About a month ago, Claire and I wrote to a bunch
of organizations on the internet, asking about
support groups by email and opportunities to
contact other people with facial cranial
differences.
Claire was born with a large lymphangioma involving
most of the right side of her face and eye. She
has had several surgeries, but there is still a
noticeable difference on the affected side. She
is now 10 years old And has had to put up a lot
of meanness and teasing etc from her peers. She
has been asking for an opportunity to meet with
other people who have experienced this, as she
describes herself as feeling sad and alone.
Here in Canada we have (had?) About Face
which was centered in Toronto. Two weeks ago
we called and left a message....no response.
Tried again today and both the 800 and regular
phone number are no longer in service.
Thanks and we appreciate any help and suggestions.
Pat & Claire