Medical Stories - Multiple Sclerosis: Out of Mind

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  • čas přidán 8. 03. 2023
  • Multiple Sclerosis has often been called the disease of young white women, but new studies have produced some startling information about the previously unrecognized impact of MS on African Americans. In this episode of Medical Stories, we follow two extraordinary people through their challenges in coping with MS.
    Dawn, a brilliant PhD candidate, left her studies behind over 20 years ago. Tyler, son of NFL hall of famer Earl Campbell, had his own NFL dream cut short when his health took a turn no one saw coming. The stories of these two influencers will bring you to tears.
    Featuring renowned experts, Dr. Mitzi J. Williams from Joi Life Wellness Group in Atlanta, GA, and nurse practitioner, Sophia D. Woodson from University Hospitals in Cleveland, OH.
    Medical Stories is an engaging Public Television docuseries with four Emmy Award wins and eight Emmy nominations. We take viewers on an inspiring journey of untold stories, often with an emotional twist that will not be found on any other medical program. Highly cinematic in style, and very down-to-earth in content, our documentary stories are anchored in the courage and hope of those waging battle against illness. With compassion and sensitivity, we step into the lives of families across the country and present the unvarnished experiences of the people we profile and their loved ones, along with explanations and commentary from leading experts in America’s medical community. Our mission is to help educate, raise awareness and increase knowledge of those who are searching to learn about specific medical issues.
    Please subscribe to our CZcams channel and look for Medical Stories on your Public Television station.
    Check your local PBS listings today!
    Or visit medicalstories.tv/ to learn more about this very popular documentary series.
    Follow us on Facebook: / medicalstories.pubtv.pbs
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    #MedicalStories #MedStoriesTV

Komentáře • 40

  • @donnamoore8479
    @donnamoore8479 Před rokem +22

    My fraternal grandfather had a condition that caused him to walk with a cane, then use a wheelchair .I only knew him bedridden for years. Back then there wasn't the title MS. My maternal great grandfather was the same. Now my sister and I both have been diagnosed with MS for since 1993 and 2001.

  • @tomw588
    @tomw588 Před 2 měsíci +4

    I’ve had MS for at least seven years. I have no loss of mobility and I have a business working at height. I tried various diets but I refused all medicines. But I just got worse whatever I tried. Now I’m (mostly) carnivore and I do a lot of earthing / grounding. I can’t believe how good I feel from the grounding. I’m saying this only to reach out to anyone who suffers from this terrible disease.

    • @scores718
      @scores718 Před měsícem +1

      Hi Tom. What is earthing-grounding? Ty. Ppms 35+ yrs

    • @sherriaaroundtheworld4133
      @sherriaaroundtheworld4133 Před měsícem

      @tomw588 I was just diagnosed with MS this week, after I woke up with right sided facial droop and right arm numbness and tingling. I thought I had Bell’s Palsy so I went to the ER. Multiple MRIs confirmed MS. I have been doing ketovore for a year, lost 70 pounds by walking, sprinting, strength training and grounding/earthing. The doctors said based on my lesions size and location, they would expect to see me completely paralyzed on my right side, but all I actually had was very mild droop and mild weakness and numbness and tingling in my arm. My doctors are amazed and say it’s probably due to my ketovore diet and lifestyle.

    • @josiektv1681
      @josiektv1681 Před 14 dny

      Also, adding Vitamin B12 helps the nerves

  • @JustSayin916
    @JustSayin916 Před 6 měsíci +15

    Grateful for the inspiration and for this important focus on MS in the black community. Thirty years ago, a friend went to a nationally recognized MS center and was told she couldn't have MS because black people don't get MS. She went elsewhere and was immediately diagnosed with the disease.

  • @magicsamart2343
    @magicsamart2343 Před 6 měsíci +5

    Amazing coverage of how MS affects the Black community! This is truly life saving and lengthening information.

  • @csaggesern743
    @csaggesern743 Před 8 měsíci +5

    Powerful reporting on this horrible disease.

  • @petercole8798
    @petercole8798 Před rokem +5

    Such a nightmare.. how they handle this is amazing.

  • @51colibri
    @51colibri Před 8 měsíci +2

    So happy this people have a good support system.
    When the First Lady say “ I didn’t know the family suffering with you”.
    Not trying to get anyone’s pity, but some of us, we are literally abandoned completely by our families, n eventually because our condition friends started leaving to.
    I’m the first n my family with this condition, but like him I don’t think im the only one.

