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WOMEN LISTEN, Inc. - A group of women cancer survivors, Alaska Home Meetings Retreats Upcoming Events Cancer Haiku Healing Boxes Jan's Cards and Survivor Fairies Who We Are/Photo Album Coping Tips/Things I Wish I had Known
The information on this webpage is not intended to served as medical or psychological advice or to take the place of care by your physician or mental health provider.
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Jan Porterfield Go to Jan's CardsLink to purchase apparel, cards and other wonderful things with Jan's art www.cafepress.com/janporterfield Jan's bio about herself, written in about 2004: I’m 55 years old, married with a 15 year-old son. When I was diagnosed with cancer I was teaching preschool. I kept teaching for about a year—through surgery, radiation and my first round of chemo. I stopped working when my cancer metastasized. The chemotherapy made me too tired and my energy was too unpredictable to be able to continue teaching. I was very sad to leave the preschool. I loved what I did and was good at it. But it just wasn’t possible. Since I stopped working I have become a serious watercolorist. I find that painting helps me relax and takes me out of myself. Last year I had a painting accepted for the Alaska Watercolor Society show. I was thrilled. I have had many interesting jobs: research, university teaching, and, of course, teaching preschool (my favorite). I was born and raised in Kansas. I went to in Britain in 1976 to do research in services for people with disabilities and stayed 11 years. I met my husband on a vacation in the States and moved to Alaska in 1988 to marry him. I was diagnosed with colon cancer in November 2000 when I had a routine colonoscopy. Since then I have been in and out of treatment. I am currently getting chemotherapy. I joined the LISTEN group when it was just starting in July 2002. The group was originally for women with breast cancer but since I knew most of the other women from life before cancer, they invited me to join. At the first meeting I attended, a woman who had just been diagnosed with breast cancer was there. She was worried about losing her hair and wondering about hats, scarves and wigs. She asked what it was like to be without hair. Everyone who was without hair spontaneously whipped off headgear—right in the middle of a busy coffee shop. It was a great moment with lots of laughing. And the woman who was concerned said she now knew she’d be OK—hair or no hair. Surprising to me, I have not lost my hair. I’m on different drugs than the breast cancer drugs. When I knew I would be getting chemo I almost got my head shaved. I didn’t want to wait around for my hair to fall out. I didn’t know that not everyone who gets chemo becomes bald. The LISTEN group is open to women with any kind of cancer. We especially like to have women who have completed treatment come to the group. They inspire us. A few women who have never had cancer come to the group: Muff Zellmer, a nurse practitioner who works with Dr. Judith Whitcomb (a breast surgeon), Jean Bodeau, an acupuncturist who treats chemotherapy side-effects, Andy Dunham an artist who started coming when her daughter had cancer, Jean Shadrack, another artist and Andy’s friend. Jean and Andy have brought art activities to our retreats. They are warm, caring women who are especially sensitive to women who are newly diagnosed. I think the group is very helpful to women with are newly diagnosed. We can help them know what to expect and answer questions. We understand how scary it is and empathize. I come to the group meetings almost every Friday. I like being with other women who have cancer. I can be open about my fears without freaking them out (as sometimes happens with family and other friends). This group is also fun. I’m not a real group person and don’t think I’d like a formal group—but LISTEN is perfect for me. We often don’t even talk about cancer—we talk about whatever is going on in life—children, husbands, creative activities, work or whatever is on our minds. We plan retreats, tell funny stories and laugh. We help each other deal with chemo and radiation side effects, give each other advice on dealing with medical staff, and the emotional ups and downs of having cancer. Some people come to the meetings every week, others come occasionally, still others come after they are first diagnosed for a few meetings and then stop coming. This is a group you can come to when you want to. You are always welcome but there is no pressure to keep coming. Note: Jan passed away on June 21, 2007. Her husband, Jeff Friedman, suggested we print her obituary, which is included below.
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