The animal world is full of age-related curiosities. Tiny aquatic creatures called hydras don’t age at all, while small dogs live twice as long as big ones. Pets may be the first to benefit from medicines that slow aging, which could pave the way for similar drugs for people.

Making the right choices around what we eat, how much we exercise and how we manage our stress can add a decade or more to our lives. In this episode: A science based blueprint for building your own fountain of youth.

Keith and Laura get tested to find out if they’re genetically predisposed for longevity. Another test promises to reveal their biological ages. Have stress and disease conspired to make them older than they should be? Plus, more hallmarks of aging: weakened immunity, chronic inflammation and methylation.

Scientists have identified several drugs that appear to slow aging. Some are already widely used in humans to treat other diseases. But how do you get a cure approved when regulators don’t see aging as a disease? And wouldn’t it take decades to prove the pill prolongs human lifespan? This episode explores the hits and misses on the path to a fountain-of-youth pill.

Why do we age, and how can we reverse it? We meet a researcher whose discoveries overturned everything we thought we knew about aging. We learn about the levers that cause aging to speed up or slow down. And we meet the 11-year-old scientist at the centre of it all.

Today’s aging science is built on shaky foundations, from Ponce de Leon’s legendary quest for the fountain of youth, to surgeons who transplanted monkey testicles into men. We also look at cryonics and mind-uploading -- speculative science that purports to bring people back from the dead.

Are we on the verge of medical breakthroughs that will extend healthy human life by decades? Some scientists say the first human to reach 150 years is already alive. Is it you?

If there were a pill that could add decades to your life, would you take it? Unlocking the Fountain is a podcast about the mysteries of aging and the scientific quest to slow, stop or reverse it. Hosted by Keith McArthur, coming September 28.

Bryson's family struggles with the trials of pandemic life. A death in the community underscores the need for a cure — and promising new research might make one possible.

After months of waiting, the “Bryson mouse” is finally ready for lab tests that will provide new insights into treatments and cures. And Bryson’s parents explore two possible versions of Bryson’s future.

Bryson’s parents travel to Boston/Cambridge, the global capital for rare disease research. Their goal: to ask private biotech companies to help in their search for a cure. Scientists provide new clues, but also raise difficult questions.

Finding a cure for Bryson no longer seems impossible. And that raises new questions about the ethics of this journey. Bryson’s family seeks out new perspectives and learns why “cure” is a loaded term in the disability rights community.

Scientists in Toronto get to work building a mouse with Bryson’s precise genetic variant. Plus, the family travels to Atlanta to provide blood samples for a researcher to create DNA-based “mini-brains” in his lab. Could this cutting edge science provide clues to unlocking Bryson’s brain?

Bryson’s family travels to meet other GRIN1 patients, including Bryson’s GRIN-twin Olivia. And research on mice offers new hope for finding a cure. But a new illness means that the family now needs two medical miracles.

Bryson’s parents explore CRISPR, a new technology with the potential to cure dozens of diseases once thought incurable. But gene editing comes with risks — not just for individual patients, but for the human race.

From violent seizure-like episodes to insensitive comments from strangers, Bryson has a hard life. But after years of searching, doctors finally provide a diagnosis. The news changes everything for Bryson’s parents and provides a possible path to new treatments — or even a cure.

Bryson seems like a perfectly healthy baby. But soon doctors confirm his parents’ worst fears: something is wrong with Bryson’s brain. Despite dozens of tests over nearly a decade, doctors come up empty in their efforts to find a diagnosis.

Bryson is a beautiful, happy boy. But a mysterious illness means he can’t walk, talk, or feed himself. Scientists working at the cutting edge of genetics believe they know what’s causing Bryson’s disease — and think it could be reversed. Motivated by the hope for a cure, Bryson’s parents search for the miracle key that could unlock Bryson’s brain. Hosted by Keith McArthur, coming April 2020.