Rethinking Vestibular Schwannoma

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  • čas přidán 27. 08. 2021
  • Rethinking Vestibular Schwannoma brought to you by the Medical Student Neurosurgery Training Center.
    Join Dr. Matthew Carlson from the Mayo Clinic Department of Neurological Surgery as he discusses the history, presentation, and treatment of Vestibular Schwannomas.
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Komentáře • 57

  • @fjames2230
    @fjames2230 Před 2 lety +2

    Thank you for sharing this. I appreciate the approachable lecture style for a very complicated topic.

  • @user-wj8gd9gl8y
    @user-wj8gd9gl8y Před 2 lety +4

    Thank you for presenting this training. So many physicians know very little about AN and have no idea how to deal with their patients. As a patient myself, post SRS, I love your enthusiasm about the topic. God bless!

  • @GuillRoy10
    @GuillRoy10 Před 2 lety +7

    Really, really, I hope the clinics, hospital and doctor of all world continuie investigating and developing more information for combat this type of tumors, you're great! Thanks a lot! Saludos from México!! :)

    • @BrainSpineGroup
      @BrainSpineGroup  Před rokem +1

      Thanks for sharing your comment!
      Our channel has a lot great new things coming soon, and our live broadcast starts Tuesday 12 noon EST next week! Subscribe for notifications and join us live every Tuesday & Thursday with Dr. Rad!

    • @maris7457
      @maris7457 Před 9 měsíci

      ya. i have the charity for raising awareness for this in my beneficiaries on my bank acct. it's rly needed

  • @zoeduckering7509
    @zoeduckering7509 Před 2 lety +1

    Thank you, very informative.

  • @simplymeconnie4003
    @simplymeconnie4003 Před 2 lety +11

    Thank you for this. I had a 6cm one removed in 2016, and GK on the growing 2cm left behind in late 2019. I learned a lot in those years, but this is by far the most informational video I have seen

    • @kristenalmonte1110
      @kristenalmonte1110 Před 2 lety +1

      I am going through this right now. Did you do gamma knife or surgical removal? I'm trying to decide what to do.

    • @simplymeconnie4003
      @simplymeconnie4003 Před 2 lety +2

      @@kristenalmonte1110 Do NOT have surgery if you don't have to. I had translab 6 years ago. I am left with 2cm of the 6cm. Go with radiation if you can. I had it for the regrowth. It still sucks, but no chance of living with constant 11/10 pain like I woke up with this morning.

    • @kristenalmonte1110
      @kristenalmonte1110 Před 2 lety +3

      @@simplymeconnie4003 Thank you for your input. Yes, in my research in most cases people are left deaf as well. Was unsure if that was all types of surgery since I thought there were 3 kinds. Mine is 2.5 cm and I am unsure exactly where it is until I see the neurosurgeon on 5/25. I just found out I even had it this past Tues. I have ringing & hissing. I am assuming it may grow and I have to do the gamma knife now while it is small and I have minimal symptoms.

    • @khouse1554
      @khouse1554 Před 2 lety +2

      @@kristenalmonte1110 any update? I have this and I’m only 27 :/ scared

    • @BrainSpineGroup
      @BrainSpineGroup  Před rokem +3

      Thank you all for sharing with each other. We’re all glad our channel is able to bring patients together to discuss shared experiences - going through all this is a lot!
      Our channel has a lot great new things coming soon, and our live broadcast starts Tuesday 12 noon EST next week! Subscribe for notifications and join us live every Tuesday & Thursday with Dr. Rad!

  • @kobenoah1
    @kobenoah1 Před 2 měsíci

    I just found out i have one. 16mm. I think I must have had it for about 15 years. I’ve been slowly going, deaf in that air, and it finally got to the point where I was tired of saying what all the time. Having people have to repeat themselves when talking with them.

  • @Me-lb8nd
    @Me-lb8nd Před rokem +1

    Very interesting!

  • @dllee5930
    @dllee5930 Před 5 měsíci +1

    very interesting I am not a doctor but could follow your presentation pretty well.

  • @zorro248
    @zorro248 Před 2 lety +2

    Very helpful. I’m having my 2.7cm AN removed surgically in a couple of weeks and this helps clarify some details.

    • @BrainSpineGroup
      @BrainSpineGroup  Před rokem

      Thank you for sharing your story! We’re glad this video helped clarify some things for you.
      Our channel has a lot great new things coming soon, and our live broadcast starts Tuesday 12 noon EST next week! Subscribe for notifications and join us live every Tuesday & Thursday with Dr. Rad!

    • @varun31779
      @varun31779 Před rokem

      Hi, hope u r doing well, may what were the symptoms in your case?

    • @photo_art
      @photo_art Před rokem +2

      Hi, thanks for sharing, as it’s been over a year, how was the surgery ? If you don’t mind me asking, any issues ?

