I have cervical instability which on top of that all of the symptoms you outline in most of your vagus nerve videos and the multiple physicians I’ve seen here in west Texas have no idea why I’m having the in-compasanating symptoms. This is so incredibly true to what I experience sporadically. I’ve looked into prolotherapy and have found it is not covered by insurance. I wish to God some one some where could properly diagnose me. It is embarrassing for me to even to have to interact with my family much less anyone else. I lose complete control of my body whenever I wake up with these symptoms.
Great presentation. Like many ADHD patients I have had so many of these symptoms over such a long while. I have found success with chiropractic functional neurology- but it is so hard to explain to people the reality of these symptoms. Yes- moving the eyes is an issue. Yes- afterimages. Yes- looking at something and not seeing it.
I was hit by a stolen car going 120mph and went over a cliff. I broke c5/6 with anterior wedge fracture and now have retrolithesis and multiple other issues. I have been in eye therapy at our local university Abi/tbi eye therapy center and have prism glasses- but the bigger problem is that these symptoms don't stay consistent. I have binocular vision dysfunction- are there any contraindications for treatment? Cases you wouldn't accept? And I am in Arizona- so if I came for treatment, I understand it can take 8-10 treatments? Would this require multiple visits? Are you working to teach other providers your treatment approach? Thank you so much for all of your dedication, hard work and information you share!!
Hi karlabarr, Thank you for your kind words. Hope you can get care for your case close to home for now by someone who understands cervical instability. We wish you all the best in health!
The doctors I saw kept bringing up my anxiety meds which i never took in a way to discard my claims of symptoms as just mental illness no more im seeing a specialist like Dr Hause ASAP I WAS that guy that was labeled crazy !
I was a professional therapist for 25 years- very well respected until a car accident and broken neck- when I tried to seek treatment, I got the same thing 🙄 my teeth felt like I needed root canals- so I went to the dentist who only said my teeth were fine and acted like I was crazy- turned out it was from the trigeminal nerve- so disgusting a dentist didn't know this and they find it easier to label you as crazy when they don't know or understand
All these symptoms are characteristic of Lyme and co-infections. Lyme and other tick infections will eventually cause all kinds of nerve dysfunction. Bartonella is an epidermic and is especially detrimental to the brain and eye. You all need to get blood work done for Lyme.
Dr Hauser, I need this so bad. I've been dealing with this since July and doctors keep saying it is just anxiety. I need imaging to show is there is a problem or not. But I live in California :(
Hi Ryan, Thanks for sharing and sorry to learn about what you've been dealing with since last summer. We understand travel is not feasible for everyone, but if it were in the future, feel free to reach out to us directly for a more thorough case review. We wish you all the best in navigating your options closer to home. Take care.
That happened to me (a mix of both cases). A neurologist said I have MS. Maybe, but is it possible it's really my vagus nerve? My neck is stiff, the symptoms came strongest after whip lash from car accident and since the whiplash, I have what I call nocturnal focal seizures. But my neurologist blames EVERYTHING on MS now that he labeled me. I have always been extremely flexible since before kindergarten. I had my thyroid out at 23 yrs old. I'm 53 now. The car accident 2 yrs ago created intense memory loss including forgetting my 5 children's names. I had to think of the first letter of their name to bring their name to memory. I couldn't remember numbers or details longer than 3 seconds. Yet, I knew who I was, whete I was and the date. I lost short term memory capabity so had to quit some classes I was taking for functional nutrition. I had strange eye issues and unexplainable anxiety and nightmares. I have had virtually zero care over these issues. I have refused drugs for MS so the doctors don't want to treat me at all. They basically leave me feeling like it's my fault I have symptoms. However the only drug my insurance will pay for has a side effect of liver cancer. My mom just died of liver cancer so to me, I don't see it as a sensible option when strict diet control shows benefits. I eliminated gluten, dairy, pork, MSG, artificial sweeteners, most lectins such as nightshade veggies, beans, etc, and