Excellent video! Love the introduction too that frames it. Especially the clarification that it doesn’t matter how long you have had symptoms, recovery from NCD begins the day you realize this is a neural circuit/mind-body condition that you CAN recover from.
This is a really important video. Trying to get better in an abusive situation is very challenging. I’m so glad you are talking about this as is the mindful gardener and Sam Miller and Dan. This information is badly needed.. thank you 🙏
Agree re: day one is first day you knew what is going on. I would say I'm about 90% better in several months, thanks to you (and me taking steps in line with your advice). But I had had symptoms for almost 1-1/2 years before I found your channel.
You are an absolute star. I have had off balance since may after a couple of panic attacks about blood pressure. It was all in my head in the end but it has left me with the feeling. I slowed down on work as a supply teacher but symptoms have got better or I have learnt to cope with them working with kids and stood up all day. My question is, have you ever seen a link with over use of the voice as my vocal folds now seem to take a battering and I have a croaky voice alot (only do two days a week and used to work full time a few years ago). I'm going to ask the ENT which is looking at my balance which I actually understand cant do anything about the dizziness due to be thinking it's neural circuit dizziness but just thought I would ask you.
The EGO can and will use specific conditions as a safety mechanism in order to prevent the patient from moving forward, keeping them in their comfort zone.....and let's not forget that you become addicted to Cortisol which keeps being released into your system due to your stressful environment or simply the fact that you are, or have been, stuck in fight or flight over such a prolonged period of time due to their specific circumstances.
Hey dr yo, thank you so much for all your videos they’re really helping my bad mental state right now. I’m 19 from Scotland and have been diagnosed with vestibular neuritis which started on the 14th of January, was wondering if it’s still normal to be dizzy everyday with vestibular neuritis? I’m hoping it doesn’t turn into pppd, thank you
Dr Yo, I had completely normal calorics and overall testing in October, I started to experience different symptoms and went to a vestibular specialist who has redone all testing. I now have a positive VHIT and my calorics have fallen on both sides to a 5-7 (they were in the double digits in October). They are still considered normal by the reference range but my Dr says the lowest end of normal. Doesn’t the VHIT in conjunction with the new calorics mean bilateral vestibular hypo function? I am supposed to have VEMP testing this week and will ask for a repeat of the rotary chair but am very anxious about bvh.
Yo me encuentro en el número 8,yo quiero recuperarme de los síntomas,pero como bien dice Yo, ¿como mandar un mensaje de seguridad a nuestro cerebro,si realmente estamos viviendo una situación abusiva que nos mantiene en un estrés crónico?,mi pensamiento es,nada en esta vida es eterno,y se qué mi sistema nervioso volverá a la normalidad cuando me libre de esta situación. Mientras tanto tengo las herramientas que la doctora Yo me ha dado para poder ser funcional manteniendo a raya mis síntomas y poder hacer mi vida,estoy convencida de que me recuperaré cuando mi tranquilidad no esté en peligro.
This is a very, very well done video. I watch your content religiously and this is as good as anything you've ever put out.
Excellent video! Love the introduction too that frames it. Especially the clarification that it doesn’t matter how long you have had symptoms, recovery from NCD begins the day you realize this is a neural circuit/mind-body condition that you CAN recover from.
This is a really important video. Trying to get better in an abusive situation is very challenging. I’m so glad you are talking about this as is the mindful gardener and Sam Miller and Dan. This information is badly needed.. thank you 🙏
Excellent video Dr. Yo❤
Thank you 🙏🏾 anything helps at this point…. The more tools the more success💯
Agree re: day one is first day you knew what is going on. I would say I'm about 90% better in several months, thanks to you (and me taking steps in line with your advice). But I had had symptoms for almost 1-1/2 years before I found your channel.
Great content!! Could persistent eye floaters even in healthy eyes that you can’t neuroadapt to…be a symptom?
What an adorable dog❤❤❤What is his name?
Can vestibular migraines be constant and cause brain fog?
You are an absolute star. I have had off balance since may after a couple of panic attacks about blood pressure. It was all in my head in the end but it has left me with the feeling. I slowed down on work as a supply teacher but symptoms have got better or I have learnt to cope with them working with kids and stood up all day. My question is, have you ever seen a link with over use of the voice as my vocal folds now seem to take a battering and I have a croaky voice alot (only do two days a week and used to work full time a few years ago). I'm going to ask the ENT which is looking at my balance which I actually understand cant do anything about the dizziness due to be thinking it's neural circuit dizziness but just thought I would ask you.
The EGO can and will use specific conditions as a safety mechanism in order to prevent the patient from moving forward, keeping them in their comfort zone.....and let's not forget that you become addicted to Cortisol which keeps being released into your system due to your stressful environment or simply the fact that you are, or have been, stuck in fight or flight over such a prolonged period of time due to their specific circumstances.
Hey dr yo, thank you so much for all your videos they’re really helping my bad mental state right now. I’m 19 from Scotland and have been diagnosed with vestibular neuritis which started on the 14th of January, was wondering if it’s still normal to be dizzy everyday with vestibular neuritis? I’m hoping it doesn’t turn into pppd, thank you
Dr Yo, I had completely normal calorics and overall testing in October, I started to experience different symptoms and went to a vestibular specialist who has redone all testing. I now have a positive VHIT and my calorics have fallen on both sides to a 5-7 (they were in the double digits in October). They are still considered normal by the reference range but my Dr says the lowest end of normal. Doesn’t the VHIT in conjunction with the new calorics mean bilateral vestibular hypo function? I am supposed to have VEMP testing this week and will ask for a repeat of the rotary chair but am very anxious about bvh.
Is vestibular migraine is neural circuit
Yes. 1 min. 46 sec. She says it in the vlog.
#Vestibular migraines are neural circuit disorders. That doesn’t mean they’re imaginary. #pppd #mdds
ruclips.net/user/shortspHHSdPKnWBE?feature=share
Yo me encuentro en el número 8,yo quiero recuperarme de los síntomas,pero como bien dice Yo, ¿como mandar un mensaje de seguridad a nuestro cerebro,si realmente estamos viviendo una situación abusiva que nos mantiene en un estrés crónico?,mi pensamiento es,nada en esta vida es eterno,y se qué mi sistema nervioso volverá a la normalidad cuando me libre de esta situación.
Mientras tanto tengo las herramientas que la doctora Yo me ha dado para poder ser funcional manteniendo a raya mis síntomas y poder hacer mi vida,estoy convencida de que me recuperaré cuando mi tranquilidad no esté en peligro.
So many commercials lol