My fiance just released an album dedicated to his mother who has MS. Half of the proceeds will go straight to the MS society. Support good music for a great cause! Please!
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
The Key to the lock is the sea squirt which cures Multiple Scloresis which I suffer from. Watch Run from the cure to find out to heal yourself reguardless of the kind
There is now a Reformed Multiple Sclerosis Society that is urging for the medical community to check out Dr Paolo Zamboni's discovery that MS is caused by poor blood drainage from the brain. The answer to restore this blood drainage from the brain is angioplasty. Watch the before & afters for this surgery called CCSVI on youtube- simply amazing. In just 24 hours a world of difference. Standing on one foot eyes closed in just 24 hours!
Can this research be applied to CIDP (chronic inflamatory poly[rediculo]neuropathy)? If the t-killer cell's migration over the bbb is blocked won't these circulating t-cells attack periferal nerves? Finally, why do some CIDP patients have antibodies in the CSF and some (about 20%) do not?
Omega 3s, low saturated-fat diet (<10g/day), vitamin D (5000IU/day), and a multivitamin. Takes time to regenerate the brain with the right fat (15 weeks to 2 years), but it will help build myelin and reduce inflammation in the long run.
@AWDESIGNS8 im so sorry m8 i read that in a swedish evening newspaper onfurtonatly im as curius as u are ,i cant find the link , but i called the university hospital of lund and the top neurologist didnt know anything about it. btw i also asked alot about stem cell therapy for ms , and sadly the doctor said dont believe everything u see on youtube, they had some tests with in sweden and he said it could even make it alot worse then before the start of the therapy.
I like this and the idea of myelin repair, and the work of the foundation.... I am just a little guy in a big big world of you research guys - but my research as taken me to a different place.... I have been working on the research of many other researchers who have no idea as to what I am doing - but I applied there work to my research... Now I need you big guns to understand this nuts work into myelin repair through "smell" (olfactory) and "taste" (gustatory)....
What if the key is gravity? What if myelin repair requires gravity to remain influencial by maintaining correct alignment with the direction of fluid flow? Could ms be posture related? Do people with ms experience more problems sleeping flat and when sitting incorrectly? Do people with ms find they have more problems emerging over night and experience them when trying to get out of bed in the morning? Does high humidity comprimise circulation and induce relapses? Is ms a circulation problem?
after tons of research and endless interviews and multiple healing research,it seems that MS is actually easy to heal...it is self inflicted by the patient, starting with their own soul becoming detached from their nervous system and then of course their own muscles and body.All patients I have seen so far need to love themselves again and the healing process will commence.If you want help ...CALL ME...this is FREE !!!!! You have nothing to lose......call me...860 391 1650 in the USA
@JetDriver1111 u should pay more respect for people with it and back it up with real scientific proof otherwise i beg u with biggest sincerity shut da fuck up sir!
@Potalot your name should be smokes pot alot....douche bag..I've forgotten more than you will ever know about this shit...not to mention my family member has MS...MD's know only part of the problem, I know the other half...when you have 5 degrees under your belt, come see me...until then , go smoke another joint asshole...
@JetDriver1111 wow thousands of doctors and scientists could not figure out this disease but you and your mombo jumbo soul bullshit u should use your belt that u have 5 degrees under and strangle your lying piece of shit self u fucking cunt!!! kids have better imagination then u!! did even accour to u that people with ms starts to hate themselfs bc of the condition ? u take stpidity to new levels and btw pot is given to ms patients
anyone with ms who can speak on a phone to me should call me..I may be able to help you...this is not a joke nor a business scam...860 873 8757..leave your number I will call you back if i am not there..
hi my name is raklita im froum romania , i have 23 age and 2 yers back i got this desasees caled mutiples sclerosis(MS) if u can help me plz contact me of my mobile +40751565180 ... thx
@1971blinson they are doing research for it not a cure other wise there would be no ms. i think and i did look it up it helps the symtoms of ms. thats all you want to stop that did any get the ccsvi and then take a brain and spine mri at it read no lesions any more then i can say it is a cure other wise its not.
ScienceDaily (July 1, 2009) — Scientists have uncovered new evidence suggesting that damage to nerve cells in people with multiple sclerosis accumulates because the body's natural mechanism for repair of the nerve coating called "myelin" stalls out.
Check our my exclusive video of Montel Williams talking about being diagnosed with MS and the one pill he always makes sure he takes! Recorded 6/27/09! Don't miss it!