  • @tlmy915
    @tlmy915 Před 6 měsíci +4

    I have 2 nephews which are brothers that have been diagnosed with MS. One has lesions affecting his brain the other has lesions on his spine.

    • @donnamoore8479
      @donnamoore8479 Před 6 měsíci +2

      Hello, my sister has brain lesions, I have more spinal lesions, therefore I can't move my legs and have used a wheelchair for about 20 years now. But life is so good. She can take a few steps but her thinking and memory are a concern. She uses a wheelchair as well.

  • @rabina1100
    @rabina1100 Před 8 měsíci

    Thank you

  • @shirleehughes8125
    @shirleehughes8125 Před rokem +5

    God blessings to you 🙏 for you

    • @donnamoore8479
      @donnamoore8479 Před rokem +2

      He has already blessed me. In a way my having MS has greatly drawn me to a better spiritual life. He has supplied all my needs, He has become a close and dear friend. It isn't what happens to you it's how you choose to handle it. Take care

    • @hoosierbaddy3052
      @hoosierbaddy3052 Před 6 měsíci +1

      @@donnamoore8479 absolutely! 💯

  • @estherbarnslater7613
    @estherbarnslater7613 Před měsícem

    I need to tell my story of MS

  • @q8forme943
    @q8forme943 Před 4 měsíci +1

    Am Arab I have it also
    No one had it before in my family

  • @marlo9380
    @marlo9380 Před 3 měsíci

    Can an mri be done with no contrast? My kidney can't handle it

    • @Blakberi73
      @Blakberi73 Před 3 měsíci

      yes. you can receive an MRI w/o one

  • @Incredible_World_2023
    @Incredible_World_2023 Před 9 měsíci

    Is it same as GBS?

  • @kellio8087
    @kellio8087 Před 4 měsíci +3

    The doctor said smokers and obese people are prone to getting ms. Perhaps its because those are stressor's on the body same as chronic stress, overworking or working out too much which can cause lowered immune system and inflammation that then causes the immune system to attack too much and go haywire. I fixed my symptoms before it got worse by putting myself on an anti-inflammatory diet and supplementing to heal my nervous system and eliminated all stress. I've been fine for 2 years.

    • @denisek292
      @denisek292 Před 4 měsíci +2

      Blaming someone for developing MS is not cool, okay?! It makes me very angry when someone, who obviously doesn’t have MS, blames those people that do have MS. In fact, a very close friend of mine, w/ MS, is having a PET scan today to see how far his stage 4 cancer has progressed. Reading your comment makes me wish it wasn’t he that was having the PET scan, but someone else?!

    • @kellio8087
      @kellio8087 Před 4 měsíci

      @denisek292 no one should feel like it's their fault. When things go wrong for whatever reason, the body sometimes cannot recover. I'm very sorry for the misunderstanding. If you will, look up on CZcams, Aaron Boster MD " how stress influences multiple sclerosis outcomes "

    • @BlasianGoddessTM77
      @BlasianGoddessTM77 Před 4 měsíci

      @@denisek292You okay? 😮

    • @analauracaceres1392
      @analauracaceres1392 Před 3 měsíci +4

      Well, smoking, obesity and stress are bad for anyone that's a well known fact, but with MS no one knows what is the cause, you can't just reduce it to that, I wasn't either of those things and still I got it. If you have a diagnosis you shouldn't leave it at an anti inflammatory diet, you need inmunosupresors if you want to stop it.
      I follow the diet also as an extra help.

  • @briankerrison8504
    @briankerrison8504 Před 2 měsíci +1

    I go along with EBV being the cause of ms.. it lays dormant..until we become stressed & rundown.. apparently there is a protein that matches a protein in our myelin.. so our immune system reacts to EBV (pox virus) flare up.. & attacks our myelin neural coatings..
    the ratio of females being 2x more prevalent.. is they are open & suffer more stresses, proportionally too a man.. harsher environments (colder) also take a part in physical & mental stresses.. it all just makes sense.. that EBV is the underlying course of ms.. as for diet.. yes we all need a healthy varied diet..to hold our fitness & immunity at optimal levels..🤔🤔

  • @danielasutherna8191
    @danielasutherna8191 Před 7 měsíci

    I want to appreciate Dr Madida on CZcams for treating my Dad of his Multiple sclerosis with their natural meds....

  • @danielasutherna8191
    @danielasutherna8191 Před 6 měsíci

    I want to appreciate Dr Madida on CZcams for treating my Dad of his Multiple sclerosis with their natural meds🌿.