in my opinon all the below etc. dosages are different in different medications what is made for most people is entirely too high a dose for me when it does not work for others and visa versa. it is all dependant upon who can do or take what. doctors i believe want a one size fits all, teh nature of ms as I have found it to be is definately not like that.
everyone is different, some meds work for some persons, others are not tolerant of some meds, it is all indifferent. no one ms patient is the same as the other for the simple reason that, one person is attacked nuerologically in one place where another is in another place. everyone is different, along with tolerance of medications. all different allergies etc. some persons can take penecillan others cannot. some can take this or that personally? most everything i cannot. without advers affects.
some people just have the most uncommon of what is it luck? in the world. if it isnt one thing its another? who knows. a battle for life is what I can say and is exactly what it is.
Other issues that take place, different things, conditions, surgeries, scarring etc. all different things from different things that happened, not relevant, common sense. however laymen not allowed to have a brain? not sure. affected not stupid.
I found it took a number of years with chronic extreme migraines befor the first lesion was even seen on a mri. relevant or not? i do not know but with the vision issues the opthalmic migraines the pressure in the eyes that was found etc. all of it, in my opinion has some relevance.
No understanding what so ever in regards to the various areas, either reductions of inflamations or inflamation attacks, etc. no understanding what so ever what a person with ms actually endures on a constant on going chronic basis. it leave s alot to be desired of actually what is in dire need of being understood. along with the ten other nuero ailments closely related to MS. and the difficult nature of diagnosing or what used to be. you can have swelling with migraines without lesions showing
It really would not hurt the further understanding of what cognitive means. It does not mean your a vegetable. it does not mean a full blown gone out of your mind person, cognitive has various levels of impairments. I have found there is extremely very little understanding regarding cognitive impairments.
a objective? proactive? self secured, medical professional to listen to someone who has researched, not to be a smart ass, but rather in the effort of ones own care, along with the what is suggested quality of care of medical professionals. It stands to reason that if a persons is strving to stay alive and become an asset, that what works is heard. In ms. I found, therapy, message, chiropractic, ice, heat, meds, diet, management of the many facets that R due human respect, R a prt of MS. care
ok in trying to keep up with the video and answer per the video, skipped some things, the bottom line with MS. if persons were fortunate enough to be diagnosed early on, many treatment plans are successful. however later diagnosis hasnot afforded all persons this luxury, therefore it is quality of life that is not only assistive however is also a managemnt or otherwise control model. socio economic, strain on systems, etc. regardless there are areas that can be assistive or addressed. it takes
a diffferent topic for a different issue of course. However, socio economics were related to the potentials for becoming disabled, vs. illness. Not at all consistant with reality.
aspects of future directions. There are several answers in each of these studies. however one such study I found most compelling were the issues of socio economics and the relevance to potential future possibility. not necessarily genetically relevant. some successes came from some of the most depressed of socio economic conditions of which became facinating to me as the original topics in the psychology lessons did not correlate with these findings.
by entertaining drugs without reason or cause. with the aspect of being ill, why would someone want to become ill. if we look at studies of students that are treated differently or from socio economic conditions self worth is a question there, and how a person is created or made to feel. then, we look at students that are of the socio economic dynamics so to speak that are successful and entertain drugs and alcohol without regard to the responsibilities of future and future risks. then the asp
is what some have been dismissed as persons who have actually been a self diagnostic or self medicating persons who do not get diagnosed and are not properly cared for. Is one reason persons who entertain drugs so tospeak is one question i have. why did they entertain the activity of drugs and alcohol? is there a reason why a person would attempt to self medicate in areas of drugs on their own? in some yes, just for fun, others? hopeless alcoholics etc? why? i have to ask why someone would live
relapsing has alot to do with control of the illness. It is my opinion the illness is constant however as control and management of the illness that is an off and on relationship, in some persons have a great deal to do with the quality of life of the illness. in C. it is not rickets. high previous disposition is genetic however onset of some and not some, is related to continual exposures to onsets of or some who aquire or do not aquire the illness. there is a great loss in what i believe .
inherited and genetic predisposition in my opinion is in fact related to the placental barrier crossing related to and then a continued exposure to the predispositions.
stress is a contributing factor to the exacerbation process. stress reduces the immune system responses. stress is directly related to immune system response.
