Friday, December 16, 2011

This Girl can die if she brush her hair and Holds a balloon! (soft-skill)


Combing is a daily job for every girl right? But this activity does not apply to Megan Stewart. Scottish Girl can die when she comb her hair, and she also threatened to touch the balloon. Megan Stewart has a rare disease, the name of the disease is Brushing hair syndrome. The disease is known to her mother when she was preparing her to face her first day at primary school. Sharon told how she found her daughter sick. She was combing her daughter's hair in the living room when suddenly she fell and her lips turn blue. "i think she's getting all of a sudden heart attack as never experienced before, so we call the paramedics" said 41-year-old-mother. Megan was rushed to the hospital. Megan is allergic to static electricity. if there is a static electricity in  her body, like the activity combing hair or touching the balloon, it would appear fatal reactions. Doctors at York hill Hospital in Glasgow said the syndrome is very rare. They only heard one case of this syndrome. Megan was born with a weight of just 1.05 pounds and as big as the palm of the hand of a man. She was suffering from diaphragmatic hernia, or there is a hole in her diapgragm. This means the stomach moves up into the chest, which only allows one room for the lungs to develop. Strange condition causes Megan to avoid static electricity in their daily lives. "when we comb her hair we had to lay her down and covered her hair with water to stop the static electricity. she cannot rub a balloon on her head during party. Mrs Stewart gas experienced a difficult pregnancy and six months pregnant when diagnosed with pre-eclampsia. she was forced to undergo an emergency Cesarean section to save her daughter. Thanks to the expertise of the doctors at Bells hill Maternity Hospital, Lanarkshire, Mrs Stewart could recovered, but little Megan spent the next 18 months at York hill hospital. Megan also had asthma and a condition called dorsal stream dysfunction, which makes it difficult to see fast moving objects, like a ball. even so, her life is still normal. Megan is now waiting for a surgery and plans to follow the activities of charitable fundraising for York hill on October 8th "she's really brave against all odds. she's a little miracle" said her mother. 

Sources:
tribunnews.com













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