Help Lewi Make His Album & BEAT CF
Donation protected
Help Lewi beat Cystic Fibrosis & make records:
Picture the gooey green slime from Nickelodeon. The suffocating gunk, the thick way it drips and droops. Got it? Now imagine that slime seeping into your lungs, clogging your airways, making it impossible to breathe. That deep breath you just took?
That’s a mere dream for the 70,000 people worldwide who suffer from Cystic Fibrosis.
Or as Lewi, who has had cystic fibrosis since birth, knows it: “65 roses.” That’s how many kids explain their disease – because this lovely term sounds similar to the frightening cystic fibrosis, which is a terminal genetic disease that causes the body to produce clogging mucus. This mucus infects the lungs, digestive system, pancreas, kidneys, and reproductive system, decreasing their function and reducing the sufferer’s lifespan. Currently, a cystic fibrosis patient is lucky to live to 40. Lewi is now 22. Like thousands of sufferers and their families, he dreams of a cure.
That’s the dream that Lewi and his team want to make a reality. Cue lights, camera, and action.
Drumroll please…introducing: Let Lewi Live. This movement will:
Help Individuals:
· Lewi is a hip-hop artist who is working with renowned producer Damizza (producer for Mariah Carey, Snoop Dogg, Michael Jackson, etc.) to create a professional album
· Immediate proceeds from this movement will help fund Lewi’s album production and medical treatments, as well as a documentary of Lewi’s journey
Help Society:
· The documentary will raise awareness and funds for Cystic Fibrosis, and many proceeds from Lewi’s album will go towards cystic fibrosis research to find a cure
· The success of this movement and Lewi’s success will show others with cystic fibrosis and life-threatening diseases that anything is possible. That even people with debilitating diseases can achieve their dreams and change the world
Ready to change the world? Make a donation now and receive updates about Lewi’s progress! Time is one of many things sufferers of Cystic Fibrosis do not have much of, so please spare a moment to donate to the movement and increase your awareness of this terrible disease. As Lewi constantly says: “I have Cystic Fibrosis. It doesn’t have me.” As you take a deep breath, please remember your healthy lungs are a luxury.
Please don’t let Cystic Fibrosis claim Lewi and the tens of thousands of sufferers – please join the movement today.
Picture the gooey green slime from Nickelodeon. The suffocating gunk, the thick way it drips and droops. Got it? Now imagine that slime seeping into your lungs, clogging your airways, making it impossible to breathe. That deep breath you just took?
That’s a mere dream for the 70,000 people worldwide who suffer from Cystic Fibrosis.
Or as Lewi, who has had cystic fibrosis since birth, knows it: “65 roses.” That’s how many kids explain their disease – because this lovely term sounds similar to the frightening cystic fibrosis, which is a terminal genetic disease that causes the body to produce clogging mucus. This mucus infects the lungs, digestive system, pancreas, kidneys, and reproductive system, decreasing their function and reducing the sufferer’s lifespan. Currently, a cystic fibrosis patient is lucky to live to 40. Lewi is now 22. Like thousands of sufferers and their families, he dreams of a cure.
That’s the dream that Lewi and his team want to make a reality. Cue lights, camera, and action.
Drumroll please…introducing: Let Lewi Live. This movement will:
Help Individuals:
· Lewi is a hip-hop artist who is working with renowned producer Damizza (producer for Mariah Carey, Snoop Dogg, Michael Jackson, etc.) to create a professional album
· Immediate proceeds from this movement will help fund Lewi’s album production and medical treatments, as well as a documentary of Lewi’s journey
Help Society:
· The documentary will raise awareness and funds for Cystic Fibrosis, and many proceeds from Lewi’s album will go towards cystic fibrosis research to find a cure
· The success of this movement and Lewi’s success will show others with cystic fibrosis and life-threatening diseases that anything is possible. That even people with debilitating diseases can achieve their dreams and change the world
Ready to change the world? Make a donation now and receive updates about Lewi’s progress! Time is one of many things sufferers of Cystic Fibrosis do not have much of, so please spare a moment to donate to the movement and increase your awareness of this terrible disease. As Lewi constantly says: “I have Cystic Fibrosis. It doesn’t have me.” As you take a deep breath, please remember your healthy lungs are a luxury.
Please don’t let Cystic Fibrosis claim Lewi and the tens of thousands of sufferers – please join the movement today.
Organizer
DAMIZZA PRESENTS
Organizer
Santa Barbara, CA
