I cannot thank you enough. I have been dealing with PPPD symptoms for almost three years. I have had a panic disorder since I was 12. Three years ago I became extremely dizzy gradually. It was debilitating at first and got better over time but is always there. I still can’t walk into a Walmart because it triggers my dizziness from the visual stimuli and their lighting and I literally feel like I will fall over. I’m still unsure if it was caused by my panic disorder or some sort of inner ear issue. But I am beyond thankful that I finally have a proper diagnosis.
Thankful you addressed trying to re program the brain in the end and not just taking pills, so far all western medicine has is the bandaid 🩹 resolution of SRNI’s. Doing my best to shake my 3PD, going on month 9. 🤞🏼👊🏼
I have been diagnosed with Menieres auto immune disease. I found high stress sets it off and well as high salt. The ENT doctor said more than 2000 mg salt a day. Also high sugar foods set off the vertigo. I dont eat cotton candy anymore but before , I would get vertigo if I ate it. I also have neuropathy in my toes and Hashimoto's. Thankyou for this video.
I've had debilitating dizziness for almost three years now. I've spent thousands of dollars, tried every diet under the sun as well as a ton of different supplements. One doctor said it was vestibular neuritis and another said it was BPPV that wasn't obvious until he put the video goggles on me. Other doctors didn't know, some said it was anxiety and another said it might be caused by my stopping taking anti-anxiety medication. Three days ago I started using wild yam cream and I am finally starting to feel improvements. My dizziness has decreased along with the edema I have had for many years. For me, it's apparently hormones, something I never even considered.
@@AJ88874 I use a VERY tiny amount of it, like only enough to cover the tip of a fingernail because I am super sensitive to everything. You just alternate where you put it; one day on the wrists, one day the inner thigh, etc...there are some videos explaining it more in depth. Just three weeks a month then skip the week of your cycle. Unless you are a man then I don't know if would even help you lol.
@@Rose-gc8og Hi Rose! Yes, I feel a lot better. I'm not 100% but I'd say I'm about 85% better than I was 5 years ago. I don't know that I will ever fully recover but I'm thankful that I can function and have more good days than bad. Balancing my hormones seems to have helped a lot of things for me. Best of luck!
I’m a 23 year old male. I have PPPD. Have gotten many tests and was told it’s anxiety. I do have severe anxiety and visual stuff too like floaters, visual tracers, etc. but the dizziness is pretty much 24/7 minus when I’m sleeping or on my phone.
Gates Brain Health I hope PPPD is something someone can recover from. I can absolutely agree. pppd and anxiety go hand in hand and fuel off eachother. All my neurotransmitters are wired to feeling dizzy. At least that’s my theory.
Damn im 25, i only feel this rocking and swaying whenever im laying down, sitting on toilet, and standing straight for like 1 minute. Sucks everyday for 5months straight now
Wow thank you for this posting. I live in UK I’m 49 I have scoliosis broken spinal rod also sickle trait just been diagnosed jan 22nd this year. I started off vertigo issues September 2019 just increased since then. Currently having neuro physio due to double vision etc most of the symptoms I have but not nausea or vomiting. Was on stemistil then on Topiramate tablets 50mg had to stop those due it effecting my speech. I’m on cocadomol30mg 4mtimes a day due to my back. No ear problems had several tests done. Now the neurologist want to put me on Candestartan 2mg then build up to 16mg. Not started yet. Yes I’ve have loads of outside factors with stress and anxiety but I’m not officially diagnosed with depression anxiety etc. I’m symptomatic at any time yes everything I do effects me including trying to eat dinner I can get headnswaying and then my fork or spoon misses my mouth. I get dizzy doing anything I just carry on with I’m doing. My disassociated feeling is definitely have that I wake up feeling hung over stairs trigger me having a shower can cause dizziness. It’s horrible to have never thought this would happen it’s changed my mood totally. Sorry if this comes out mixed up. I don’t drink or smoke or drive a car I don’t have a drug addiction where I inject it. I’m 5ft 3 weigh165lb currently. Yes I’ve had tingling in both feet. Neck pain I do suffer from heartburn as well. What you have said is almost 98% me. Oh sleeping is very difficult I suffer from spinal pain flare up every night. My rod is broken on the left but major pain on the right. I’m a medical junky so hearing this I understand it fairly well. Motion sensitive yes definitely me as well sitting or waking laying down I get dizzy. My vision has altered huge amount short sight is what I have but cannot get a eye test as I get double vision very quickly. Same with physio my double vision is strong my eyes turn into my nose if you get me. Last a few mins most of the it occurs. I have not had head or ear injury no trauma at all. So thankyou so much for this posting again it has help me to understand what I have more.
Oh trying to find what triggers me is complex no consistency at all. Frustrating but as time goes by hoping for answers to come up. Concentration is poor memory long and short poor as well. I also,take Sumatriptan for my migraines 50mg it works very well and clears up my brain fog but the brain fog does return after a couple of days.
I have pppd since 1year...tinnitus started after i stopped talking etizolam.. I quit vertin ssri or benzo quite a low doze. 0.25mg these drugs make u more dizzy.. Now since 3 months i am not using any drugs.. I am going for cycling... Still visual and motion unbalance is there.. The recovery is very very slow...u cant notice but it will built ur confidence.
I cannot thank you enough. I have been dealing with PPPD symptoms for almost three years. I have had a panic disorder since I was 12. Three years ago I became extremely dizzy gradually. It was debilitating at first and got better over time but is always there. I still can’t walk into a Walmart because it triggers my dizziness from the visual stimuli and their lighting and I literally feel like I will fall over. I’m still unsure if it was caused by my panic disorder or some sort of inner ear issue. But I am beyond thankful that I finally have a proper diagnosis.
