2843 E. Grand River Avenue – #230 East Lansing, MI 48823 [email protected] 303-783-0924

Coping with Fatigue

Tips on Treatment-related Fatigue- Video
from Dana Farber Cancer Institute

https://www.youtube.com/watch?v=su3z_2eY12c&feature=youtu.be

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Inform – Inspire – Empower

Our Mission is our Passion:

“What we can do today can affect what happens tomorrow”

  • Annual Patient/family/ Caregiver LMS Education/Advocacy Programs
  • Annual LMS research funding for promising LMS research projects
  • Founded by the NLMSF: The Annual International LMS Research Roundtable
    Think Tank of the Sarcoma Research Community in support of advancing
    LMS-specific precision research initiatives
  • Continuously bridging partnerships/collaboration with organizations to increase/strengthen resource assistance support
“The information in the NLMSF’s three websites helps shape the journey and build hope.”
Foundation Resource/Support Contact:
Annie Achee (303)  808-3437 or (303)  783-0924  Email: [email protected]

The National LeioMyoSarcoma Foundation (NLMSF) is a 501(c)(3) Non-Profit Charitable Organization and a member of the GuideStar Exchange.

National LeioMyoSarcoma Foundation – NLMSF

2843 E. Grand River Avenue – #230
East Lansing, MI 48823

Sarcoma Coalition Member Seal

Sarcoma Coalition – We are here for you.

The Sarcoma Coalition brings together advocacy groups throughout the United States,
to build bridges of collaborative resource advocacy and support and Sarcoma Research
Community alliances.

By working together, the Sarcoma Coalition members extend their advocacy strength
and provide a united presence for patients and their families/caregivers.

“Achieving More Together!”

Disclaimer

Information provided on the NLMSF website and Facebook page as well as any referenced information links are provided for informational purposes only and do not represent medical advice or opinions. All information provided has a referenced source indicated for further access to the information being provided to followers. Followers are responsible for interactions with this website, the Facebook page, and any links relative to the medical information offered/posted.

Q & A Patient / Clinician Disclaimer:

Please be advised that only general questions may be directed to a volunteer clinician, and to only expect a general response – one that does not take the place of your medical care team/oncologist’s guidance and care.

Please do not include personal information such as your full name, date of birth, personal medical information in any emails sent through the Foundation’s open Facebook group or webpage on its website. No one can diagnose your condition from email or any other written communication and communication via the Foundation’s Facebook group / website cannot replace the relationship you have with your health care provider(s).

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