Sarcoma Alliance seeks volunteers across the country

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The national nonprofit organization will update its volunteer program to accommodate more people with different skills.

Ali Olig has gone from volunteer to Sarcoma Alliance board member.

Ali Olig has gone from volunteer to Sarcoma Alliance board member.

The Alliance has amazing, committed volunteers, but we can always use more and would love to have volunteers in every state.

The Sarcoma Alliance gives education, guidance and support to people affected by the rare cancer called sarcoma, and it has found people want to give back, board member Alison Olig said today.

“The Alliance has amazing, committed volunteers, but we can always use more and would love to have volunteers in every state,” says Olig, who will help revamp the volunteer page on the Alliance’s website to include an interactive application and a more extensive list of needs. She volunteered for the task at the Alliance’s annual board retreat last week in Hermosa Beach, Calif.

“Our goal is to match an individual volunteer's skills and interests with our volunteer needs.”

Needs include: updating website content, hosting or assisting at fundraising events, shooting photos or video, starting a support group, talking to other patients, monitoring the discussion board, and writing grants, she says.

“We also encourage interested individuals to propose their own volunteer ideas, as we are always open to new, creative forms of assistance!”

The latest creative idea: Some crafty volunteers have offered to sew tote bags out of sunflower material, says board member Suzie Siegel of Tampa, a survivor of leiomyosarcoma. “The Alliance has made the sunflower a symbol of hope for sarcoma patients.”

The Alliance is looking for other volunteers, as well as sunflower material, she says. The tote bags will include information on sarcoma and resources, such as the Alliance’s Assistance Fund, which helps reimburse patients who seek a second opinion from an expert in sarcoma.

“I think the tote bags will definitely be appreciated by sarcoma patients,” says volunteer Sandy Williams, of Huntington Beach, Calif., a survivor of malignant fibrous histiocytoma. She has begun the hunt for materials.

“When I was first diagnosed, I was flying blind. I made many mistakes, including having my first surgery done by a general surgeon.” After he saw the tumor, she says, “he realized it was way above his abilities and he sewed me back up.

“Getting information on second opinions is life-changing and life-saving.”

Alliance board member Kellie Flynn of Tustin, Calif., agrees. That’s why she volunteered to help administer the Suzanne Renee Leider Hand-in-Hand Assistance Fund, named after the Alliance's founder.

“This is a cause near and dear to my heart on many levels,” says Flynn, who also had leiomyosarcoma. “I truly believe that I had a terrific doctor in that he checked his ego at the door and told me that he would not be treating me, but that he would gather the appropriate doctors and seek counsel from those doctors who were knowledgeable in sarcoma.

“Also, it is extremely important to me to support Suzanne's legacy. I am very close with Sharon Leider, Suzie's mother. I believe her vision was revolutionary in establishing the Assistance Fund.”

Flynn has volunteered for sarcoma patients for years, having facilitated a sarcoma support group at the Gilda's Club in Chicago and helping with Ocean of Hope, an Alliance fundraiser that consists of ocean races.

“I chose to participate in the Alliance because I feel that I am one of the lucky ones who survived this rare and aggressive cancer and feel compelled to make a difference in the lives of others. I had sacrificed a lot during my diagnosis and treatment, both with my health and my finances, to make sure that I had the appropriate care I needed for a fighting chance to beat this disease. It was a huge price to pay. I went in to business for myself to repay my medical debt and begin a new life for myself. I am now in a position, both personally and professionally, to give back."

Olig, of San Rafael, Calif., was diagnosed with alveolar rhabdomyosarcoma, a pediatric cancer, at age 13. “I cherish each day as a gift not to be taken for granted. I advocate on behalf of childhood sarcoma patients and raise awareness of the long-term side effects that often plague survivors.”

Alliance board members are all volunteers. Siegel says the national nonprofit has many volunteers in California because it was founded in Marin County and has its largest fundraiser in Los Angeles County.

The Alliance hosts a website for the newly diagnosed, long-term survivors, family and friends. Services include a Peer-to-Peer Network, live chat room, blog, Facebook page, YouTube channel and discussion board. Sarcoma is a cancer of connective tissue, including muscle, bone, fat, nerve, cartilage and blood vessels. It can occur anywhere in the body at any age, from newborn on up.

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Suzie Siegel
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