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National LeioMyoSarcoma Foundation

helping to empower and educate about leiomyosarcoma a rare smooth tissue cancer

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Newly Diagnosed

What is LMS?

Definition/Diagnosis

New Diagnosis/ Treatment

Next Steps

NLMSF-SPAEN Publication on evidence

based unmet needs in LMS research and treatment

Finding a Sarcoma Center of Excellence

LMS Tumor Assessment

Treating LMS by stage/ Follow Up care by Stage - according to NCCN Guidelines for Sarcoma Treatment

Molecular Tumor Testing

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Donate to NLMSF Today!

Help Shape the Future of Survival:

https://nlmsf.org/donate-leiomyosarcoma-research/

Please enter your loved one’s name in the memo if you would like to donate in his/her name.

Contact Us!

Phone
303-783-0924
303-808-3437

Email
annieachee@aol.com

Mailing Address

1685 So. Colorado Blvd, Unit S, Suite 447,

Denver, CO 80222

Follow Us!

“The information in two more NLMSF websites created for you, help shape the journey, and build hope.”

leiomyosarcoma.info & nlmsflifechange.com

My family has been touched by Leiomyosarcoma, not once, but twice. I know the heartbreak of this rare disease, and I believe that being aware of what to look for and asking the right questions is so important on this journey.

Learn More About Peri’s Message

Bridging collaborations through advocacy, with organizations to amplify resources and support for patients and families.
“Achieving More Together”

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Information provided on the NLMSF websites and social media, as well as any referenced links, are provided for informational purposes only and do not represent medical advice. Clinicians volunteering with NLMSF will only address general questions and not offer specific medical guidance. Please do not share any personal information via NLMSF’s public forums.

Readers are responsible to use all information as guidance only and to discuss with their own medical team.

Copyright © 2021 · National Leiomyosarcoma Foundation

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