The National Leiomyosarcoma Foundation (NLMSF)- dedicated to patient support /advocacy/education/LMS research support - The LMS Intern'l Research Roundtable
Giving Tuesday is tomorrow!
๐ Visit https://t.co/5wMKMDZxqe to learn more and make a Giving Tuesday contribution that brings hope forward.
๐ Visit https://t.co/QaQO3nzJYY to make a purchase with a donation toward fighting LMS.
DECEMBER 14 - Dr. John Mullinax from Moffit Cancer Center will discuss Cutaneous LMS and also his perspective on the recent global meeting discussing LMS research. Join Dr. Mullinax by sending a note to [email protected] to receive the zoom link. The Program is at 7pm ET.
TODAY SURVORSHIP CARE PLANNING CLINIC - to help patients get the most out of quality of life during and after treatment. send a note to join the meeting today: noon PT, 1 pm MT, 2 pm CT 3 pm ET send a note to [email protected] and a link to the virtual session will be sent
@CMCaAlliance We will actually be in Ireland - and would love to meet you if you have time to connect with us Nov 1 - 7. We are at a sarcoma meeting that ends Nov 4 but staying on a bit longer. Please email me [email protected] - would love to meet you all! Blessings!
@CMCaAlliance What a lovely group! Would you like to reach out to us here in Denver Colorado? This is the National Leiomyosarcoma Foundation - helping ALL sarcoma patients! We have noted that Liposarcoma and Undifferentiated Pleomorphic Sarcoma patients Please email me at [email protected].
It's National Leiomyosarcoma Awareness Day! There are many ways to share your support whether it be sharing this to your story or making a donation. We appreciate all of your support and let's make today great! Feel free to comment how you are spreading awareness today!
It's a big month for us as we try to spread awareness! Please use and share the link below so we can help make a difference. Thanks for all your support. #sarcomaawareness#leiomyosarcoma#rarecancer
Here is the link to be shared as well: https://t.co/GP8znuAPeM
It is Leiomyosarcoma awareness month! It is important to bring awareness to this rare cancer! Thanks for your support in helping us spread the word and make a difference! #cancerawerness#leiomyosarcomaawareness
The NLMSF LifeLine Buddy Program offers one-on-one support for an LMS patient/survivor or caregiver. Being paired with someone who has been in a similar phase of LMS diagnosis/treatment journey can be a โlifelineโ to help build courage, strength, and resilience.
There are many ways to navigate LMS and we have resources for you! Check out our website where you can find NLMSF Reliance Resource Podcasts and Powerful Tools for Caregivers! #StrongerTogether
We want to talk about mental health and cancer to close out mental health awareness month! Cancer affects more than just your body; it also affects your emotions and feelings. . We have resources to help you or your loved ones find the strength and support you need.
The National Leiomyosarcoma Foundation is partnering with Count Me In to inform patients about this exciting project and to encourage patients to participate at NO COST. Our goal is to bring patients and researchers together, to accelerate discoveries in cancer research.