We support research and education to enable better treatment and outcomes for Leiomyosarcoma cancer patients.
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We aim to create a network of researchers and experts to coordinate and focus research efforts, encourage collaboration, and share best practices, ultimately leading to improved outcomes for LMS patients.
We are dedicated to funding research into the prevention, diagnosis, and treatment of LMS, with the goal of improving patient outcomes and developing the next generation of medical experts and researchers.
We provide up-to-date, accessible information about LMS through leaflets, our website, social media, and patient information sessions.
We offer a safe and supportive community for those affected by LMS through local and online support groups and forums.
We actively work to increase awareness of LMS within the community and among medical professionals, advocating for better diagnosis and treatment options.
Access to clear and up-to-date information about LMS and the latest research developments.
Opportunities to connect with other LMS patients and families through support groups and online forums, fostering a sense of belonging and shared experience.
Resources to help you advocate for yourself and make informed decisions about your treatment and care.
By funding research and fostering collaboration, we are actively working towards better treatments and improved outcomes for LMS patients.
To support more research into Leiomyosarcoma and linked Sarcoma subtypes, please donate here.