Dermatologists...And/or advise for grand/parents child diagnoised

Hi all,

May I please ask if have any referrals and advise, etc. Thanks

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Replies to This Discussion

Permalink Reply by ayshia2000 on July 27, 2017 at 3:49pm

Are there any up coming workshops?  would like to attend to know more for my granddaughter. Thank you

Permalink Reply by leah on July 29, 2017 at 4:55pm

Hi Ayshia, Thanks, please see main page for upcoming meets I posted (1 next weekend and another in Sept). And leaders/groups (CAP, NAAF, etc) I encourage you contact asap, since I recall you saying short amount of time your granddaughter and daughter will be here. Plus I feel best to meet with parents of children and people with experience with, I just know for myself as an adult and other adults. Those should have referrals and advise with a child with alocepia. I also message you and put this post up for others in community to see if they have any info for you too. Please keep checking and if I hear anything more I will tell you as well. Here's link to main page http://www.alopeciaworld.com/group/seattleareaalopecians

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