2843 E. Grand River Avenue – #230 East Lansing, MI firstname.lastname@example.org 303-783-0924
Reaching For the Cure Together
Cancer Cell Line Project
ANNOUNCED APRIL 9, 2017:
THE RARE CANCER RESEACH FOUNDATION AND THE NLMSF HAVE PARTNERED TO INCLUDE LMS AS ONE OF THE
RARE CANCERS REPRESENTED IN THIS PILOT PROGRAM:
The Cancer Cell Line project is an opportunity for patients to contribute to research in a big way – a personal way.
If a patient is facing a biopsy or surgery to extract an LMS diagnosed tumor – tissue from the procedure(s) can be offered to the Rare Cancer Research Foundation (RCRF) through a simple consent form. The RCRF takes care of the rest of the coordination to make sure your de- identified tumor sample is sent to the Broad Institute of MIT / Harvard laboratories for cell processing and hopeful growth.
To learn more about how to be empowered ti direct your cancer tissue sample to research projects, for the development of research models.
This opportunity offers a huge opportunity to “move the needle” forward for potential research initiatives across the globe. Researchers can access de-identified data for research initiatives / studies they wish to pursue.
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
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).