As someone who lives with ms a world free of it would mean that I wouldn't have to worry about if I will still be alive and healthy when my son gets married and has children. That would be my greatest dream come true. I have been in remission with very few and not too life adjusting occurrences for 16 years and am still going strong. I still have hope for the future and still live my life fairly normaly. I just decided that I wasn't going to allow it to rule my life.
High Saturated Fat diet -> young age (active thymus) -> exposure to herpesviridea or other neurovirus -> high permeability of BBB caused by poor, brittle structure from high saturated fat diet, low levels of vitamin D -> T cells in CNS -> sensitization of T Cells -> later onset of MS -> recovery -> anything that can cause a proper situation for episodes (stress, Epstein Barr, etc.) -> disability
but, to be honest, i think there won't ever be a cure for it - because pharmaceutical-industry, as well as foundations/societys don't really want to ure us!
we are a source of profit! and until they make up to 20 billion $ each year with our medication, they on't let us get healthy again! it is simple as that. money, interest, profit, it's all worth more than my life and the live of all MS patients... i have no hope in a "world without MS" - but i wish...
Where can I get assistance to diagnose MS? I have no medical insurance, I do not work & I am suffering immensely. Currently, I have all but one symptom of MS. I am very apprehensive but I am certain based on the information I have read that I must have it. Please if anyone can assist in helping to me find services to obtain diagnosis, please contact me. Thank you very much. I will be most greatful.
You state you want to keep us moving. Why the ban on simple angioplasty? Why deny us the option of obtaining some relief when we have proof that our veins are stenosed. You can't keep us down forever. The National Money Sucker Society will be out of a job. Criminal negligence by no allowing us the option to obtain a simple procedure that has been approved since 1979 just because we have MS like symptoms. You would rather us continue on this slow-tortuous death. Pay that CEO $450,000 while we die
@pdye39 Angioplasy? You mean the CCSVI? Not enough is known about it. and not enough research is done for most insurance companies to even approve payment. I think your anger should be taken to the those who pay or do not pay in this case for a procedure that isn't clinically proven
@noellezsassy you are so wrong you are a moron with NO experience to say that! I HAD MS for 15 years I Had the Liberation I am MS Free! so much for your theories! ROLF!
And lastly, thank you for reminding me that there are wonderful people all over the world working to rid the world of MS. An internationally shared goal is a beautiful thing indeed.
CCSVI will help MS
Lynneheal 3 months ago
As someone who lives with ms a world free of it would mean that I wouldn't have to worry about if I will still be alive and healthy when my son gets married and has children. That would be my greatest dream come true. I have been in remission with very few and not too life adjusting occurrences for 16 years and am still going strong. I still have hope for the future and still live my life fairly normaly. I just decided that I wasn't going to allow it to rule my life.
MrsAngelaGrogan1 11 months ago
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High Saturated Fat diet -> young age (active thymus) -> exposure to herpesviridea or other neurovirus -> high permeability of BBB caused by poor, brittle structure from high saturated fat diet, low levels of vitamin D -> T cells in CNS -> sensitization of T Cells -> later onset of MS -> recovery -> anything that can cause a proper situation for episodes (stress, Epstein Barr, etc.) -> disability
seekirk 1 year ago
I believe in cures and one day there WILL be one!!!!!! Love you meaghan
1114cara 1 year ago
in A World Free of MS, the National MS Society is full of people without a job! good thinking Sherlock!
gekiryudojo 1 year ago
i have MS and it's a horrible desease!
but, to be honest, i think there won't ever be a cure for it - because pharmaceutical-industry, as well as foundations/societys don't really want to ure us!
we are a source of profit! and until they make up to 20 billion $ each year with our medication, they on't let us get healthy again! it is simple as that. money, interest, profit, it's all worth more than my life and the live of all MS patients... i have no hope in a "world without MS" - but i wish...
m0rbusPolytox 1 year ago
@mackrockettere contact the Society at our toll free number. We can provide information and referral services 1-800-344-4867.
NationalMSSociety 1 year ago
@NationalMSSociety SHAM...cough cough........ sorry, I'm sick off all your BS!
Daniel7681 1 year ago
Where can I get assistance to diagnose MS? I have no medical insurance, I do not work & I am suffering immensely. Currently, I have all but one symptom of MS. I am very apprehensive but I am certain based on the information I have read that I must have it. Please if anyone can assist in helping to me find services to obtain diagnosis, please contact me. Thank you very much. I will be most greatful.
macrockettere 1 year ago
You state you want to keep us moving. Why the ban on simple angioplasty? Why deny us the option of obtaining some relief when we have proof that our veins are stenosed. You can't keep us down forever. The National Money Sucker Society will be out of a job. Criminal negligence by no allowing us the option to obtain a simple procedure that has been approved since 1979 just because we have MS like symptoms. You would rather us continue on this slow-tortuous death. Pay that CEO $450,000 while we die
pdye39 1 year ago 2
@pdye39 Angioplasy? You mean the CCSVI? Not enough is known about it. and not enough research is done for most insurance companies to even approve payment. I think your anger should be taken to the those who pay or do not pay in this case for a procedure that isn't clinically proven
noellezsassy 1 year ago
@noellezsassy you are so wrong you are a moron with NO experience to say that! I HAD MS for 15 years I Had the Liberation I am MS Free! so much for your theories! ROLF!
gekiryudojo 1 year ago
As someone who is living with MS, I thank the makers of this Video and to all those who are living with MS. Keep fighting the good fight
Mickroofer 2 years ago
World-communication and validation is indeed healing.
Thanks for posting.
Hope 2010 is a Year of Fellowship; thanks for the inspiration.
Also, liked your comments on Pastorgeorgec
Happy New Year and may God continue to shine His blessings on you and all of us that are suffering in silence.
Highest Personal Regards, Dr M
DysautonomiaMD 2 years ago
necesito los videos subtitulados...alguien podria decirme como puedo hacer?
MariaFruniz3 2 years ago
Thank you for making this video.
Thank you for posting this video.
And lastly, thank you for reminding me that there are wonderful people all over the world working to rid the world of MS. An internationally shared goal is a beautiful thing indeed.
rudybeardog 3 years ago