Yet again INFLAMATION strikes . Tell what is wrong with you and i'll tell you whats INFLAMED . cuz that is always the problem. Someting gets inflammed and you feel like sh!t . However., WHAT is making us inflammed to begin with?? ENVIRONMENT. is my guess. (;
My wife was diagnosed with MS 12 years ago. This disease has gradually affected her ability to walk, keep her balance and in the last year has caused severe headaches. The last symptom is a problem with her eyes that causes a jerking effect leading to sever dizziness and nausea. Anyone have any possible ways to relieve this?
parttygnome, I was diagnosed with MS 1.5 years ago. I'm fortunate to live 30min. away from Dr. Burt Berkson. His program is amazing. He prescribe Low Dose Naltrexone (LDN), Alpha Lipoic Acid, vitamin D, Magnesium, Selenium, B complex, Multi-vitamin, Omega 3. High raw vegetable diet, Low on processed foods and exercise. It's a wonderful plan, but the problem is it's hard to get a dr. to prescribe LDN. Good luck.
parttygnome, one more thing. If you choose to take supplements, make sure they are not Chinese. The good brands are Metabolic Maintenance, Carlson and Biotech. In that order, IMO.
Our Case Western lab uses mesenchymal stem cells in their work, which are a variant of adult stem cells. There's a Wiki article on mesenchymal cells for more info.
Is this research going to lead to a cure ? ow soon do you think ? i have had ms since 1990 and I can't wait to heal .. where us the best place to get support ? US?
The closest analogy for what we are working toward is how insulin works as a treatment for diabetics. A myelin repair therapy wouldn't cure MS, but would dampen the symptoms to help users lead a normal life.
Is it true that I, a MS patient since '75, can not be helped with Stem cell therapy? I am so confused as to what I learned in all of my sciences. Why won't it help a person who has had MS for over 5 yrs?I am very angry, yet very, very sad about this. Its as if meds R the only thing 4 me the rest of my pitiful, breaking down life!!!!WHere is the medicimal pot, cause I cant stand the thought of this?
The Myelin repair foundation doesnt wanna find a cure. Imagine if they find a cure. All the labs, all the jobs, all the money, everything having to do with MS will go away. They dont wanna a cure, just like the greedy freakig drug companies. The only people that really want a cure for MS are the people with MS.
I can certainly understand your frustration with the lag time toward finding a cure or a really effective treatment. But I disagree strongly with the rest of your statement.
Our founder has MS. Many of our volunteers have MS. They have a totally personal stake in our research, and all of us are committed to finding a myelination treatment for the sole reason that it will help everyone who suffers from this disease - ourselves included!
Also, as a non-profit, MRF will put any additional funds from licensing our drug targets back into research for more therapeutics. That's our mission, and that's what we will continue to do.
I urge you to visit our website and learn more about the passion of our team and the reason why we have embarked on this mission. We are in this to find a better and more effective treatment for everyone with MS.
Best of luck, and I am happy to answer any questions anyone may have.
We at MRF are not trained to diagnose or treat any symptoms of MS.
I have heard that some MS patients have seen improvements from using the Best Bet Diet (see MSRC's website).
Best,
Justine
The information is not provided for the purpose of giving medical advice or recommending specific treatment options. The Myelin Repair Foundation urges you to consult one or more licensed physicians who are trained to diagnose and treat the symptoms of MS and other neurological diseases.
yea but, cant they just apply all their resources to a new disease. there are no shortages of disease.
Business is always booming. especially if you have the reputation that provided a cure. lets say you cure MS. then tackle lupus, I would definitely donate to the guys with the track record of success. plus you have to administer the cure to all the new cases.
This has been flagged as spam show
My fiance just released an album dedicated to his mother who has MS. Half of the proceeds will go straight to the MS society. Support good music for a great cause! Please!
itunes.apple.com/us/album/jnewryep/id476015357
Blessings
JessicaSunshineMusic 1 week 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 2 months ago
The Key to the lock is the sea squirt which cures Multiple Scloresis which I suffer from. Watch Run from the cure to find out to heal yourself reguardless of the kind
qualisarx 5 months ago
This has been flagged as spam show
There is now a Reformed Multiple Sclerosis Society that is urging for the medical community to check out Dr Paolo Zamboni's discovery that MS is caused by poor blood drainage from the brain. The answer to restore this blood drainage from the brain is angioplasty. Watch the before & afters for this surgery called CCSVI on youtube- simply amazing. In just 24 hours a world of difference. Standing on one foot eyes closed in just 24 hours!
