If an individualized treatment plan from a functional neurologist is the crux of one's recovery then what information does your course provide that is above and beyond the benefit of a personalized assessment by a chiropractic neurologist? Thanks.
As you mentioned in your other comment Michele, committing to being assessed and treated by a board certified chiropractic neurologist can be a substantial financial cost especially when seeing the ones that offer the more thorough examination protocol; some people won't be able to afford it, which it goes without saying, is a real shame, however others might consider it, but perhaps don't have enough knowledge themselves to commit to that venture. It took me 2 years of researching this topic before I booked the trip myself - the course combines and condenses the 20+ pieces of complex literature that I consumed over that time. Because I had built a significant wealth of knowledge on the topic before I saw the team in the states, I was able to ask better questions, get very personalised presentations/explanations from them and also know what activities would help me to improve/set me back when arriving home, which has allowed me to build on the progress I've made since arriving home from the clinic. The course breaks down the neurological link between 3 key sensory pathways and how their function/dysfunction influences the function of the ANS. This is one of the main reasons why sufferers with these types of conditions can't just 'push their bodies a little more each day to recover' - it's because breakdowns in certain neuronal pathways are causing the body to have to make adaptations, making it expel more energy, which forces the individual to want to 'shy away' from engaging in particular activities/exposing themselves to overwhelming/unfamiliar environments - this doesn't just mean engaging in crazy things like concerts/supermarkets/shopping malls etc, but also simple activities like talking and standing up. So people basically have to stabilise (get these systems under control) before progressing with their recovery. I also go more in-depth into my own recovery and share why I believe this is the pathway that provides the most longevity for sufferers of Autonomic syndromes. Yes, you're right you don't need the course, because being assessed by the right practitioner is the key in my eyes, but I think it's up to the individual whether they'd like to be more informed on the topic before committing to making that decision.
@@chris_gascoigneThanks for this overview! The comment you're referencing, from a different video, is my experience that, "most chronically ill people don't have the financial resources for bespoke assessment and treatment by a highly specialized medical professional." It breaks my heart to know so many people with complex chronic illnesses will continue to struggle because current medical systems aren't designed to identify, assess and treat many complex chronic illnesses.
100% with you there Michele, it breaks my heart too; the current conventional health system just isn't good enough, which reflects in the increasing numbers of people getting sick. More resources definitely need to go into actually identifying root causes rather than attacking the effects of these root causes. People currently putting up with these terrible conditions deserve a second chance at life, it's just sad that there's such an enormous gap between the supply and the demand
@@davisrochold1908 I plan to keep making videos on this channel Davis, so I hope they can offer you some value and direction in helping you to find a solution
Yes it surely has psychosomatic symptoms. Some psychiatrist say that guts its the second brain but proper diet, mild excercise and a normal sex life helps a lot.... of course a steady environment in work in the house in your community also help and some meditation all together have a positive impact!
I think those things are definitely important, the way I see it though, is, are those things enough to get somebody out of a debilitating chronically ill state? And often the answer's no, because the underlying issue is actually outside of the person's conscious awareness/control, which is why a thorough examination to identify the location of the dysfunction is often necessary
Certain foods can produce more symptoms in the gut lottie, but by taking this approach you're building up your body's resistance to a wider variety of foods, so that you don't have to rule so many foods out of your diet (if you wish)
I haven't looked up much on it John, but I believe nicotine can impact certain neuro-hormonal pathways to the brain. That could potentially alter activity within the brain, which could then in turn impact digestion
I was diagnosed with UC over a decade ago, but the issues I mention specifically in this video first started for me in 2016 whilst I was being given 3 separate IV antibiotics in hospital Daniel. Those antibiotics seemed to disrupt the balance of the neurological systems, which makes sense, as one of them is a known ototoxic drug, meaning that it is known to be toxic to the otolith, which is a certain component of the vestibular system itself
Hey Chris. This might be a tricky question to answer but I'd love to be able to message back and forth about it if necessary. I'm very interested in visiting a chiropractic neurologist or functional neurologist or something to try and fix my debilitating gut condition and fatigue. Is there something specific that caused you to travel to Michigan to The Keiser Clinic - or would I be able to do something in the UK (I'm UK based)? Like I say, I can message back and forth if it's easier to talk that way. Many thanks, Flynn
What are these neurofunctional hi exercises?
If an individualized treatment plan from a functional neurologist is the crux of one's recovery then what information does your course provide that is above and beyond the benefit of a personalized assessment by a chiropractic neurologist? Thanks.
