Jul
23

Montel Williams Explains How He Deals With His Multiple Sclerosis (Part 2)

Posted by admin Comments (25)

(Part 1) www.youtube.com (Part 2) www.youtube.com (Part 3) www.youtube.com (Part 4) www.youtube.com


More What Is Multiples Sclerosis

    25 Responses to “Montel Williams Explains How He Deals With His Multiple Sclerosis (Part 2)”

    1. laziruss says:

      5:08 I’ve done that as well. It’s the worst feeling

    2. ambc98 says:

      i soo wish more people would listen i have ms 7yrs montel is a great man and im a good person i havent had the best i keep faith

    3. ramona7609 says:

      I have all these symptoms for years but in my world no one cares so I just carry on and live with it. I will finally get an MRI this winter though. My only fear is that they will tell me there is nothing wrong with me.

    4. DisabledActivists says:

      Hi Ramona.. If the doctor doesn’t believe you are experiencing these symptoms, don’t get upset. You have to continue to get second opinions until you find a doctor who will treat your symptoms. Montel was misdiagnosed by know-it-all docs for years.

    5. Entropy56 says:

      MS takes one apart piece by piece.
      I have a saying…”Break your arm you have one problem. Get MS you have 100 problems.”

    6. glorthoron3791 says:

      everyone, look into Raw Food effects on MS. It works. I have a friend who is already improving after several weeks.

    7. lenief says:

      I tried to convince my sort-of sister-in-law of this. Wouldn’t have it.

      You’re invited to the address below
      WhereDoYouGetYourProtein.
      blogspot.
      com

    8. hashcr says:

      Orah is not a good interviewer!

    9. Johangela71 says:

      i think people who post things that are not scientifically proven to help MS, should refrain from posting. i have had it for 16 years and have heard a lot of stupid advice.

    10. Johangela71 says:

      take interferons to slow progression or glatimir acetate -Copaxone if you are allergic to interferons. reduce stress in life. have a treatment team: Neuro-Ophthalmologist, Neurologist, and PCP. eat healthy and vitamin D3 is important because most ms patients have a D deficiency. excercise to a point, not a breaking point.

    11. Johangela71 says:

      DisabledActivists you are great !

    12. Johangela71 says:

      please ignore false cure alls and to rule them out ask yourself does this stop the lesions forming on the brain and spinal cord…does it protect the blood barrier in the brain from the T-cells entering & attacking…..read & protect your health. criteria has changed for diagnosis. if you are positive on one test for ms legally DR is supposed ti give you a RX.

    13. sn1pe352 says:

      I am an MIT Physics student whos studied electrical engineering and electrophysiology and I believe i have found an absolute simple curing for MS using Physics, if you or someone you know has MS please msg me…also if you have HIV AIDS i have cures so msg me

    14. sn1pe352 says:

      I understand where youre coming from but Im not like other people, please research Transcranial Magnetic Stimulation for MS Treatment (From my understanding of the disease and physics I can promise you it will only help) also check out Megadoses of Intravenous Vitamin C treatment

    15. fingerbob74 says:

      I think I have the progressive form which my father had and died from 4 years ago! I have noticed progressive deterioration since sept 2005! no official diagnosis yet but I know there’s something up! I got 1 negative mri scan back in May of
      2006!

    16. lura32000 says:

      @sn1pe352 smart guy

    17. drewfuss2121 says:

      I think Montel pretty much said it all. Oprah didn’t have to interview too much, anyway.

    18. 9gabbycats says:

      Is Montel informed about CCSVI?

    19. 2ndSamuel710 says:

      Montel should be outspoken against vaccinations & recognize ‘jab’ years ago caused him MS- Big Pharma owns media would put target on his back. Guess such stand would cost him $ & position. Word Pharmacy comes from Greek word Pharmakeia means magic, sorcery, witchcraft, poison. Autism & MS. NO vaccination EVER proven safe or effective. Infectious disease already on steep decline BEFORE vaccinations introduced. Jew Jonas Salk saved world of polio? Puke. Spare me. Lies. Revelations 18:23 sorceries

    20. ADreamAsLovely says:

      Watching this makes me so proud of him and honored to watch this. You can tell that it means everything to him to be able to talk to a large audience about his experience with ms and how to help people. God bless him.

    21. watzgoodinthe711 says:

      i wish he could get the CCSVI procedure done

    22. mszeee says:

      I didnt know MS was soo painful, OMG thank you for this insight. I cant imagine living with this kind of pain everyday everyday, day in and day out all year wow thats a lot of pain and I dont do well with it. Can someone please find a cure

    23. HiMyNameIsJessica says:

      does anyone know anything about the Italian Doctors new ms “cure”? Please if anyone has any information about getting this done or contacting the doctor or anything please please let me know. My dad has ms.

    24. HCN says:

      Hi myname isjessica,
      I had the procedure done in May, there is significant improvement…but its gonna take time…tons of energy though but for me I have major gait disturbance and balance issue
      ok the procedure is done in Delhi,India.( too amoung other countries…i’m an Indian so I know!)
      the procedure is done at Max Hospital, New Delhi. octore name is Dr. Shakir Husain. His contact email is drshakir@gmail.com. The only thing is that u’ll have to tell him that u r interested in the procedure and what to have it performed (its experimental so he wants the patient to want it!)
      now there is also a possibility of people habving their jugular veins not blocked…but thats very few people …( now that can happen coz of sleep apnea)
      if u have anymore questions shoot me an email at abster79@gmail.com
      HCN

    25. Wolferocks2 says:

      After reading all I have on this one page alone, I find that mediocrity in research is perhaps worse than being diagnosed with Multiple Sclerosis. Ask yourself one question, “Are the side effects of drugs like Avonex, Copaxone or Rebif worse than not being able to walk, talk, kiss your spouse, child or grandchild?” Side effects are different for each individual as are the clinical attacks of MS. To not treat it, to not research logical treatment options and to actually consider treatment options as described here is an enormous attack of illogical thinking. I see comments from television personalities and I laugh. Of course they can experiment with treatment options. Of course they can have the finest diets planned out for them on a daily basis, of course they can because they do not have monetary difficulties as most of the people in the world. Think about it people.

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