Strange! Why statins raise lipprot*a? Mine goes down- 10 points in one year.

😢

I wish all doctors had his pleasant manner

Alot of woman have been sexually abused and DONT HAVE FND, most people have gone through trauma at one point in their life AND DONT HAVE FND. Of course if you gather fnd patients and RESEARCH them that they have had trauma and or sexual abuse, why? because you will find this with ANY group of people! Yes trauma can trigger it but it has nothing to do with fnd. I wish they would go beyond talking about this as mental health problems, its so repetitive and going around in circles. So many research papers with 'fluff' and the same information. It's like a dog vomiting and eating his own vomit again and again. Yes, I have FND.

Everyone Lied, Organisations let me down, I panicked and got FMD, I was, and still am fighting dental fraud

GABA increases Klotho production at a very low dose 6mg/kg mice, human equivalent dose is .48mg/kg mixed with water and drunk throughout the day.

❤ Love you, Fredrik ! ❤ Tank you !

You mention relative risk reduction, but not absolute risk reduction. Why?. Also, this all asumes that all Ldl is bad. If it is that bad, then why do we have it in the first place?

I was diagnosed with FND on Wednesday, this video has been so helpful. Thank you

very informative sir. Thank you!

And then theirs me! Diagnosed with FND and yet over ten years later diagnosed with PSP! Thank you!

Fascinating. Thank you for uploading this. I found Professor Raal's presentation very compelling.

This video was quite helpful and informative however functional symptoms don't always require attention. Especially considering the fact functional symptoms can impact a person 24/7. A functional symptom has no known physical cause and refers to abnormal functioning of the body. Functional symptoms also aren't caused by physical and/or psychological risk factors, those risk factors simply increase the chances of you developing a functional disorder. If those physical and psychological risk factors were truly the "cause" everyone would have functional symptoms. "Psychological trauma is to FND what smoking is to stroke, a risk factor but not the cause." - Professor Jon Stone, Consultant Neurologist and Honorary Senior Lecturer at the dept. of Clinical Neurosciences, University of Edinburgh

My hand shake alot

I'm 69, became disabled from FND at age 62 but it took years to figure out this diagnosis. My symptoms are textbook FND. The more I've learned, the more I've been able to improve my quality of life. I'm a veteran so I've had access to lots of programs and services, mostly focused on PTSD. I wish we had FND informed providers near me like you do in UK. Throughout my ordeal I refused opiates and benzo medications, thankfully. My best results have been from Biofeedback and gentle yoga. Especially the yoga. It was a big leap forward when I realized my body can operate well when controlled by habit thinking, just not with conscious focus of thoughts. Frankly, i thought I was nuts untill I saw some wonderful videos like this one to enlighten my point of view. The more I've learned and thus acquired more of a sense of control, my anxiety levels decreased which lessen the conscious focus. When I can stay calm, my habit thinking controls my movements, at times surprising me. :) It may be controversial but I think cannabis helps because it calms me and distracts my conscious focus. Thank you for this video and reading my comments.

Chronic fatigue syndrome/ME is not a psychiatric illness, it is a complex neuro-immune disorder! Chronic fatigue might be a symptom of a psychiatric illness. Please make this difference in your next lecture? Thanks

incredible talk, wow

Wow, what an amazing presentation!

How do I find out if I am Lp(a) null? I have done a DNA test through 23 and me. Is the data already in there to be found? In my case I have good reason to doubt my non-detect Lp(a) level is genetic as the literature states. I am wondering if my non-detectable level Lp(a) might be an epi-genetic effect of my rare combination of diet (low carb/carnivore and OMAD) and exercise metabolic regime (long distance thru-hiker who spends months on-trail hiking 10 to 12 hours per day). None of my 3 siblings have Lp(a) levels that are non-detect. With respect to Lp(a), the literature does not speak to the effects of a zero carb/carnivore diet or daily high intensity long duration exercise. From what I have been able to discern, my combination of diet and exercise constitute a metabolic regime for which there is no published data or research. My Lp(a) is non-detect (<8.4 nmol/L). The lab flagged the non-detect result with an * asterisk footnote stating "Results verified by repeat testing". Small LDL-P is also non-detect (<90 nmol/L). Large HDL-P = 14.5 umol/L HDL-P = 36.9 nmol/L LDL-C = 126 mg/dL HDL-C = 90 mg/dL Triglycerides = 37 mg/dL Cholesterol (Total) = 222 mg/dL Fasting Insulin = 2.6 uIU/mL C-Peptide = 1.5 ng/mL In my case, I am 59 with a history of insulin resistance and a host of associated metabolic problems. I now live on a zero carb/carnivore diet and eat on a One Meal A Day (OMAD) intermittent fasting schedule. I am now insulin sensitive and all metabolic problems have been reversed. No medical problems. No medications. Blood work and vitals are all very good. I had my blood work done after 3 months on-trail hiking the Appalachian Trail (2,200 miles) from Georgia to Maine. I maintained my zero carb/carnivore diet and OMAD eating schedule (with no snacks) on-trail. I hike 10-12 hours per day covering 12 to 15 miles carrying a 35 lb pack over hilly steep mountainous terrain. Heart rate is near maximum for several hours a day during ascents. My resting heart rate is in the 40s.

