My Nonprofit Reviews

Being knowledgeable of the NLMSF and its mission and purpose, I find this Foundation to be very proactive, responsive to the needs of patients,families,caregivers all over the world. Their three websites, the programs they offer, the upcoming live / free SUPPORT HELPLINE - starting Sept. 1 - all point to the direction of effective advocacy to help those needed help after being diagnosed with LMS, navigating treatment, and after treatment - survivorship. A truly worthy Foundation to be recognized!

NLMSF has worked tirelessly to create a foundation that personally reaches patients in need of a community that is there for them. NLMSF is always available through phone calls or the internet to personally assist patients with their treatment plans or to just have someone to talk to. Recently a chat room was set up for patients to exchange thoughts and feelings with each other which was very successful.

NLMSF is truly dedicated and committed to finding innovative ways to find funding for a cure for this truly underfunded rare form of cancer. They have also been able to bring top scientists, clinicians and researchers onboard to interact with each other as well as the sarcoma community at various conferences around the country.