all table sugar. I eat mainly grass fed/grass finished meat and butter. I only use sea salt or Himalayan salt and olive oil for cooking. I eat all organic and consume spoonfuls of coconut oil at a time. I eat green Olives a lot ( a jar a day) because I need extra sodium for some reason. I regularly consume cacao mixed with coconut milk to soften and monk fruit to sweeten, pistachios, green tea, blueberries, plain Greek yogurt, and coffee pretty much every day. I bounce between 112 lbs and 126 lbs. Sometimes in a single week depending on water retention. All symptoms worsen during my menstrual cycle. I have very low blood pressure dropping to 57/38 one time at my doctor's appointment. I think I have hypoglycemia but no tests have been done. I can't consume sugar or I react but I can eat 100% raw honey if the bees consumed yellow clover. I can't eat fiber or my system jams. I take in some fiber foods in nuts and Olives etc as stated above but if I eat cruciferous Veggie, I get destroyed for days. I feel toxic/drugged or poisoned when constipated. I control it all pretty well however everything you say about the vagus nerve sounds right to me. I have swallowing paralysis as I attempt to swallow. My jaw feel misaligned some days and I get slightly nasal sounding but no congestion. Ugh! My doctors avoid me like the plague because I won't take a single drug including Tums or Tylenol. I choose chemical free so I always know what my body is saying. I always feel like I have a knot inside my left should blad and sometimes pressing on my neck, right below my skull takes headaches away. I told my doctors I feel like my brain is being pushed into my ears when I get brain fog, but they don't even comment then move on to their next step to get the appointment over. I have low nutrient absorption. I test low on iron, Zinc, copper, vitamins A, D, and E and did have my gull blades removed. I demanded these tests. They refused forever saying my problems didn't have to do with vitamins. Yet all my levels were SUPER low! They still don't care except about the iron. My B vitamins test great. I have stopped consuming calcium, coffee and polyphenals close to times I eat iron plus eat pistaccios for copper before consuming iron. That seems to have fixed my iron. But I also have frozen feet though warms to the touch. I get invisible tremors throughout my body then get narcolepsy followed by passing out and waking with a focal seizure (feeling of falling plus heart issues). Even after waking, I can't stop the falling sensation or heart issues for a few minutes. Plus I can't always respond by waking. I feel paralyzed.I know it's happening but can't move. I can force movement but feel like my body is 500 lbs. However, sometimes I feel like my brain is leaving my body like I'm about to die, so I force myself to quickly sit up and come to. Then walk it off for about a minute. I don't feel right so go back to sleep. It returns up to 4 times in a row.
I have these: 1. Some minor pain swallowing water or other liquids. 2. Ringing in the ears for minutes (duration is different every time it starts). 3. Some facial pain 4. Some pain the back of my neck. 5. When I drive, my left arm starts to hurt from the inside at around the shoulder area, bicep, and forearm. 5. Minor headache that feels like ringing 6. I was playing video games and I started feeling dizzy and I had to stop. 7. Blurred vision at times. 8. Pressure in the forehead and nose.
Hi vidfreak727, Sorry to hear that, and everything you've listed makes sense to us from a potential structural cause in the neck. We hope that you are able to work with a provider who can help you determine if you have a structural reason for your symptoms. These are symptoms that are very common for us to help in our center. If you would like us to evaluate your case in more detail and potentially see you here, we'd be happy to help. Wishing you all the best in health!
@@CaringmedicalProlotherapy how would you be able to? I’m in California. I’d love to be able to travel to Florida but I have no money for that right now. I also am with Kaiser through my employer.
What do you do if you have iris coloboma- the eye is not connected to the optic nerve, crooked spine, chest pectoral bone sticking out and difficulty swallowing? I don't know how I came across your channel, but I'm glad I did and subscribed. I hope you can help me🙏 Definitely have the symptoms you described Thanks
I’ve been diagnosed with CCI, and have been experiencing visual disturbances for 7 months now. I watch many of your videos and wondering if people with CCI that get your prolotherapy treatments have good success with vision improvement/reduced pressure behind the eyes?