This is very helpful, I’ve been diagnosed with fibromyalgia and I have spinal cord injury, thats more than 20yrs old. I often wondered if some of my fibro symptoms were FND related. I get sudden headaches that trigger bad shaking of my body, I loose control of body function of my legs to the point of falling down, and sometimes bladder. MS and epilepsy have been ruled out. And talking at times I trip over my words, my fibro fog gets extremely bad. My whole body gets shuts down. Full total system overload. And stress is a huge trigger for the tremors I experience. I’d like to make comments on the Australian FND Hope, but they’ve disabled their comments. Can a GP diagnose FND, or does a Neurologist need to. Our hospitals are back logged with a 18mth to 2yr wait to see a specialist. You’ve provided a plethora of crucial information on this vlog. Thank you.

Very good talk.

Very interesting, and as someone who is still waiting to see cardiology, reassuring. Thank you

He is lip smacking.😟

Thanks awfully.

excellent lecture Thank You..

Thank you for this video and to Dr Glenn Nielsen particularly. I have diagnosed FND for 14 years and as with most with FND my symptoms have progressed and evolved. I started with paralysis (waist down), and gait issues. This has evolved to less of these symptoms but, more to speech, tremor and facial paralysis. Both before and current problems also affect excretory systems too. Given that I know is that flickering lights and bright white car headlights (or bright white lights in general), trigger my facial paralysis, cognitive reasoning and the closing of my left eye; I have often wondered if a clinically introducing a flickering or white light whilst undergoing a fMRI may help to distinguish what is going on neurologically in greater detail. I also know that heat, inability to take breaks when needed and high stress affects my gait and speech and cognition. I am sure these have already been extensively studied explored but, I am very interested in helping others with FND and helping the advancement of treatment and education. Best wishes and once again, thank you. Dan

My mother's lp(a) done after she got MI(2006).. Was17mg/dl!

There is no mention of severe and enduring mental illness and the risks of CVD. This is shocking considering those with SMI have a reduced lifesoan of 10 to 20 years.

Slides are not clear

No question exercises are the gold standard of promoting health- and life span that nothing else can replace as effectively as well as safely as far as known so far.

It was great working for Dr. Baranzini's Lab

What are all the exact tests that need to be performed to diagnose FMD and by who? I had a diagnosis of MS when I was 17 and now I’m 47. I’m still walking around the house with with walker but use electric wheelchair to go out. I Have the same issue with my hip abductors, and a few other things that were mentioned. Over the years I was also diagnosed with Raynauds disease.

I have neglogical movements disorder i need helo understanding dont know enough

My FND symptoms started a few weeks after my first and only Astrazeneca jab which was mandated for over 60s in Australia. I was walking 7000 steps a day until then that was 2 years ago. Still looking for answers which I may never get. Thank you for this very interesting and informative video.

I’m a CHF patient. This drug class is miraculous!!! I couldn’t complete a stress test. I could nearly walk due to shortness of breath. I had many thousands of PVC’s a day. My BNP was abnormal. 3 months into this treatment, my BNP is normal. My Holter is normal. I can walk over 10,000 steps. I could barely across my suite. These drugs reverse heart failure!

4:43 compares Ocrevus to a known less effective drug Interferon Beta 1 A to make it look good.

Ocrevus didn't help my PPMS so I'm in Mexico for HSCT in 5 days (a treatment which is effective in rebooting the faulty immune system of many with MS with cyclophosphide. Rituxan is used after the chemo.)

Invaluable

Fantastic information for someone who has AF thank you

Very interesting. Since Ocrevus is the only dmt currently available for PPMS, I'll have to continue taking my chances with it. Hopefully the BTK inhibitors get FDA approval soon.

Would CAR-NK therapy spare the B-cells unlike CAR-T?

This is great!.. Thanks for posting.

why was there a rise in MS during the pandemic?

how does one know whether there is inflamation present still?

My neuro psych has just diagnosed me with FND. I'm in Australia

This was a really informative lecture about how FND can be treated, hopefully Australian professionals will listen to your research. I also found it sad and confronting in regards to how early death can occur however I understand this as my lifestyle has completely changed in 4 years, going from a completely busy on the go person to an extremely idle, exhausted person

Here we go again. Scare the hell out of people--but do not worry we are developing magic drugs that will come to the rescue and make big Pharma billions of dollars. Its all about the health of your endothelium--get that right by getting fasting insulin down HbA1c down, blood pressure down uric acid down.Get rid of your intra-abdominal (liver and pancreas) fat. Get your triglycerides down and your HDL up. All of this can be done by diet and exercise and time restricted eating. If you do that you will have healthy blood vessels with healthy endothelium and Lp(a) and LDL-C will not matter, because there is no damaged endothelium for them to attack. But no, modern medicine targets the particles which end up in the damaged blood vessels because that's where the money is --in drugs! Take these expensive drugs for 5 years and instead of 3 out of 100 having a heart attack 2 out of 100 will have a heart attack. Wow we have decreased the heart attack rate by 33%. So carry on eating a SAD diet and we will give you an anti-dote which you need to take for the rest of your life because lifestyle does not affect your Lp(a) levels, only drugs will do that! The studies that scare you are of course done in the metabolically sick people who are that way because the USDA determines your diet even though they represent the people making and selling the food! Guidelines by eminence, not by real evidence, just big Pharma sponsored trials that ask the wrong questions!

Anyone know of any lpa trials?

Anybody here have FND with sensory symptoms? Like numbness, tingling, prickly sensations, heat sensitivity?

Jardiance