  • @sirajallie4682
    @sirajallie4682 Před měsícem

    Thank you for your info...need to know as you are very easy to communicate need your help to help others in particulary with other health issue's as im not a dr but i have matter that relate

  • @lolfunvids3103
    @lolfunvids3103 Před 5 měsíci

    I know this video is older, but are there still any books available? Recently diagnosed with a 0.9cm vestibular schwannoma and I am looking for all the information I can get. I am not one to only trust the advice of one doctor etc. as stated many have opinions and I want to be very involved in the treatment of my situation. Thank you for this informative and amazing video!

  • @jeffmui3727
    @jeffmui3727 Před měsícem

    I have 11mm. After consulting with ENT, they suggested to get it removed.

  • @poparada
    @poparada Před 5 měsíci +1

    Thank you for this presentation. Do you still have books to give out? I’d be interested in reading.

  • @michelebruxinha
    @michelebruxinha Před rokem +2

    Thanks for the video, it's very helpful. My dad has a vestibular schwannoma and we're trying to find all information we can to know what to do, including information about a procedure called gamma knife in Brazil to see if he can have it killed instead of removed, sparing him from a 7hs surgery plus a week in hospital. I'm not a doctor, but a biologist, so I understand a bit of how the human body works and I'd be very interested in the book you said to study it, if possible.

    • @BrainSpineGroup
      @BrainSpineGroup  Před rokem

      Thank you for sharing your dad’s story! We genuinely hope your dad and his doctors are able to find the best and right treatment for him as an individual.
      Our channel has a lot great new things coming soon, and our live broadcast starts Tuesday 12 noon EST next week! Subscribe for notifications and join us live every Tuesday & Thursday with Dr. Rad!

  • @puppetman1496
    @puppetman1496 Před 2 lety +1

    Good8 day

  • @sherrylapiro5930
    @sherrylapiro5930 Před 4 měsíci +1

    I would love to get your book. I’m having major memory issues. Is this normal?

  • @maris7457
    @maris7457 Před 9 měsíci +1

    the giveaway for my tumor was when i wasn't able to smile fully on that side of my face anymore. sooo apparently it wasn't a true vestibular schwannoma? lol (: it was almost 3 cm, originated in the ear canal, and was causing midline shift. baseline only 1 of 3 signals in my ear were working at the start of surgery and it was lost during surgery. i also had heavy hemmorhage in my cerebellum to the point where it compressed my 4th ventricle, and i had a stroke in my pons. it left permanent damage/scars in that area and i have seizures/epilepsy in that region now that i've just started medication for because it was getting dangerous (affecting heart/breathing)

  • @estherbarnslater7613
    @estherbarnslater7613 Před 3 měsíci

    Thank you sir, I have been tumors, right and left. How do I get copy of your book?

  • @dllee5930
    @dllee5930 Před 5 měsíci +1

    do you think Cawthorne's head exercise are even practical if you have Vestibular Schwannoma??

  • @anjalimishra7821
    @anjalimishra7821 Před 3 měsíci

    My friend is having a neoroma in right and left region both of 2 mm but it has pus involving cerebral linings what should be the tt plan?

  • @las174
    @las174 Před rokem

    connection to cell phone use?

  • @quietguy3969
    @quietguy3969 Před rokem +2

    I have a 1.5cm AN with complete deafness in my left ear. I also suffer from vertigo quite often and am unstable while standing still and walking. I have tinnitus all the time and loud noises make it worse. it grows about .5cm per year so far.

    • @BrainSpineGroup
      @BrainSpineGroup  Před rokem

      Thank you for sharing - living with those symptoms must be such a challenge. We’re here cheering for you and your doctors to come up with the best treatment plan possible.
      Our channel has a lot great new things coming soon, and our live broadcast starts Tuesday 12 noon EST next week! Subscribe for notifications and join us live every Tuesday & Thursday with Dr. Rad!

    • @chocolateidol9040
      @chocolateidol9040 Před 9 měsíci

      The doctors won’t remove it?

  • @bill6656
    @bill6656 Před 2 měsíci

    Could they be caused by older "Brick" style phones?

  • @marionjones2244Bible
    @marionjones2244Bible Před 2 lety +1

    I have this so can you send me a book. I’m a patient of Cedars Sinai in California

    • @BrainSpineGroup
      @BrainSpineGroup  Před rokem +1

      Glad the video helped - sorry we don't have books right now.

  • @johannacenteno5885
    @johannacenteno5885 Před rokem +1

    May I have a copy please

  • @hiraomer7062
    @hiraomer7062 Před 2 měsíci

    Can you send me copy

  • @tsangs3363
    @tsangs3363 Před rokem

    I have a 14mm....😢

    • @marciwhitman3513
      @marciwhitman3513 Před 10 měsíci +1

      That is a very very small tumor. You are very lucky to have found it this small. More than likely the course of treatment would be to watch and wait. But it's best to see a neurosurgeon so that he can do an exam and determine what is the best treatment for you based on your symptoms and the positioning of your tumor. It's also best to see an ENT and to get a hearing test. My tumor is 1.7 cm and yours is 1.4 cm. I just recently had radiation done and I just had my MRI after that three months later. There has been no new growth. I'm due to get another MRI in November to compare the findings.