antibiotic if the person is not allergic to the penecillan vk worked to assist, to reduce the infectious agents related to the inflamattory processes. As was explained to me, most persons are immune to penecillan vk because of the foods we eat, as most meats are treated with this normal version of antibiotic usage.
sure nmss does, however they wanted the passage of the marijuanna, montel also involved in this has in fact been passed however used in conjunction with other medications, is effective however I found the dosages to be excessive or suggested dosages to be excessive in the use of marijuanna and efficacy. I found that they did not advance because the suggested amount is excessive. 10 marijuanna cigarettes a day? that is excessive in my opinion. the steroids I can no longer take. response bad now
stretch exercises is important however, pushing the body is a increase in the ms exacerbations. it is not transferable. it is what the persons are exposed to, and or genetics, otherwise is not contagious.
reducing the movement does reduce the exacerbation of. The continued pushing of a person does in fact, reduce the increase or excelleration of the disability related to the ms. problem? no quality of life. sedentary? is not desired in anyone s life in my opinion.
It also makes sense to me that to include inflamation, or concerning inflamation that ice packs to reduce the inflamation, that ice packs reduce the inflamation to include the severe migraines that also go along with ms I personally believe is due to the lesions forming on the brain, neck spinal cord, etc.
It is my opinion, that medications such as lyrica, nuerontin, baclofens, etc. are nothing short then the spead up process to murder, drown people, etc. with ms. to get rid of persons faster? a drain on the insurance companies? etc. My toe was stuck up for years. I could not wear a pair of shoes for more then a two month period of time without going thru the shoes, no matter the leather or what they were made of.
i find them to be extremely arrogant mean and take great delight in persons agony. by way of all the broken fibers and the nerve pain that people suffer. I have never seen a more sick and dettrimental society of what is supposed to be medical professionals in all my life.
while in the state that i am currently in, these people love to torture people. they enjoy greatly and fully the extent of persons pain, they are sick deprived and ignorant more then any medicine has ever experienced in the history of medicine.
my research was in fact done over time and in the note taking of what was actually going on inside the body and how to keep the so to speak attack mode reduced, ie: reducing the number of lesions, however a chronic or constant activity in the background. it still exists. however reducing damage is key to the continued quality of life or reducing the amount of disability a person sustains regarding the illness.
of the body whose being attacked. The next method found ie: the ms or relevant illness is related to the central nervous system. calming hte central nervous system that is in constant hyper mode so to speak, then needs to be calmed by what works to calm the central nervous system. see mayo clinic also substantiated this very art of quality of life methods regarding MS.
I began this theory based on my impression that illness is a response to a foreigne entity entering hte body and the bodies defense mechanisms attempting to rid itself of the foreign or correct the attack on the body, via the immune system response. The problem becomes greater as the immune systems response continually goes into a chronic or in laymens terms, attack mode. it is a if you will chronic fight inside the body where no one else in the entire world can imagine what is going on inside
foreigne material in the system. One reason it became a part of my research to treat the inflamation, especially after being allergic to what medicine uses to treat inflamation, allergy medicines to treat the inflamation. It does work I did use different doses for different MRI's and found a reduced inflamation of lesions on MRI's. This does not mean the activity is not still in the back ground attacking the nerves, it just means that the inflamation is reduced.
severed nerve endings and fibers. in the eyes, ie: floaters, the left is a picture of development of the fibers? change in the fibers that are in the system entering the blood? the problem is that the blood brain barrier is not supposed to cross or be able to enter the other. It is my suspicion however that this happens by inflamation caused by the nerve breaks and entry into blood system. so someone to understand this would be like a swelling of a splinter in a finger so to speak almost
I have been personally more and more successful then thousands of years of research and stupid doctors with their insanity of what they think they know. so thank you. diabeties? another line of crap. then if you get the treatments that work? ppl. like to steal your ins. and label you and when it is a problem no one gives a shit about your identity. the cognitive, etc. everyone is a doctor. but dont have a clue about anything. quality of life is not respected or even a concern.with most doctors.
every bit of the opening credits? the biggest joke and lie any one ever came out with, should be made to excuse yourself, be smacked in the hand or what ever allowed you to put such lies up on the screen. in fact I am so pissed off at the lies related that I am turning this off right now, you are all liars after 30 yrs of pure hell you know what you are all welcome to do with what you do not know about real life, thank you since you have no problems with no experience you can grow up a little
Help Jeff Johnson raise money to find a cure for Multiple Sclerosis. Visit his fund raising home page at nationalMSsociety website and add /goto/jeffjohnson to the URL
that is nationalMSsociety AND dot org AND /goto/jeffjohnson
I know few people suffering from MS...it is truly horrible. But I must say I've noticed that they become stronger and better persons - probably facing incurable disease all people start thinking about what's really important in life...
