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So SFN has to be painful ? if I have the symptoms for 10 years, but they're not painful, they are rather annoying, they are not getting worse, what could it be

So, in essence it looks like ALS but with much longer clinical hx, sensory and other systemic symptoms.

Health is the foundation of good development. International cooperation 🕊️🤝in the field of research and new solutions is a step in building the best system. For good future. For good cooperation. Great respect from 🇵🇱🕊️🤝

Can decades of benzo use followed by cold turkey withdrawal cause or worsen "idiopathic small fiber polyneuropathy?"

Poor presentation

Very useful information! Thank you Dr. Martinez!

I need your help plzzzz. I am from india and my father have MFS since 5 to 6 days we have taken immunoglobulin 5 day treatment, but there is no chahge in conditions. He can here us slowly move he's feet and arm but not enough power to pull up the feet. Plzzzz guide me what to do next........

how cruel

Very informative presentation

Amazing presentation !

The only to see😅 I tut dish🎉 😂😂 Moommyfyss😅ceo😅koi😂😂😂w

good luck Shota

Why pain and itch changes locations in the body?

I have TLE and you described it perfectly but i would add it feels like leaving your body and seeing yourself from a third person view, or visual hallucinations. I also rub my fingers and can't look in the mirror

Congratulations Unni

Is there a different type of Dopamine Agonist recommended with Parkinson’s Plus?? My father who a certain type of Parkinson’s Plus - is having terrible reactions to Carbodopa/ Levidopa.. hallucinations, severe constipation- but without it lacks dopamine and not getting out of bed the same.. So needing something else as a Dopamine Agonist that doesn’t cause the horrific REM disturbed sleep issues and more.. Any recommendations are appreciated 🙏🏽

Where is cbd oil? Niektóre osoby reagują dobrze tak jak wszystkie inne leki zalezy od danej osoby. Mam diagnozę a ci mi wciskają nieskuteczne leki jak na depresję nie mam depresji a lek nic nie pomaga lekarze nie pomogli mi przez 37 lat w Niemczech i Anglii dawali mi leki na depresje co jest głupotą tych z listy nie chcą mi dać jeszcze. Nielegalnie zamówić bo się żyć nie da bez leków jak pracować. Niektórzy neurolodzy nie widzieli niczego a mi drżą nogi ręce głowa głos. To tragedia dla ludzi którzy nie mają diagnozy albo ich leczą na co innego. Jak żyć gdy lekarz drugi rok odmawia mi recepty ale walą na depresję od razu jak cukierki to tragedia

You did not list b6 toxicity in your video. It is one of the most common causes of SFN right now and doctors are never knowledgeable about it.

Is there any cure for this disease.. we are just getting treated here.. please help!

Hey. My old doctor 😂😂

Functionsl disorders are not psychiatric.

very helpful lecture mam.....

Covid did this to me. I had the mild case. Loss of smell and taste, not other symptoms. Then few months later I am in the wheel chair.

Much informative. ❤alot of thanks to u.

Tq mam

Do you offer rotations in Neuroradiology and/or Diagnostic Radiology?

Also, he had meningitis as a baby and my grandfather is epileptic. Would these be factors?

Hi there, Im now convinced my son has this. We have had every test and all clear no problems, 3 years of tests and doctors. I noticed today he is out of it when his pain hits- he can't converse with me. He speaks gibberish. I thought that was because of the pain but today it looked more like a seizure and he fell asleep afterwards. this happens every couple weeks.

Hello thanks for the video. I'm very interested by the RLS videos , because since one week ago, i know that i'm a RLS person. First traitment for me, since one week, i take Sifrol 0,18 mg. Coul you tell me where can i download the slide, please ?

What test did you use for ttg6? Was it Cyrex Array 3?

Thank you for this comprehensive presentation.I have been a Doctor for 3 decades and this past year developed symptoms of fasciculations , cramps , weakness etc . I have seen 3 neurologists all suspect that I have ALS but the last Neurologist did what the others did not do . she put a tuning fork on my limbs and noted a loss of vibration sense in both feet, she still suspected ALS .However the penny dropped .and after exploring the differential diagnosis.I discovered I have other symptoms such cold paresis, intention tremor .fertility issues , bladder neck obstruction , Gynaecomastia etc . I am awaiting to have an extensive assessment in a specialist centre in The Netherlands and hope to get a clear answer.

Doctor i have a seronegative celiac disease. I was diagnosed with 3c Marsh atrophy in 2018. Last year i took another endoscopy and I still had a Marsh 3a atrophy ( i have been dking a ketogenic diet). Now i receiced my last endoscopy result and i have been diagnosed with gastroparesis, incontinent Cardias, iron and folate deficiency. I have been diagnosed with the Babinski reflex 6 years ago Is Babinski related to Ms, Gluten Ataxia or ?

Sir i want some help on HOMICIDE POISONING.

Rao shaab rocks❤

thank you for this presentation Doctor! very Informatiove!!! * minimize though the "amm" filler words .

This is the best presentation on Kennedy disease that I have heard on KZbin. Excellent work.

This is bad 😢

Thanks a ton. Excellent presentation!

Very good presentation. Thanks alot!

Treatments are terrible, we need regenerative treatments for neuropathy like IVIG, no more of these bandaids, no thank you I’m getting IVIG, I’ll advocate for change to how treat neuropathy, we can’t keep doing the same thing over and over again, it’s insanity

Thank you

इस बीमारी का क्या उपाय है

New studies linked ADEM with COVID-19 , reference Amy T Waldman, MD

❤❤ video is very nice

Well done.

The video was informative but it was hard to hear at times. It had an eco and it kept cutting out unfortunately.

I have watched several of these videos and it's interesting that they say sudden movements can cause muscle spasms. I notice upon waking up from sleep in the morning I sometimes move my leg suddenly and it almost seems as though I hyper-extend it and that sets off a severe painful muscle spasm. Now I try to be conscious of how I move my legs in the morning when first waking up and try to move them slowly if I can catch it before it happens. I have also had myoclonus a few years ago whenever I started falling asleep which started before the muscle spasms, and sleep studies found that I had central sleep apnea and Biot's respiration. I could not tolerate CPAP and it actually made it worse. This seems to support the theory that muscles fight against each other in this condition. My treating professionals at the time never considered this diagnosis. I was put on low flow oxygen at night and that did resolve the respiratory part. I also am hyper-reflexive. One year I fell 7 or 8 times and it was like a tree falling as they describe. I never knew why. My legs just stopped responding and I fell forward without being able to brace myself. I have had alot of stiffness which affects my back and hip area, and often have to twist from side to side with my knees bent first in order to get out of bed. Nobody put 2 and 2 together but this might very well be what the underlying condition is.

So many thanks...I have suffered with SPS since 1988, and after watching your video and educating myself I was able to provide a profile of my case to my family doctor. I was having vibration in my larynx. A trial of 5 mg of Valium has eradicated my contractions, my hunchback, my pain in my foot and arm that felt like they were going through a meat griner. Investigations can now begin, and I can share the results with you if it would help you. I have the P.E.R.M. diagnosis that began with an anoxic event and had been given the diagnosis of anoxic encephalopathy requiring intubation. I had 2 children as a disabled person. My body is riddled with deformities so my condition is end-stage but maybe I can be useful diagnosing other people inflicted with this crippling syndrome.

Very good 👍 👏 👌 😀 ☺ 🙌 👍 👏 👌 mamu ji