As you mentioned in your other comment Michele, committing to being assessed and treated by a board certified chiropractic neurologist can be a substantial financial cost especially when seeing the ones that offer the more thorough examination protocol; some people won't be able to afford it, which it goes without saying, is a real shame, however others might consider it, but perhaps don't have enough knowledge themselves to commit to that venture. It took me 2 years of researching this topic before I booked the trip myself - the course combines and condenses the 20+ pieces of complex literature that I consumed over that time. Because I had built a significant wealth of knowledge on the topic before I saw the team in the states, I was able to ask better questions, get very personalised presentations/explanations from them and also know what activities would help me to improve/set me back when arriving home, which has allowed me to build on the progress I've made since arriving home from the clinic. The course breaks down the neurological link between 3 key sensory pathways and how their function/dysfunction influences the function of the ANS. This is one of the main reasons why sufferers with these types of conditions can't just 'push their bodies a little more each day to recover' - it's because breakdowns in certain neuronal pathways are causing the body to have to make adaptations, making it expel more energy, which forces the individual to want to 'shy away' from engaging in particular activities/exposing themselves to overwhelming/unfamiliar environments - this doesn't just mean engaging in crazy things like concerts/supermarkets/shopping malls etc, but also simple activities like talking and standing up. So people basically have to stabilise (get these systems under control) before progressing with their recovery. I also go more in-depth into my own recovery and share why I believe this is the pathway that provides the most longevity for sufferers of Autonomic syndromes.
Yes, you're right you don't need the course, because being assessed by the right practitioner is the key in my eyes, but I think it's up to the individual whether they'd like to be more informed on the topic before committing to making that decision.
@@chris_gascoigneThanks for this overview! The comment you're referencing, from a different video, is my experience that, "most chronically ill people don't have the financial resources for bespoke assessment and treatment by a highly specialized medical professional."
It breaks my heart to know so many people with complex chronic illnesses will continue to struggle because current medical systems aren't designed to identify, assess and treat many complex chronic illnesses.
100% with you there Michele, it breaks my heart too; the current conventional health system just isn't good enough, which reflects in the increasing numbers of people getting sick. More resources definitely need to go into actually identifying root causes rather than attacking the effects of these root causes. People currently putting up with these terrible conditions deserve a second chance at life, it's just sad that there's such an enormous gap between the supply and the demand
I would like to take you me course l, however, way to expensive can’t afford it
@@davisrochold1908 I plan to keep making videos on this channel Davis, so I hope they can offer you some value and direction in helping you to find a solution
@@chris_gascoigne thank you
@@chris_gascoigne have you thought about publishing your course on Udemy?
Yes it surely has psychosomatic symptoms. Some psychiatrist say that guts its the second brain but proper diet, mild excercise and a normal sex life helps a lot.... of course a steady environment in work in the house in your community also help and some meditation all together have a positive impact!
I think those things are definitely important, the way I see it though, is, are those things enough to get somebody out of a debilitating chronically ill state? And often the answer's no, because the underlying issue is actually outside of the person's conscious awareness/control, which is why a thorough examination to identify the location of the dysfunction is often necessary
@@chris_gascoigne what about carnivore and meditation with some everyday light exercise....?
I feel like fibre is what irritates me.
Certain foods can produce more symptoms in the gut lottie, but by taking this approach you're building up your body's resistance to a wider variety of foods, so that you don't have to rule so many foods out of your diet (if you wish)
Me too
This must be why smoking is what keeps me from flare ups, I think its disgusting the nhs treat flare ups with cortisol steroids.
I haven't looked up much on it John, but I believe nicotine can impact certain neuro-hormonal pathways to the brain. That could potentially alter activity within the brain, which could then in turn impact digestion
@@chris_gascoigne Well its put me in remission, the last 5 or so years of trying to quit have made me really bad. Looks like I'm stuck with it.
What caused this to happen to you in the first place ?
Crohn's disease ?
I was diagnosed with UC over a decade ago, but the issues I mention specifically in this video first started for me in 2016 whilst I was being given 3 separate IV antibiotics in hospital Daniel. Those antibiotics seemed to disrupt the balance of the neurological systems, which makes sense, as one of them is a known ototoxic drug, meaning that it is known to be toxic to the otolith, which is a certain component of the vestibular system itself
Hey Chris. This might be a tricky question to answer but I'd love to be able to message back and forth about it if necessary.
I'm very interested in visiting a chiropractic neurologist or functional neurologist or something to try and fix my debilitating gut condition and fatigue. Is there something specific that caused you to travel to Michigan to The Keiser Clinic - or would I be able to do something in the UK (I'm UK based)? Like I say, I can message back and forth if it's easier to talk that way.
Many thanks,
Flynn
Hey Flynn, best to send me an email - chris_unbeatableblueprint@yahoo.com and I'll try to get back to you when I have the opportunity
I don't agree
Which part don't you agree on J?