Since its inception in 2002, TAAASPS is the only worldwide organization dedicated exclusively to finding a cure for this insidious cancer that attacks children and young adults.

We are a non-profit 501(c)(3) organization, with no overhead and no administrative expenses. Our mission is to act as an advocate of medical research in ASPS, by increasing funding to support, discover and develop new treatments to save ASPS patient’s lives.

All funds raised are applied directly to the development and FDA approval, of a cure or other viable treatment for ASPS.

We are affiliated with the National Organization of Rare Diseases (NORD).

You are invited to surf our web and join us in this difficult quest. Please do not hesitate to call us 718 523-7752 or send us an E-mail info@alveolarspsarcoma.net with any question/s you may have.

Together we will win this battle!!!

• Read the following report. Show it to your oncologist. - Long survival for patients with ASPS: Aggressive surgery and appropriate diagnostic techniques (Report from The Memorial Sloan Kettering Cancer Center in NY)
• NORD update on Medicare Waiting Period
  

• [Clinical Trials ] Clinical Trials and ASPS Links pages updated. Sept 21, 2007
• [Up-coming events ] Post gala information. Dec, 17 , 2006
• [Up-coming events] Annual Gala at the Copacabana Club invitation posted! Oct, 21 , 2006
• [Up-coming events] Annual Gala at the Copacabana Club event updated! Sept 20, 2006
• Website updates box created!