Run for Rare 2022

Driven by the vision of creating a support group for patients and families with genetic and incurable rare skin conditions and building an inclusive society for them due to the visible difference that comes with the conditions, non-profit support groups Rare Skin Conditions Society Singapore (RSCS) and DEBRA (Dystrophic Epidermolysis Bullosa Research Association) Singapore were founded by patients, their parents and caregivers, doctors, nurses, social workers and volunteers.

By building public awareness about rare skin conditions, RSCS and DEBRA hope to build a more inclusive society where individuals with rare skin conditions from all walks of life are accepted, loved and respected for who they are and for their contribution to society, regardless of their visible difference.

With your donations, we can effect a positive change for these individuals by supporting them with resources, assistance, hope and most importantly, kindness. Join us in helping them live their lives to the fullest by  donating here