Most of us can only imagine what Sahana Collins is experiencing each day of her life. Her rare condition, known as Epidermolysis bullosa, creates blisters on her skin that easily become wounds upon contact. Sadly, there is no cure yet. Only regular treatment help lessen its painful effects.
In this video, Sahana admits she feels depressed, asking questions to herself like why does it have to be her. But she continues to fight on and gets strength from her mom. More than that, a number of celebrities are in support to fund the research for Epidermolysis bullosa and its cure.
Nowadays, we are made aware by rare diseases only when strong people like Sahana step up and speak about it. The support we can give, no matter how big or small, makes all the difference. This little girl’s story can serve as an inspiration to keep fighting against seemingly insurmountable conditions.
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