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GIVEAWAY: 2 tickets to Baltimore Bar Guild’s + Cystic Fibrosis Foundation’s annual Ryes Up
1 week in Grace Bay, Providenciales, Turks & Caicos, the OBX of the Caribbean
When Steve and I returned from Europe, I promised him that he could choose our next trip for so kindly allowing me to drag him across the continent. He wanted a super relaxing beach vacation and had heard great things about Turks & Caicos, so off we went! A few things before we get into …
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StitchFix #15 (or the one in the office when the wifi was out)
I was planning to post this Stitchfix tonight, but the wifi went down in the office, so why not have a little fashion show? I asked my co-workers for their opinions on each item and also texted them to Steve, because I know you all care about his opinions. So, which do I keep? What …
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Ground & Griddled to open at Remington food hall, R House, this fall
Ground & Griddled to open at Remington food hall this fall
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Guest post from my husband: The 5 best pranks I’ve played on my wife in 5 years of marriage
I was planning to write a post about what I've learned in five years of marriage and I asked Steve to share his thoughts. Instead, he wrote about the five best pranks he played on me in the past five years ... and it was better than my post.
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2014 in review
The WordPress.com stats helper monkeys prepared a 2014 annual report for this blog. Here's an excerpt: The concert hall at the Sydney Opera House holds 2,700 people. This blog was viewed about 55,000 times in 2014. If it were a concert at Sydney Opera House, it would take about 20 sold-out performances for that many …
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My 30th Birthday Wish… For 30 More
I am so excited to help Katharine launch #For30More! Keep tuning into both of our blogs for details.
As most of you know, at 16I was diagnosed with cystic fibrosis,a life-threatening genetic disease that affects the lungs and digestive system.Even 13 years later I’m still a long way from fully dealing with what it means to have this disease and the implications it has on my future.
Right now, my life looks like many other 29 year olds?. I have a wonderful husband, fabulous family and friends, and a job that I love. But unlike most people my age, I have to do time-consuming daily treatments, spend countless hours at the hospital, and worry about what my future looks like.
When I was born in 1984, the life expectancy of someone with CF was just 25 – onSeptember 26th I’ll turn 30! And I can’t wait to celebrate the many things this wonderful life has allowed me to do.
But I’m not finished…
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