He is leaving UTSW at the end of July 2021 and opening his own practice in Frisco, a suburb of Dallas TX. I hope you can see him. In real life he is just like in the videos, cheerful, friendly, caring. Great doctor.
I actually have an appointment with him in August.. Iive 20 min away. But he does do Telehealth too.. I can't wait to meet him in reading his book too. It's so informative.. I'm really nervous about the appointment.. I'm so scared of meds abd I have a med phobia.. And health anxiety.. This is a horrible disorder but I do believe in mind body disorder.. And stress and anxiety since a child has caused this.. Sensory overload is the worst..
@@janiceince6221 how did your appt go ? Dr Beh seems very expensive and no insurance accepted and he follows a strict “check the boxes” protocols like all the other drs I’ve seen instead of listening to the lived experience and going from there. 😢
Ya he’s my doctor. He is very caring and returns emails when i’m in a bad way and personally answers my questions. I’ve been through dozens of doctors for my VM and he’s very caring
I'm so thankful to have found these sessions! It's been 10 years for me. Told it's BPPV but VOT hasn't worked, I keep getting attacks and they then said vertiginous Migraines and now feel like the ENT doc can't figure it out to stop these and has referred me out to a headache specialists. I feel like I have to figure this out myself as I cannot function when these attacks hit and can last for months. I need to get this book by Dr Beh!
“When you wrote something like this it’s relatable” lol relatable???? I was crying during the whole chapter 1 of the book!!! Finally Someone is able to explain how I feel…
I have VM but basically no vertigo. Many other symptoms. But not that. I had dizziness early on in that I felt I needed for my head to be supported, but not classic vertigo, unless triggered by a therapist. So my VM falls within the less classic parameters and then is hard sometimes to get a good diagnosis from a new physician.
A million things out there, (most of them money makers, sorry) but many folks ignore the basics: diet, stress, sleep, supplementation, and exercise. Being aware that migraine is a threshold disease. Be your own physician. No one knows your body better than you do. For vestibular, watch the sodium/potassium balance. Stress is a MAJOR trigger in any kind of migraine. The body gets depleted and out of balance. Returning to homeostasis is key to healing.
you are absolutely right! Stress is a major trigger in any kind of migraine. The only thing it worked for my migraine was alectro-acupuncture. No medication worked for me.
If you have not yet read Dr. Beh’s book on Vestibular Migraine I cannot recommend it highly enough. Packed full of great info. and you will not regret it.
Iv had a migraine since my 1st period Then pri menopause I got vertigo and the migraine was nearly ever day for 3 years. I tried some preventive meds some I could not take. Some never worked I went to see a Neurologist and he said I had vestibular migraine and he would try me on botox. But then the migraine got less and I thought that my hormones must be settling down So I never had the botox. But last March they came back with a vengeance. My life stopped again. Iv been taking magnesium and b2 for 3 months and the vm has been less . But iv had a migraine for seven days now. This morning I had no migraine I was so happy But by 4 pm its back and very painful. I am waiting for botox but it was supposed to be in march then it got put back to may Then November and now they don't no when Am number 43 on the list and the hospital say theirs no staff . Am in the u.k Am so fed up I want some life. Vm is so debilitating. I also have chronic fatigue syndrome. Which iv had 16 yrs also I have shingles for 16yrs. And no one cares. I did try the head set celfy but it made the migraine worse. Please could you tell me what others are available. Thank you 😊
Is it common to have vestibular migraine or migraine related dizziness and have no nystagmus? I’ve had therapists try maneuvers to try and see nystagmus and I don’t have it. A lot of the head maneuvers therapists have done don’t trigger dizziness just nausea.
Article: "Migraine - More than a Headache" by Drs. Michael Teixido and John Carey (www.hopkinsmedicine.org/otolaryngology/_docs/migraine%20patient%20handout.pdf)
I have vestibular migraine and my neurologist in Atlanta doesn't know about EMDR and doesn't treat PTSD. Have any of you tried EMDR for PTSD-related issues? For my dizziness, I have had very positive results from acupuncture and supplements listed in Dr. Beh's book, but still have photophobia, phonophobia, and osmophobia exacerbated by stress/lack of sleep.
Please get me out of this MdDS hell after four years and counting. I need it to stop. I went to Mount Sinai and gyrostim in Asheville. I have done almost everything.
I watch every video featuring Dr. Beh. He seems like the most caring doctor. He listens to his patients. I wish there was a Dr. Beh in every state.
He is leaving UTSW at the end of July 2021 and opening his own practice in Frisco, a suburb of Dallas TX. I hope you can see him. In real life he is just like in the videos, cheerful, friendly, caring. Great doctor.
I actually have an appointment with him in August.. Iive 20 min away. But he does do Telehealth too.. I can't wait to meet him in reading his book too. It's so informative.. I'm really nervous about the appointment.. I'm so scared of meds abd I have a med phobia.. And health anxiety.. This is a horrible disorder but I do believe in mind body disorder.. And stress and anxiety since a child has caused this.. Sensory overload is the worst..