he may know about the history but I am the Expert Because I have lived with MS for 16 years and last October 2010 I was Liberated from CCSVI in Serbia and I am now free of MS and can run and do everything I am 51 with MS and can run! you need to wake up Mr Jock OC,MD,FRCP(C),MAPC,LLD(HON) DSc, FRCP (LON) you have a lot of titles but you are Blind
CCSVI Clinic Receives Joint IRB Approval for Aftercare Protocol Study.
The joint application between Noble Hospital and CCSVI Clinic has been approved through the IEC Institutional Review Board (IRB) that will allow researchers to use patient data to study their new extended and enhanced aftercare treatment protocol. Please Call 888-419-6855 to know more about participating in the study. Log on to ccsviclinic. ca for more information. Email apply -at- ccsviclinic. ca
in my opinon all the below etc. dosages are different in different medications what is made for most people is entirely too high a dose for me when it does not work for others and visa versa. it is all dependant upon who can do or take what. doctors i believe want a one size fits all, teh nature of ms as I have found it to be is definately not like that.
boxerpup7 2 months ago
everyone is different, some meds work for some persons, others are not tolerant of some meds, it is all indifferent. no one ms patient is the same as the other for the simple reason that, one person is attacked nuerologically in one place where another is in another place. everyone is different, along with tolerance of medications. all different allergies etc. some persons can take penecillan others cannot. some can take this or that personally? most everything i cannot. without advers affects.
boxerpup7 2 months ago
some people just have the most uncommon of what is it luck? in the world. if it isnt one thing its another? who knows. a battle for life is what I can say and is exactly what it is.
boxerpup7 2 months ago
Other issues that take place, different things, conditions, surgeries, scarring etc. all different things from different things that happened, not relevant, common sense. however laymen not allowed to have a brain? not sure. affected not stupid.
boxerpup7 2 months ago
I found it took a number of years with chronic extreme migraines befor the first lesion was even seen on a mri. relevant or not? i do not know but with the vision issues the opthalmic migraines the pressure in the eyes that was found etc. all of it, in my opinion has some relevance.
boxerpup7 2 months ago
No understanding what so ever in regards to the various areas, either reductions of inflamations or inflamation attacks, etc. no understanding what so ever what a person with ms actually endures on a constant on going chronic basis. it leave s alot to be desired of actually what is in dire need of being understood. along with the ten other nuero ailments closely related to MS. and the difficult nature of diagnosing or what used to be. you can have swelling with migraines without lesions showing
boxerpup7 2 months ago
It really would not hurt the further understanding of what cognitive means. It does not mean your a vegetable. it does not mean a full blown gone out of your mind person, cognitive has various levels of impairments. I have found there is extremely very little understanding regarding cognitive impairments.
boxerpup7 2 months ago
a objective? proactive? self secured, medical professional to listen to someone who has researched, not to be a smart ass, but rather in the effort of ones own care, along with the what is suggested quality of care of medical professionals. It stands to reason that if a persons is strving to stay alive and become an asset, that what works is heard. In ms. I found, therapy, message, chiropractic, ice, heat, meds, diet, management of the many facets that R due human respect, R a prt of MS. care
boxerpup7 2 months ago
ok in trying to keep up with the video and answer per the video, skipped some things, the bottom line with MS. if persons were fortunate enough to be diagnosed early on, many treatment plans are successful. however later diagnosis hasnot afforded all persons this luxury, therefore it is quality of life that is not only assistive however is also a managemnt or otherwise control model. socio economic, strain on systems, etc. regardless there are areas that can be assistive or addressed. it takes
boxerpup7 2 months ago
a diffferent topic for a different issue of course. However, socio economics were related to the potentials for becoming disabled, vs. illness. Not at all consistant with reality.
boxerpup7 2 months ago
aspects of future directions. There are several answers in each of these studies. however one such study I found most compelling were the issues of socio economics and the relevance to potential future possibility. not necessarily genetically relevant. some successes came from some of the most depressed of socio economic conditions of which became facinating to me as the original topics in the psychology lessons did not correlate with these findings.
