California Girl Who Could Barely Open Her Mouth Due To Rare Syndrome Gets 'Life-Changing' Treatment ibtimes.com - get the latest breaking news, showbiz & celebrity photos, sport news & rumours, viral videos and top stories from ibtimes.com Daily Mail and Mail on Sunday newspapers.
Dorothy McKay, obituary penbaypilot.com - get the latest breaking news, showbiz & celebrity photos, sport news & rumours, viral videos and top stories from penbaypilot.com Daily Mail and Mail on Sunday newspapers.
Even during a global pandemic, miracles can happen.
A local family who could ve spent the holidays in a hospital in Baltimore is grateful to be at their home in New Galilee with their newborn baby, Matthew.
Matthew was still in utero in the summer when the Brommer family found out he had Nager Syndrome, a rare genetic disorder characterized by craniofacial malformations which can include facial abnormalities such as a small, setback jaw.
Due to this diagnosis, the Brommer family was set to move to Baltimore during the 37th week of mom s pregnancy so Matthew could be delivered at Johns Hopkins Hospital. But when mom s water broke more than a month early in mid-August, everything changed.