Hi I have EDS(genetically tested) and I have many of your mentioned issues also i had tribble tinnitus and then I start to have vertigo. I had standard MRI and was dismissed that is just anxiety.Anyway cut long story short... One morning when ringing in my head and vertigo was so bad that there is no way I could go to work I put my neck brace on and In 30 min my life changed !!! there was no ringing no vertigo and my vision was perfect! Took my brace off and ringing comeback ,but not so strong. So for now I keep wearing my neck brace on/off until I can get proper diagnosis and have to tell to my GP what tests she have to send me for , lol
@@CaringmedicalProlotherapy patient just wants answers from the experts just to be asked "Do you have any feelings of harming yourself or others" its disgusting !
Flashes of lightning when you turn your head is due to a vitreous detachment and you still have some traction from bands of vitreous tugging on the retina. Anyone can see this just by putting pressure on the globe. Can you share some cases of lowering intracranial pressure with addressing the neck?
Your videos are always so insightful and put everything I feel in to context. I have bouts of pulsing vision upon movement, sometimes accompanied by whooshing in the ears at the same time and visual snow. I have bilateral internal jugular vein compression from c1 and elongated styloids. Next step is catheter venogram and venoplasty. I’m praying that after 3 years I am finally on the right path. The first patient you mention is me. Derealisation, feeling detached from my surroundings, numb brain feeling like flow of circulation is being blocked off to the brain. So fascinating to watch. Thanks for sharing your knowledge and expertise to the world
Thank you for your kind words, Natalie. So happy that you have been connecting with the content and being able to then connect the dots in your own case. We hope you get the relief you need! If travel to Fort Myers is an option, our team would be happy to review your case and see if you sound like a good fit for our center. Wishing you all the best in healing! Take care, Natalie.
@@harshpunkFX hi. I am the same day in day out. I was happy and healthy for 32 years then this started when I was heavily pregnant, 3 years ago. When did this start for you?
I have pressure in my eyes, black dots in my vision, almost static fuzzy vision, dizzy disorientation from my eyes and the almost unreal derealisation feeling
Have been struggling with these symptoms plus peripheral neuropathy, constant dry cough and stutter step. I have been diagnosed with Parkinson’s. Had cataract surgery in one side. Got glasses prescription updated twice. Nothing helps
i’ve got eye pain, increased pressure, sinus pressure, university the eye pressure, pressure in my face and nose. am i a candidate for caring medical? damn straight i am. your prolotheropy could really change my life. i will get prolotheropy happen somehow. listen to this guy! listen to this guy! listen to this guy! listen to this guy!
I get the same anxiety an my neck always has tension I feel pressure in my head an dizzy an eye sight it gets bad when I drive an like brain fog as well an I had blood test an CT scan done wish was something that can be done
how can i find someone in the uk that understands this and can perform this procedure , i am having most of these symptoms and its making my daily life miserable . thanks
We are so sorry to hear this. We know how frustrating it can be and unfortunately we hear this from a lot of our UK patients. If you find that you can travel to FL we would absolutely love to help you, but we understand it is not feasible for all. We wish you all the best on your continued research!
During the day my eyes are normal and moistured, but at night when I lay down my eyes start to dry up badly to the point of eyelids and eyes stock together, I always keep a saline solución for every time I need to open my eyes and get up it's more severe on the right eye...what can be the problem!
I've been following you for awhile and find your vids helpful. I have lots of weird symptoms. My eye doc believes I may have visual snow, also ghosted images (some), swallowing problems, vibration feelings in my head along with some other weird things. One thing in particular -- my hairdresser keeps telling me to hold my had straight - it leans, according to her. My ENT told me to straighten my head as well when he was doing a procedure. Maybe my spine might be shifting - maybe nothing more than always holding my work phone between my head and shoulder. In any event, I wish you were here in Phoenix area. I do not know what kind of doc I should be seeing in addition to all the ones I am already seeing for everything - Cardiologist for AFIB, Pulmonary for Pulmonary Hypertension, ENT for swalloing problems etc etc Any advice?
Hi Gavin, Thanks for sharing and sorry to hear about your neck issues. Glad you are looking into some options for addressing it and the symptoms that are commonly associated with cervical instability. We hope that you are able to get in to see a specialist soon for a treatment plan. If you feel that you need our team in the future to possibly see you here in our center, you are welcome to reach out to us directly. Wishing you all the best in healing!
My eyes do all weird things. I have balance issues and severe dizziness like im on a boat and sinking into the lounge and bed. Whoozy head, depression, anxiety, dissociative disorder. Is there any way to find someone in australia who deals with cervical instability who does the same tests as caring medical?