boxerpup7 2 months ago
by entertaining drugs without reason or cause. with the aspect of being ill, why would someone want to become ill. if we look at studies of students that are treated differently or from socio economic conditions self worth is a question there, and how a person is created or made to feel. then, we look at students that are of the socio economic dynamics so to speak that are successful and entertain drugs and alcohol without regard to the responsibilities of future and future risks. then the asp
boxerpup7 2 months ago
is what some have been dismissed as persons who have actually been a self diagnostic or self medicating persons who do not get diagnosed and are not properly cared for. Is one reason persons who entertain drugs so tospeak is one question i have. why did they entertain the activity of drugs and alcohol? is there a reason why a person would attempt to self medicate in areas of drugs on their own? in some yes, just for fun, others? hopeless alcoholics etc? why? i have to ask why someone would live
boxerpup7 2 months ago
relapsing has alot to do with control of the illness. It is my opinion the illness is constant however as control and management of the illness that is an off and on relationship, in some persons have a great deal to do with the quality of life of the illness. in C. it is not rickets. high previous disposition is genetic however onset of some and not some, is related to continual exposures to onsets of or some who aquire or do not aquire the illness. there is a great loss in what i believe .
boxerpup7 2 months ago
inherited and genetic predisposition in my opinion is in fact related to the placental barrier crossing related to and then a continued exposure to the predispositions.
boxerpup7 2 months ago
with or without MS.
boxerpup7 2 months ago
stress is a contributing factor to the exacerbation process. stress reduces the immune system responses. stress is directly related to immune system response.
boxerpup7 2 months ago
antibiotic if the person is not allergic to the penecillan vk worked to assist, to reduce the infectious agents related to the inflamattory processes. As was explained to me, most persons are immune to penecillan vk because of the foods we eat, as most meats are treated with this normal version of antibiotic usage.
boxerpup7 2 months ago
sure nmss does, however they wanted the passage of the marijuanna, montel also involved in this has in fact been passed however used in conjunction with other medications, is effective however I found the dosages to be excessive or suggested dosages to be excessive in the use of marijuanna and efficacy. I found that they did not advance because the suggested amount is excessive. 10 marijuanna cigarettes a day? that is excessive in my opinion. the steroids I can no longer take. response bad now
boxerpup7 2 months ago
The therapies are useless if not in fact started at onset of the illness. started later in the illness has proven ineffective
boxerpup7 2 months ago
stretch exercises is important however, pushing the body is a increase in the ms exacerbations. it is not transferable. it is what the persons are exposed to, and or genetics, otherwise is not contagious.
boxerpup7 2 months ago
reducing the movement does reduce the exacerbation of. The continued pushing of a person does in fact, reduce the increase or excelleration of the disability related to the ms. problem? no quality of life. sedentary? is not desired in anyone s life in my opinion.
boxerpup7 2 months ago
It also makes sense to me that to include inflamation, or concerning inflamation that ice packs to reduce the inflamation, that ice packs reduce the inflamation to include the severe migraines that also go along with ms I personally believe is due to the lesions forming on the brain, neck spinal cord, etc.
boxerpup7 2 months ago
It is my opinion, that medications such as lyrica, nuerontin, baclofens, etc. are nothing short then the spead up process to murder, drown people, etc. with ms. to get rid of persons faster? a drain on the insurance companies? etc. My toe was stuck up for years. I could not wear a pair of shoes for more then a two month period of time without going thru the shoes, no matter the leather or what they were made of.
boxerpup7 2 months ago
i find them to be extremely arrogant mean and take great delight in persons agony. by way of all the broken fibers and the nerve pain that people suffer. I have never seen a more sick and dettrimental society of what is supposed to be medical professionals in all my life.
boxerpup7 2 months ago
while in the state that i am currently in, these people love to torture people. they enjoy greatly and fully the extent of persons pain, they are sick deprived and ignorant more then any medicine has ever experienced in the history of medicine.
boxerpup7 2 months ago
my research was in fact done over time and in the note taking of what was actually going on inside the body and how to keep the so to speak attack mode reduced, ie: reducing the number of lesions, however a chronic or constant activity in the background. it still exists. however reducing damage is key to the continued quality of life or reducing the amount of disability a person sustains regarding the illness.
