“State legislators want to create two different healthcare policies for kids with autism: one that generously covers the privately insured, and the other that gives minimal coverage to the poor and publicly insured, but both using state funds,” says Idil Abdull of Burnsville and mother of a 10-year-old son with autism.At age 11, when Abdull came to the United States from her native country of Somalia, she knew very little English and very little about American politics. “The only thing I knew about America was Superman and Rocky [the movie], she says.”Some 20 years plus since arriving on North American shores, Abdull is now very fluent in both English and the parlance of American politics. “If nothing else, I know how to be loud,” she says.Like many other families, Abdull says she went through a period of denial about autism. “I couldn’t say the word for many years, because in Africa there is shame around having a disability like autism. But fortunately, I was able to get the help I needed for my son, and he has made great strides in meeting developmental milestones.“At age two, he walked on his toes, and by age three he still couldn’t talk. Continue Reading