BFB 2010_0144Registration opened – and they were off!  Blue Footed Boobies flocked in by the numbers creating a virtual team, taking action and raising funds for our sixth annual Walk with Love.

We know what you’re thinking…the WHAT flocked in?  Blue Footed Boobies?  The same question buzzed through the DSLRF office, and like we are doing with breast cancer, we decided to get to the bottom of this and get some answers.

We took a moment to get to know the leaders of this fantastic flock; Jeanne Rees and Liz Gardner, and we invite you to enjoy their amazing story:

DSLRF: Blue Footed Boobies?  Where did this name come from and why did you choose this to represent your Walk with Love team?

Liz: I met my first Blue Footed Booby during a once-in-a-lifetime trip to the Galápagos Islands in 2007, where I fell in love with these tenacious, powerful, lovely birds with funky, blue clown-feet. After my breast cancer diagnosis in 2008, I was desperate to reclaim that slice of invincibility that I had lost after undergoing several surgeries.  I registered for a breast cancer walk, creating my team, the Blue Footed Boobies, with the intention to gather friends and family to join me, and to have the Boobies’ awesome spirit infuse our every step with strength, joy, and LOVE. After walking three annual breast cancer events in a row, raising nearly $100K for breast cancer research, and skiing to raise money for the American Cancer Society, the Boobies, who have grown from one to nearly thirty, are proud to gather again for the Dr. Susan Love Research Foundation’s Walk with Love. Once a Booby, always a Booby. With Boobies all over the country, the Blue Footed Boobies are walking for everyone, everywhere!

DSLRF: There is definitely power in numbers.  Who are the Blue Footed Boobies and how did you come together?

Jeanne: We are all associated with a boarding school, Northfield Mount Hermon, in western Massachusetts.  There was an enormous amount of support from the NMH community for us as we walked in our first fundraising walk in 2009.  The following year another woman in the community was diagnosed with breast cancer.  She and other people whose lives had been touched by breast cancer (as survivors, caregivers, relatives, and friends) joined the group:  13 of us walked again in 2010.

Living and working at a boarding school means there are few lines between your professional and personal lives.  We live and work in a wonderful community in which people care about and take care of each other.  I think that the success of our group (in recruiting others to walk, in raising money and doing the actual walk) can be attributed to this sense of community.

In the fall of 2011, a student came to NMH whose father had recently been diagnosed with brain cancer.  She decided to start the Cancer Support Team, a group of students who have done many events to raise money and awareness for all types of cancers.  This year she is actively working with us to recruit students to join the Blue Footed Boobies for Walk with Love.

DSLRF: Jeanne – Your life has also been personally touched by breast cancer.  Can you tell us about this?

Jeanne: I was diagnosed with cancer in my right breast in the fall of 2002.  My surgeon was Susan Troyan, a remarkable woman who trained with Dr. Susan Love.  In the spring of 2006, a tumor was found in my left breast.  Following my second diagnosis, my oncologist suggested genetic testing – and I turned out to be BRCA2 positive.  With this in mind, I decided to have my ovaries removed in 2008.  In December of 2010, I then discovered that I had uterine cancer, followed by a third diagnosis of cancer in my left breast.  I have been extremely lucky; all of my cancers have been detected incredibly early. I have had wonderful care and wonderful doctors, and an amazing circle of friends who have supported me.  I also have an incredible husband and two wonderful sons!

DSLRF: Why DSLRF?  Why Walk with Love?

Jeanne: For the Boobies, we are inspired by the Foundation’s focus on finding the cause(s) of breast cancer and preventing it.  This is where the research should be. There would be no need to find a cure if the disease didn’t exist.  We are committed to being a part of something bigger – and we believe in the work that the Dr. Susan Love Research Foundation is doing.  Looking for possible causes seems to be outside the “mainstream,” and the Foundation’s progressive approach may finally get us there.  I live in a community of approximately 400 people and more than 20 women have been diagnosed with breast cancer in last 20 years – there is something going on here and we need to figure it out.  This is why the Blue Footed Boobies are teaming with Love for this year’s Walk with Love!

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If you’d like to support the Blue Footed Boobies in achieving their fundraising goal, visit their team page!

To learn more about Walk with Love and register to participate, visit

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One Response to Blue Footed Boobies Team with Love

  1. Bonnie Wallace says:

    This is directed to Jeanne Rees (Blue Footed Boobies):

    Our 39 year old daughter, Lori, was diagnosed with cancer in her right breast, which had very aggressive cells, lympho-vascular invasion, but negative lymph nodes, in early 2011 (stage 2b)). Her youngest son was almost 5 years old. We subsequently learned that we carry the BRCA2 genetic mutation. Following chemo., she had a bilateral mastectomy with reconstruction (using “tummy fat” to construct new breasts). In 2013, she underwent an oopherectomy/hysterectomy.

    Recently (early Feb.) she discovered a lump, and learned that she has cancer in numerous lymph nodes on the opposite side. She has begun Faslodex injections, following which (hopefully, the tumors will have shrunk considerably) she will begin radiation, all at Stanford Hospital. We are all devastated, of course, and taking things one step at a time. The doc.’s at Stanford are not completely in agreement between undiagnosed original cells (stage 3), or metastasized cells (stage 4), but seem to agree on the fact that the treatment will be the same.

    I imagine that because of this feature on the blue Footed Boobies, you may have been inundated with e-mails galore. If you have not been snowed-under, and have the time, would you be willing to share a bit more of your story with our family and, possibly, help our daughter feel a bit more encouraged. She’s being very positive, and willing to do what it takes, especially with a son so young (now almost 8), but she’s also terrified (inside) and I can tell that she thinks ” this is it”! They’ve told her that she’s lucky because they’ve discovered it early, again, but also, that the statistical median survival at this stage is 2 to 3 years. Her oncologist says she thinks Lori will probably survive longer, because of her general health, and because they’ve begun treatment pretty early, again.

    Lori is part of a young survivors group, and has known a number of members who have passed away within months to a couple of years following rediagnosis. Very scary!

    It was so hopeful to learn of your experience with this nasty disease, and that you are still here supporting the “fight”. Lori vehemently objects to that word, saying that it implies that if someone stricken with cancer dies, it was the individual’s fault, for not fighting effectively . I have to say that I now agree with her.

    I hope that you can somehow get my e-mail address through Dr. Susan Love’s Research Foundation. I give them permission to share it with you, herewith. March14, 2014
    With appreciation,

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