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Mihaela Boban, Croatia,  None

Mother of a beautiful girl with a PWS on her left side of the face. At the beginning of our journey nobody knew what was on her face, we went to so many medical examinations with no luck. Thanks to VBF and support groups on Facebook, we found Dr. Linda and learned everything about our birthmark, and now we are seeing Dr. Geronemus in New York and finally we are satisfied that we are doing the best for our child. As a parent who did not know that PWS exist, we are very grateful and it is very important for us to share awareness.

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