Embarking on a 60-Mile Walk while Battling Breast and Ovarian Cancer

For Ashley L., sharing her story is a part of her healing journey.  

In October 2022, Ashley decided to be proactive and get her first mammogram since her mother was diagnosed with breast cancer at age 50 and is also BRCA 1 positive. At just 35 years old, this routine procedure led to a stage 1 breast cancer diagnosis with abnormal webbing that is only present in 6% of breast cancer patients. Shortly after, she learned that she, like her mother, was BRCA positive, another finding she needed to process.  

In the following months, Ashley faced one life-changing, frightening event after another: 

November 2022: Right breast removal including the nipple, spacer in place 

December 2022: ACL surgery 

January 2023: Stage IV ovarian cancer diagnosis 

February 2023: Treatment begins at new hospital, City of Hope, with new doctors 

Current Day: Ashley continues to receive infusions every three weeks and takes a chemo pill every day, which will go on for some time. Eventually, she will need to remove the left breast and nipple to prevent the return of the breast cancer and to prevent it from acting as a gateway for the BRCA gene.  

As she continues her battle with breast and ovarian cancer, Ashley refuses to allow her diagnoses to define her. “I love trying new things, going on adventures, and I make a really big point to give myself space to have bad days,” she shared. She finds normalcy in her work as a Director of Staffing in property management, a career she finds extremely rewarding, and cherishes her time with friends, family, and her German Shepard, Ms. Harley. Through the hardships of treatment, Ashley remains steadfast in her passions of travel, painting, and writing, even recently publishing a children’s book! 

Another favorite pastime of Ashley’s is walking, so when she saw an ad for the Susan G. Komen 3-Day® online she knew that she wanted to participate. As an active participant in other fundraising walks, Ashley decided to embark on the Komen 3-Day to not only raise money for breast cancer research, but to also enjoy the personal accomplishment of walking 60 miles.  

Since signing up, she’s found the Pink Bubble to be a tremendously supportive community as she copes with both breast and ovarian cancer. “The Pink Bubble makes me feel not alone, supported and has helped me identify things I was concerned about physically through treatment,” she shared. In the meantime, she can’t wait to experience the 2024 San Diego 3-Day among likeminded people who are committed to ending breast cancer forever! 

Youth Corps Fundraising Ideas!

Fun, creative, inclusive, forward-thinking, altruistic; Youth Corps, we’re talking about you!  

You are an integral part of the Susan G. Komen 3-Day®, bringing fresh perspectives, innovative ideas, and an unmatched enthusiasm for making a difference. Whether this is your first Komen 3-Day as Youth Corps or you’re a returning veteran, we need your help to continue the fight against breast cancer. With your innovation and determination to leave a positive mark on this world, we’re confident that the cures for breast cancer are just around the corner. Not only does your fundraising collect money for research and patient care, but it puts you in the powerful position to influence your peers. Remember, it is going to take all of us to end this disease and we need your help! 

If you don’t know where to begin, take a deep breath and remember that you’re already changing lives just by showing up! So, let’s have some fun with fundraising and turn anything you love into an opportunity to raise money and advocate for the breast cancer cause. Unlike previous generations, you thrive in the digital world having grown up with the internet and social media as everyday essentials. As you continue your fundraising for the 3-Day®, why not use these skills to go beyond the boundaries?  

Here are some fun ideas to get you inspired!

HARNESS THE POWER OF POP CULTURE — From Taylor Swift to Naruto, the opportunities are endless! Get in your fundraising era by making and selling friendship bracelets. Host an anime viewing party or a trivia night where everyone brings a donation. Get creative and have fun with it! 

UTILIZE SOCIAL MEDIA — TikTok; ever heard of it? With your parents’ permission, share why you’re participating in the 3-Day and ask for donations. You can also do a challenge, where for every $10 raised, you learn a new dance or eat a bite of an onion. Want to kick it up a notch? Go to the mall with a parent or guardian and ask them to record while you share your story and ask people to donate. At the end of the video, share how much you raised and how much more you need to raise until you reach your goal!  

INCORPORATE SPORTS — If you’re on a sports team, this is the perfect place for a fundraiser with assistance from your coaches and parents! At your next game or meet, host a “pink out” where the proceeds from tickets and concessions go to your 3-Day fundraising account. Advertise with pink flyers that contain a brief statement speaking to your participation in the 3-Day Youth Corps. Maybe your team can wear a pink accessory in solidarity with the breast cancer cause.  

COLLABORATE WITH SCHOOL ORGANIZATIONS — There are so many organizations throughout every school district that are always looking to contribute to a good cause. Many organizations such as musical theater and the PTA already host events, so ask to hold a concession stand or raffle entirely for 3-Day donations. You’ll be surprised by how many people will want to help! 