2ndSamuel710 5 months ago
Can this research be applied to CIDP (chronic inflamatory poly[rediculo]neuropathy)? If the t-killer cell's migration over the bbb is blocked won't these circulating t-cells attack periferal nerves? Finally, why do some CIDP patients have antibodies in the CSF and some (about 20%) do not?
edwardschlosser1 6 months ago
Omega 3s, low saturated-fat diet (<10g/day), vitamin D (5000IU/day), and a multivitamin. Takes time to regenerate the brain with the right fat (15 weeks to 2 years), but it will help build myelin and reduce inflammation in the long run.
seekirk 11 months ago
XMRV XMRV XMRV XMRV
omv08 1 year ago
a swedish reasercher has cured Multiple scleroisis with milk acid bakteries
Potalot 1 year ago
@Potalot look that up didnt find anything like that
AWDESIGNS8 1 year ago
@AWDESIGNS8 im so sorry m8 i read that in a swedish evening newspaper onfurtonatly im as curius as u are ,i cant find the link , but i called the university hospital of lund and the top neurologist didnt know anything about it. btw i also asked alot about stem cell therapy for ms , and sadly the doctor said dont believe everything u see on youtube, they had some tests with in sweden and he said it could even make it alot worse then before the start of the therapy.
Potalot 9 months ago
@Potalot thanks for writing back sweden i want in usa so your saying stem cell wouldnt work would just make my ms worse
AWDESIGNS8 9 months ago
I like this and the idea of myelin repair, and the work of the foundation.... I am just a little guy in a big big world of you research guys - but my research as taken me to a different place.... I have been working on the research of many other researchers who have no idea as to what I am doing - but I applied there work to my research... Now I need you big guns to understand this nuts work into myelin repair through "smell" (olfactory) and "taste" (gustatory)....
datadatado 1 year ago
What if the key is gravity? What if myelin repair requires gravity to remain influencial by maintaining correct alignment with the direction of fluid flow? Could ms be posture related? Do people with ms experience more problems sleeping flat and when sitting incorrectly? Do people with ms find they have more problems emerging over night and experience them when trying to get out of bed in the morning? Does high humidity comprimise circulation and induce relapses? Is ms a circulation problem?
AndrewKFletcher 1 year ago
after tons of research and endless interviews and multiple healing research,it seems that MS is actually easy to heal...it is self inflicted by the patient, starting with their own soul becoming detached from their nervous system and then of course their own muscles and body.All patients I have seen so far need to love themselves again and the healing process will commence.If you want help ...CALL ME...this is FREE !!!!! You have nothing to lose......call me...860 391 1650 in the USA
JetDriver1111 1 year ago
@JetDriver1111 u should pay more respect for people with it and back it up with real scientific proof otherwise i beg u with biggest sincerity shut da fuck up sir!
Potalot 9 months ago
@Potalot your name should be smokes pot alot....douche bag..I've forgotten more than you will ever know about this shit...not to mention my family member has MS...MD's know only part of the problem, I know the other half...when you have 5 degrees under your belt, come see me...until then , go smoke another joint asshole...
JetDriver1111 9 months ago
@JetDriver1111 wow thousands of doctors and scientists could not figure out this disease but you and your mombo jumbo soul bullshit u should use your belt that u have 5 degrees under and strangle your lying piece of shit self u fucking cunt!!! kids have better imagination then u!! did even accour to u that people with ms starts to hate themselfs bc of the condition ? u take stpidity to new levels and btw pot is given to ms patients
Potalot 9 months ago
anyone with ms who can speak on a phone to me should call me..I may be able to help you...this is not a joke nor a business scam...860 873 8757..leave your number I will call you back if i am not there..
JetDriver1111 1 year ago
hi my name is raklita im froum romania , i have 23 age and 2 yers back i got this desasees caled mutiples sclerosis(MS) if u can help me plz contact me of my mobile +40751565180 ... thx
raklitasolo 1 year ago
ccsvi is not a cure. People need to stop overstating the findings..
Oozingmachismo24 2 years ago
@Oozingmachismo24 but if it is hope for some thats ok to dont give up hope
AWDESIGNS8 1 year ago
an Italian researcher has discovered a cure for MS. MS is a vein blockage disease, and can be cured by ccsvi...google it
1971blinson 2 years ago
@1971blinson they are doing research for it not a cure other wise there would be no ms. i think and i did look it up it helps the symtoms of ms. thats all you want to stop that did any get the ccsvi and then take a brain and spine mri at it read no lesions any more then i can say it is a cure other wise its not.
