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Let us help you and your teen resolve FND: www.teenfndacademy.com/tfa-yt

Let us help you and your teen resolve FND: www.teenfndacademy.com/tfa-yt

I've struggled with FND since sophomore year of high school, possibly since third grade because I had functional seizures almost everyday in third and fourth grade. I'm 19 now. I have plenty of reasons why I want to get better. I have been medicated, I've tried CBD oil, I've done therapy, I've been to five neurologists, I've seen countless doctors, and no matter what it doesn't stop. I know I have PTSD and I've had traumatic incidents since being diagnosed with FND, but I still can't figure out why I'm getting better.

Great video! hanks so much. My 16yo was diagnosed w FND 2 months ago and while she has been complaining of some pain related to scoliosis for a couple of years, that pain has become chronic now. The scoliosis curve has been reduced through non-invasive means but her experience of chronic pain continues. She's got some hard work ahead of her, as does the rest of the family. Thanks again

Let us help you and your teen resolve FND: www.teenfndacademy.com/tfa-yt

Very helpful video

YES! Thank you for this!!!

Let us help you and your teen resolve FND: www.teenfndacademy.com/tfa-yt

Hardly qualified to present upon, as is a neurological condition in the WHO's ICD-11-DSM-V hardly relevant in consideration

Very well done video. I will be sharing with other parents. Thank you!

Let us help you and your teen resolve FND: www.teenfndacademy.com/tfa-yt

Let us help you and your teen resolve FND: www.teenfndacademy.com/tfa-yt

Feeling overwhelmed and unsure of where to turn? Discover how Teen FND Academy™ can help you restore balance and get your life back on track. Click below to learn more about our supportive programs and start your journey towards a brighter future! www.teenfndacademy.com/?

Still feel like shit evey day.just not as bad as when I first got it but I do still have to live with it 2 years later and its likely I'll live with it forever since I'm not getting any better

FND is a easy diagnosis for doctors I have seen 3 consultants within 3 minutes they said FND nothing we can do without letting you tell them my symptoms a utter disgrace

Feeling overwhelmed and unsure of where to turn? Discover how Teen FND Academy™ can help you restore balance and get your life back on track. Click below to learn more about our supportive programs and start your journey towards a brighter future! www.teenfndacademy.com/?

Feeling overwhelmed and unsure of where to turn? Discover how Teen FND Academy™ can help you restore balance and get your life back on track. Click below to learn more about our supportive programs and start your journey towards a brighter future! www.teenfndacademy.com/?

Iam an adult with fnd 2 yrs now, I ran across your video awhile back. I belong to an fnd support group on fb, when I come across parents with teens struggling with fnd I always tell them to look you up😊 as you maybe can help you have good inf. Thanks for being you

Dear Doctor Jin Lee, Have you ever wondered why your video views, likes, comments, and SEO scores are so low?

40 years old i developed FND after surgery for spinal issues. It has been 7 years of unimaginable pain and loss of motor function. I have recently started Kentamine assisted psychotherapy and find its helping a little so im keeping my hopes up. I do wish i was able to find mor knowledgeable help here in NY

Thank you.

You’ve got a real talent! This is amazing! 🎉

Very helpful video

Every time I watch your videos, I’m blown away!❤❤❤❤❤

Ma'am doing SEO and promotion will get new views and subscribers to your channel, now if you give me the task of SEO and promotion of your channel videos then I can organically bring more views and subscribers to your channel.

My daughter has hEDS and FND. I also have hEDS. I would love to chat with you about EDS. I love that you made the video but you don't have all of the information correct about EDS.

What is the name of the study?

Thank you for this video and connecting FND and EDS. We went years trying to figure out what was going on with my child. She just turned 13. She LOVES dancing and gymnastics and would aways contort her body. But as she got older she started to get a lot of pain all over her body. She has been diagnosed with FND, Dystonia, Non epileptic seizures ,HEDS, AMPS, Migraines,POTS,ADHD, anxiety disorder,mood disorder,anemia, Gerd, Oral allergies, seasonal allergies, eczema, learning disabilities,asthma, borderline diabetic and is in the process of getting tested for EOS. She had some trauma with Covid and going back to school and separation anxiety. She said she only felt safe with her family at home. She is in chronic pain and fatigue, she was hospitalized for a month for rehabilitation at a children’s hospital. She gets CBT therapy for two hours once a week and physical therapy 3 times a week. This has been a roller coaster of test after test missing a lot of school. I hate seeing her in pain. Some days are better than others. I finally got her an appointment for an FND Clinic. But it’s been rough for her and our family. Thank you for putting out this information. I do my best researching and educating myself to get my daughter the help she needs. She has a great support system and I’m very thankful for that.

