NO ONE SHOULD FACE SARCOMA ALONE.

The Northwest Sarcoma Foundation was founded on April 12, 1996, by Ernest U. Conrad, III, M.D. during his tenure at the University of Washington Medical Center. The foundation was started with a large financial gift from the McClary family after the loss of his beloved wife and mother of their small children. Through the help and support of others, 501(c)3 paperwork was filed, and we received our IRS determination letter in June 1997.

 

In 2000, the first fundraising event was held: the Hike, Bike, and Trike. In 2006, the foundation gets a new Executive Director. With guidance from the founder and board of directors, the Executive Director helped develop the foundation into what it is today. Under her tutelage, Help$ grants were developed, the Hike, Bike, and Trike events evolved into the Dragonslayer Walks, the Stories from the Vineyard, now the Knight Life Gala, were born, and we made our first investment into research.

 

As the 2008 crisis was gripping the US, the Northwest Sarcoma Foundation launched their Help$ Foundation grants for adults. In its inception year, the program provided 30 grants to patients across the PNW totaling $7,500 in Help$ grant support. By 2009, the number of grant requests doubled and the foundation quadrupled the amount given, which was a total of $31,500. Also, in 2009 the Westerholm family began a legacy in memory of their daughter, Jenna, who lost her battle to embryonal rhabdomyosarcoma. The Jenna Foundation Help$ grants were created in her memory; these grants provide for pediatric patients. Between these two grant programs, we now serve over 100 patients yearly, exceeding over $100,000.

 

In 2011, we made our first investment in Sarcoma research. Sarcoma treatment advancements have been made with the research grant support from the Northwest Sarcoma Foundation. Somewhere along the way, the Sarcoma Journal Club program advanced past the living room of Dr. Conrad to a larger opportunity to bring our PNW researchers and physicians together to network and discuss some of the latest research in Sarcoma.

 

As 2020 shut down the world, we took to heart the needs of the Sarcoma community who became quarantined in their homes along with everyone else. Through the brainstorming help and financial support of a donor who lost her husband to Sarcoma, the Care Package program was developed and launched in 2021. We started the virtual Researcher Update Nights, allowing Sarcoma researchers to share their knowledge and experience with our supporters, who then are able to ask questions about how research is developing. We were also able to launch the virtual Casual Chat program to support patients and survivors, caregivers, and those who have had someone pass away from Sarcoma. We are looking forward to our next historical advancements for the Northwest Sarcoma Foundation. We encourage you to be a part of our history.

 

The foundation serves anyone affected by Sarcoma in the Pacific Northwest, which includes the states of Alaska, Idaho, Montana, Oregon, and Washington. However, we have virtual programs which have a broader reach across the globe. The foundation was established to be a place of support and education for those who are living with Sarcoma or other rare bone tumor disease. In addition, the site is intended to offer support to friends, family, and caregivers. Because the information on this site is provided for educational purposes only, nothing found here is intended to replace medical advice. A physician should always be consulted about medical and health-related issues.

 

Any reference to other resources made by the Northwest Sarcoma Foundation is not an endorsement of any individual, agency, or organization. Northwest Sarcoma Foundation may not necessarily agree with all information provided on other websites but has found some value may exist for patients and family members.