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Montel Williams - Guests Living With Multiple Sclerosis PART #01.avi

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Uploaded by on Dec 19, 2009

Guests talk about living with Multiple Sclerosis. 06-02-2008

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Education

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  • I keep wondering how much function I have permanently lost because of physician ignorance?? EBV in 1981, chronic neck/back pain soon after. I have had very brisk reflexes, can't walk heal to toe for at least last 15-20 years. Pain, headaches, stiffness, pain, muscle wasting, pain, numbness, can't lift my arms, pain.... Now, for the past 6 years, I am in bed 24/7. The internet is my only lifeline. I keep reading about the bad effects of MS drugs, and I think it scares me more than the MS!!

  • and begging for pain relief!!!!!

  • I am 99% sure I have MS, and have had it for at least 30 yrs. And I'm STILL waiting for a diagnoses!!! But I FINALLY got a doctor to order a MRI of my brain in Dec. 2011,which shows lesions in the pons. I am leaving for a 15 hour drive to Cleveland Clinic in just a few hours from now.

    I have been ignored, referred to psychiatrists, psychologists, pain management for meditation and biofeedback, accused of drug seeking. Literally THROWN OUT of several hospital emergency rooms while crying..

  • By the way pain pills are awful on your. Liver it ruins it

  • I've got ms im a lady 33 yrs old had it 8 yrs been on avonex7 yrs its making my hair fall out beep takeno time with me I want Ldn @ copanax I pray my girls don't have my genes she's a strong girl. God bless.

  • Montel I have MS but cant take the Meds because of my Liver and my heart, so I take pain pills and sleep alot, till i have a remittion. I have had migraines since i was 6, I had a problem with my eye and my eye surgeon found my MS.

  • I Have MS,Thank You Lord for keeping me!Ive had it since 2003&God has been keeping me from giving up&my illness has not worsen I n my life.Thank You Lord:-)

  • I have RRMS, and I feel hopeful for the first time in years. I created a chat group called M.S. (Millions Strong to raise awareness of CCSVI.). It contains valuable resources to learn about new surgical procedures for people who suffer from M.S. I feel like if I help get the word out these procedures will be recognized, and that people who suffer, like I do, can be helped.

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