Very nice videos but your channel videos need a lot of work then your channel views subscribers will increase a lot

This is very interesting. Can they do other activities of any kind to entertain themselves while doing the breathing, or does that interfere with the purpose? It seems hard for a teen to just focus on breathing for 20 minutes at a time, even working up to it slowly?

You made it sound like those were three magic solutions. For some people, they lessen the symptoms but don't cure anything.

If you’re like many families I talk to, you are not alone. Join the Teen FND Academy Parents Hub FREE Facebook Group to learn more about how you can actually help your teen resolve FND. Yes, it is possible to recover from FND completely-as long as you and your teen take the right approach with the right guidance.

The Teen FND Academy is fully online, allowing you and your teen to start the healing journey NOW. We use a comprehensive parent-teen team approach, so you both will learn exactly what to do-and how to do it-to resolve FND and get your lives back.

Come hang out with us in the Teen FND Academy™ Facebook Group and connect with families who are on the same journey! 💙

Join our Teen FND Academy™ Facebook group today and grab this free resource to start making a difference in your teen’s journey. Our supportive community and expert insights will empower you with the tools and knowledge you need to help your teen thrive, both academically and personally.

Join our supportive Facebook group for parents of teens struggling with FND. It’s a great place to connect with other parents who are on a mission to find the right solution for their child’s FND. Let’s work together to find hope and make a difference for your family!

This is really useful thank you. I am seeing a neurologist because I was not diagnosed when I was younger. The only issue I have found my neurologist has not really explained anything and I only had a few 10min appointments over 2 years. She told me I can't have tourettes because I use a wheelchair and I found out from my doctor that she wants me to do a gastric emptying to make sure there's nothing else for FND. She also had me take medication without explaining why and when I said i didn't think it was helping certain tics she just said to take half in morning and half in evening, next appointment she said the same thing even though I was doing what I was told. Your video has given me more explanation than the past 2 years...

Assistive devices were never intended to cure disorders. I have FND, and I use a custom wheelchair. I’ve been paralyzed for over a year, and it’s kinda the only way I can get around. If my parents removed my wheelchair, that would be neglect. No child deserves to have to drag themselves on the floor 💀💀💀

I have FND, I'm an adult. I know that not all FND sufferers can cope with being on their own during an episode. I need to be coddled, cuddled, soothed, to be told it's okay and "I'm here". Caressing and being distracted by touch helps me a lot. If I'm left alone, I don't like it. I need someone to comfort me. After an episode, having someone not acknowledge what had happened makes me feel like it's not worth talking about or it's being ignored. I prefer to speak about it and them making sure I'm okay. I feel like if someone left me during an FND episode, and not talking about it afterwards, I feel neglected

Thank you for this! My teen daughter has FND. And we are so grateful for your encouragement and information.

This is truely beautiful

Due to FND & Iron deficiency without anemia (IDWA), our daughter was unable to attend school for 2 months. Once IDWA improved, she was able to to do 2 months of homebound school (4 hours/week). Then school was out for the summer. This year our daughter started high school & she went back in person. It hasn’t been easy, but we’re using your FND Action Plan with the school to inform them what to do & not do. Your videos & materials have been so helpful. Thank you so much! 😃😃😃

Very nice and instructive video

Very NIce Video

A very educational video

I would suggest you hold off on the fancy trip to Disneyland until the child with fnd is exhibiting more good days and less reliance on assistive devices or desire to have days off school.

Thanks for the tips but how can I get moving with Pots if I just end up passing out when I do physical exersize?

Myofascial paid syndrome is the most common manifestation of chronic pain. It is very effectively treated with dry needling and electrico-microcurrent. Activity pacing does not help it.

As a sufferer you got frustrating right for us, is debilitating having to deal with it, your nerves doing unexplained things, i wouldn't wish this on anybody, people who don't understand be kind and if you know someone suffering with fnd tell them you are there for them and that you love them. A hug can be everything having to fight the battle everyday

The diagnosis of FND should be considered a good diagnosis- it is something which can be successfully treated!