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LIVE with The Landman’s
September 14, 2020 @ 6:00 pm - 7:00 pm EDTFree
Join us LIVE on Facebook for
“LIVE with the Landman’s,” a talk with Jenna and Lauren Landman about their dad and creating the Myositis Empower Walk in his memory, and ways we can all be involved.
Monday, September 14, 2020, at 6:00 PM Eastern Time
Join MSU and Lauren and Jenna Landman, creators of the Myositis Empower Walk in loving memory of their dad, Robert “Bob” Landman for a discussion about their family journey during and after Bob’s diagnosis and subsequent death due to dermatomyositis. We will talk about how they were inspired to do something and took action to make it happen. And, we will discuss how you can be a part of the Myositis Empower Walk, Saturday, September 19th, in-person or virtually.
The Myositis Empower Walk is Saturday, September 19th, from 10:30 AM – 12 PM Pacific Time (1:30 PM – 3 PM Eastern Time). We hope you will join us, either in person in Henderson, NV, or live online on the MSU Facebook page.
See ways to get involved at https://understandingmyositis.org/empowerwalk.
About joining this talk
REGISTRATION IS NOT AVAILABLE for Facebook events. To join us, at the time of the event, visit our public Facebook page to watch the LIVE stream and comment and ask questions in real-time.
About The Landman Family
When Robert “Bob” Landman became ill he was misdiagnosed several times. When he finally got the diagnosis of dermatomyositis, it was too late for any of the medications to be effective and Bob passed away due to complications.
Since, Gladys, Jenna, Lauren, and Chad have been involved to help MSU promote awareness and raise money to continue to further our mission by creating the Myositis Empower Walk. The inaugural Myositis Empower Walk was held on May 19, 2019, in Henderson, Nevada, just outside of Las Vegas, where it will be held again this year.
What a great legacy Bob leaves for other patients continuing to fight this rare disease, and or families and friends to get involved to make a difference.