The National LeioMyoSarcoma Foundation
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                                                                                                      LMS on the 98.1 WOGL Philadelphia

                                                                                                      NLMSF Board member, Amy Rovi, and Teresa Berger, have both lost their mothers to LMS. On September 5, 2010, both Amy and Teresa sat down to have a discussion with Brad Segall of 98.1 WOGL. We thank them all for sharing their stories.

                                                                                                      You can listen to their radio chat online below:



                                                                                                       

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                                                                                                      Teresa has an online blog called LMS Sucks to raise awareness on LMS. 

                                                                                                      She has also recently published a cookbook with recipes and stories from her mother. Teresa is donating a portion of all the book sales to the NLMSF. She also has gratiously donated some of these books for our online store. Look for these items in our
                                                                                                      Foundation Store soon!

                                                                                                      Teresa also has organized the First ever Sunset Stroll for LMS on October 10, 2010 in Abington, Pennsylvania. More event details can be found on our
                                                                                                      Events page. You can purchase tickets online.



                                                                                                      LeioMyoSarcoma makes the National News

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                                                                                                      September 3, 2010: Vicki Kelly is a survivor of LMS- and recently her story was featured on the National Fox News. The follow up article written by Jessica Ryen Doyle can be found here.

                                                                                                      We applaud Vicki for sharing her story with the world.

                                                                                                      National LeioMyoSarcoma Foundation - Copyright 2011