Does anyone take them because of your kids special needs. We are still dealing with what to do for Eli to deal with the Subclavian Steal Syndrome. The doctors here have absolutely NO experience in surgery to correct it. It's very complicated and makes me not be able to breath and feel like I'm going to pass out whenever I think about it. I can't really afford the dr visit or meds (my hubby and myself are not covered 100% like the kids are). However, I may be reaching a point that it's necessary. But as I told a friend the other day, I just keep thinking "when things get better I won't need it". And that's what keeps me from getting any. Can anyone relate?