Fireworks for the Lewis-McCrory Household
by Gingersnap | damian-lewis.com | December 31, 2019
Damian and Helen celebrate New Year’s Eve with bang as they pick up some fireworks from UK based firework retailer, Dynamic Fireworks. They must have had a spectacular display as they rang in the New Year! How kind of them to pose for photos with all the store employees:
Continue reading Damian and Helen Celebrate New Years Eve – Dec 31, 2019
Billions of Stocking Stuffers
by Gingersnap | damian-lewis.com | December 16, 2019
Need some last minute holiday gifts for that Billions fan? How about a F*** You Money throw pillow or sherpa blanket for a long winter’s nap? Don’t forgot a festive crewneck sweatshirt to stay warm or that Billions ornament for your tree! Santa’s elves have been busy over at the Billions holiday store here.
Continue reading Ho-Ho-Holiday Over at Showtime Store – Dec 16, 2019
Cure EB: The Big Give Christmas Challenge
by Damianista | Fan Fun with Damian Lewis | November 27, 2018
Today is Giving Tuesday! It is a a global day of giving we celebrate on the Tuesday after Thanksgiving and kick off the charitable season! So it’s time to be thankful for all the good stuff in our lives and focus on our holiday giving.
Well, most of you know Damian Lewis is a proud patron of Cure EB.
Damian Lewis with Sohana and her mother Sharmila at BGC Charity Day 2014, source: Sohana Research Fund
Sohana Collins is a 15 year old teenager who was born with Recessive Dystropic Epidermolysis Bullosa (RDEB) which means she lacks the protein that holds her skin together. Kids with RDEB have extremely fragile skin that they are sometimes called “butterfly children.” Lots of activities we take for granted as easy routines in our daily lives are a struggle for them. Can you imagine a day where your dressing up takes up to two hours and eating and drinking cause blisters in your mouth and throat? These kids have to deal with this kind of pain every single day. Besides, they are under extra risk to develop skin cancer later in life and their life expectancy is not very long. Sohana’s parents Sharmila and James Collins founded Cure EB to raise awareness as well as funds for research to ultimately have a cure for this terrible skin condition.
Here is what Sohana says about EB.
Continue reading Giving Tuesday – Nov 27, 2018