Pinktober Guest Post: Chris Welander

Pink-to-ber n A portmanteau coinage used by many people who live with breast cancer to refer to October, the Breast Cancer Awareness Month, which is heavily dominated by marketing in the color pink and cute tags like “Save the tatas”. (See Komen, etc.)

During the month of October 2013, I am running guest posts from people with metastatic breast cancer (MBC) or who are closely involved with someone who has MBC. This was the idea of the wonderful Jody Schoger, and I think some other breast cancer bloggers are participating, too.

Chris Welander is our guest writer today. Chris is a minority within a minority: one of our youthful sisters-in-mets. Diagnosed ten years ago at only 37 years of age, Chris tells her story in a voice that is both strong and plaintive.

I was in shock.

I was first diagnosed with breast cancer in 2003 at age 37. I hit it hard with a double mastectomy, oophorectomy and 10 weeks of chemo. I had a huge breast cancer team. Raised a lot of money for mammograms Went to support groups and really assumed I beat it. I didn’t worry. My iron will plus hard years of treatment was going to fix this.

When I found out two years ago that it had spread to my hip I was shocked. More treatment, lots of surgeries. I left work, lost touch with friends. Thank God for my metastatic support group but I was still young comparatively to many of the members. I felt freaky and lonely.

Last month my cancer spread to my liver after months of completely clean scans. More shock and boy do I feel gypped! I wanted to grow old with my partner. I want to contribute to society with my career and help my mom enter her twilight years. I want to see the pyramids, cook a hundred Italian recipes and read all my bedside books. Now I just make my friends and family sad. I talk to lawyers, doctors, financial planners and make THEM sad. I feel forgotten and still have to fight for care, for my rights and to be heard.

I think all discussion about breast cancer is better than the shame in the old days of not even saying the word “breast”. So I don’t have an issue with pink-azation. But I am invisible in the breast cancer community absolutely…mostly because women can be so stubborn. Like I didn’t work hard enough. Let me tell you I did. And being younger ironically works against my survival. You know what I need now? Money for a trip, cheaper prescriptions, people to say loving things to my partner instead of always asking how I am. And a resolution that agrees metastatic patients have been ignored and that more will be done to fund treatment for us and those after us.

Can it happen? Can we will that?

7 thoughts on “Pinktober Guest Post: Chris Welander

  1. Chris, you are a strong woman with a powerful voice. I am sorry that I cannot give you all that you want and need, but I give you my attention, as will many others in reading about you and metastatic cancer. -Elizabeth

  2. I so understand feeling gypped. I am in my 50s, not as young as you, yet I feel gypped, too. I want to live for future weddings and grandchildren, to enjoy retirement with my husband. My career has been cut short, he will probably have to work longer, and I wonder if I will even be here long enough for the one grandbaby I have to remember me, much less even see his future siblings and cousins.
    I keep hearing about people not discussing breast cancer in the old days. But it was so prevalent in my family that I can’t remember a time I had not heard about it. I hope and pray for a cure, or even a prevention, so that my own daughters will not go through this. Thank you for speaking out.

  3. I can really relate to your post. I feel like I just make people sad (including myself sometimes) and they don’t know what to do with me unless there is some physical crisis happening.

  4. Pingback: Pinktober Guest Post: Chris Welander | Searching for EMWA

  5. To feel invisible amongst fellow sufferers must hurt. To be cheated of so much living must also be painful. To see your partner ignored is also painful, as they suffer with you and also need support. I hear your cry Chris.
    Prayers and blessings
    Maxine

  6. I can relate to a lot of your story; I was also diagnosed with breast cancer, stage II, in 2003; I was 39. I had a bilateral mastectomy, and that was followed by chemo and radiation. I was put on Lupron injections to shut down the ovaries. I began having a lot of pain in my left hip towards the end of 2006, in April 2007, I had a diagnosis of bone mets, and they were not only in my hip, but spread throughout my pelvic bones too.

    My mom has often talked about losing her own mother to breast cancer, in the 1940’s. My mom was only 12 years old when she lost her mother. She remembered at that time, people only spoke about cancer in whispers. My grandmother had found a lump under her arm, and she waited a year before she saw the doctor about it. She had a mastectomy, but she died from complication from the surgery before she was fully recovered.

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