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It's a very well edited and filmed video. There's many fully functional RUclipsrs who couldn't do such a fantastic job.

This was so beautiful. Thank you for sharing . 🙏🏾

I love to see other young people with mobility aids! I’m 25 and use them because of Ehlers Danlos syndrome. Thank you so much for sharing your story!

When I had to start using a walking stick. I decided to bling it out and get different colors and designs on it to match my outfits and a happy state of mind. ❤

You are spot on!!!!!

Just found your channel. You are adorable. I can relate to many of your struggles. It looks like you are doing so well now and I am so happy to see that. May God bless you always!!! ❤

What a beautiful way to start 2025 - it must have meant so much to your grandma. So happy to see that you have recovered from FND. Do you mind sharing what helped you most with recovery. I have been diagnosed with FND symptoms began a few weeks after my 1st covid jab over 3 years ago and despite seeing several doctors and physios etc. Symptoms continue to get worse. Thanks for your videos and wish you and your family a Happy New Year. Stay safe specially while walking alone in the park.

I have been diagnosed with FND after months of being to several neurologists and having a multitude of tests which were all negative. My symptoms began over 3 years ago l, a few weeks after my 1st and only Astra-zen jab. Greatest regret of my life. Paralysis has got worse over time - permanently on a walker and require additional help too. So glad to read in your update that you are getting better Clarity. Thanks for sharing your story.

eat 300 grams steak, 70 g liver, 130g beef or lamb or pork fat, and 30g lambs brain a day

Hi Clarity, it is lovely to see you looking well. Your grandma is lucky to have you. What a lovely thing to do for her. The fireworks display looked stunning. Scary thought that you were so near those nasty men. It looked so calming in the park, it definitely soothes the senses. My sister lives in Australia too. What an uplifting message that you read, very inspiring. I realise that this comment is getting long and as you know I have forgotten what I have wrote at the beginning and then I'm hoping this makes sense. (FND go away lol) But wanted to comment as I just wanted to let you know that I always enjoy your videos even though I might not be able to comment I give you a thumbs up. I wish you all the very best for 2025. Wishing you good health happiness peace and lots of love ❤️ love Andrea xxx

This disorder is becoming an epidemic. It needs to be investigated more. You're lucky to have had someone speak up for you.

Send you love girl, I’m about to hear that you are recovering very fast. Do yoga, and gym (if doctor allows), yoga is very good for the nervous system as per my understanding

After five years of undiagnosed symptoms (including constant exhaustion / fatigue and intractable vomiting) - I finally got a diagnosis of Myalgic Encephalomyelitis, a progressive, degenerative neurological condition associated with Chronic Fatigue Syndrome…. And then, I woke up to extreme pain at the left trigeminal nerve at the mandible - excruciating pain, and tremors, weakness, tingling - and as I jumped into the shower, preparing to rush to the doctor (about 04:30) I was terrified to discover that the symptoms were knife-edge divided between my left and right side - like a distinct line bisecting my entire body, dividing left / right - similar symptoms on both sides, but the right substantially worse. Having been in care since the early symptoms of the ME, I have a standing order for labs at the local clinic, so I decided to take a sample in, and see if there were ANYONE who could see me; oddly, the lab was closed, but my primary doctor was in the office, and had just had her first appointment cancel - did I want to see her? Duh. She sent me immediately by ambulance to the ER for imaging; despite there being no “bleeders,” the on-call ER doc diagnosed as Functional Neuropathy - and basically told me it was in my head. My clinical neurologist tried to convince me of this - and my response was that, if she could explain the mechanism by which I was awoken from a dead sleep with late-stage Parkinson’s symptoms and ungodly pain at the trigeminal nerve was the result of my grief of having lost my mom unexpectedly a few weeks prior - well - you should write a paper - otherwise, I think more imaging is in order. She ordered the FMRI and CAT scans immediately. After several visits to UW Neurological, Virginia Mason Neurological Research Clinic, and a gaggle of endocrinologists, urologists, gastroenterologists, and other specialists - not any closer to finding out why - only an entire year spent bedbound, atrophying until I simply forget who and where I am - as degenerative nerves include the most important of them - the neurons and axons in the noggin. The complex PTSD and chronic depression, while preexisting, are probably what ultimately does me in - because this isn’t really living. My entire point is not to complain, or compare - only to advise others that - despite being preternaturally healthy for 55 years - sudden, unexpected illness can, and does destroy lives, and the current state of healthcare / insurance in the US is designed to profit off suffering, with no actual attempt at curative care, but *managed care* - because that’s where the profit margins are. I’m not saying that what Luigi did is right - only that I understand. 🤨😒

You should make some vlogs sometimes so we get updates and see how you are doing and how far you have recovered or not, so people with FND can see what can happen. And not guess the worst.