Hi Angela P, We do not know of anyone doing all of the types of tests we do. We are a unique center and always working with technology representatives to look into new tests and which types of tests can best show various anatomy that is being affected in our patient population. We are constantly researching and working on this aspect of our practice because the types of complex cases we see here really need this level of dedication to the field. We do try to discuss what we're learning and seeing in our patients in our videos, research articles, and blogs to try and help others even if they cannot be seen in our center. But we do understand that it can be frustrating to not have other centers like this everywhere and that many patients feel they are trying to piece together their own case because no local doctor is able to put it all together for them. Sorry that you have been experiencing this and we wish you all the best in your quest for answers and finding the ideal treatment for your symptoms.
Can u help me out? I was testing my fever and I think I pushed the tester thing too far in my ear... My ear feels full but I got my ear looked at and there’s not that much ear wax. I do have a cold so is it just a cold symptom? It didn’t feel full straight away when I did it. I posted this on another video but I figured u might not see it. I can live with this problem, I can hear but it’s just weird. Also whenever I swallow or yawn my ears pop, is that normal? Sorry for all the questions I’m just a bit worried.
Dr hauser I am still having issues. I have eye ball pain. Blurry vision. Vertigo being seen by a neurologist here in Florida. I’m suffer from all sorts of symptoms from cervical insatiably but he says I have mood disorder. Because I tell him all of my issues. He put me on topamax which has helped but I still get symptoms and side effects. Now he sending me to physical therapy. Which I know won’t help. He never did a MRI to see what is going on. He only looked at the one from the emergency room. I am desperate to get more answers i am suffering. I feel like a dementia patient. It’s terrible. He doesn’t listen to me. He checks my reflexes and sends me on my way . Please help!!
@@safariprint1972 hard to explain here but really helped me . I did it twice a day for three weeks and it was a game changer. Google it for details. Also check with your doctor if it’s appropriate for you...as I’m not a doctor
THIS IS EVERYTHING I’VE BEEN EXPERIENCING FOR THE LAST YEAR. Thank you. Thank you.
Bless Doctor Hauser! Hes a Great man!
Too many doctors today are quick to brush off patients claim of weird going ons
Agreed. Everything can't be fibromyalgia right?
You are such a relief when we hear cases similar to ours
We are so happy to hear that!
I have cervical instability which on top of that all of the symptoms you outline in most of your vagus nerve videos and the multiple physicians I’ve seen here in west Texas have no idea why I’m having the in-compasanating symptoms. This is so incredibly true to what I experience sporadically. I’ve looked into prolotherapy and have found it is not covered by insurance. I wish to God some one some where could properly diagnose me. It is embarrassing for me to even to have to interact with my family much less anyone else. I lose complete control of my body whenever I wake up with these symptoms.
Your only a 2 hour flight away do wat is necessary for your health! I fly from Los Angeles .. I waited a lil too long lost everything wife left me!
You go Dr hauser. Thank God for you.
Hi Charlotte, Thank you for your kind words. Wishing you all the best in health!
I am going to work for you as soon i finish medical school. PLEASE dont retire.
Dr Hauser.. Tina here again... This is me again!! I feel ALLL THOSE sensations... i def need you!!!
Great presentation. Like many ADHD patients I have had so many of these symptoms over such a long while. I have found success with chiropractic functional neurology- but it is so hard to explain to people the reality of these symptoms. Yes- moving the eyes is an issue. Yes- afterimages. Yes- looking at something and not seeing it.
These videos should be incorporated into recurrent training for all MDs, DO’s DC’s #healthy lifestyle reports #athlete
I was hit by a stolen car going 120mph and went over a cliff. I broke c5/6 with anterior wedge fracture and now have retrolithesis and multiple other issues. I have been in eye therapy at our local university Abi/tbi eye therapy center and have prism glasses- but the bigger problem is that these symptoms don't stay consistent. I have binocular vision dysfunction- are there any contraindications for treatment? Cases you wouldn't accept? And I am in Arizona- so if I came for treatment, I understand it can take 8-10 treatments? Would this require multiple visits? Are you working to teach other providers your treatment approach? Thank you so much for all of your dedication, hard work and information you share!!
