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Disclaimer: 'MS Views and News' DOES NOT endorse any products or services found on this blog. It is up to you to seek advice from your healthcare provider. The intent of this blog is to provide information on various medical conditions, medications, treatments, for your personal knowledge and to keep you informed of current health-related issues. It is not a substitute for the advice of your physician. Should you or your family members have any specific medical problem, seek medical care promptly.


Tuesday, November 14, 2017

A MS Patient's story: How I'm Living Well With MS, a Decade After My Diagnosis

I wanted to help myself win against MS, but I’m so glad I didn’t stop there.

     Kendra and David Lyons pose at their fitness and wellness center in Murrieta, California.
              Robert Randall

It’s been more than 11 years now since my diagnosis with multiple sclerosis (MS), and nearly 10 years since I stepped back into the gym on my mission to beat MS through bodybuilding and fitness.

So far, it’s been a remarkable ride, with highlights ranging from competing in a bodybuilding competition in 2009, to starting the MS Fitness Challenge (MSFC) charity in 2012 (in partnership with my wife, Kendra) and receiving the Health Advocate Lifetime Achievement Award from Arnold Schwarzenegger in 2015.

MS Fitness Challenge Reaches Across the Globe

I am particularly excited to see how far the MS Fitness Challenge — a charitable program created to educate people with multiple sclerosis on fitnessnutrition, and maintaining a positive mindset — has expanded since Kendra and I founded it.

I am now working with and helping people with MS as far away from my base in California as South Africa and Switzerland, designing personal fitness programs, motivating people to fight MS through changing their lifestyle, and supporting them in their efforts to conquer this disease.

At the same time, I am waging my own war with MS on my preferred battlefield — the gym — and training for an award I will be receiving from the International Bodybuilding & Fitness Federation as I head toward my 60th birthday in 2018.
It's an honor and a privilege to serve as an encouragement to so many people with MS worldwide and to be acknowledged for my accomplishments on this journey with and for MS.

I never look at this MS voyage as one I am on alone or that is about me. The thousands of amazing and courageous people with MS I have met along the way have made this a “family” effort to positively impact lives. I am humbled, I am grateful, and I am blessed beyond belief to have you all in my life. Sharing my life, my triumphs, and my struggles with you has had such a positive impact on me and continues to do so. It has inspired me to continue to create more ways to connect with and be of service to the MS community, as well as driven me to keep setting new goals in the gym.

MS Symptoms Continue to Pose Their Own Challenges

MS Views and News is MAKING an IMPACT for those, affected by Multiple Sclerosis
MS Views and News provides beneficial Multiple Sclerosis education, information, resources and services. 

Thanks to Caregivers Who Share Our MS Load

Nov 14, 2017

The MS load we carry is heavy. Some of us, unfortunately, must carry it alone. But many of us are fortunate to have someone with whom we can share the weight.
It’s National Family Caregivers Month and a new survey shows just how heavy that load can be. Caregivers, it will come as no surprise, are carrying their own problems and needs.

  • Nearly half (49%) of unpaid caregivers surveyed have feelings of depression.
  • Nearly half (45%) of unpaid caregivers surveyed feel that their physical health has suffered as a result of their caregiver duties.
  • Nearly half (45%) of unpaid caregivers surveyed often don’t have time to book or attend medical appointments for themselves.
  • 41% of female unpaid caregivers report that being a caregiver has put pressure on their financial situation, as compared to 28% of male caregivers.
  • Almost half (47%) of female unpaid caregivers do not feel supported at all by the local community, and a third (33%) of unpaid caregivers do not feel supported at all by their local health system. Just 40% of unpaid caregivers feel supported by their employer in their role as a caregiver.

MS Views and News is MAKING an IMPACT for those, affected by Multiple Sclerosis
MS Views and News provides beneficial Multiple Sclerosis education, information, resources and services. 

Sunday, November 12, 2017

Updated Clinical Trials @ Sunrise Neurology - in Sunrise, Florida

               Click banner to access Infinity Clinical Research Website