How are you doing now and if better… what did you do to help?
Thankful you addressed trying to re program the brain in the end and not just taking pills, so far all western medicine has is the bandaid 🩹 resolution of SRNI’s. Doing my best to shake my 3PD, going on month 9. 🤞🏼👊🏼
hola que ejercicios haces?
I have been diagnosed with Menieres auto immune disease. I found high stress sets it off and well as high salt. The ENT doctor said more than 2000 mg salt a day. Also high sugar foods set off the vertigo. I dont eat cotton candy anymore but before , I would get vertigo if I ate it. I also have neuropathy in my toes and Hashimoto's. Thankyou for this video.
I've had debilitating dizziness for almost three years now. I've spent thousands of dollars, tried every diet under the sun as well as a ton of different supplements. One doctor said it was vestibular neuritis and another said it was BPPV that wasn't obvious until he put the video goggles on me. Other doctors didn't know, some said it was anxiety and another said it might be caused by my stopping taking anti-anxiety medication. Three days ago I started using wild yam cream and I am finally starting to feel improvements. My dizziness has decreased along with the edema I have had for many years. For me, it's apparently hormones, something I never even considered.
Wild Yam Cream? How do you take it and amount?
@@AJ88874 I use a VERY tiny amount of it, like only enough to cover the tip of a fingernail because I am super sensitive to everything. You just alternate where you put it; one day on the wrists, one day the inner thigh, etc...there are some videos explaining it more in depth. Just three weeks a month then skip the week of your cycle. Unless you are a man then I don't know if would even help you lol.
@@monicafeuerborn oh i just saw that it’s for women’s hormone lol yea I’m a guy... don’t think it would help😢😅
@@monicafeuerborn hi May I know do you feel better?
@@Rose-gc8og Hi Rose! Yes, I feel a lot better. I'm not 100% but I'd say I'm about 85% better than I was 5 years ago. I don't know that I will ever fully recover but I'm thankful that I can function and have more good days than bad. Balancing my hormones seems to have helped a lot of things for me. Best of luck!
I’m a 23 year old male. I have PPPD. Have gotten many tests and was told it’s anxiety. I do have severe anxiety and visual stuff too like floaters, visual tracers, etc. but the dizziness is pretty much 24/7 minus when I’m sleeping or on my phone.
Interesting. You have a very similar clinical presentation to other individuals I have worked with, particularly the visual tracers.
Gates Brain Health I hope PPPD is something someone can recover from. I can absolutely agree. pppd and anxiety go hand in hand and fuel off eachother. All my neurotransmitters are wired to feeling dizzy. At least that’s my theory.
@@briangonzalez5360 Yes I know what you mean!
Damn im 25, i only feel this rocking and swaying whenever im laying down, sitting on toilet, and standing straight for like 1 minute. Sucks everyday for 5months straight now
@@briangonzalez5360 hi how are u feeling? Have u tried getting on an SSRI?
Wow thank you for this posting. I live in UK I’m 49 I have scoliosis broken spinal rod also sickle trait just been diagnosed jan 22nd this year. I started off vertigo issues September 2019 just increased since then. Currently having neuro physio due to double vision etc most of the symptoms I have but not nausea or vomiting. Was on stemistil then on Topiramate tablets 50mg had to stop those due it effecting my speech. I’m on cocadomol30mg 4mtimes a day due to my back. No ear problems had several tests done. Now the neurologist want to put me on Candestartan 2mg then build up to 16mg. Not started yet. Yes I’ve have loads of outside factors with stress and anxiety but I’m not officially diagnosed with depression anxiety etc. I’m symptomatic at any time yes everything I do effects me including trying to eat dinner I can get headnswaying and then my fork or spoon misses my mouth. I get dizzy doing anything I just carry on with I’m doing. My disassociated feeling is definitely have that I wake up feeling hung over stairs trigger me having a shower can cause dizziness. It’s horrible to have never thought this would happen it’s changed my mood totally. Sorry if this comes out mixed up. I don’t drink or smoke or drive a car I don’t have a drug addiction where I inject it. I’m 5ft 3 weigh165lb currently. Yes I’ve had tingling in both feet. Neck pain I do suffer from heartburn as well. What you have said is almost 98% me. Oh sleeping is very difficult I suffer from spinal pain flare up every night. My rod is broken on the left but major pain on the right. I’m a medical junky so hearing this I understand it fairly well. Motion sensitive yes definitely me as well sitting or waking laying down I get dizzy. My vision has altered huge amount short sight is what I have but cannot get a eye test as I get double vision very quickly. Same with physio my double vision is strong my eyes turn into my nose if you get me. Last a few mins most of the it occurs. I have not had head or ear injury no trauma at all. So thankyou so much for this posting again it has help me to understand what I have more.
Oh trying to find what triggers me is complex no consistency at all. Frustrating but as time goes by hoping for answers to come up. Concentration is poor memory long and short poor as well. I also,take Sumatriptan for my migraines 50mg it works very well and clears up my brain fog but the brain fog does return after a couple of days.
I have pppd since 1year...tinnitus started after i stopped talking etizolam.. I quit vertin ssri or benzo quite a low doze. 0.25mg these drugs make u more dizzy.. Now since 3 months i am not using any drugs.. I am going for cycling... Still visual and motion unbalance is there.. The recovery is very very slow...u cant notice but it will built ur confidence.
What is the treatment of PPPD?
Check out The Steady Coach for help with this!👍