2843 E. Grand River Avenue – #230 East Lansing, MI firstname.lastname@example.org 303-783-0924
Reaching For the Cure Together
SIDE EQ-Patients Registry
SIDE EFFECTS AND SYMPTOM MANAGEMENT RESOURCE ASSISTANCE
The Free, Interactive platform, which enables patients to track and manage their side effects – knowing in advance, in preparation for cancer treatment, hearing from others during cancer treatment – to improve the quality of life and thrive after treatment is completed.
Patients and caregivers can input, track, and share their side effects through a personalized dashboard as well as learn helpful tips and best practices from top healthcare professionals and other patients. A win-win for patients to learn from each other – share information that can help and receive supportive information from the medical community as well. The LINK: https://www.mysideeq.org/
This helpful program is brought to you through the collaborative partnership with the Life Raft Group who originated SIDEEQ, and the National Leiomyosarcoma Foundation – keeping its promise to bridge resources to assist patients and their families. We are grateful to the LifeRaft Group.
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).