HI everyone! First of all, thans for the existance of this web site once again... it's really important for us to have someone "like us" to talk to.... to share our doubts and fears, to share our vitories and new challenges! I'm portugese and here in my country with don't have yet any kinf of association or nacional support group... Like in many many countries and states, i think that we should have one! becaus of that i'm trying to difuse this new facebook group that i created in order to join all together the people in Portugal that soffer of ALOPECIA ( AA, AT or AU). Family and close friends, dermatologists, and people related to this disease are also invited!
Please share this group -
https://www.facebook.com/groups/490303304382176/#!/groups/490303304382176/?fref=ts

It's the beginning portuguese alopecians! ;)
join me at ALOPECIA PORTUGAL ( facebook group )

To the alopecians around the world! we're together! ;)
thanks
best regards
Catia Ferreira