Sounds like me down to a T. Always had perfect 20/20 until a few years ago. Plus the awareness issues.
Sounds VERY MUCH like my experience!
I've had this for years
Thank you! Youre an amazing Doctor! I just wish I had money to see you!
Hi karlabarr, Thank you for your kind words. Hope you can get care for your case close to home for now by someone who understands cervical instability. We wish you all the best in health!
The doctors I saw kept bringing up my anxiety meds which i never took in a way to discard my claims of symptoms as just mental illness
no more im seeing a specialist like Dr Hause ASAP
I WAS that guy that was labeled crazy !
I was a professional therapist for 25 years- very well respected until a car accident and broken neck- when I tried to seek treatment, I got the same thing 🙄 my teeth felt like I needed root canals- so I went to the dentist who only said my teeth were fine and acted like I was crazy- turned out it was from the trigeminal nerve- so disgusting a dentist didn't know this and they find it easier to label you as crazy when they don't know or understand
I pray one day I can see you.
I need to get better.
I'm tired of feeling sick.
We hope you will get the healing you need whether through methods at our clinic or another. Hang in there, Maria.
@@CaringmedicalProlotherapy thank you.
God bless you all.
All these symptoms are characteristic of Lyme and co-infections. Lyme and other tick infections will eventually cause all kinds of nerve dysfunction. Bartonella is an epidermic and is especially detrimental to the brain and eye. You all need to get blood work done for Lyme.
Dr Hauser, I need this so bad. I've been dealing with this since July and doctors keep saying it is just anxiety. I need imaging to show is there is a problem or not. But I live in California :(
Hi Ryan, Thanks for sharing and sorry to learn about what you've been dealing with since last summer. We understand travel is not feasible for everyone, but if it were in the future, feel free to reach out to us directly for a more thorough case review. We wish you all the best in navigating your options closer to home. Take care.
hi Ryan I live in San Diego too did u ever get yours fixed
Severe Adrenal fatigue can also cause pupil issues
That happened to me (a mix of both cases). A neurologist said I have MS. Maybe, but is it possible it's really my vagus nerve? My neck is stiff, the symptoms came strongest after whip lash from car accident and since the whiplash, I have what I call nocturnal focal seizures. But my neurologist blames EVERYTHING on MS now that he labeled me. I have always been extremely flexible since before kindergarten. I had my thyroid out at 23 yrs old. I'm 53 now. The car accident 2 yrs ago created intense memory loss including forgetting my 5 children's names. I had to think of the first letter of their name to bring their name to memory. I couldn't remember numbers or details longer than 3 seconds. Yet, I knew who I was, whete I was and the date. I lost short term memory capabity so had to quit some classes I was taking for functional nutrition.
I had strange eye issues and unexplainable anxiety and nightmares. I have had virtually zero care over these issues. I have refused drugs for MS so the doctors don't want to treat me at all. They basically leave me feeling like it's my fault I have symptoms. However the only drug my insurance will pay for has a side effect of liver cancer. My mom just died of liver cancer so to me, I don't see it as a sensible option when strict diet control shows benefits.
I eliminated gluten, dairy, pork, MSG, artificial sweeteners, most lectins such as nightshade veggies, beans, etc, and all table sugar. I eat mainly grass fed/grass finished meat and butter. I only use sea salt or Himalayan salt and olive oil for cooking. I eat all organic and consume spoonfuls of coconut oil at a time. I eat green Olives a lot ( a jar a day) because I need extra sodium for some reason. I regularly consume cacao mixed with coconut milk to soften and monk fruit to sweeten, pistachios, green tea, blueberries, plain Greek yogurt, and coffee pretty much every day. I bounce between 112 lbs and 126 lbs. Sometimes in a single week depending on water retention. All symptoms worsen during my menstrual cycle. I have very low blood pressure dropping to 57/38 one time at my doctor's appointment. I think I have hypoglycemia but no tests have been done.
I can't consume sugar or I react but I can eat 100% raw honey if the bees consumed yellow clover.