@@janiceince6221 how did your appt go ? Dr Beh seems very expensive and no insurance accepted and he follows a strict “check the boxes” protocols like all the other drs I’ve seen instead of listening to the lived experience and going from there. 😢
Ya he’s my doctor. He is very caring and returns emails when i’m in a bad way and personally answers my questions. I’ve been through dozens of doctors for my VM and he’s very caring
@@AndyPittman1988did he help u?
I'm so thankful to have found these sessions! It's been 10 years for me. Told it's BPPV but VOT hasn't worked, I keep getting attacks and they then said vertiginous Migraines and now feel like the ENT doc can't figure it out to stop these and has referred me out to a headache specialists. I feel like I have to figure this out myself as I cannot function when these attacks hit and can last for months. I need to get this book by Dr Beh!
“When you wrote something like this it’s relatable” lol relatable???? I was crying during the whole chapter 1 of the book!!! Finally Someone is able to explain how I feel…
I have VM but basically no vertigo. Many other symptoms. But not that. I had dizziness early on in that I felt I needed for my head to be supported, but not classic vertigo, unless triggered by a therapist. So my VM falls within the less classic parameters and then is hard sometimes to get a good diagnosis from a new physician.
A million things out there, (most of them money makers, sorry) but many folks ignore the basics: diet, stress, sleep, supplementation, and exercise. Being aware that migraine is a threshold disease. Be your own physician. No one knows your body better than you do. For vestibular, watch the sodium/potassium balance. Stress is a MAJOR trigger in any kind of migraine. The body gets depleted and out of balance. Returning to homeostasis is key to healing.
you are absolutely right! Stress is a major trigger in any kind of migraine. The only thing it worked for my migraine was alectro-acupuncture. No medication worked for me.
If you have not yet read Dr. Beh’s book on Vestibular Migraine I cannot recommend it highly enough. Packed full of great info. and you will not regret it.
Is this book only good for vestibular migraines?
Canyou please clarify all the acronyms you all are using? Thank you!
I loved the video! Thank you so much. Any suggestions for me to visit a specialist in London? I have BPPV and VM with no pain. Many thanks 🙏
Where in Texas are you located?
Does vestibular migraine cause head pressure and face pressure too?
I've been feeling that too
Yeah mostly in my forehead.
@@FJano12 I mostly feel it in my nose area accompanieed by constant lightheadedness/dizziness
@@LebJamal23 same
Same my head feels heavy and scalp so sensitive to much 😢
If you have VM and Tumarkins, would you say that this must be a case of Menieres too?
Can you suggest anyone near Greenville sc
Iv had a migraine since my 1st period
Then pri menopause I got vertigo and the migraine was nearly ever day for 3 years.
I tried some preventive meds some I could not take.
Some never worked
I went to see a Neurologist and he said I had vestibular migraine and he would try me on botox. But then the migraine got less and I thought that my hormones must be settling down So I never had the botox.
But last March they came back with a vengeance. My life stopped again.
Iv been taking magnesium and b2 for 3 months and the vm has been less . But iv had a migraine for seven days now.
This morning I had no migraine I was so happy
But by 4 pm its back and very painful.
I am waiting for botox but it was supposed to be in march then it got put back to may
Then November and now they don't no when
Am number 43 on the list and the hospital say theirs no staff .
Am in the u.k
Am so fed up I want some life. Vm is so debilitating.
I also have chronic fatigue syndrome.
Which iv had 16 yrs also I have shingles for 16yrs. And no one cares.
I did try the head set celfy but it made the migraine worse.
Please could you tell me what others are available.
Thank you 😊
electro-acupuncture helps ...it helped me a lot!
Is it common to have vestibular migraine or migraine related dizziness and have no nystagmus? I’ve had therapists try maneuvers to try and see nystagmus and I don’t have it. A lot of the head maneuvers therapists have done don’t trigger dizziness just nausea.
I don't have it.
Can you add the link for the article Dani references to give to patients as a warm up to VM?
Article: "Migraine - More than a Headache" by Drs. Michael Teixido and John Carey (www.hopkinsmedicine.org/otolaryngology/_docs/migraine%20patient%20handout.pdf)
@@BalancingActResources Is it possible to send the link again? I am not able to access the article. Thank you!
@@BalancingActResources This link does not work...
I have vestibular migraine and my neurologist in Atlanta doesn't know about EMDR and doesn't treat PTSD. Have any of you tried EMDR for PTSD-related issues? For my dizziness, I have had very positive results from acupuncture and supplements listed in Dr. Beh's book, but still have photophobia, phonophobia, and osmophobia exacerbated by stress/lack of sleep.
Any suggestion for a dr in Phoenix as I have m s and the neurologist doesn’t do this diagnosis
You are in luck. Dr. Beh has mentioned Phoenix neuro otologist Terry Fife MD as a renowned expert on PPPD and vestibular migraines. Best wishes!
Did you know the word "Cephaly" is the greek word for head? Yes, indeed. Kefali is the greek pronounciation.
Why can’t you help people in Utah
Please get me out of this MdDS hell after four years and counting. I need it to stop. I went to Mount Sinai and gyrostim in Asheville. I have done almost everything.
So sorry you're not feeling well. Perhaps give this provider directory a try: vestibular.org/healthcare-directory/
Asian Elon Musk?