accomplish. Even though my life looks vastly different than before, this has led to other possibilities that I can only describe has a blessing from God. One thing I have learned from this disability is that I don't have to understand it, but I know God has ordained it. Thank you for sharing your story and journey through FND. God Bless.

I've been fainting regularly, couldn't move for hours, tired all the time etc. The doctors don't know what's wrong with me, but they've only done ekgs and blood tests and nothing else because my parents waited 6 months to take me to a doctor. I'm debilitated and unable to do my schoolwork. We still don't know whats wrong with me, though my heart rate is always high (resting around 110, it's jumped up to 195 resting before). I want the doctors to take me seriously and have answers.

Hi! I was also diagnosed with FND on Oct 10. I can’t walk forward but I can walk backwards. We got this 💪

Have you ruled out pandas/pans? Many people are being misdiagnosed and get FND diagnosis when they actually have pandas/pans.

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Do you drive?

8:12 Exactly my story up to this moment in your video. I have no faith.

Woou increíble videos, gracias por mostrarnos las luchas diarias del FND, a mi también me diagnósticaron, gracias, haces que no me sienta sola en esta lucha, te envío un gran abrazo guerrera❤❤❤❤

"optimism is intentional" Dang! No idea why I needed that. Thank you so much!!! 😊 Earned a sub

Just can’t across your videos after seeing you have FND, I’m nearly diagnosed, just wonder is there hope for this? Do you feel better now? Thanks.

i dont ever leave video comments, but i'm shocked that your videos aren't more popular yet. you're incredible at sharing your perspective on life and illness in these videos! i'm of a similar age as you and hoping to go into healthcare while also dealing with a chronic illness, so i hold these videos close in my heart

what are you triggers for flares??

this is such a bueatiful work of art. thank you for filming this. i wish you all the best for the future.

You are beautiful ❤

❤

Ok

My symptoms started in 2021 but were mild Dr told me it was anxiety more I have tics,faint attack,limb weakness, problems with speech I know it's fnd its getting a Dr to believe me

I have been diagnosed with fnd

I developed FND from a covid reinfection in May 2022 as well as ME/CFS. It's completely changed my life - housebound over two years now

Thank you Clarity for sharing your experience with FND. You are a geeat inspiration. I developed FND soon after my 1st and only covid jab. Was there any connection between the timing of your covid vaxes, and developing FND symptoms, in case you took any jabs.? Would appreciate a reply very much. Thanks.

Inspirational video. Thank you for sharing your story. May I ask if your symptoms began after the covid jabs. I was 68years old when I had my 1st jab 3 years ago. Symptoms started soon after and after several tests that all came back normal, I now need a walker even to get around my home. I'd rather risk dying of covid than risk any more vaxes. Recently diagnosed with FND. Hope you find ways of getting better Clarity. You are a very brave young lady and thanks again for sharing your story.

My Daughter was diagnosed with FND October 22. Went to bed a bit run down with a cold, and next moring could barely walk with collapsing episodes. Battery of tests, and eventually we paid for a private diagnosis. This got worse with unconscious handgriping, arm movements, tics and tourettes outbursts etc. Only had a couple of what Id call seizures. Nearly 2 years later she's doing a lot better. She had to suspend college for a year while we all refocused, but she's walking, doesnt need the wheelchair any more etc. It's still with her, and heat and loud noises can be a problem, but considering how bad it got we're so proud of her progress abd recovery. Walking issues..weirdly she could dance flawlessly, and we found any type of distraction helped normalise her movement. Good luck to you and stay strong 🙏👍❤

Love watching your inspiring video ❤

What a brave inspiring young lady you are. Thankyou for raising awareness on this delibating condition ❤

So good Gorgeous Clarity that was calming.

girl this is so real thanks for sharing <33

I feel this on so many levels, but im glad ❤ because all these things happened for a reason.

