you don t know jack about ms

You Don't Know Jack About Multiple Sclerosis (MS) | Mental FlossDiane, living with MS"I found new ways to do the things I used to do. How to get a three-wheel bike to join my husband on walks." "I found new ways to do the things I used to do, like getting a three-wheeled bike to join my husband on walks." Find a program near you. Becky"I have renewed confidence to move forward, one day at a time." "I have renewed confidence to move forward, one day at a time. "Connect with our MS team of experts and get access to educational resources. Valerie. I walked for the first time in three years." "I walked for the first time in three years. "Involve today to help us provide more life-changing experiences to people with MS, such as Valerie. Founder Jimmie Heuga"Support about what you can do." "Continue what you can do. " Jimmie was a pioneer in the philosophy of health through exercise and nutrition, allowing those who have MS to lead healthier lives. Jack Osbourne, star of "You don't know Jack about MS", opens on his MS journey 2 December 2018 Jack Osbourne just became a father. Your daughter, Pearl, was three weeks old. Suddenly, he began to lose his vision. "I developed optical neuritis. I didn't know what it was at that time, but I went to the eye doctor. I think the eye doctor knew what he was, but he wasn't a neurologist, so he couldn't tell me. He sent me to the hospital to have an MRI. There were spine cracks, blood tests, and all that. Then they gave me the news: 'You have MS.'"First to his diagnosis, Jack's life had been rather careless when it was his health and well-being. He was 26 years old at the time, 9 years sober, and his career as a television personality was taking off. A diagnosis of MS is difficult to process. Jack, a proud father ready to start this new chapter in his life, had trouble wrapping his head around what just landed on his shoulders. He has contacted his support partners to receive advice. "One of my best friends was one of the first I called. I said, "Dude, I can't see, I can't do all these things, I don't know what's going to happen." And he looked at me and said, "From him. Don't let him win. You can find a way to make this work with you. That was the kind of advice I needed. "Jack's support group knew it would not respond well to a soft hand. Recognizes that it subscribes more to the style of "affective love" of affectionate concern. "I called my other friend the day I left the hospital, when I was still in shell shock. I called him and said, "John, I'm in a bad way. I have MS. He looked at me and said, "And?" I remember saying, 'Really?' He asked me, "Can you breathe?" I said, "Yes... "Are you still sober? Have you lost anything? Not yet. "Then you are good today. "Jack adapted. Along with Teva Neuroscience, Jack creates the web series (YDKJ). Webisodes provide information and resources for those who are newly diagnosed or currently living with multiple sclerosis. YDJK also highlights how Jack manages his health and well-being while living with MS. "I'm doing a campaign that I could have used when I needed it most. It doesn't matter what my job is. If I were a carpenter in Kentucky, I would still need the same information. I wanted to do a campaign that I could have used and benefited. Some webisodes focus on common misconceptions that people have about MS, others speak about nutrition and exercise, but all show that while RRMS is part of Jack's life, it doesn't control it. A webisode that epitomizes this theme is "Movement and Substance" – the second webisode of the series. During this webisode, Jack discusses how, before his MS, he loved doing high-impact exercises. A fan of rock climbing and weightlifting, Jack never considered anything like yoga as exercise. Going to yoga with your family helped you see exercise in a different way. Since then he has learned to incorporate this experience into a new vision of the world." Whether it's a work-related theme, travel, exercise or a resistance event, I have to say, "Well, I want to do this. That's why I think it's good. Is this going to affect my MS? If you do, can I make it? If so, how? ' I always ask these questions in the evaluation process." The episode also shows how Jack has re-evaluated his diet. While registered dietitians agree that there is no single food plan for people living with MS, adopting healthy foods and living habits are linked to improving a person's quality of life. Jack discusses how he found his own food plan, based on what food makes him feel good (and what he doesn't). YDKJ is developing its next season and will have a webisode that almost all those living with MS can relate to: avoid the doctor. "I have a very bad tendency to "head in the sand" when it comes to going to my doctor's appointments... I haven't had a magnetic resonance in a few years, so let's do an episode about making sure you go to your doctor's appointments every six months!" Now a father of three, Jack is proud to have helped to educate others and raise MS awareness. He has worked with his neurologist and other health experts to develop a treatment plan that works for him. Instead of living in the future, Jack focuses on the present. "Now I can, so I'm going to... A moving body will keep moving." Viewers can find all the webisodes of line. To listen to the full interview with Jack, along with his personal stories and experiences, look at him! This podcast is available to download or transmit online and your favorite podcast app. Photos courtesy of James Branaman. Sign for our NEWSLETTER© 2020 can make multiple sclerosis. All rights reserved. Multiple sclerosis can be done is a non-profit organization 501 (c)(3). Charitable Organization Number: 74-2337853 Sign up for our newsletter

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