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Myositis Empower Walk
Hanes X-Temp Raglan T-shirt
- Sizes S - XXXL
- View Sizing Guide
About this campaign
Purchase your Myositis Empower Walk shirts, also the official MSU awareness shirt for 2020, and join The Landman Family, together with Myositis Support and Understanding (MSU), for the 2nd Annual Myositis Empower Walk, Saturday, September 19, 2020, created in loving memory of Robert “Bob” Landman.
The 2020 Myositis Empower Walk will be in-person (with precautions) and virtual! There will be many fun ways to get involved, and we are introducing individual and team Empower Walk fundraising.
Join The Landman Family on September 19, 2020, from 10:30 AM - 12:00 PM Pacific Time, at Discovery Park, 2011 Paseo Verde Pkwy, Henderson, NV 89012. Or, join us online and go LIVE to the Myositis Empower Walk at Discovery Park on MSU's Facebook page, and be a part of this special event no matter where you are in the world!
Stay tuned for updates on MSU's website and social networking sites, and on the official Myositis Empower Walk Facebook event page.
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 Myositis Support and Understanding (MSU) promote awareness and raise money to continue to further our mission. What a great legacy Bob leaves for other patients continuing to fight dermatomyositis and all forms of myositis, which are rare diseases.
Read "Our Dad was More Than His Dermatomyositis" to learn more about who Bob Landman was. He was certainly much more than his illness.
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Share Why You Support "Myositis Empower Walk"
Supporters
I have dermatomyositis
My small contribution to the good works of my friends at MSU.
I was diagnosed with dermatomyositis in April 2018. Understandingmyositis.org has been a great resource for me.
I am supporting this campaign because I dedicate my professional life to caring for myositis patients , finding better treatments and finding a cure for myositis. MSU is a patient centered organization that is so valuable for myositis patients.
In Memory of Robert Landman
Making advances in myositis research is my career goal.
Debi and I are looking forward to participating in this great event once again. Thank you for everything you do to organize this event.
I love love love Gladys and her family !♥️