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Bobbi Jo Beitz – On becoming a cancer thriver

Bobbi Jo Beitz – On becoming a cancer thriver

Bobbi Jo Beitz - On becoming a cancer thriver

Active all her life, playing competitive fastball and hockey since she was young, Bobbi Jo
Beitz assumed the numbness she felt in her right heel was a sciatic nerve issue. She could
never have imagined that it would turn out to be something entirely different.
“Of all weird things, it started with some numbness in my right heel and then it started
getting a little more numb in my saddle region,” says Bobbi Jo. “I was going to the
chiropractor and when I mentioned to him about the numbness, he got really serious and
excused himself for a minute.”


At the urge of her chiropractor, Bobbi Jo visited her family doctor in October 2019 and got
scheduled in for an EMG and MRI in January 2020. Not long after, both tests got expedited
by her family doctor. “I remember them saying there was evidence of nerve damage and I
thought, ‘Okay, let’s figure this out.’ I did not have a thought of cancer.”


In the coming weeks, Bobbi Jo would learn she had a 6.8-centimetre mass in her sacrum
and a 2.8-centimetre lump in her left breast, with the latter discovered by a CT scan. On
December 5, 2019, Bobbi Jo was diagnosed with metastatic breast cancer (MBC).
“I was mad,” says Bobbi Jo upon hearing her official diagnosis. “I was so mad because all
my life I’ve been active. There are all those risk factors which increase your chance of
getting cancer. I never smoked. I rarely drink. And of all those risk factors, there was only
one that I ticked off and that was having kids after the age of 30.”


With her family by her side, where she found nothing but positive support, Bobbi Jo rallied
her strength to move forward. “Whenever you hear someone talk about stage four you
automatically think doom and gloom, one foot in the grave. But it’s not doom and gloom
and one foot in the grave,” says Bobbi Jo.


Not the type of person to dwell and hide, Bobbi Jo sought out information to learn more
about her diagnosis and turned to the Canadian Cancer Society’s Cancer Information
Helpline (CIH), finding the experience to be therapeutic and wonderful. CIH is a national,
toll-free service available to anyone in need of support and looking for cancer information.
“The lady I spoke with – she was amazing. She was so compassionate. When I spoke with
that lady, she listened to every single word I said. She was so nice, and I was grateful
because it wasn’t that you were just a statistic. She made me feel important, even if it was
just something small.”


Bobbi Jo continues to live her life with the hope that one day, there will be a cure. Its why
research is so important to her because it can help people like her live longer. “There’s a lot
that I’ve still got to see. Every little bit helps and every little bit counts. It goes to a good
cause to help people.”


Today, she keeps herself busy by finding new hobbies, including taking up piano lessons,
bird watching, photography and joining a dragon boat team made up of breast cancer
thrivers and survivors to live her life to the fullest while she can amidst a pandemic.
“There’s a lot of things that I haven’t been able to do. I used to play hockey and now I can’t
because it would be a little too dangerous and the chemo – not to mention the cancer itself
– has weakened my bones. But I found other things to do to keep myself busy. Life takes
some funny turns, but you just got to go with that bend!” says Bobbi Jo.


Bobbi Jo hopes to inspire and be of help to people on similar cancer journey’s, especially
those who are newly diagnosed. An advocate for the MBC community, she wants to create
more awareness about MBC.


“Everyone has heard of breast cancer but I’d never heard of metastatic,”
remarks Bobbi Jo. “Treatment is ongoing. I want people to know it’s scary, but sometimes
it’s the words that are scarier more than anything. While cancer sucks, it is not all scary and
gloomy.”


Selena Randall found a lump in her breast in the spring of 2018. After completing a
mammogram and a biopsy, she received a diagnosis of triple negative, stage one breast
cancer. Selena said upon receiving her diagnosis that, “being told that I had triple negative
breast cancer was pretty scary, women die from triple negative breast cancer more than
some of the other cancers, so it was scary to have a diagnosis with an aggressive form.”
The first step in Selena’s treatment was a referral to a surgeon to have the lump removed. The
day prior to meeting the surgeon, Selena found CancerConnection.ca through the Canadian
Cancer Society website, and reached out to the forum to find out what questions she should
ask during the meeting.


Selena recalled that “at a time when I was feeling really vulnerable, I had found a community
and when I reached out, it felt like I received hugs back.” After her surgery, Selena had to wait
to undergo chemotherapy and radiation treatments. “The waiting period between my surgery
and hearing about what my chemotherapy treatment plan would be – that was really hard,”
Selena explained. “The forum was really helpful because anything that can make the process
easier helps reduce your anxiety”. On the CancerConnection.ca forum, Selena was able to
connect with other people affected by cancer as well as survivors, offering her supportive
words and helpful answers to her many questions.


“Reading the stories and connecting with people who had the same type of cancer was
really helpful,” Selena recalled. “It was great to learn hints and tips on how to cope with the
treatment, how to cope with chemotherapy, and how to manage the fatigue.” During her
chemotherapy and radiation treatments, Selena experienced many side effects and found
solace in receiving advice from others on the forum who had been through similar
experiences. “You get information that just does not come from your oncologist,” Selena
explained. “I have neuropathy from my treatment, but I didn’t know what neuropathy was or
what it would feel like, and my oncologist couldn’t tell me because she didn’t know what it felt
like, she could only describe what others had said.”

After four months of chemotherapy and twenty radiation treatments, Selena officially became a breast cancer survivor in 2019. She then spent some time being a mentor on the CancerConnection.ca forum and enjoyed
helping others while staying connected. “I was fortunate to become a mentor on that
platform so that I could give back as well,” Selena states. “When you see the same questions
that you were raising come up, you can empathize because you’ve been there, and you can share what worked.” CancerConnection.ca is a supportive online community designed to help patients find connection, share experiences, and exchange information.

If you or a loved one have been diagnosed with cancer and are looking for support, visit
CancerConnection.ca to join the community, or go to Cancer.ca to learn more.