2843 E. Grand River Avenue – #230 East Lansing, MI 48823[email protected] 303-783-0924
Reaching For the Cure Together
Survivorship Care Planning Information
The 2016 Commission on Cancer Program Standards required that all accredited cancer centers deliver treatment summaries and care plans to an increasing percentage of patients who have been treated in their facilities. An overview of care plans can be found at Blueprints of Hope and a list of clinic and program resources follows.
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 – 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!”
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).