Відео

Thank you! Great explanation!

Dr. House brought me here! 😂

makasih ya dok huhuhuhuhu :'(((

This guys the real deal.

So... I'm recovering from grade 3 and 4 retinopathy due to prolonged hypertension. My vision has been effected. What foods and vitamins can I take to help with my recovery?

My eyes checked out by retina specialist bc I see white flashing things when I blink. There is no issue, even no issue w the gel. He’s sending me to a neuro-ophthalmologist. Anyone get this?

Who needs textbook when we have you!

I was diagnosed with classical ehlers danlos syndrome.. after multiple organ prolapses. I also have other things… then I come back with FBN1 mutation. 🫡 I actually met one other woman like me with both. She’s in Scotland 🤍

Wow ty

You are a great teacher. Your lessons are memorable

Great job! Thank you doc

Only explanation on the internet about these tests that made complete sense!! A+++++++++++++++

verdade

hello i was having ptosis since 2009 and diagnose in 2022 with ocular myasthenia gravis and tested acetyl choline receptor negative and no thymoma in ct scan test . the neurologist prescribed pyridostigmine only and said no need to take steroid . I just want from your advice what should i do, please dr.Andrew

some of the best teachers I never paid for. Respect from Pakistan Sir. One day I will meet u and thank you wait for it

It's really clear and helpful concept explanation, your channel is really a youtube gem. thank you for teaching with such passion dr.Lee.

My ventricles are slit and my shunt is disconnected but the neurosurgeon I saw said I don’t need it anymore. My vision is “blanking” out sometimes (not going black) and narrows at times, though

Thank you Dr. for ACKNOWLEDGING that MANY patients can and do suffer long term/indefinitely, without acknowledgment or support from mainstream medicine bc the CDC is failing by not putting the 2 missing bars back on the Western blot test which they REMOVED in the 90s for vaccine which failed. The CDC needs to get on the stick with Tick borne diseases. (Not only Lyme.) Keep it up!

Can’t take this Drew Carey guy seriously…Whose blood is it anyway? 😂

Experiencing this for 4 years. Nothing was found. It gets progressively worse. First i saw only 1 ghost image above the actual thing. One mont ago a second one developed bellow. Since today I’m seeing one in almost every direction. Please if anyone finds a cure, tell me.

Thanks Doctor. Always seeking more knowledge to better treat patients.

Thanks sir

🎉amazing

Good

Thank you!

My child is just diagnosed with ocular melanocytis in one eye (sclera, iris (heterochromia, and fundus). I have amblyopia since always, did not react to early treatment, and just found out I have unilateral hemianopia in the amblyotic eye (because I am studying the eyes for the first time). I also have vague heterochromia, and suspect melanosis/melanocytis in the optic nerve in the amblyotic/hemianopic eye. Is it hereditary? Should we be tested? Are there specific genes to look at?

_I am so happy for my Sister, she got cured of her Multiple Sclerosis just few weeks of using Dr Madida Sam herbal supplements🍃🌿🌿._

My daughter just got diagnosed with Paresis of accommodation, bilateral. Is that the same as paralysis? She also has convergence excess and Deficient saccadic eye movements. Vision therapy is being suggested. I’ve heard good and bad things

This was by far the best explanation on the internet, and in less than 6 minutes. Love it, thank you.

This was great

Thanks a lot sir.

what about cta with contrast? thanks for the video

Hello. I as well as several people have had photopsia after 360 retinal laser. No retinal detachment. I was wondering your thoughts on this?

You did not MENTION muscular input to the brain. Leg CONSTANTLY trying to gain balance when on a moving platform ( a boat a sea) comment please

Hello Dr Lee, I am a 56 year old male with a Trochlear Schwannoma, my understanding is this is the rarest of tumors. This tumor is causing me to have Trochlear Palsy in my left eye. I have seen Neuro Ophthalmologist at both Mayo and Barnes in St Louis. I have chosen a wait and watch approach rather than surgery or radiation due to its location adjacent to the brain stem. This location make surgery a non option and radiation a dangerous approach. Would love to hear your opinion on my situation?

What the management for tectal RAPD

Brilliant!!

Thank you so much,this is just what I needed, a precise, easy to understand video. I have had high LDL since my thirties, I am 63 now and it is 9 now, I am allergic to statins so am booked in to get checked for FH, I can't check on family history as they have all passed.

I’m been suffering with this for years, makes me really unwell. I’ve also just recently been diagnosed with bilateral vestibular loss & pppd. I’m worried I’ll never get my life back . Been told it’s going to be hard to treat as I have ME/CFS and Central sensitivity syndrome on top of everything else. Starting vestibular rehabilitation next month to see if it helps with anything 🤞🤞

Superb

În limba română

Thank you! I was diagnosed with Cadasil but before the blood test to confirm this diagnosis my neurologist wanted me tested for MS because she never heard of Cadasil and my brain MRI showed all the typical lesions. Thank goodness for the radiologist who flagged my MRI in his notes to rule out Cadasil! I googled it and it made sense from for my mom’s side of the family where many family members died young of strokes and Drs couldn’t figure out what was wrong with them, including my mom. She was also mis diagnosed with MS. Unfortunately there is no treatment or cure for Cadasil, but the worst part is when drs want to prescribe the wrong medications (blood thinners) to us not knowing that will cause our brains to bleed! My mom died not knowing she had Cadasil and had been placed on all the wrong meds after her strokes.

ive been having this for years since my teenage that time i thought i had a vision problem i always tell my mom maybe i need glasses, now im 30 years old, it happened to me just today so i came again looking for more information about, because today it got worst, it usually takes few minutes but this afternoon it took way longer than before. it doesnt happen everyday, sometimes i dont experience it for months. ive discovered something is that everytime i drink too much coffee it happen, i dont usually drink coffee but sometimes when i sleep just 3 or 4 hours i do drink coffee at work, i dont know why but everytime it happened to me ive had coffee and im more sure about this today

and ofcourse there is no treatment

I have semi facial myokiyamia what is the solution plz tel me sir last 2 months I have this issue am so scared

Bloody brilliant

pen is running out of ink

Great thanks sir.

I had Horner Syndrome in 2019 after cluster type headache sent me to ER. CT scan, MRI, nothing showing internally. Obvious ptosis, miosis, and severe pain behind eyeball on one side. Took weeks for pain to go away but still deal with ptosis and miosis that comes and goes. Had obvious anhidrosis on side where pain originated, just on forehead. Anhidrosis has gone, no more cluster headache since that day. Thanks for the video, very informative and interesting for me!

short and sweet.thanks sir