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Hello, It's really great ❤

Dr. Hussain was part of the team that cared for my husband in his last days back in 2013. My husband did pass away from complications from a stroke. Dr. Hussain was very kind and I have not forgotten him. I am happy to see this good man is successful in his career all these years later.

Do we patients with a symptomatic arachnoid cyst get an excuse for more than 40 years of medical gaslighting by you and your colleagues worldwide?... And finally, outdated and incorrect information that is still published is removed. I almost died, my arachnoid cyst was monitored since the late 1990s... I did not even get a painkiller, my arachnoid cyst was the size of a mango... in 2014 the symptoms became worse and I had to suffer from hydrocephalus until 2021. proptosis, midline shift over 7 mm, mass effect... more than 7 years of hellish pain... I suffered permanent brain damage due to late intervention. I'm not the only one in the world who has had to fight so hard to get help. most of my fellow patiënts are going through hell with doctors sending us away. many of us have been left handicapped for life by intervention far too late. We deserve a sincere apology. I am one of the arachnoid cyst warriors. I am from the Netherlands.

I had this procedure performed on me 4 days ago. The only reference point I had of the pituitary macroadenoma was a brief glimpse of the original mri from 20 months ago. Having now seen this video I understand why my nose is so heavily splinted and packed! I also now know what an incredible job my surgeon did on and for me. For a patient, a brain tumour like this is an abstract experience. It was there, it’s now gone, fortunately it was non-symptomatic though it would have become so over time. Thank you for the video, a unique view of what happened in my head on a Wednesday afternoon in August.

I'm 49 and barely figuring this out because a physical therapist finally gave me a name for my hypermobile joints. I'm constantly popping in my back hips, knees, and feet, I'm double jointed but not so flexible. I was supposed to wear braces do to bowl leggedness as a child and had supposed growing pains at 10, TM J since 15, hernia, spasms, and bruising, no one believed me, as I've been diagnosed with fibromyalgia, I have IBS, I constantly have spranged ankles now.

Dr. Souweidane removed my 11 mm cc a week ago today. I feel great. No cognitive deficiencies I am aware of. Dr. S is a great man and his staff is awesome. I was discharged the day after. A day and a half later we went and walked the Metropolitan Museum of Art. I am so grateful.

Dr. Souweidane removed my colloid cyst one week ago today. I was discharged the next day. I have no residual memory deficits. Sight headache. Only taking Tylenol otc. Mine was discovered incidentally also. I wanted it out because of my age (70) and good health now and wanted to control who and how it was removed. Not many do doctors are trained in Endoscopic removal. I did not want it removed by craniotomy. I traveled from Florida to NYC just to have this doctor do this surgery. No regrets at all. Excellent doctors, nurses, hospital.

So after the surgery the headache gone

I ' ve been so interested to hear ALICIA speaking english and she does it pretty well, Is there another video?

My son is currently in the Smiths Falls Hospital with this. We are all very worried awaiting his MRI results. He had a very bad headache last weekend and was told he had a migraine and sent home. I think it may have popped however he still feels some pressure in his head but no pain right now.

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Candace Pert is my guru. I listen to her audiobooks on repeat. She has helped me in my quest for self-knowledge and understanding. Thanks you for this presentation. looking forward to reading the biography.

How can I contact Dr. Jared knopman? My husband just had this procedure 3 weeks ago.

Dr. Stieg Are there neuro surgeons in Califorina who can evaluate my headaches and the constant moving of this lump in my head? I feel a lump that moves from the top of my head to now to the left side.

That's not true.

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Very informative and well put together!!

I can’t believe more people haven’t seen this! As a left-handed woman who comes from a left-handed family you are describing my biggest frustrations living in this society.

The Work-Work balance is a real deal💯

Awesome, so happy this young man is doing well and I am certain the Dr Steig had to have a wonderful feeling that this young man reached out to him after all these years !

Amazing!! 👏🏻👏🏻👏🏻

That's a great lecture and thank you everyone. From an EDS patient prospective, I found out that NASID was not effective at all because Prolo therapy approved the opposite as promoting some tiny inflammation at some defected ligaments / Tendons came out with a very effective results as it helped in tightened these ligaments / Tendons and that's what we wanted to do for long term treatment plan. Dr. Moustafa Ibrahim

Please remove the 'music'! It makes understanding much more difficult!

