Beschermde donatie
Dear Family & Friends,
My sister, Fete passed away on Tuesday, June 26th, she was 34 years old. She was diagnosed with her inevitability when she was 13, telling us she would be lucky to live until 40 with this disease. She was right. She suffered from a rare autoimmune disease called Systematic Sclerosis also known as Scleroderma. It took away weight, changed her face, deformed her hands and feet, and lastly affected her gastrointestinal system as well as her lungs. She fought pneumonia’s, infections, and death as long as she could. She fought to the end with a feeding tube, traych collar, malnourishment, and no voice.
This disease took over our lives, but most importantly hers. She never stopped trying.
We are asking you to try to donate as much as you can, even if it’s a dollar...it adds up. We need to find a cure for a disease that doesn’t have enough people fighting for it. We ask you, for our angel up in heaven who is looking down on us praying that no one else go through what she went through. Let’s start here. God bless you always.
*please note, I am her sister, Luljeta Dervisevic raising money on her behalf for the Scleroderma Foundation. The funds will be sent via check to the Scleroderma Foundation or however else they accept funds. Since they are currently not affiliated directly with gofundme.com we will send a check via Reach For the Cure Campaign. Please click the link below to get more information:
http://www.scleroderma.org/site/PageServer?pagename=donate_home#.W0exu9X0mpp
My sister, Fete passed away on Tuesday, June 26th, she was 34 years old. She was diagnosed with her inevitability when she was 13, telling us she would be lucky to live until 40 with this disease. She was right. She suffered from a rare autoimmune disease called Systematic Sclerosis also known as Scleroderma. It took away weight, changed her face, deformed her hands and feet, and lastly affected her gastrointestinal system as well as her lungs. She fought pneumonia’s, infections, and death as long as she could. She fought to the end with a feeding tube, traych collar, malnourishment, and no voice.
This disease took over our lives, but most importantly hers. She never stopped trying.
We are asking you to try to donate as much as you can, even if it’s a dollar...it adds up. We need to find a cure for a disease that doesn’t have enough people fighting for it. We ask you, for our angel up in heaven who is looking down on us praying that no one else go through what she went through. Let’s start here. God bless you always.
*please note, I am her sister, Luljeta Dervisevic raising money on her behalf for the Scleroderma Foundation. The funds will be sent via check to the Scleroderma Foundation or however else they accept funds. Since they are currently not affiliated directly with gofundme.com we will send a check via Reach For the Cure Campaign. Please click the link below to get more information:
http://www.scleroderma.org/site/PageServer?pagename=donate_home#.W0exu9X0mpp
Organisator
Elvis Dervisevic
Organisator
Staten Island, NY