The views were 666. Felt weird so here I am, watching so it becomes 667 lol 😂

I am touched with grief and sadness to see someone of such young age needed to go through such struggle. I too find comfort and inspiration in your attitude to "rock it out" despite your current circumstances. Thank you for this beautiful emotional ying & yang today. Wishing you a beautiful and meaningful life journey ahead.

Keep strong.

Ηave you done the vaccine?

This reminds me a lot of Gluten Ataxia. The symptoms over lap quite a bit.

I was misdiagnosed with FND & Fabrication of Illness. I actually have dysautonomia/POTS and severe ME + MCAS & hEDS triggered by vaccine injury. The thing that caused my seizures was a combination of Adrenal insufficiency/ very low cortisol, low blood volume & chronic potassium deficiency. I almost died because it was never tested for until I went private… yet i was told by NHS neurologist that i just needed psychiatric therapy. Make sure your vitamin levels are optimal and hormones have been checked & also consider researching vaccine injury if you had vaccine within 3 months of onset (you won’t get far with just googling as heavily censored topic.) Regardless of your trigger, there are many people, especially young women, presenting similar symptoms to you. So you are never alone.❤

Amazing videography

UPDATE: Hi everyone! I’ve noticed my video has been resurfacing again recently and I’m blown away by all the love, support and kind words you’ve shared. I just want to take a moment to thank every single one of you from the bottom of my heart. Back in Dec 2023, being diagnosed with FND and becoming disabled overnight at 22 was one of the most challenging, confusing and isolating experiences of my life. Now that it’s 2025, I wanted to give you an update on where I’m at! I’m incredibly grateful to share that I’ve recovered about 95% of the way. It’s been a long journey that required faith, perseverance and help from many areas-but it truly was a holistic transformation. If you’re curious to see more about my journey or behind-the-scenes updates, I’ve been sharing over on Instagram (@claritymromero). I have an FND highlights over there so feel free to check it out if you’d like! Thank you again for being such a supportive, uplifting community. You’ve truly made a difference in my life. I don’t feel so alone anymore. I love you all so much! ❤️❤️❤️

Was this result of a vaccination?

Have you considered medical marijuana ?

My heart definitely goes out to you, i have been dealing with this since May of 24. I have been in the ER multiple times for seizures, the last time was literally Christmas night which I was so upset about because I didn't want to ruin Christmas for my family. Doctor's often dismiss me, they send me home every time. I don't know if they think I'm faking or what. I now have two mobility aids my cane and my rollator walker. Thank you for this video I feel less alone.

Try protein shakes..high protein daily

How come she'd not shaking putting on makeup? Is there medication for this,?

Low blood pressure?

we are not a conquered people.

YOU KNOW WHAT SO IF YOU HAVE TO WALK WITH A CANE, OR WALKING STICK. ATLEAST YOU CAN WALK. DON'T BE EMBARRASSED CAUSE YOU NEED THE HELP OF A CANE, OR WALKING STICK.

Omg I have never heard of this before! Thanks for sharing! I randomly stumbled across this video!

Thank you for educating people about this - you are an incredibly strong woman. Those who are healthy have no idea as to the struggles of those who are not. I see many unsympathetic comments on other videos when talking about disability - some people mention that people should prepare financially to avoid the economic devastation this can cause - this is nonsensical, no one can prepare for a catastrophic illness or accident. Even a former highly successful professional can be wiped out financially by catastrophic illness. Without a support system like family who are willing and able to help, this can completely destroy a person. This is a huge issue with older, disabled, childless people who struggle on SSI/SSDI and can barely afford basics.

I became disabled overnight with FND at the age od 21. It took everything from me. I had to quit a professional sport career and give up on my dream of studying medicine. I'm 32 now and still haven't recovered, unfortunately. I relate strongly to your comment about looking at others through a window as I've spent many years doing just that.