I can't eat fiber or my system jams. I take in some fiber foods in nuts and Olives etc as stated above but if I eat cruciferous Veggie, I get destroyed for days. I feel toxic/drugged or poisoned when constipated. I control it all pretty well however everything you say about the vagus nerve sounds right to me. I have swallowing paralysis as I attempt to swallow. My jaw feel misaligned some days and I get slightly nasal sounding but no congestion. Ugh! My doctors avoid me like the plague because I won't take a single drug including Tums or Tylenol. I choose chemical free so I always know what my body is saying.
I always feel like I have a knot inside my left should blad and sometimes pressing on my neck, right below my skull takes headaches away. I told my doctors I feel like my brain is being pushed into my ears when I get brain fog, but they don't even comment then move on to their next step to get the appointment over.
I have low nutrient absorption. I test low on iron, Zinc, copper, vitamins A, D, and E and did have my gull blades removed. I demanded these tests. They refused forever saying my problems didn't have to do with vitamins. Yet all my levels were SUPER low! They still don't care except about the iron.
My B vitamins test great. I have stopped consuming calcium, coffee and polyphenals close to times I eat iron plus eat pistaccios for copper before consuming iron. That seems to have fixed my iron. But I also have frozen feet though warms to the touch. I get invisible tremors throughout my body then get narcolepsy followed by passing out and waking with a focal seizure (feeling of falling plus heart issues). Even after waking, I can't stop the falling sensation or heart issues for a few minutes. Plus I can't always respond by waking. I feel paralyzed.I know it's happening but can't move. I can force movement but feel like my body is 500 lbs.
However, sometimes I feel like my brain is leaving my body like I'm about to die, so I force myself to quickly sit up and come to. Then walk it off for about a minute. I don't feel right so go back to sleep. It returns up to 4 times in a row.
I started off like the first patient and now feel like the second patient agent 2 years
I have these:
1. Some minor pain swallowing water or other liquids.
2. Ringing in the ears for minutes (duration is different every time it starts).
3. Some facial pain
4. Some pain the back of my neck.
5. When I drive, my left arm starts to hurt from the inside at around the shoulder area, bicep, and forearm.
5. Minor headache that feels like ringing
6. I was playing video games and I started feeling dizzy and I had to stop.
7. Blurred vision at times.
8. Pressure in the forehead and nose.
Hi vidfreak727, Sorry to hear that, and everything you've listed makes sense to us from a potential structural cause in the neck. We hope that you are able to work with a provider who can help you determine if you have a structural reason for your symptoms. These are symptoms that are very common for us to help in our center. If you would like us to evaluate your case in more detail and potentially see you here, we'd be happy to help. Wishing you all the best in health!
@@CaringmedicalProlotherapy how would you be able to? I’m in California. I’d love to be able to travel to Florida but I have no money for that right now. I also am with Kaiser through my employer.
Can the neck problem cause confusion and changes in behavior?
What do you do if you have iris coloboma- the eye is not connected to the optic nerve, crooked spine, chest pectoral bone sticking out and difficulty swallowing? I don't know how I came across your channel, but I'm glad I did and subscribed. I hope you can help me🙏 Definitely have the symptoms you described Thanks
6 months ago I started getting 99% of this and the “Specialist’s in FL panhandle are lost.
I’ve been diagnosed with CCI, and have been experiencing visual disturbances for 7 months now. I watch many of your videos and wondering if people with CCI that get your prolotherapy treatments have good success with vision improvement/reduced pressure behind the eyes?
I’ve had blurry vision for 2 years the doctor said I have 20/20 !!!!! This is crazy!!!!!
Same-I believe it’s related to my TMJ and now cervical issues . 😢
Hi I have EDS(genetically tested) and I have many of your mentioned issues also i had tribble tinnitus and then I start to have vertigo. I had standard MRI and was dismissed that is just anxiety.Anyway cut long story short... One morning when ringing in my head and vertigo was so bad that there is no way I could go to work I put my neck brace on and In 30 min my life changed !!! there was no ringing no vertigo and my vision was perfect! Took my brace off and ringing comeback ,but not so strong. So for now I keep wearing my neck brace on/off until I can get proper diagnosis and have to tell to my GP what tests she have to send me for , lol
Is it a special kind of neck brace, i would like to try as well
See a Chiropractor. 👍
Please dr make a video of blurry/tired eyes after eating
Oh my thank you for that 0:53 0:53
It's sad that people wanting relief are labeled that
Yes, sadly it happens far too often, in what we've seen.
