Hi!
I am a fourth year speech pathology student from Australia.
I am currently researching information about the emotions and reactions of parents when they learn that their child has a craniofacial anomaly.
I would really appreciate any informaiton about what your reactions were when you learnt that your child has a craniofacial anomaly and how your reaction was delt with by health care professionals. (For instance did they explain what support services where available? etc)
I would also appreciate information about additional information that you didn't receive that you think would have been helpful in coping with this situation
Thanks
Sophie Ferizis