Wednesday, 1 November 2017
It's World Epidermolysis Bullosa Day!
It's Word Epidermolysis Bullosa Week and to celebrate this, we've put together a video montage of the efforts that has been put in so far in caring for these butterfly children.
Again, EB children needs lifelong support, be it physical or psychologically. We welcome you to join us in caring for these children.
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It's Word Epidermolysis Bullosa Week and to celebrate this, we've put together a video montage of the efforts that has been put in s...
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EB is a lifelong disease with no definitive treatment or cure at present, despite intensive ongoing research. The EB spectrum can vary fr... -
We are so grateful to have The Star do a coverage on Epidermolysis Bullosa. And who better to talk about this other than Dr Sabeera Begum, ...
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