@@CaringmedicalProlotherapy patient just wants answers from the experts just to be asked
"Do you have any feelings of harming yourself or others"
its disgusting !
Flashes of lightning when you turn your head is due to a vitreous detachment and you still have some traction from bands of vitreous tugging on the retina. Anyone can see this just by putting pressure on the globe. Can you share some cases of lowering intracranial pressure with addressing the neck?
Your videos are always so insightful and put everything I feel in to context. I have bouts of pulsing vision upon movement, sometimes accompanied by whooshing in the ears at the same time and visual snow. I have bilateral internal jugular vein compression from c1 and elongated styloids. Next step is catheter venogram and venoplasty. I’m praying that after 3 years I am finally on the right path.
The first patient you mention is me. Derealisation, feeling detached from my surroundings, numb brain feeling like flow of circulation is being blocked off to the brain.
So fascinating to watch. Thanks for sharing your knowledge and expertise to the world
Thank you for your kind words, Natalie. So happy that you have been connecting with the content and being able to then connect the dots in your own case. We hope you get the relief you need! If travel to Fort Myers is an option, our team would be happy to review your case and see if you sound like a good fit for our center. Wishing you all the best in healing! Take care, Natalie.
Hi how r u now I am seeing same symptoms
@@harshpunkFX hi. I am the same day in day out. I was happy and healthy for 32 years then this started when I was heavily pregnant, 3 years ago. When did this start for you?
I have pressure in my eyes, black dots in my vision, almost static fuzzy vision, dizzy disorientation from my eyes and the almost unreal derealisation feeling
Hi it's what I'm experiencing did you get help?
@@nmash6835 no I'm still looking for answers, I've had loads of tests n stuff but still nothing!
visual snow ?
Have been struggling with these symptoms plus peripheral neuropathy, constant dry cough and stutter step. I have been diagnosed with Parkinson’s. Had cataract surgery in one side. Got glasses prescription updated twice. Nothing helps
i’ve got eye pain, increased pressure, sinus pressure, university the eye pressure, pressure in my face and nose.
am i a candidate for caring medical?
damn straight i am. your prolotheropy could really change my life.
i will get prolotheropy happen somehow.
listen to this guy!
listen to this guy!
listen to this guy!
listen to this guy!
Ever seen somebody's heart reaction on the monitor to Wi-Fi and how it reacts to different strength levels
I have ALL those symptoms
I have Lyme….I have all these symptoms.
Can you recommend any dr like yourself in Cape Town South Africa?
Steven Stavrou in JHB.
😔 hope you take FL Blue
Have you tried the cawthorn cooksley gaze stabilisation exercises
I get the same anxiety an my neck always has tension I feel pressure in my head an dizzy an eye sight it gets bad when I drive an like brain fog as well an I had blood test an CT scan done wish was something that can be done
how can i find someone in the uk that understands this and can perform this procedure , i am having most of these symptoms and its making my daily life miserable . thanks
We are so sorry to hear this. We know how frustrating it can be and unfortunately we hear this from a lot of our UK patients. If you find that you can travel to FL we would absolutely love to help you, but we understand it is not feasible for all. We wish you all the best on your continued research!
I live in Pennsylvania though only problem
During the day my eyes are normal and moistured, but at night when I lay down my eyes start to dry up badly to the point of eyelids and eyes stock together, I always keep a saline solución for every time I need to open my eyes and get up it's more severe on the right eye...what can be the problem!
I've been following you for awhile and find your vids helpful. I have lots of weird symptoms. My eye doc believes I may have visual snow, also ghosted images (some), swallowing problems, vibration feelings in my head along with some other weird things. One thing in particular -- my hairdresser keeps telling me to hold my had straight - it leans, according to her. My ENT told me to straighten my head as well when he was doing a procedure. Maybe my spine might be shifting - maybe nothing more than always holding my work phone between my head and shoulder. In any event, I wish you were here in Phoenix area. I do not know what kind of doc I should be seeing in addition to all the ones I am already seeing for everything - Cardiologist for AFIB, Pulmonary for Pulmonary Hypertension, ENT for swalloing problems etc etc Any advice?
