Getting Back Up…Again (and Again and Again and Again)
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Getting Back Up…Again (and Again and Again and Again)

Lupus limits us enough as it is. But I don’t think it’s our biggest enemy.

Convention is the enemy. The little voice that tells you to stop dreaming, and start settling because you’re a broken human being and shouldn’t expect much. The voice that tells you to be afraid of everything. I know I’m sick of hearing it – what about you? Continue reading »

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Crazy, Sexy Food

I’ll come right out and say it; I love food. I love experimenting with flavors (perhaps a little too enthusiastically for my mother’s taste) and techniques. Eating is fun; every meal can be as familiar and comforting or new and unusual as I choose. And, living in New York City, I have an entire globe’s … Continue reading »

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Toughing it Out with Lupus

I hear this a lot from both other lupus patients and non-lupus people who just want throw advice my way. They frown upon taking a day off, limiting activities, taking medications, or anything else that is less than having a “normal” life, because this implies, in some way, that you’ve surrendered to your illness and are letting it rule you.

In my humble opinion, that’s bullshit. Continue reading »

Making Your Craziest Goals Attainable
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Making Your Craziest Goals Attainable

People would chide me for not being considerate enough (or fearful enough) of my health or telling me outright the big old “NO!”. This wasn’t just limited to physical activities, but also to any situation that might put “stress” on me – even becoming an excuse to deliberately keep information from me that might be upsetting (such as my mother needing shoulder surgery). And, deep down, I would wonder if they were right. Maybe I should just stay home, twiddle my thumbs and stare at the ceiling for the rest of my life. Safe. Protected. Bored out of my skull. Continue reading »