The post Here We Go Again appeared first on Living with Scleroderma.

Last Wednesday night marked the beginning of Passover, when we always host the first seder for our extended family. Al’s first cousins always host the second seder. This is a family tradition that dates back to Al’s mother and her youngest sister, who alternated hosting the two festive meals every year, when we join Jews […]

The post Until Next Year appeared first on Living with Scleroderma.

When I am not writing about living with scleroderma or helping my clients with marketing and communications strategy, I pursue my own writing. Fiction, that is—historical fiction, in particular. Back in 2014, I began working on a novel set in World War I about a mother whose estranged daughter runs off with her beau to […]

The post And Now for Something Completely Different appeared first on Living with Scleroderma.

I didn’t realize it at the time, but at the end of December, I wrote my 700th post on this site. I launched Living with Scleroderma on January 3, 2012, and have been posting nearly every week since, with time off for good behavior when on vacation. That’s a lot of posts. While there always […]

The post 700-plus appeared first on Living with Scleroderma.

Daylight Savings Time crept up on me this past weekend. Really, is it already time to set the clocks forward an hour? I find this adjustment jarring. I’d rather just let the sun tell me what time it is. According to Harvard Health, we’d all be better off sticking to standard time. But DST has […]

The post Fast Forward appeared first on Living with Scleroderma.

Nights here have been clear and cold, and the moon is waxing brightly. As I write on Monday morning, I’m anticipating tonight’s stunning view, when the moon will be full, a huge silver plate in the sky—that is, until 12:44 a.m. Tuesday morning, when a two-hour total lunar eclipse will begin. As the moon passes […]

The post Spring Beckons appeared first on Living with Scleroderma.

As I write on Monday afternoon, all is white outside, once again. We are in the midst of a blizzard that has slowed down our corner of the world. Maybe a foot-and-a-half of snow when this is over later today, maybe a little less, maybe a little more—on top of all the snow that hasn’t […]

The post White Out appeared first on Living with Scleroderma.

Nearly every night for the past 11 days, I have been reveling in the Milan Cortina Winter Olympics. Watching these amazing athletes’ extraordinary feats has been the best antidote to horrible headlines and stress. It has also helped me get through my bout with the flu and the lagging fatigue and residual, annoying cough. I […]

The post Olympic Interlude appeared first on Living with Scleroderma.

And so, despite my best efforts, I caught the flu, too. I thought I was being really careful taking care of Al, who quarantined in our home. Wore a mask, brought him meals, the whole bit. He came down with it last Sunday. By mid-week, I was still doing fine, even went to Pilates on […]

The post Tag, I’m It appeared first on Living with Scleroderma.

Despite our vaccines last fall, the flu has found its way into our home. On Sunday afternoon, Al came back from running errands, went upstairs and went to bed. He never does this. He roused for supper and ate well, then lay down on the couch. Definitely out of character. So I dug out a […]

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