'I Wish My Son Had Cancer': Dad Stands By Brutally Honest Awareness Campaign

He knew his candid comments would cause a firestorm, but Alex Smith will do whatever it takes to help find a cure for his son’s little-talked-about fatal disease.

Smith’s 8-year-old son, Harrison, has Duchenne muscular dystrophy (DMD), a genetic disorder that has no treatment or cure, and causes progressive muscle degeneration and severe heart and lung problems, according to Parent Project Muscular Dystrophy (PPMD).

Harrison likely won’t be able to walk by the time he hits adolescence and probably won’t live beyond his 20s. His dad is committed to educating the public about his devastating prognosis.

harrison fund

So when Smith’s organization, "Harrison's Fund," was chosen by creative agency AIS London to develop an ad campaign, the vehement advocate decided to share some of his darkest thoughts with the group, Smith wrote in a recent Guardian op-ed.

After having extensive conversations about the experience, AIS and Smith agreed on an unconventional and controversial tag line.

"I wish my son had cancer," read the ad placed in the London Evening Standard and the Independent last year.

The campaign was met with expected backlash, but more than a year later, Smith has no regrets.

"I felt a cancer diagnosis would have more options, more of a chance, a chance to try something -- a chance that those with DMD still don't have," Smith wrote in his op-ed.

Duchenne muscular dystrophy is the most common fatal genetic disorder diagnosed in childhood and affects approximately one in every 3,500 live male births, according to PPMD.

Muscle weakness can begin to happen when a child is as young as 3, and those with the condition usually didn’t survive beyond their teen years, according to the Muscular Dystrophy Association. Research breakthroughs have helped people with DMD to now live into their late 20s and early 30s.

These are the encouraging breakthroughs that give Smith hope, and drive him to continue to raise funds through his organization to support researchers working to find a cure.

They’re the breakthroughs that also drove Smith to help develop the off-putting campaign.

harrisons fund

"[There are] no slim chances, no drugs to help, just the certainty of a very short life, marred by a progressive debilitating condition that will leave him unable to move, until his heart or lungs give up their battle to keep going," Smith wrote in a blog on his fund’s website. "Funding for cancer research is epic in its vastness and reach, led by some incredible charities, doing amazing work … My hope is that this advert if nothing else will open up a conversation, make people think, look wider than the big players, with the big presence and big budgets and just perhaps join me to help children like Harrison and rid the world of Duchenne."

Smith is just one of the vocal voices in the Duchenne community that is determined to help support more bolstering research.

After undergoing a treatment called "eteplirsen," 12 boys with DMD saw their muscle function and breathing stabilize, Tracy Seckler, co-founder and executive director of Charley’s Fund -- a nonprofit that works to raise funds for DMD research -- wrote in a blog post for HuffPost. Still, even after the drug showed promise after two years of testing, the FDA didn’t provide clear guidance to the drug company on how to expand access to the drug for kids in need.

That’s when advocates decided to take matters into their own hands and devised a White House petition, which required collecting 100,000 signatures in 30 days in order to elicit a response the administration. It collected the names in 27 days in March and advocates are asking for the drug to be fast-tracked.

While Smith supports the traditional fundraising and petitioning route, he also sees value in pushing the limits.

Some of Smith’s critics took issue with the fact that his ad clumped all cancers together -- not taking into account that many have low survival rates and little research funding.

harrison fund
Harrison hugging his 6-year-old brother, William.

The committed dad replied personally to all of his critics, but still stands by the need to incorporate "shock value" into advocacy work when the issue calls for it.

It’s a tactic that’s used for a number of causes but hasn’t quite made its way into a sphere that often relies on heart-wrenching videos and adorable lemonade stands to raise awareness and funds.

"If what you say shocks and is based on honesty and truth," he wrote, "it rises above the cookie-cutter adverts and distinguishes itself from other items on the page."



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