boxerpup7 2 months ago
of the body whose being attacked. The next method found ie: the ms or relevant illness is related to the central nervous system. calming hte central nervous system that is in constant hyper mode so to speak, then needs to be calmed by what works to calm the central nervous system. see mayo clinic also substantiated this very art of quality of life methods regarding MS.
boxerpup7 2 months ago
I began this theory based on my impression that illness is a response to a foreigne entity entering hte body and the bodies defense mechanisms attempting to rid itself of the foreign or correct the attack on the body, via the immune system response. The problem becomes greater as the immune systems response continually goes into a chronic or in laymens terms, attack mode. it is a if you will chronic fight inside the body where no one else in the entire world can imagine what is going on inside
boxerpup7 2 months ago
foreigne material in the system. One reason it became a part of my research to treat the inflamation, especially after being allergic to what medicine uses to treat inflamation, allergy medicines to treat the inflamation. It does work I did use different doses for different MRI's and found a reduced inflamation of lesions on MRI's. This does not mean the activity is not still in the back ground attacking the nerves, it just means that the inflamation is reduced.
boxerpup7 2 months ago
severed nerve endings and fibers. in the eyes, ie: floaters, the left is a picture of development of the fibers? change in the fibers that are in the system entering the blood? the problem is that the blood brain barrier is not supposed to cross or be able to enter the other. It is my suspicion however that this happens by inflamation caused by the nerve breaks and entry into blood system. so someone to understand this would be like a swelling of a splinter in a finger so to speak almost
boxerpup7 2 months ago
I have been personally more and more successful then thousands of years of research and stupid doctors with their insanity of what they think they know. so thank you. diabeties? another line of crap. then if you get the treatments that work? ppl. like to steal your ins. and label you and when it is a problem no one gives a shit about your identity. the cognitive, etc. everyone is a doctor. but dont have a clue about anything. quality of life is not respected or even a concern.with most doctors.
boxerpup7 2 months ago
every bit of the opening credits? the biggest joke and lie any one ever came out with, should be made to excuse yourself, be smacked in the hand or what ever allowed you to put such lies up on the screen. in fact I am so pissed off at the lies related that I am turning this off right now, you are all liars after 30 yrs of pure hell you know what you are all welcome to do with what you do not know about real life, thank you since you have no problems with no experience you can grow up a little
boxerpup7 2 months ago
reality hurts! MS is still among the diseases without cure..sad
happinesson 2 months ago
Aww ;(
katheryncruz24 3 months ago
This has been flagged as spam show
Help Jeff Johnson raise money to find a cure for Multiple Sclerosis. Visit his fund raising home page at nationalMSsociety website and add /goto/jeffjohnson to the URL
that is nationalMSsociety AND dot org AND /goto/jeffjohnson
Ekorn999 3 months ago
Nice video...and now give us something like "Future without Multiple Sclerosis". That would be really good... :(
RedleafResort 4 months ago
historical development of disease
PersonalHumility 5 months ago
I know few people suffering from MS...it is truly horrible. But I must say I've noticed that they become stronger and better persons - probably facing incurable disease all people start thinking about what's really important in life...
IVEDCtube 5 months ago
Horrible disease... I believe that positive thinking and care can truly help people in need.
ethnolink 6 months ago
I have epilepsy and I think i have this.
It is getting hard to walk. I just fall down.
duvexy 10 months ago
he may know about the history but I am the Expert Because I have lived with MS for 16 years and last October 2010 I was Liberated from CCSVI in Serbia and I am now free of MS and can run and do everything I am 51 with MS and can run! you need to wake up Mr Jock OC,MD,FRCP(C),MAPC,LLD(HON) DSc, FRCP (LON) you have a lot of titles but you are Blind
gekiryudojo 11 months ago
This has been flagged as spam show
CCSVI Clinic Receives Joint IRB Approval for Aftercare Protocol Study.
The joint application between Noble Hospital and CCSVI Clinic has been approved through the IEC Institutional Review Board (IRB) that will allow researchers to use patient data to study their new extended and enhanced aftercare treatment protocol. Please Call 888-419-6855 to know more about participating in the study. Log on to ccsviclinic. ca for more information. Email apply -at- ccsviclinic. ca
Gregmills007 11 months ago
This has been flagged as spam show
@Gregmills007 this is not spam
gekiryudojo 11 months ago
This is nice video about the historical development of disease. :)
nirajrm 1 year ago