Rudy Santos

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In his heyday, Rudy Santos would draw crowds of fascinated onlookers as “Octoman,” the headline attraction of travelling fairs.  Attached to his abdomen are an extra leg, arms, shoulders, what appears to be an ear, and a patch of hair.  His own right leg is deformed and he is unable to walk without crutches

These grotesque deformities are symptoms of a rare condition called "parasitic twin," the result of conjoined twins not fully separating in the womb.  In other words, Mang Rudy has lived his entire life with the remains of his would-be twin attached to his body.

After two decades of earning a living as a freakshow attraction, Mang Rudy settled down to live a quiet life with his wife Evelyn and teenage daughter Riza.  Wanting to live a normal life, the family put up a small sari-sari store in Zamboanga.

Unfortunately, their dreams were dashed when their small stall slowly lost business.  Evelyn made the difficult decision of leaving her family behind in Zamboanga to work as a domestic helper in Manila.  Because Mang Rudy’s limited mobility made it difficult for him to work, the family scraped by on daughter Riza’s meager earnings as a bakery employee.

The GMA program "Wish Ko Lang" learned about Mang Rudy’s plight from a letter he sent to the show.   The program flew Evelyn back to Zamboanga to reunite the family.  Upon seeing her mother, Riza embraced her tightly, crying,  “Mahirap ang walang mama. Parang ako ang naging mama.”  Mang Rudy was at a loss for words when his wife embraced him and said, "Ngayon maalagaan na kita, ang payat-payat mo na!”

"Wish Ko Lang" treated the Santos family to a summer getaway in a popular resort in Dapitan.  They were then presented with a sari-sari store package to help revive their business, which would be newly named, “Ang Tindahan ni Octoman.”  The program also gave Riza a scholarship to any four-year-course at Ave Maria College, a gift that Mang Rudy said was the best of all.

Tom Staniford

BRITISH paracyclist Tom Staniford has discovered he is one of just eight people in the world with a rare syndrome.

Tom Staniford, 23, is unable to store fat under his skin, losing all the fat around his face and limbs during childhood having been born a normal weight. In spite of his wasted frame, Staniford's body thinks he is obese, meaning he has type 2 diabetes. His hearing also became impaired in his childhood, requiring him to wear hearing aids since the age of 10.

Staniford’s condition - MDP syndrome - was not identified until recently, when a research team went to work mapping and analysing his DNA, in a quest to isolate the gene mutation responsible.

This was only possible after a second person with the same condition was found.

Using the most recent genome sequencing technology, scientists from England, India, Italy and the US were able to identify the single genetic mutation responsible for the rare condition.

"All Tom's features can be explained by this one specific change," says Exeter University scientist Professor Andrew Hattersley, who believes the genetic mutation would have occurred in Staniford’s father’s sperm very early in Staniford's life.

Staniford has not let the condition hold him back from achieving several goals, including being British national paracycling circuit race champion in 2011, as well as a degree in law and French.

He hopes to become Paralympic circuit race champion at Rio 2016.

Staniford does concede, however, that his condition presents particular challenges to training: "I have just 40% of the muscles of an average male. I struggle to metabolise sugar and carbohydrates efficiently due to the diabetes - and I struggle to recover due to lack of immediate fuel sources, low testosterone etc.

"My muscles have a very narrow margin of efficiency and they're also tight, stiff and inflexible because I don't have fat to perform that role.

"This is why I have to constantly experiment and attempt to find, through trial and error, what works."

Staniford is not one to dwell on the rarity of his condition, but says: "[It] is reassuring to know that there are other people with the condition and that we can lead relatively normal lives.”