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Myositis Empower Walk

Organized by Jerry Williams and Jenna Landman
Po42766087 front
Myositis Empower Walk Fundraiser - unisex shirt design - front
Myositis Empower Walk Fundraiser - unisex shirt design - back
Myositis Empower Walk shirt design - zoomed
Myositis Empower Walk Fundraiser - unisex shirt design - front
Myositis Empower Walk Fundraiser - unisex shirt design - back
Myositis Empower Walk Fundraiser - unisex shirt design - front
Myositis Empower Walk Fundraiser - unisex shirt design - back
Hanes X-Temp Raglan T-shirt

Myositis Empower Walk shirts were so popular we are offering them again!! Purchase as gifts or for yourself! Proceeds support MSU, in loving memory of Robert Landman.

verified-charity
All funds raised will go directly to MYOSITIS SUPPORT AND UNDERSTANDING ASSOCIATION
5 items sold of
150 goal
9 Days To Go
$24
Hanes X-Temp Raglan T-shirt, Unisex - White / Deep Royal
Hanes X-Temp Raglan T-shirt
Unisex - White / Deep Royal
  • Myositis Empower Walk Fundraiser - unisex shirt design - small
  • Myositis Empower Walk Fundraiser - unisex shirt design - small
  • Myositis Empower Walk Fundraiser - unisex shirt design - small
Organized by Jerry Williams and Jenna Landman

About this campaign

The Myositis Empower Walk shirts this year are a huge hit! We have been asked to provide them one more time, so be sure to get yours now as this will be the last chance. These are great to give as gifts, or just for you to share awareness. The shirts have UV protection. This is the official MSU awareness shirt for 2020.

Check out the 2nd Annual Myositis Empower Walk, held on September 19, 2020, and learn more about this fast-growing annual community and fundraising event created in loving memory of Robert “Bob” Landman by his family.

The 2020 Myositis Empower Walk was in-person (with precautions) and virtual! We also introduced individual and team Empower Walk fundraising. We want to thank Team "We Love Mary B." for your spot on the TOP of the fundraising.


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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Supporters

Caitlin Castillo 1 item
Linda Rabinowitz 1 item

As a Myositis patient, I want to raise awareness of these rare diseases and what better way than to wear my, wait for it, a-wear-ness! (please forgive me there lol) I'm also incredibly thankful to the beautiful Landman family and all that they do <3

Rebecca Hassien 1 item + $10

To help with future research. I wish I was able to work so that I could afford to give more.

Lynn Wilson 1 item
Jerry Williams 1 item

I have myositis and know so many who do. We are grateful for every person we can help, and for every penny raised. Thank you to the Landman's for all of their hard work on the Myositis Empower Walk!

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