Friday, August 21, 2009
Tuesday, August 11, 2009
Thursday, August 6, 2009
Dad's Blog
Many of you know that back in November my Dad was diagnosed with an incurable and rapidly progressive neurological disease called Multiple System Atrophy (MSA). After the shock wore off, and after a lot of research, he’s decided to travel to a clinic in Germany next month for experimental stem cell treatment to slow down or hopefully even halt the disease. He’s started a blog to chronicle his treatment and to help educate others who may be interested in doing the same. After a few short days, he’s had hundreds of hits.I’m proud of him for doing this, and for the straightforward, open, and strong way he’s facing this illness. My Mom too. The subtitle of his blog says it all “I Have This Disease – It Doesn’t Have Me.”
Check out the blog and, please hope, pray, cross fingers, light candles, sacrifice small animals – whatever you do to send good vibes for successful treatment.
Sunday, August 2, 2009
Can-can show
Sunday, July 26, 2009
The West Wing!
How cool is this? I couldn't get us tickets to the public White House tour, but I did get my parents a private tour of the West Wing of the White House from a very nice man I know who works there. The tour lasted about an hour, and they went all over the place, including the Rose Garden, the Oval Office, and the press room. And, they saw Malia (or Sasha, whichever daughter is the older one) playing with Bo the dog in the Rose Garden.
Happy Birthday Lily!
Lily turned 5 years old on Thursday, and Grandma Fran and Grandpa Steve came up to celebrate with her. Here are some of Grandma Fran's photos:
Carvel cake. Mmmmm. There's only half a cake because we couldn't wait and had some the night before Lily's birthday.
Licking the plate(s) clean.
Carvel cake. Mmmmm. There's only half a cake because we couldn't wait and had some the night before Lily's birthday.
Licking the plate(s) clean.Sunday, July 19, 2009
I really hope we're not related
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