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3rd Annual Myositis Empower Walk

Organized by info@understandingmyositis.org
Po50551572 front2
3rd Annual Myositis Empower Walk Fundraiser - unisex shirt design - front
3rd Annual Myositis Empower Walk Fundraiser - unisex shirt design - back
3rd Annual Myositis Empower Walk shirt design - zoomed
3rd Annual Myositis Empower Walk shirt design - zoomed
3rd Annual Myositis Empower Walk Fundraiser - unisex shirt design - front
3rd Annual Myositis Empower Walk Fundraiser - unisex shirt design - back
3rd Annual Myositis Empower Walk Fundraiser - unisex shirt design - front
3rd Annual Myositis Empower Walk Fundraiser - unisex shirt design - back
3rd Annual Myositis Empower Walk Fundraiser - unisex shirt design - front
3rd Annual Myositis Empower Walk Fundraiser - unisex shirt design - back
3rd Annual Myositis Empower Walk Fundraiser - unisex shirt design - front
3rd Annual Myositis Empower Walk Fundraiser - unisex shirt design - back
3rd Annual Myositis Empower Walk shirt design - zoomed
3rd Annual Myositis Empower Walk shirt design - zoomed
Augusta 50/50 Raglan T-shirt

Buy shirts in this campaign for delivery before the LIVE event in October!

verified-charity
All funds raised will go directly to MYOSITIS SUPPORT AND UNDERSTANDING ASSOCIATION
$1,920 raised
159 items sold of
100 goal
Thanks to our supporters!
$28
Augusta 50/50 Raglan T-shirt, Unisex - White / Gold
Augusta 50/50 Raglan T-shirt
Unisex - White / Gold
  • 3rd Annual Myositis Empower Walk Fundraiser - unisex shirt design - small
  • 3rd Annual Myositis Empower Walk Fundraiser - unisex shirt design - small
  • 3rd Annual Myositis Empower Walk Fundraiser - unisex shirt design - small
  • 3rd Annual Myositis Empower Walk Fundraiser - unisex shirt design - small
  • 3rd Annual Myositis Empower Walk Fundraiser - unisex shirt design - small
Organized by info@understandingmyositis.org

About this campaign

Order your Myositis Empower Walk shirts in this campaign to receive them in plenty of time to have them for pictures, videos, and to pack to travel to Vegas, or to wear when you join via the interactive live stream, October 2nd for the 3rd Annual Walk!

Join MSU and the Landman family on Saturday, October 2, 2021, at Discovery Park, 2011 Paseo Verde Pkwy, Henderson, NV 89012. Or, join us online and go LIVE (interactive live stream) to the Myositis Empower Walk at Discovery Park on MSU's Facebook and YouTube page. We want you to 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 website, which we are building over time.

The Myositis Empower Walk was created in loving memory of Robert “Bob” Landman by his family to support the mission and vision of Myositis Support and Understanding (MSU).

This year, we will be honoring the life of Stella Clapp. Stella passed away earlier this year and she was living with inclusion body myositis. Stella helped so many people newly diagnosed with myositis, providing them with love, support, and encouragement. She touched our lives at MSU and we are honored to share her with all of you. Stella's family will join us live in Vegas.

The Myositis Empower Walk is a community-building fun walk and MSU's signature fundraising event created in 2019 by the Landman family. Stay tuned for ALL of the details that are coming soon, including Spirit Week! For now, purchase your shirt and then CREATE YOUR FUNDRAISING TEAM!

The week before the walk join us for Spirit Week and join us in honoring the life of Stella Clapp. There will be many fun ways to get involved, and we are expanding individual and team Empower Walk fundraising. Stay tuned for updates on MSU's website and social networking sites, and on the official Myositis Empower Walk Facebook event page.

Supporters

Benita K Moyers 1 item
Shinese Harvey 1 item + $5

I am recently diagnosed. I want to learn more about this disease, and I know more research needs to be done. Please support! #DermatomyositisWarrior

LINDA HEDLESTON 1 item

My Granddaughter and I, both have Dermatomyositis. We need a cure!

Tawn Montes 3 items
Monica Freeman 1 item + $10

I lost my mom to dermatomyositis in 2014. She ended up in a nursing home at age 58 and passed away at age 65. It’s rare and it’s a terrible disease. My mom got it while taking the cholesterol lowering drug, Lipitor. We miss her everyday.

Nancy Thomson 2 items

In honor of all the Myositis warriors! And my family (The Landmans) who are working so hard to bring awareness and help others!

Frank 1 item
RSW Holzman 2 items
Ashley Gutierrez 1 item

I am recently diagnosed with dermatomyositis

BRITTANY LEE 1 item

This group has changed my life and made me feel not alone.

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