musings about the actor and the characters he brings to life
Damian continued his meaningful work in 2025 as a devoted patron of two charities, Cure EB and the Sir Hubert von Herkomer Arts Foundation (Sir HvH Arts). His support is continuous; year after year, he gives his time, energy, and voice to raise awareness and funds, ensuring both organizations continue their life-changing work. And as always, seeing Damian show up for these causes remains a true highlight of the year. Continue reading “TOP Damian Lewis Moments 2025: Cure EB and Sir HvH Arts”
It’s EB Awareness Week – a week to raise awareness about this terrible skin condition and the impact they have on patients’ lives. The primary target of the campaign is the general public; however, it is very important to raise awareness among policy makers, researchers, health professionals and anyone who has an interest in Epidermolysis Bullosa. And we would like to take this opportunity to raise awareness as well as funds to find a cure for EB, one of about 7,000 rare diseases for which there is no cure.
Well, most of you know Damian Lewis is a proud patron of Cure EB.
The kids that are born with Recessive Dystropic Epidermolysis Bullosa (RDEB) or EB for short lack the protein that holds their skin together. They 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. Continue reading “Do it Like Damian Lewis: HELP Raise Awareness for EB on EB Awareness Week!”
Today is Rare Disease Day, a day to raise awareness about rare diseases and the impact they have on patients’ lives. The primary target of the campaign is the general public; however, it is very important to raise awareness among policy makers, researchers, health professionals and anyone who has an interest in rare diseases. And we would like to take this opportunity to raise awareness as well as funds to find a cure for EB, one of about 7,000 rare diseases for which there is no cure.
Well, most of you know Damian Lewis is a proud patron of Cure EB.
The kids that are born with Recessive Dystropic Epidermolysis Bullosa (RDEB) or EB for short lack the protein that holds their skin together. They 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. Continue reading “Do it Like Damian Lewis: HELP Raise Awareness for EB on Rare Disease Day!”
Damian Lewis is the proud patron of two charities, Cure EB and Sir Hubert von Herkomer Arts Foundation (HvH Arts). In the photo above, you see him with two formidable ladies: On the left is Debbi Clark, the founder and CEO of Sir HvH Arts, and on the right is Sharmila Collins, the founder and CEO of Cure EB. And Damian making time for these charities, attending their events and working to raise funds for them is always a TOP MOMENT of the year!
Continue reading “TOP Damian Lewis Moments 2024: Cure EB and HvH Arts”
Today is Rare Disease Day, a day to raise awareness about rare diseases and the impact they have on patients’ lives. The primary target of the campaign is the general public; however, it is very important to raise awareness among policy makers, researchers, health professionals and anyone who has an interest in rare diseases. And we would like to take this day to raise awareness as well as funds to find a cure for EB.
Well, most of you know Damian Lewis is a proud patron of Cure EB.
The kids that are born with Recessive Dystropic Epidermolysis Bullosa (RDEB) or EB for short lack the protein that holds their skin together. They 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. Continue reading “Do it Like Damian Lewis: HELP Raise Awareness for EB on Rare Disease Day!”