See a Chiropractor. 👍
Opthmos here just shrug. Really? So what kind of doctor DOES investigate this
Why do the great Drs always have to be so far away? 😭😭😭
Traveling to their office is a fraction of the cost of the actual office visits/treatments 😳
Could fasciculations in the the legs also be a symptom ?
I have this in my calves and all the eye symptoms
what about c1 and c2 instability ... does it affect?
❤
Can you advise similar doctor in uae
Do u take insurance
Anyone know why all of my ear muscles in both ears move when I move my eyes??
Dude this is legit me omg
Dear lord Jesus i have all that !
I wish o could afford u I go to a chiropractor they are going to send me to a vertigo specialist
I have DDD on C5 C6 and C7 can this cause vision problems and I get heart palpitations
Hi Gavin, Thanks for sharing and sorry to hear about your neck issues. Glad you are looking into some options for addressing it and the symptoms that are commonly associated with cervical instability. We hope that you are able to get in to see a specialist soon for a treatment plan. If you feel that you need our team in the future to possibly see you here in our center, you are welcome to reach out to us directly. Wishing you all the best in healing!
@@CaringmedicalProlotherapy thank you doc I'm from South Africa and here they don't go that extra mile they do normal vital checks and send you home
I've been feeling very off balance especially in the dark it's ten times worse
Sir please help.
My eyes do all weird things. I have balance issues and severe dizziness like im on a boat and sinking into the lounge and bed. Whoozy head, depression, anxiety, dissociative disorder. Is there any way to find someone in australia who deals with cervical instability who does the same tests as caring medical?
Hi Angela P, We do not know of anyone doing all of the types of tests we do. We are a unique center and always working with technology representatives to look into new tests and which types of tests can best show various anatomy that is being affected in our patient population. We are constantly researching and working on this aspect of our practice because the types of complex cases we see here really need this level of dedication to the field. We do try to discuss what we're learning and seeing in our patients in our videos, research articles, and blogs to try and help others even if they cannot be seen in our center. But we do understand that it can be frustrating to not have other centers like this everywhere and that many patients feel they are trying to piece together their own case because no local doctor is able to put it all together for them. Sorry that you have been experiencing this and we wish you all the best in your quest for answers and finding the ideal treatment for your symptoms.
Have you tried the cawthorn cooksley gaze stabilisation exercises
Can u help me out? I was testing my fever and I think I pushed the tester thing too far in my ear... My ear feels full but I got my ear looked at and there’s not that much ear wax. I do have a cold so is it just a cold symptom? It didn’t feel full straight away when I did it. I posted this on another video but I figured u might not see it. I can live with this problem, I can hear but it’s just weird. Also whenever I swallow or yawn my ears pop, is that normal? Sorry for all the questions I’m just a bit worried.
Probably your Eustachian tubes are compressed by muscles tightness in your neck, TMJ... relax, and Diet... no gluten no sugar no dairy...
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Sounds alot i have, ugh
Dr hauser I am still having issues. I have eye ball pain. Blurry vision. Vertigo being seen by a neurologist here in Florida. I’m suffer from all sorts of symptoms from cervical insatiably but he says I have mood disorder. Because I tell him all of my issues. He put me on topamax which has helped but I still get symptoms and side effects. Now he sending me to physical therapy. Which I know won’t help. He never did a MRI to see what is going on. He only looked at the one from the emergency room. I am desperate to get more answers i am suffering. I feel like a dementia patient. It’s terrible. He doesn’t listen to me. He checks my reflexes and sends me on my way . Please help!!
Have you tried the cawthorn cooksley gaze stabilisation exercises
@@charlescarter2072 no what is it?
@@safariprint1972 hard to explain here but really helped me . I did it twice a day for three weeks and it was a game changer. Google it for details. Also check with your doctor if it’s appropriate for you...as I’m not a doctor
Also get to the bottom of your emotions too. I found that that really helped me. I joined some 12 step groups to help me with childhood trauma (Aca)
@@charlescarter2072 ty will do.