Mr Gladstone's life was 'completely changed' when he was diagnosed with myeloma blood cancer during a routine test.

When Peter Robson went to the doctor for a routine check-up, he never imagined the results would change his life forever.

Scans revealed his vertebrae had been gnawed away, his jaw fractured and his ribs punctured.

“It was like termites were eating away at the bones from the inside,” Robson said.

Shocked and confused, the Gladstone man was sent to a haematologist (specialist in blood disorders) who discovered he had multiple myeloma, a rare type of blood cancer that affects plasma cells. did.

“Went home [from the scans] “So I got a call and they said, 'Peter, you should go to Brisbane now,'” he said.

“Well…at that exact moment, my life changed forever.”

Mr Robson worked full time as a welding inspector on large commercial projects in central Queensland before moving into the world of chemotherapy, radiation and stem cell transplants to save lives.

His wife Tricia said the family was in “complete shock”.

“I think we were all in a state of fear and anxiety because we had no idea what we were going to find,” Robson said.

“It was a shock…a complete shock. And you end up in a spiral of emotions, not being able to control what's going on.”

A new treatment that gives hope

It's been nine years since Robson was diagnosed with multiple myeloma, and although there is no cure, treatments continue.

Kathryn Huntley, director of health services at the Leukemia Foundation, said myeloma patients had weaker bones and more bruising.

“The exact cause of myeloma development is not actually known, and unfortunately, our actions are limited when it comes to screening and prevention to thwart the possibility of myeloma developing. “There's nothing we can do,” she says.

“While it affects the blood, it also affects the strength of the bones, and the secretions that result from myeloma can weaken the bones.”

Huntley said new treatments and research are allowing people to live longer with the disease.

CAR T-cell immunotherapy, in particular, is providing a glimmer of hope for patients.

“I have worked in this field for more than 20 years and have seen the introduction of new treatments extend the lives of people with myeloma…but the work is not done.” said Huntley.

“He's a fighter.”

Mr Robson's next appointment with a specialist is next week.

Health checkups can be a stressful time for the family, especially after nearly dying from the disease last year.

The myeloma was eating away at the bones in his left arm so badly that he needed surgery and another stem cell transplant.

Mr Robson said: “Peter went into cardiac arrest and almost died from it.”

”[But] He is a fighter and has always kept his outlook very positive and taken everything in his stride. ”

Ms Robson said the impact had completely changed their lives, both emotionally and financially.

“We've been on a long journey trying to get back to some kind of normalcy…but the truth is, we'll never be back to normal,” she said.

“I don't know whether to be happy or sad or anything. You really don't know what's going to happen every day. So I just want to give a big shoutout to the Leukemia Foundation.”

Mr Huntley said an estimated one in 12 Australians are diagnosed with blood cancers such as leukemia, lymphoma and myeloma each year.

She said medical research was key to finding treatments for myeloma and improving the quality of life for the 20,000 Australians living with the disease.

“The Leukemia Foundation not only invests in research so that we can find treatments that can ruin the lives of people diagnosed with myeloma, but also helps people overcome the challenges of facing years of treatment. I’m here for it.”

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