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YOU CAN HELP US BUILD
STRONGER WINGS
 

DEBRA SINGAPORE

Dystrophic Epidermolysis Bullosa Research Association, Singapore (DEBRA Singapore), is a support group for patients living with congenital epidermolysis bullosa, a rare skin condition that in its most severe forms affects all of the body's linings, the skin, the linings of the mouth and oesophagus, and even the eyes.

Our goals are to : 

  • Increase awareness of Epidermolysis Bullosa (EB)

  • Provide resources, support and funding for EB patients and their families

  • Create and strengthen networks for professionals involved with EB care or research, in Singapore and around the world

  • Be a regional centre of research excellence, and medical and diagnostic support

  • Foster the development of new Debra groups and mentor newly established ones.

Special Thanks to our Sponsors 

One of our ongoing challenges and initiatives is to raise the awareness level of EB in our communities and nationwide. If you would like to help us raise EB awareness, here are some ways you can make a difference.

ANNOUNCEMENT

 

BUTTERFLY VIRTUAL RUN

In 2020, we can't run to help the Butterfly children. But, now more than ever, we can stand as one Pledge S$25 to cover a distance of 5km. Wherever you are, record your run/walk/swim/cycle - submit your performance to us and receive a beautiful limited edited DebraSingapore face mask. Go the extra mile of the Butterflies!

HEADQUARTERS

100 Bukit Timah Road

KK Women's and Children's Hospital

Singapore 229899

Tel: +65 6513 7310

Email: debrasingapore@gmail.com

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