You guys don’t even know how to pronounce it. AYlers-danlos, not ERlers-danlos

This was a great lecture. Thoroughly enjoyed and learnt.

i don't think it's img friendly

I’m so proud of you bro. TM

excellent

Thanks a lot John. I hope I can understand my dad's treatment better now

THERES NO SUCH THING AS A COMMON SENSE democrat Like unicorns....THEY DONT EXIST

Thank you for this very informative presentation, very helpful 🙏.

I've just gone through this 2 weeks ago! Was in intensive care for 15 days! The treatment was amazing! Quick diagnostice,ctc Scans,cocktail of meds,Quick interventuion. Sonar Scans 2 away. After 14 days had last ctc scan and home! I must say i am so lucky as I am home now,a slow recovery, 3 months, but I feel no impediments,yet, just a little slow with memory for now. I thank the medication services in The Czech Republic in Brno Svarmty Anna

RUclips channel video has a bad SEO score of Due to this your subscribers and views are not increasing, and the titles, descriptions, and keywords SEO should be done correctly only then you will get good results. the same problem in Video every.

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Hello Doctor ,,I'm 49, I have a bigger CBT 10*6*7.6 cm ,, what can I do, I'm living In Libya?

For me, definitely hearing loss, a little tinnitus, get light headed or muzzy headed and weird taste.

'promosm'

I have this… only 2mm at the moment that I’m aware of … I’m terrified. I have all the symptoms and have for 3 years now, no fluid build up but life has been difficult

I know this video is old at this point so nobody is likely to respond, but what happens with the removed vomer/cartilaginous septum afterwards? is the patient just left with, like, half of their septum or was there another procedure done to replace it? I know at 5:12 it's stated that the removed septum may be used for reconstruction, but is this meant as reconstruction of the septum or reconstruction of the sella? Would be amazing if anyone could answer this!

Very nice demonstration Sir for budding skull base Surgeons

I have Hemifacial spasm over 5 year now and when I smiled is show crooked, I’m very worried. Can you help me how can I get my mouth normal again, I have vestibular schwannom tumors too.my eye stop twitching but my mouth is I can feel the never on my face. I do boxto every three month .

Really i have colloid cysts i live uk Can you help me

Dr. Stieg, I have had what I would call Type 2 TN on v.2 and v.3, but no MRI or MRA scan find a problem. However, the pain is pretty darned obvious to me! Now, we toss in one more factor that may be a contributing cause. Just last week I had an angiogram and it did show something quite condemning to me--an 80% blocked artery. FYI, I'm 83 and swim regularly, play the tenor sax and restore old cars, so I'm not exactly dottering old man with one foot in the grave. My doctors are now saying rest, don't bend over, and resist your normal level of activity. I am not very happy about all of this. Could my TN-pain like systems be due to a blockage in my brain?

Very nice. These are identical conclusions that Tao/zen/buddhism came to as well.

I hate that they want to Gatekeep on fusion surgery out of fear that someone wouldnt heal well. Come on, Sir, that train left the station. It really cant get worse only better. That is the reality when you are looking fir a fusion. Its your last ditch chance. Dont gatekeep that. Before my fusion I had no quality of life

I developed a mild foot drop two weeks ago following a lumbar fusion on disc 4 and 5. I had tingling if the toes and pain in my calf after surgery. That has gone, but I realize lifting my toes and foot up while my heal is on the ground is challenging. Is there any exercise I can do to help with restoring proper movement in my foot?

I wrote a book about Synesthesia in 2014, inclusive of the use of this disease (or largess) in criminal justice system.

I am in my late 50s and I precisely remember myriads of moments from my childhood to the present day. Those are the episodes where I had emotional connection to the events or situation. My guess is that emotions (good or bad) preserve and perpetuate memories on limitless spans because the recall is pushed to the limbic area as opposed to the analytic grey matter that would otherwise discard "non-important memories by analytic prioritization." I am not a specialist in the field so this was my lay interpretation.

Thank you ... this is very interesting ... may i ask why some of us are sensitive to the frequencies from cell Towers ... I know its not thermal ...we are all biologicly different ...just like some are alergic to peanuts ...our Brains are electrical and the interferance from EMF ... can and is torture ... can anything be done to stop this my body has become exhausted from these Frequencies...... Thank you in advance

I'm 84!!!! My whole life. Weak ankles had to be wrapped as toddler so I could walk. Asthma and allergies at 10 and now have COPD. At 15, both knees dislocate playing football. Continue to dislocate thru life even with many surgeries. Develop IBS in 20s. Constant joint pain. Many anxiety and depression issues over the years. Carpal tunnel surgery. Open heart surgery in 70s. I can't believe the connections with connective tissue disease. These symptoms are shared by my children and my sister's children. WoW.