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The Power of Advocacy

September 22, 2020 @ 7:00 pm - 8:00 pm EDT

The Power of Advocacy webinar

September 2020 Myositis Awareness

High Fives from the Heart: #MyositisLIFE in a Pandemic World

Keeping you informed during the COVID-19 pandemic

Register to join us for

The Power of Advocacy 
with Holly Jones and Rhonda Rogers, the Myositis Warrior

Tuesday, September 22, 2020, at 7:00 PM Eastern Time

Webinar Details

Meet two people with myositis who are living their lives with purpose and positivity. Holly Jones, polymyositis (PM) and interstitial lung disease (ILD), and Rhonda Rogers, inclusion body myositis (IBM), will talk about their journey from diagnosis to advocacy and how the lessons they are learning can help each of us.

Join to be inspired to get involved. We can all do something to help advance myositis education and research.

About joining this webinar

REGISTRATION IS REQUIRED. Click the Register button above to get started. After registration, you will receive an email containing all information needed to join the webinar at the scheduled time and date.

Be sure to check your spam and junk folders if you do not see the email.

About Holly Jones

Holly JonesHolly Jones is not your average stay at home wife and mom. Living with Polymyositis for over 16 years has not stopped Holly from accomplishing her life goals. Having to leave college after one year due to hospitalization, Holly returned and graduated with an Associate of Applied Science Degree in Business Administration. Today, she is what we would call an up-and-coming Social Media Boss/Entrepreneur. She is the creator and host of the Facebook Live talk show, Krazy N Christian where she speaks on trending topics and important information that helps build the community.

Her Facebook page, Polymyositis: Bringing Awareness, informs, educates, and brings encouragement to those living with the rare disease. Holly’s YouTube channel, MyoLife, showcases her everyday walk with Polymyositis. She gives her audience an insight into what she has and is currently experiencing as a patient, a wife of 14 years, a mother of two daughters, and a friend. Despite the setbacks in her life, like having a rare disease that caused her to relearn everyday skills, to losing a baby and both parents before the age of 30, Holly has turned her tears into triumph. Holly summarizes life using these words, inspired by Philippians 1:27-30, “Live your life in such a way, for those who don’t know God, will come to know God because they know you.”

About Rhonda Rogers

Rhonda Rogers, Myositis WarriorRhonda received her initial Myositis diagnosis of polymyositis (PM) in 2003. She tried all sorts of treatments in her search for relief and improvement but kept getting worse. Eventually, she found her way to Dr. Namita Goyal, Myositis specialist and researcher at the University of California, Irvine, in 2015. It was Dr. Goyal who gently told Rhonda she didn’t have PM, but IBM, Inclusion Body Myositis. Dr. Goyal added there was no cure or even a treatment. For once, Rhonda was speechless.

As most newly diagnosed individuals do, Rhonda attended the University of Google and began her quest to learn about this “other” form of myositis. And after exhaustive searches, she eventually found other myositis patients through the Myositis Association, and Myositis Support and Understanding. Yes, IBM is a rare disease, but at least she wasn’t alone.

Rhonda started identifying with the fighting spirit displayed by the Myositis Warrior, often found on Myositis Support and Understanding Facebook posts. She drew strength from people who shared experiences and asked for advice about life with Myositis. Then in 2019, Rhonda decided to BECOME the Myositis Warrior and attended the original Comic-Con in her hometown of San Diego. She wore a cape that said Myositis Warrior, so she fit right in and felt at home with the superhero crowd, even though she was not as famous as Batman.

But real superheroes have a mission. To do good. To be strong in spirit. And to act. Rhonda is now recruiting other Myositis Warriors who are ready to have their Myositis voice be heard. She hopes you will become a Myositis activist too.

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MSU Facebook page

Be sure to visit and “Like” our public Facebook page for special events, articles, videos, and patient and caregiver opportunities.Visit us on Facebook »

September Myositis Awareness Activites

High Fives from the Heart: #MyositisLIFE in a Pandemic World

Historically, Myositis Awareness Day is September 21st of each year, however, we have celebrated the month of May for the past 2-3 years. This year, we are using both May and September with our theme, “High Fives from the Heart” as MSU turns 5-years-old and we continue our focus of empowering, supporting, educating, and assisting the myositis community. Join us for fun, educational activities and events all month long.Learn more »

Upcoming support and education sessions

Event starts in . . .

2020/09/22 19:00:00



September 22, 2020
7:00 pm - 8:00 pm EDT
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MSU Zoom Video Session
Video session using Zoom


Myositis Support and Understanding (MSU)


Event Audience
Open to the public

© 2021 Myositis Support and Understanding Association (MSU). All rights reserved. | View our Privacy Policy, Terms, and Non-Discrimination policy. MSU is a charitable organization with 501(c)(3) tax-exempt status. Federal ID #47-4570748.

The best way to prevent catching or spreading coronavirus is thorough hand washing, social distancing, and social isolation. Should you begin experiencing symptoms of coronavirus, which include fever, cough, and shortness of breath, please contact your doctor immediately. View COVID-19 resources and updates, and stay tuned to your state, local, and federal health agencies, along with the CDC.

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