NEW TLC SERIES "TWO IN A MILLION" BRINGS PEOPLE TOGETHER WHO SHARE THE SAME RARE MEDICAL CONDITIONS

Tales of shocking medical stories and life-changing bonds begin on Wednesday, April 6

New York, NY - Imagine living with one of the rarest medical conditions in the world; having no one to confide in who understands the pain, struggles, and isolation of everyday life. In each episode of the new TLC series TWO IN A MILLION, premiering on Wednesday, April 6 at 10/9c, two people who share the same medical struggles meet and spend one week together, sharing hardships and incredible triumphs, visiting world-renowned doctors, and finding answers to important questions. This new series follows the powerful journey of those who live with some of the world's most unusual disorders, and brings unique insight into the intimate journey of these extraordinary people. The connections they make are powerful beyond imagination.

Meet the remarkable people who find out they're TWO IN A MILLION:

A condition so rare there are fewer than 100 cases worldwide, both Giovanni and Owen suffer from Schwartz Jampel syndrome. This extremely rare medical condition means the young boys have muscles that are permanently and painfully contracted, respiratory issues, and painful fixed joints. The boys' mothers found each other on Facebook, and thought their sons looked like twins! Both families cannot wait to share tips on surgeries, parenting, and living with SJS day-to-day.

Bobbi of Arizona and Kenny of New Jersey, both suffering from lamellar ichthyosis. Also known as 'the fish scale disease', this skin disorder causes scaling of the skin that can lead to deadly infections. Their skin builds up rapidly and sheds as large, thick scales. Both Bobbi and Kenny go through a grueling daily skin route of bathing, exfoliating and moisturizing that can take up to 2 hours. Will they both find the support and understanding they are looking for?

Tiffany and Destiny have the one of the most severe types of osteogenesis imperfecta. Before the age of 3, they had broken over 300 bones between them. Now 21, both girls are feeling constrained by their condition and want to learn how to become independent adults. Together, they travel to Chicago and learn how to drive a specially adapted vehicle - an exciting first taste of the independence they crave.

Both Austin and Elena's mothers were told their children may not survive infancy, but both proved the doctors wrong. Austin and Elena have Goldenhar syndrome, a rare disease in which development of the ear, nose, soft palate, lip, and jaw can be incomplete. They also have respiratory issues, as well as hearing and vision loss. After undergoing many painful reconstructive surgeries, Austin and Elena's families would like to meet to support each other through future struggles and find the one friend that their children can truly confide in.

TWO IN A MILLION is produced by Raw for TLC.

About TLC

Offering remarkably relatable real-life stories without judgment, TLC shares everyday heart, humor, hope, and human connection with programming genres that include fascinating families, heartwarming transformations, and life's milestone moments. In 2015, TLC was a top 10 cable network with women and had 26 series averaging 1 million P2+ viewers or more.

TLC is a global brand available in more than 93 million homes in the US and 332 million households in 189 markets internationally. A destination online, TLC.com offers in-depth fan sites and exclusive original video content. Fans can also interact with TLC through social media on Facebook, Instagram, Pinterest and @TLC on Twitter as well as On Demand services, YouTube and mobile platforms. TLC is part of Discovery Communications (NASDAQ: DISCA, DISCB, DISCK), the world's #1 pay-TV programmer reaching 3 billion cumulative subscribers in 220 countries and territories.