SHOWCASE YOUR TALENTS — If you’re an artist, dancer, or have another special skill, use it! Sell crafts at a farmers’ market or host a paint party with friends, partner with your dance studio to hold a special donation-based class, or anything else that showcases your talents.  

Regardless of how you choose to fundraise, remember that every dollar makes a difference. You are unstoppable and by putting yourself out there to ask for donations, you’re helping to create a world that is free from breast cancer. We can’t wait to see you rock yellow in the Pink Bubble! 

July Pink Bubble Story of the Month: Beth B. 

Beth B.: My Story— 4 Words Plus 1  

“A lot can happen in three days” has been running on a continuous loop through my head over this past week. May 12th was my first Mother’s Day without my mom. May 13th was the day phase 2 of treatment began. May 14th was the one-year anniversary of John’s death. It was an incredibly difficult three days for me, exacerbated by radiation burns in my throat which have made it very difficult to swallow and to eat. Thankfully, that has started to ease. 

I never wanted to become the story, but when I was originally diagnosed in 2011, I let myself become the story. I thought it was a way to show people what it’s like to have cancer, to live with cancer, and to live beyond a cancer diagnosis. It also lit a fire in me; a fire to fight, survive, and pay it forward. Every. Single. Day. Publicly sharing your story is daunting for many people [but] it is empowering for me. It puts cancer in its place. Everyone [with cancer] has a story [and] if telling my story helps just one person, then it’s worth it. It is all worth it. To anyone facing a cancer diagnosis, tell your story; tell one person, tell a friend, a stranger, tell me, tell ten people, tell 10,000 people… just tell it. Telling your story prevents cancer from being something sacred or secret and puts the power back in your hands. It also introduces you to all us survivors and thrivers. We are here and we can’t wait to meet you.   

My original story began on November 4th, 2011, with 4 words, “You have breast cancer.” 

“You have a lump.” 

“We found something suspicious.” 

“You have breast cancer.” 

“Lumpectomy, mastectomy, chemo, reconstruction.” 

“You are a survivor.” 

For the last 12+ years, I have lived my life as a survivor. I went to all my follow-up appointments, followed all the rules, I walked and walked and walked, raised money for the cause, [and] lived my life out loud. But there was always a sword hanging over my head because breast cancer is never truly gone. It hides. It lurks. It may stay hidden, [or] it may burst back into sight. It is a dirty, sneaky beast. 

On April 13, 2024, my story became 4 words plus 1, “You have METASTATIC breast cancer.” 

“There is no cure.” 

“There are treatment options.” 

“There are clinical trials.” 

“I will fight this.” 

“We will fight this.” 

“I am a thriver.”  

There are an estimated 168,000 women in the US living with metastatic breast cancer (MBC) and the 5-year survival rate continues to improve, thanks to advancements in treatments that help people like me live longer, and with a better quality of life. Kisquali, the drug I started taking last week, was approved by the FDA in 2018. To anyone who questions why I walk, why I have walked since 1997, why I will always walk (including this November in San Diego), why together we have raised close to $250,000, why Susan G. Komen 3-Day® participants have raised close to $1 billion—this is why. The money we raise goes to fund research [which leads] to clinical trials [which leads] to better treatment options. While there currently is no cure for MBC, people are living longer, better lives with the current drug options.  

I’m sure you’re asking where I am now.  

On May 6th, I completed 10 rounds of radiation to shrink the tumors on my spine. Memorial Sloan Kettering completed blood work which included genetic mapping of my tumors and determined I have no genetic mutations which means I do not qualify for clinical trials. My treatment was transferred up to Albany to my original oncologist and his team. On May 13th, I began phase 2 of treatment which consists of hormone therapy shots of Fulvestrant every three weeks. My current pathology is identical to my original pathology which means this is treated as breast cancer even though it is in my spine, liver and lymph nodes. Kisquali is an oral medication that blocks certain enzymes that feed my cancer which I started this last week. I take three pills a day for 21 days then I get a week off and start all over again. This will continue for the rest of my life or until another protocol is developed. I will also get Prolia injections every three months to strengthen my bones which can be impacted by these medications. This treatment protocol will be so much easier than chemo and with far fewer appointments. 

With this diagnosis, I will continue to live my life out loud. I do this for those who don’t want to, or just can’t tell their stories. This diagnosis is so much harder, but I want and need people to know I’m here if they need me. I want people to understand what MBC is and what it means, to see us Thrivers living with this chronic, not terminal, disease; and we will NOT back down.