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I've been diagnosed 15yrs ago with cluster tic syndrome by Dr Steven Graf Radford at cedar Sinai in la. It started right after FESS sinus surgery in 2001. Is there any new treatment for CTS? THANKS BRAD

This does help me thank you.

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Guys let's be very careful. They are some issues that are more spiritual than physical or medically. This man in this video is going through what is called partial spiritual possession. There is a jinn or unclean spirit alive inside his belly. The only way to get it out of your stomach is by placing a Bible or Quaran on top of your stomach . That spirit is unclean and can't stay under a "holy book ". It usually passes from one person's stomach to another likely through sexual comtact. Signs to know it's a jinn. Involuntary throbbing as shown in the video , feeling weak or drained and having a dull uncomfortable pain on that spot. Feeling it throb when using holy name like Jesus , holy mary etc.

I had GBS after getting vaccinated. I was vaccinated with Pfizer. One day my legs felt heavy. It felt like my feet had magnets and the ground was made of metal. My finger tips were tingling and numb. I went to work and within an hour I knew something was really wrong. The hospital didn't find anything wrong with me and sent me home. The next morning I could not get out of bed. 911 was called and I was transported to Health Sciences center in Winnipeg where they immediately did CT scan, spinal tap, and later on a MRI. I was diagnosed with GBS. They did treatment in my arm. The treatment did not improve my condition. I had to then get a stent put in my neck and had 5 treatments of plasmapheresis. It worked almost immediately. I was transferred to the rehab hospital (rehab staff were so great). After 1 month I was determined to leave the hospital on my own two feet. I was able to beat the odds and get out 1 week before Christmas. The process was not over. I did physiotherapy for 6 months and was able to fully recover. Now I'm back to playing hockey again. I don't like how the governments pushed for vaccinations. I took it to play hockey because I couldn't if I wasn't. But the vaccine took hockey from me.

I had GBS after getting vaccinated. I was vaccinated with Pfizer. One day my legs felt heavy. It felt like my feet had magnets and the ground was made of metal. My finger tips were tingling and numb. I went to work and within an hour I knew something was really wrong. The hospital didn't find anything wrong with me and sent me home. The next morning I could not get out of bed. 911 was called and I was transported to Health Sciences center in Winnipeg where they immediately did CT scan, spinal tap, and later on a MRI. I was diagnosed with GBS. They did treatment in my arm. The treatment did not improve my condition. I had to then get a stent put in my neck and had 5 treatments of plasmapheresis. It worked almost immediately. I was transferred to the rehab hospital (rehab staff were so great). After 1 month I was determined to leave the hospital on my own two feet. I was able to beat the odds and get out 1 week before Christmas. The process was not over. I did physiotherapy for 6 months and was able to fully recover. Now I'm back to playing hockey again. I don't like how the governments pushed for vaccinations. I took it to play hockey because I couldn't if I wasn't. But the vaccine took hockey from me.

I have blepharoclonus without Parkinsonism, I’m 25. It hasn’t improved in 2 years, and it is painful…it has severely impacted my sleep.

Congratulations Lidia

Sometimes people want to be doctors they don't even know how to diagnose anything for what to subscribe what's the point of this dumb video

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I know 3 friends that got GB after covid 19 vaccination. That stat is insane!! I'm just one guy that doesn't have a lot of friends.

I wonder what could have become of me if you weren't the one who came to an interval in my life. Thank you for curing my Hsv1&2 naturally Doctor Orias. I immensely appreciate you ........

Dr. Obulor thank you so much for your dedication, expertise, and positive impact on health. I am truly grateful for all you do doctor Thanks,

Dr. Obulor thank you so much for your dedication, expertise, and positive impact on health. I am truly grateful for all you do doctor Thanks,

You not only love your work but you also show care and comfort to all your patients, I want to thank you for the extra time you took to ensure my infection is completely gone. Your medication worked successfully, Thank you, DoctorOrias

Mine are everyday 2-7 times a day. Nothing has worked, and no Dr' will see me. I haven't had a dr. Fur 4 yrs. I'm not very nice some days

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Yeah I am also suffering, there are no any enough funds to find treatment because the quantity of patients are low.

