Information please

[Dianejourno]

Hi
I am a freelance journalist researching a health article for an Australian women's magazine and I'm hoping someone can please point me in the right direction. I'm trying to find a support group for parents of, and children with, haemangioma or birthmark tumours. Or I'd like to speak with parents whose children have had, or still have, these kind of facial birthmarks.
I placed a thread a couple of months ago when I was researching unusual and speedy births and I was overwhelmed by your responses, so thank you again to all those who responded.
I can be contacted at diane@realfeaturesagency.com.au
Many thanks:wave:

[nemosmum]

I have a friend whose daughter was born with a large one on her head (near her forehead) and a couple of small ones on her neck.

Im not sure if she went to a support group? probably not as she was pretty unfazed by it.

I will pass on your email and see if she wants to contact you.:)

[Dianejourno]

Thank you, all information is helpful and much appreciated.
:)