Nat'l LMS Foundation

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

RFP for LMS-specific grant proposals: Submission to the National Leiomyosarcoma Foundation. Details here: leiomyosarcoma.info/general-resear…

We would love to see you! Join us on the 22nd of January 💜

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

Learn about what NLMSF has to offer! Visit our website for more information

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: nam10.safelinks.protection.outlook.com/?url=https%3A%…

Join us in spreading awareness this month! Check out this campaign on @Bonfire bonfire.com/nlmsf-tote/

Champion of Hope for Leiomyosarcoma Research on @Bonfire bonfire.com/champion-of-ho… Show your

Champion of Hope for Leiomyosarcoma Research on @Bonfire bonfire.com/champion-of-ho…

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 “lifeline” to help build courage, strength, and resilience.

From the National LMS Foundation (NLMSF) The  NLMSF News Tracker -  June 13, 2023 mailchi.mp/nlmsf.org/nlms…   -

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.

4 pm ET on May 23- send a note to [email protected] to join the discussion - for patients and families/caregivers - important information to share.

Register for the Webinar discussed below - here:  rarecancer.org/events/learn-a… For more questions, contact:  [email protected] Annie Achee -  NLMSF

Register for a webinar to learn how to  impact LMS research in a personal way: M A Y 19 , 2023 3:30 PM ET / 2:30 CT / 1:30 MT / 12:30 PT Save Your Spot, Register Today!   Rare Cancer Research Foundation Webinar -NLMSF collaboration enrollment process:  Pattern.org"

Register for this webinar to learn how to  impact LMS research in a personal way: M A Y 19 , 2023 3:30 PM ET / 2:30 CT / 1:30 MT / 12:30 PT Save Your Spot, Register Today!   Rare Cancer Research Foundation  Webinar -NLMSF collaboration.