Please check for PANS/PANDAS. This looks like PANS. hope you're ok <3 xx

Moral of the story, don’t take your life for granted because it can change at any moment.

ur so real

Have they check if you have any parasitic infection for you? There was some parasite only from third world countries where you traveled to.

Thanks for sharing your insights. You are so articulate, young and beautiful and wise! I am older and am in the process of purging my life from fake friends and false hopes and much of what you said resonated with me. God bless you!

Are you sure you didnt pick up a parasite, bacteria, or virus something from the water whether ingesting through food or drink or in your nose with the white water rafting? while in Bali that would cause neurological issues? It seems so strange that your life changed after this trip? Like a catalyst? Did your drs. know you went there?

Thank you for sharing your story.

Fellow FND-haver here. Thank you for this beautiful video! ❤

3 months ago my life changed overnight. Right after my 20th birthday. First I developed a vocal injury from acid damage which has continued to get worse. This is particularly devastating because I’m a singer in a band and my voice means the world to me. I can still barely talk. I thought it couldn’t get any worse until one night I was struck with the worst pain in my head I have ever felt. It came on instantly and it has been with me ever since. A constant intense pressure and pain around my whole head and face 24/7. I couldn’t sleep for weeks and was in and out of the hospital almost every day. All of my blood tests were normal, I had 7 different brain scans done that all came back normal, besides one. A 7mm cyst on my pineal gland. These are usually asymptomatic and my doctors insist that it is. They diagnosed me with chronic migraine but I know this is not the case. I’ve had migraines before, this is entirely different. Migraines don’t come on in a second and last for months. Thousands of people have very serious symptoms caused by these cysts, an unremitting pressure headache being one of the most common, but their doctors won’t believe the cyst is the cause. The only cure is a very risky surgery that only a handful of surgeons in the entire world can perform. The cyst sits right in the middle of the brain on top of the cerebral aqueduct, causing an obstruction of cerebral spinal fluid and a build up of pressure. Every moment is excruciating and it’s so dismissive be told there is no physical cause when you know for a fact there is. People don’t go from being perfectly normal to feeling debilitating unremitting pain for no reason. I used to be depressed over the smallest things and now I realize how perfect my life was. I got to sing original songs with my friends, I went to work and laughed with my coworkers, I could sleep without being in pain. Now all of that is gone and it happened so fast.

Thank You Soooo much. Your video is concise, descriptive and STILL Uplifting. Greatly appreciated 🙏 😌

This video would have helped me so much when I was first in the hospital. I know it will help others as well.

Dear ❤ Clarity, you brought so much hope to my day. I am at home and most of the time bedbound after 3 heart operations and a vaccine damage. They led to a neurological disorder. I know the seizures, sudden paralysis, loss of speech etc. This has been going on for years now. Today I will wear something nice and think about you ❤ and your courage . You are a ray of light for someone in far away Germany. ❤ I know Jesus loves us and will carry us through. We need friends and family who come, accept and love us as we are now. Blessings and Big hug. Sandy ❤

Sending love and best wishes to you. I just want to thankyou for sharing your story which has been very relatable to me and inspiring. I wish you good health and happiness and hope you have a lovely Christmas 🎄 love Andrea ❤️

Thank you so much for sharing your story ml! I got diagnosed with FND in July this year and I’m 16 years old. I haven’t seen a neurologist yet but I’m on a waiting list as I’m having worse seizures so I’m hoping it’s nothing worse than only my FND. I’m sending my love gorgeous girl, it’s a horrible illness that needs more research xx

2:10 ahhh FND.... FAKE NEURO DISEASE.... ITS MENTAL GUYS AND GALS... SHES GONNA "MEOW" SOON.... EVERYONE SHOULD UNDERSTAND HER... AND PROBABLY NOT EMPLOY HER TOO... SHES SPECIAL NOW... GET HER... HER OWN PARKING SPOT....

Je sais ce que vous ressentez je suis aussi fnd !des hauts des bas !!ma vie a totalement changé !courage je gare encore espoir c’est un combat de tous les jours chacun minutes Tout le monde ne comprends pas…

I couldn't help but feel heart broken when I saw her bike unused and rusting outside on a beautiful day as I watched a tear go down her face. 😰