Sometimes people just don’t get it, do they? Check out this report on Consumerist about a Sam’s Club in Maryland that is putting candy like Dots and Tootsie Rolls in prescription bottles labeled with an advertising message touting the pharmacy. Here is a link to the original blog post. And here is a photo of the offending “treats.”
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No, not from me. But this is something that really moved me and I felt it was worth sharing.
A co-worker today attended the Westchester County Women’s Hall of Fame Awards luncheon, at which his daughter was receiving the Merrill Lynch Westchester Leadership Award.
I think her words best relay why she was worthy of the honor and the scholarship it brings. These are excerpts from the essay she submitted as part of her application for the award:
“I have always been different. In books and movies, being different is always good. The hero and heroine are never ordinary people, they are special and gifted.
“But being different in real life is not always a good thing; most of the time it’s painful, lonely, and just plain hard. I have cerebral palsy and other learning disabilities including difficulty reading and writing.
“I would have to say that my disability, and more importantly people’s reaction to it, has had a big impact on my life and made me who I am today.
“It’s amazing how being different can be like holding a magnifying glass up to reveal those who are kind as well as those who are cruel. While I consider many of my ‘disabilities’ to be ‘abilities,’ I have had to spend much of my life learning how to be like others so I will be accepted.
“I hope to become a teacher, a special education teacher or maybe a social worker or an advocate for people with disabilities. I’d like to help other people like me get the help they deserve. Maybe I’ll even get a PhD.”
Wow. That’s some young lady.
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It’s a little bit different than the dilema plaguing many families across the nation right now. My son has too much health care coverage. This is the kind of thing you’d only get from layers of blind bureaucracy.
In a nutshell, my son has been on my health plan since my ex and I split up. No problem there. Recently, she added he husband and his son to her health care plan. Somehow, the paperwork was mixed and my son ended up on her plan too. Except we didn’t know right away. Anyway, she finds out and confirms this at her job and we discuss it. She suggests leaving him on her plan and we agree to do so. Obviously, I agree to remove my son from my plan. Seems simple.
Now, this is the kind of arrangement my ex and I have always been able to follow through on amicably. I’ve paid his health care costs for six years, and she figured it seemed fair that, given the inadvertent mess up by her health insurance carrier, we use the opportunity to have her pick up the costs to even things out. Seems fair. I know full well that health care costs are routine issues in custody disputes, and I am grateful that in this instance it has never been an issue.
Well, it wasn’t so simple. My health insurance provider says I had to make the change by Jan. 31, or I have to wait a year. I get it: That’s the rule. But that there’s no flexibility at all seems, well, bureaucratic. Oh, they are sending me an appeal request form, which will be considered and processed after a month of review.
I suppose the upside is that my son won’t be lacking for health care this year. But it strikes me as unfair that there are kids out there with no health coverage and my son is covered under two plans.
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