'Tis The Season!


© Karyn Moran Holton

Most of the time, we tend to think of giving to charities during the winter holidays. Jolly Santas are on the street corner or in front of the grocery store, ringing their bells and thanking contributors who drop some change into the red bucket. Schools have canned good drives, and kids stuff their backpacks with ancient creamed spinach from the back of the pantry. Businesses start "Angel" programs, where employees "adopt" a child or even a whole family and give them holiday gifts, shoes, and food.

Yes, that heartwarming time of year brings a sigh of satisfaction.

Harry Chapin, the renowned singer/songwriter whose songs like "Taxi" and "Cat's in the Cradle" made life (and radio!) in the '60s and '70s great, was a great advocate of programs designed to stop hunger in America. But Harry wasn't a seasonal activist. He quietly and succinctly got to the heart of the problem during the holidays when he asked the simple question: "What are those kids going to eat next week?"

Yes, I am making a pitch.

See, I figured that I would get everyone's attention now, while it's relatively quiet, and no one else is clamoring for your extra pocket change. You see, there are many great lupus-related organizations that would benefit immensely from a little monetary boost. Think of the following (as I hear your wallet crinkling from the pressure you're applying to it in an attempt to withstand my charming self):

  • The last time that a medicine was approved specifically for lupus was over 40 years ago.

  • Although more people have lupus than have cerebral palsy, multiple sclerosis and cystic fibrosis combined, we have no telethons, or celebrity lupies testifying before congress about the lack of a cure.

  • Lupus is more likely to strike women, and also more likely to strike African-Americans, yet Oprah has never done a show on lupus. (Maybe she's just not aware?)

  • Only 20% of adults 18-24 could give basic, accurate information about lupus when asked, even though it usually strikes during the childbearing years.

Hello? Is this thing still on? I think we can all agree that information must be made easily available and that awareness raising is crucial. How many times have we heard (or said) "I thought I was just tired." Or "I figured it was a sunburn." Or "My family said I was just depressed."? This kind of ignorance can cause people with lupus to neglect seeing a doctor and can cause treatment to be delayed, sometimes with terrible results.

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