Literally every symptom..along with random sweating and occasional itching.

That’s my Abby

Thank you for the program

My daughter is 19 years of age Has Rhamatoid Arthritis for 6 years All of a sudden had a seizure , than hospitalised & than diagnosed with FND. On meds now & done some counseling Was fine for a month & than took her for a holiday On holiday she had 2 seizures Can you assist me?

Good evening from South Africa My daughter 19 years of age has been diagnosed with FND. All EEG results were clear. She was fine epilepsy free for a month. Took.her on a holiday and in a week had 2 seizures. How can you help me?

Do you have an example of ABNORMAL eye movements to compare with this test?

Yeah... it's called moving somewhere colder! 🤣 At least that's what I did!

Your Video Content are Amazing and Engaging, Would you love some recommendations and suggestions for improvement

Is there something wrong if I lose my balance when eyes closed.

Is there any solution for writers cramp(focal dystonia)?

What is the eye test called?

I have been diagnosed with FND symptoms began a few weeks after my 1st and only covid jab which is now no longer in use - banned or pulled from use in most countries. I was a fit and healthy 68 year old until i had this jab. Could it have caused my FND or contributed to developing the problem? Hope you are free to give me on honest answer. Thanks in advance.

Hey Dr. Russell Teames, I'm a huge fan of your KZbin channel Desert Brain and Spine and have been following your videos for the last few months. You consistently deliver top-notch content, and your passion and effort shine through in every video. I see incredible potential for you to reach an even wider audience with a solid KZbin strategy. I'd love to schedule a short meeting to discuss how I can help you grow your channel faster. This isn't a sales call, but rather an opportunity to share ideas and offer assistance. Thanks for your time and for creating such amazing content. Keep up the fantastic work! We can find a convenient time to chat. Let me know if you're interested.

I highly suggest that anyone who gets diagnosed with FND get an evaluation for ADHD/Autism. I was diagnosed with FND in 2016 after symptoms began in 2009, after graduating highschool and beginning college. This year I discovered that I am AuDHD and after discovering some of my autistic triggers i have learned my fnd symptoms occur in response to sensory overload. If i dont remove myself from the stressor then my body does it for me.

As a sufferer and still trying to learn I would love to meet someone like this, I'm in the uk and there isn't alot to help, I would love to know the book you read and some of the breathing exercises you practiced,,, it would be a great help to us all who are struggling and suffering with fnd and maybe it can help, that's what it's all about sharing information and being together as we know how it feels

I am finding that doctors are ignoring secondary autoimmune meningoencephalitis which seems common after a initial meningitis and/or encephalitis. Since most doctors think meningitis is an infection not inflammation. Most will not check for or even know mechanical meningitis and chemical meningitis exist and infections is just one of three scientifically known causes. Merely because doctors never heard of it most will claim no such thing. That is not a scientific or medical reason, but an opinion based on lack of science and/or facts. This is autoimmune meningoencephalitis caused by initial meningoencephalitis (infectious, mechanical, and/or chemical). Even the description of patient first recieving damage fits with the symptoms described by science. I would ask if this patient experienced another form of meningitis or encephalitis or a condition that can cause it. This is something done with MS as a predective factor for developing this form of idiopathic autoimmune meningoencephalitis. More than likely autoimmune meningoencephalitis developed if patient continues to report symptoms synonymous with spine and brain inflammation (meningoencephalitis) after the intial spine and brain inflammation shock. There are no tests, scientifically speaking that can confirm this. Multiple tests must be done to rule out possible common causes first. If common causes are ruled out the test like MRI are helpful but not definitive in diagnosis due to negative MRI does not rule out inflammation. It may show but also does not like in smoldering MS. Doctors then must go by patient reported symptoms and medical history. Did patient experience spinal and brain inflammation event in the past(reference meningitis article for possible causes. If yes then a doctor after ruling out possible common causes may diagnose patients accordingly based on patients symptoms and medical history. No test give can give definitve proof of whether you jave the condition or not. MRI'S can not even give a sure result and should be taken along with other test to be as sure as possible. Doctors are commonly using MRIs alone to determine a diagnosis. This is wrong and technically malpractice considering how serious this condition. Doctors should be educated enough to know MRIs do not provide definitve proof of inflammation conditions. False negatives and positives are possible. That's why more test are done. But if only the MRI was used to diagnose then this is not scientifically or medically correct diagnoses. First if lesions are too small for MRI to see then the patient may experience all the symptoms without a MRI to showing anything wrong. MS patients can progress without new lesions or at times any lesions at all. Smoldering MS which does not show is being thought of as fueling progression. OVERVIEW OF ACUTE AND CHRONIC MENINGITIS www.ncbi.nlm.nih.gov/pmc/articles/PMC7132757/😮cv we

👍👍

Hey Dr. Russell Teames, I recently came across your KZbin channel and was impressed by the quality of your content.To grow & increase the view of your channel you need to optimize your videos. Inspite all of your efforts videos are not being viewed. Video SEO Score is very low. The title, Description, and Tags are not SEO-friendly. Videos are not shared on Social Media platforms and many other problems are found on your KZbin Channel. If your channel is optimized a little and if the videos are SEO friendly then your channel will rank very fast and your channel will grow. So immediately need Promotion,SEO for your Videos & KZbin channel. Do you want to improve those problems and grow your KZbin Channel?

🙏🙏

🙏🙏

Sir, how can we consult u?

Sir, how can the symptoms b improved?

Sir, abnormal conduction from right tibial nerve. Pots with suspected autonomic dysfunction.had moderate to severe L4, L5 S1, S2 nerve compression from years together can it lead to autonomic dyafunction? Hv a cyst in pituitary gland with loads of symptoms n vision issues. Rhombergs is alwaz positive. Now hv hypertension also n dat too postural most of the tym. Wht can be the reason for all diz. Suffering a lot

Oke

Please spread the word! A lot of us suffer with a broad spectrum of symptoms they come and go. Some are minor and others more severe. I live in a huge city and can’t find treatment.

Lol. I know that feeling now when I'm engaging with an activity and then I can now read my body and all of a sudden, OH I need to sleep NOW. Thank you so much for this chat. I relate so much to her story. I'm one year into this diagnosis tho it's been slowing coming on for 5 years prior

cathy crushed 👑

That's a cool challenge I'll try it! Edit: I thought I couldn't do it but I accidentally lifted up my left leg instead of my right one. I did it!

My what?

More content please! People helping people will make me subscribe and like almost every single time!!!! Good job👍

Need that tip! Thanks doc!

Great tip doc! 👏🔥💯

I had a simple knee surgery a knee arthroscopy, 5 years ago was told I had suffered femoral nerve damage. Still suffer from quad atrophy, weakness and can’t lift my leg after 5 years and the nerve is still damaged, was told by many specialist that the damage was so severe that it actually cause muscle damage as well not just weakness. Mri proves that there is indeed damage. Not sure why to do 🤷🏻‍♀️ I’m actually considering amputation at this point and trying to love on with my life I’m only 23 had the surgery when I was 18. As soon as surgery was done doctors dipped never se him again tried to sue him but he withheld my medical records from me and my lawyers along from my dad instill statue of limitation was done. Now I’m stuck. I’m truly lost, wanted a whole life I wanted kids and a husband but I don’t think I’m gonna ever have that now that I’m disabled feel worthless can’t work can’t walk can’t sit for very long also now do to a back injury from a fall from the knee, in other words I’m screwed sorry for the long rant