Where on the JC index should one be concerned about PML risks… 1-5 ?

Wow , 20 million dollars , My husband has Ataxia, Very little here in nz is known , about it and what to do , NZ needs help in this research . Thankyou for this .

How does coke help? My brother gets these and for about 20 years now. He fears going to sleep. He will wake up with a long one then smaller ones all night every cpl hours all night long. Its a constant brain freeze and behind one eye. He looks dead and he cant move or talk whike he has one. Its bad bad pain :(

Interesting how that mess on the EEG, looking like someone spilled ink on their page, was actually the AFTERMATH when they passed out. I thought it'd look like that while I'm convulsing, God EEG techs are amazing.

Abdominal epilepsy

Very costly 😢

This guy knows his cluster headaches.

Dear GOD please heal me from This. Heal tumors

I got GBS after my 3rd Pfizer vaccine for COVID-19. I am NEVER going to receive an M-Rna vaccine again. I was in care for many, many months. I can now walk and care for myself, but am still disabled and live with severe pain. No one is following my case in the USA!

Going to the chiropractor be like

That's what my eyes are doing!!! I'm now having B12 injections due to mthfr/genetic polymorphisms causing an issue with B12. I have SO many symptoms now - including POTS, pins & needles in my hands & feet, having trouble with my balance, walking (ataxia), proprioception, full on dizziness & lightheadedness and sometimes my speech becomes affected too. B12 deficiency is so debilitating. And often, it will not show up in ANY tests - ie all your tests will come back as 'normal'! Dizziness can cause nystagmus (obviously). Read/refer to Dr Chandy's book - 'B12 Deficiency In Clinical Practice (Doctor, you have me my life back)'. Also, I found out that deficiencies in hormones can cause dizziness and issues with your ears too - and hence your proprioception is affected - and so all of the above can cause nystagmus!

Hello. Would I be able to get permission to use this video for a commercial website? I would not be selling this video, I would just use it as a GIF for aesthetics on the company's website.

What the difference for vertical downbeat nytagmus?

I’m a 35 year old with a grade III anaplastic astrocytoma. I have three children. I had 90% resection on a golf ball size tumor on my left parietal lobe. I am currently deciding on whether or not I should do chemo and radiation. How do I apply to get in on the phase IV clinical trial?

My heart rate and blood pressure was in the toilet on the heart meds The block on the occipital did not work I had cluster 20 min later I need a Dr here that would see me during my clusters

What a new treatment please tell me als mnd please help me als mnd

Bro's HUNGRY

Hii

may be found in schizophrenia

Excellent!

I had my Syn-One test three years ago. It has been very interesting seeing the evolution that CND Life Sciences has gone through.

Until and unless this arbitrary division of disorders of nervous system into so called neurological and psychiatric one are not unified this concept of brain health is nothing but a joke

That doesn’t look so bad

My friend tenses up like being electrocuted then one minute after crashes but still awake then looks at me bewildered like he is back in the room

I’ve been having episodes for more than 10 years. People don’t understand the amount of pain they cause. It’s debilitating. Mine always follow the changing seasons. I recently went around two years without a cycle and then out of nowhere, this year, I’m having another bad cycle. Mine come on at the end of the day when I stop being active. If I stay going, they tend to be mild or not come on at all. It’s soooo frustrating. The dread of them coming on just sucks. It’s life altering.

This is Reverse ocular dipping … suggesting viral encephalitis or metabolic encephalopathy or pontine infarction…. It is not ocular bobbing

Vitamin D Regimen.

240p :(

Hello! I learned about a new drug from ARTHEx Biotech that can greatly help people who have myotonic dystrophy. Do you have any predictions as to when this new drug will be available for purchase?

creepy

Thank you!