P.E.I. woman with rare form of cancer spreads message to 'just live' - Action News
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PEI

P.E.I. woman with rare form of cancer spreads message to 'just live'

Michelle Hughes was diagnosed with a rare sarcoma cancer about a year ago. Since then, she's finding hope and figuring out how to manage the unpredictable cancer that doctors still don't know a lot about.

'I don't need to be defined within a three-year lifetime, I can do this for years and years'

Michelle Hughes at home.
'It was really frustrating and really difficult experiencing the pain over the years, but I was living my life,' Michelle Hughes says. (Laura Meader/CBC)

It wasn't long after her son was born in August of 2021 that Michelle Hughes was diagnosed with an ultra-rare sarcoma cancer.

"My first oncologist told me I have three years," Hughes said.

It's called Epithelioid hemangioendothelioma,or EHE for short.

"It's a rare, but also very unique cancer andit affects people very differently," Hughes said. "There are some people who get diagnosed and pass away in a matter of weeks ormonths, but there are some that have lived for twenty years."

When she was first diagnosed,the doctor hadn'theard of EHE.

Michelle Hughes pictured with all her children in hospital.
Hughes's son Hatton was a newborn when she was first diagnosed. (Submitted Michelle Hughes)

"It's very hidden, it's very hard to see, " Hughes said."You can't see it on ultrasound per se. Ihave cancer in my leg, liver, innumerable tumours in my lungs."

Since the diagnosis in 2021, Hughes saidshe is finding hope and figuring out how to manage the unpredictable cancer that doctors still don't know a lot about.

"I don't need to be defined within a three-year lifetime," she said. "I can do this for years and years and there's hope there."

Years without answers

Hughes had been experiencing pain on and off for years and visited dozens of different doctors looking for answers.

"It was really frustrating and really difficult experiencing the pain over the years,but I was living my life," she said."It wasn't like I was in constant pain 24/7."

It wasn't until the young mother of three collapsed, only weeks after having her son, Hatton,that ledto weeks of testing and after manyblood tests andnumerousbody scans, she'd eventually gether diagnosis.

Michelle and Ty Hughes pictured on a couch at home with their three kids.
Michelle and Ty Hughes at home with their three kids: Hatton, Adeline and Juliet. (Laura Meader/CBC)

Since that time,she has new hopefor how long she will live, andis doing what she can to keep the numeroustumours throughout her body stabilized.Hughes gets scans every three months.She has been taking experimental medication and, so far, there are no new tumours and no new growth.

"I'm kind of thankful that they didn't find it six years ago, because I wouldn't have my [children], my Juliet, my Adeline, my HattonI'm a mom and that's my purpose," she said.

It's a really, really difficult thing to comprehend that someone can have sarcoma and be flourishing. Tyrrell Hughes

She and her husbandTyrrell, or Ty,neededfertility treatments and said it was a heart-wrenching journey.Before they had their three kids, theylost a son who was stillborn, and Michelle had a miscarriage.

Now, they cherish their role as parents.

Hughes said she remainsfocused on nutrition and exercise, running almost daily pushing two kids in front of herand pulling one behind in a specialized stroller attached to her waist.

A woman running while pushing and towing a stroller.
Michelle Hughes runs with all three of her kids two in the front stroller and one in the back. (Submitted Michelle Hughes)

"She is getting a lot of feedback from her body, that exercise and nutrition that she is paying attention to is paying off massively," her husband Ty said. "It's a really, really difficult thing to comprehend that someone can have sarcoma and be flourishing."

Michelle fully admits she didn't like exercise at first, or thinking about her diet in her "past life." That perception has drastically changed.

"Exercise is what I've quickly learned is my true medicine I do it to feel alive and it feels amazing," she said.

Being active helps to reduce chronic inflammation for her, which can be a source of pain. She is also very focused on being a mom, especially with Hatton still so young.

"I believe he is here to keep me busy, he is here to show me that cancer does not define me, that 'mama'defines me.As everyone knows when you have an infant: Life doesn't stop," Michellesaid, laughing.

A rare cancer and an abundance of hope

Michelle is under the care of Dr. AbhaGupta,a medical oncologistat the Princess Margaret Cancer Centre in Toronto.

Gupta said EHE is "exceptionally rare," noting that sarcomas make up one per cent of all cancer cases and EHE cases are less than one per cent of those sarcomas.

She said she is impressed with how Michelle is doing.

"You would never know watching her running down the street with her baby, or, you know, just taking care of her familyand going about her day to daythat she has, on paper, Stage 4cancer," said Gupta.

Dr. Abha Gupta pictured in her office as part of a recent zoom interview with CBC P.E.I.
Dr. Abha Gupta is medical oncologist at the Princess Margaret Centre in Toronto, and says EHE is incredibly rare. (Zoom)

She said there is an unpredictable nature toEHE and that Hughes shows that.

"We are learning about the differences and the biology of different EHE subtypes and, thankfully, Michelle has the kind which is associated with a more indolentcourse," she said. "Absolutely, people with EHE even if they have lesions in their lungs and liver can live, hopefully, for decades," said Gupta.

"It is possible that EHE may not be the cause of Michelle's death in the future, it is just something that she has to live with."

Holding on to the motto 'just live'

Michelle holds fundraisers of all kinds, from bottle drivesto making Christmas ornaments,to help fund research. She also writes regularly on her Facebook page "My Journey to Just Live" a motto that's close to heart.

"Everyone can apply'just live' to their life," she said. "Time is a gift, nobody knows when their time is coming my mindset has changed,"

Ty and Michelle Hughes look at their lap top computer during a virtual appointment with the Princess Margaret Cancer Centre.
Ty and Michelle Hughes on a recent virtual appointment with Dr. Gupta. (Laura Meader/CBC)

Michelle saidit is possible to thrive even with an incurable cancer, adding "I don't need to be defined within a three-year lifetime, I can do this for years and years and there's hope there."

For her husband Ty, that means many more milestones to come for Michelle.

"I foresee her being at all of our children's graduations," he said,"walking our daughters down the aisle, and her and I spending the rest of our lives together."