It’s so true🙂

Hi Clarity nice to see you looking well. I really admire your strength in being so positive, in having to change your goals despite your struggles. Fnd is an awful illness which I find hard to come to terms with and then I watch how you are coping and think yes I should be like you. Hope you are OK and take care. Love and best wishes to you xxx

I have recently subscribed to your channel as I have FND too , although I'm much older than you so I'm so sorry you have this at such a young age. I find it difficult to explain this to my family and I wanted to say you have explained this perfectly. Thankyou so much for sharing & take care xxx

Love this Girl ❤so true, your so strong sending you Love and can't wait for more FND events together. #FND Warrior sisters

such high quality content for an early creator

Thank you, I really needed this💕💕

Sincerely wishing you the best. Love your optimism despite such serious challenges. You are the definition of grace under fire

Sincerely wishing you the best. Love your optimism despite such serious challenges. You are the definition of grace under fire

❤❤❤❤ it's ok anak your doing great..we're proud of you....keep up your good work in healing your FND. Love you anak. ❤❤❤❤ Fighting to all FND warriors out there. ❤

Thank you for sharing your story. This was a beautiful film. I also suffer from FND and its so difficult. It's hard watching your peers move forward while you feel left behind. It's hard grieving your past self and all you were capable of. I'm glad you've found freedom in using mobility aids, I might have to consider getting one.

Love you much nak…😊😘😘😘🥰🥰🥰😍😍😍❤️❤️❤️

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I learned recently that I am not only ADHD but also autistic, and accepting the limitations that come with those disorders. For a long time, I just thought I... sucked. I was normal, but weird. And I was fussy, picky, particular, emotional, quirky, lazy... etc. Now I have a name for my problems. However, accepting that there's just certain things I can't do, and the fact that most people in my life don't understand that I can't do certain things, and get upset with me, and judge me badly, because they think I CAN do anything I put my mind to.... it's so ... heartbreaking. I've got a different life experience than you, and we have different struggles, but I am here with you, beside you. We are sisters and we can lift each other up when the world or our bodies/brains push us down. I love you and I hope you will continue to cope easier and easier and life flows a little more smoothly. 💙

nice video give me a heart

beautifully filmed. Thank you for the reminder that life can change in an instant and our concept of 'control' is just a construct we have invented. (I was hit by a car and the life that I had before just evaporated - so I write with empathy and kindness.) thank you - you are far from alone.

Well, if nothing else, the algorithm brought me here, front page. As someone with disassociative episodes, I can only sympathise deeply, but never truly understand. I just hope. For you. For everyone who experiences anything adjacent to this. Despite the all-encompassing loneliness... that's one thing you aren't alone in 🫂 alone together

not only was this beautiful but also a jarring perspective of what it’s like to live with such a disorder. thank you for sharing this with the world, you are very strong ❤️❤️

Were you ever tested properly by a holistic practitioner for Lyme disease Bara Bartonella? the lab that’s trustworthy is vibrant. Please look into. I hope you’re feeling better soon soon.

No matter what illness you have, I would like to motivate you to cleanse your whole body. The body has self-healing powers, but these can be limited by toxins. This may also have been one of the reasons why you developed this illness. Detoxify through daily alkaline baths, vegan raw food, physical activity as much as possible, daily enemas and regular colon hydrotherapy to keep the intestines clean and prevent re-intoxication. No use of synthetic perfumes, fabric softeners, aggressive detergents and washing-up liquids, too chemical shampoo, no conditioner. Only eat when you are hungry and only enough to make the hunger disappear (don't feel full). Hypnosis to eliminate mental toxins. No new vaccinations that cause new deposits in your system or cross your brain-blood barrier and cause problems in the brain. Only drink fresh spring water, or better still distilled water and mainly water from freshly squeezed vegetable juices. Depending on your condition, take as little medication as possible (preferably none at all, of course). Of course, it will restrict your life even more and it will be exhausting. But the main reason for illness is our way of life, which is not suitable for humans. And depending on where "toxins" are located or which detoxification organs are overloaded, different diseases/symptoms appear. Incidentally, I am now also on this path. When you do it, you realise how poisoned you were. Do the test and eat nothing but water for 1 day. Your tongue will be coated, your mouth will stink, it will feel funny. These are some of the detox symptoms. Do a lot of research on the internet about the things I wrote. This is important. Doctors don't learn that. But ask your doctor if you can fast for a day to try it out. It's not a walk in the park and will take a long time, but look forward to the quality of life afterwards. I wish you all the best! And more viewers, which you definitely deserve!

Can I just say that this was beautifully filmed. I would love to follow your progress mentally as well as physically! I wish you all the best and keep in mind that grieving the body you once had as well as accepting and learning about the body you now have both have a place in the healing process.

This video is so underrated, I don't have fnd but I am neurodivergent and I understand what it feels like to be dismissed, ignored, and misunderstood. You got this :)

Commenting to help the algo and spread your story! Keep fighting and be kind to yourself!