92 Bowery St., NY 10013

+1 800 123 456 789



To put a smile and hope on the faces of children suffering from   Epidermolysis Bullosa
• To lessen their pain
• To help teach their parents how to take care of them
• To provide them with medical supplies which are not covered by medical insurance

Chairwoman of the Board of Trustees message

Dear friends,
Yasmin El Samra’s  foundation logo was one of her drawings.

I am the mother of Yasmin El Samra (1997-2012) who was born with a rare skin disease called Epidermolysis Bullosa (EB) .  I established this foundation because I felt that Yasmin came for a mission, and i have to full her mission in helping EB patients with awareness and care. 
I established the foundation in 2014 and registered in 2018.

The  foundation provides all medical supplies on monthly basis and cover all expenses covering surgeries, dental and blood transfusion  which is not covered by any medical insurance in  order  to reduce their  pain and  teach their parents  how to take care of their kids .

Every EB patient needs care, love and the right to live in our community as normal as possible with respect and dignity.

Support is at its core a positive and noble outlook on life and help is the determination of participation and a responsible commitment strengthened by financial and moral support of all children.

Let us all put a smile on their pretty faces to let feel they are not alone.
Yasmin let a LEGACY
I  would like to thank every person supporting   Yasmin el Samra Foundation Debra-Egypt

Thank you from deep of my heart.

Hanaa El Sadat