AWDESIGNS8 1 year ago
I have a bad feeling my MS is going to kill me before anything like this video describes is mastered and implemented.
whitejellyfungus 2 years ago
ScienceDaily (July 1, 2009) — Scientists have uncovered new evidence suggesting that damage to nerve cells in people with multiple sclerosis accumulates because the body's natural mechanism for repair of the nerve coating called "myelin" stalls out.
danyjr 2 years ago
Check our my exclusive video of Montel Williams talking about being diagnosed with MS and the one pill he always makes sure he takes! Recorded 6/27/09! Don't miss it!
jazyskowski 2 years ago
Yet again INFLAMATION strikes . Tell what is wrong with you and i'll tell you whats INFLAMED . cuz that is always the problem. Someting gets inflammed and you feel like sh!t . However., WHAT is making us inflammed to begin with?? ENVIRONMENT. is my guess. (;
archaedemos 2 years ago
My wife was diagnosed with MS 12 years ago. This disease has gradually affected her ability to walk, keep her balance and in the last year has caused severe headaches. The last symptom is a problem with her eyes that causes a jerking effect leading to sever dizziness and nausea. Anyone have any possible ways to relieve this?
parttygnome 2 years ago
or the jerking of the eyes (nystagumus0,i take gabapenton
trojantjl 2 years ago
parttygnome, I was diagnosed with MS 1.5 years ago. I'm fortunate to live 30min. away from Dr. Burt Berkson. His program is amazing. He prescribe Low Dose Naltrexone (LDN), Alpha Lipoic Acid, vitamin D, Magnesium, Selenium, B complex, Multi-vitamin, Omega 3. High raw vegetable diet, Low on processed foods and exercise. It's a wonderful plan, but the problem is it's hard to get a dr. to prescribe LDN. Good luck.
iamgabrielf 2 years ago
parttygnome, one more thing. If you choose to take supplements, make sure they are not Chinese. The good brands are Metabolic Maintenance, Carlson and Biotech. In that order, IMO.
iamgabrielf 2 years ago
hey peg, what about stem cells....
migo53333 3 years ago
Hi Migo,
Our Case Western lab uses mesenchymal stem cells in their work, which are a variant of adult stem cells. There's a Wiki article on mesenchymal cells for more info.
-p
myelinrepair 3 years ago
aren't B-vitamins really important for myelin repair?
maestroanth 3 years ago
Is this research going to lead to a cure ? ow soon do you think ? i have had ms since 1990 and I can't wait to heal .. where us the best place to get support ? US?
isa2222 3 years ago
Hey Isa,
The closest analogy for what we are working toward is how insulin works as a treatment for diabetics. A myelin repair therapy wouldn't cure MS, but would dampen the symptoms to help users lead a normal life.
Good luck to you.
-p
myelinrepair 3 years ago
Is it true that I, a MS patient since '75, can not be helped with Stem cell therapy? I am so confused as to what I learned in all of my sciences. Why won't it help a person who has had MS for over 5 yrs?I am very angry, yet very, very sad about this. Its as if meds R the only thing 4 me the rest of my pitiful, breaking down life!!!!WHere is the medicimal pot, cause I cant stand the thought of this?
karena321 3 years ago
If you want pot you can move to Alaska where it is legal.
"Alaska citizens have the right to possess less than four ounces of marijuana in their home for personal use."
Entropy56 3 years ago
The Myelin repair foundation doesnt wanna find a cure. Imagine if they find a cure. All the labs, all the jobs, all the money, everything having to do with MS will go away. They dont wanna a cure, just like the greedy freakig drug companies. The only people that really want a cure for MS are the people with MS.
tmmylopez 3 years ago
I can certainly understand your frustration with the lag time toward finding a cure or a really effective treatment. But I disagree strongly with the rest of your statement.
Our founder has MS. Many of our volunteers have MS. They have a totally personal stake in our research, and all of us are committed to finding a myelination treatment for the sole reason that it will help everyone who suffers from this disease - ourselves included!
(continued)
myelinrepair 3 years ago
Also, as a non-profit, MRF will put any additional funds from licensing our drug targets back into research for more therapeutics. That's our mission, and that's what we will continue to do.
I urge you to visit our website and learn more about the passion of our team and the reason why we have embarked on this mission. We are in this to find a better and more effective treatment for everyone with MS.
Best of luck, and I am happy to answer any questions anyone may have.
-Peggy
myelinrepair 3 years ago
does diet have implications on MS???
migo53333 3 years ago
Migo,
We at MRF are not trained to diagnose or treat any symptoms of MS.
I have heard that some MS patients have seen improvements from using the Best Bet Diet (see MSRC's website).
Best,
Justine
The information is not provided for the purpose of giving medical advice or recommending specific treatment options. The Myelin Repair Foundation urges you to consult one or more licensed physicians who are trained to diagnose and treat the symptoms of MS and other neurological diseases.
myelinrepair 2 years ago
@tmmylopez
yea but, cant they just apply all their resources to a new disease. there are no shortages of disease.
Business is always booming. especially if you have the reputation that provided a cure. lets say you cure MS. then tackle lupus, I would definitely donate to the guys with the track record of success. plus you have to administer the cure to all the new cases.
salonwithapeal 1 year ago