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Hingham residents step up to support North Carolina family with sick son Valeria Vazquez and Jenna Manto, The Patriot Ledger © Courtesy Shae Lewallen Shae and Ken Lewallen with their two sons before Kobe s birth. HINGHAM Shae and Ken Lewallen had a difficult decision to make when they learned their unborn son had Vein of Galen Malformation, a rare blood vessel abnormality often called VOGM. They could either stay at the hospital where they were receiving treatment in North Carolina, which had little familiarity with the disease, or they could travel away from family and friends to Boston Children s Hospital to see a doctor who specializes in the disorder. 

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