"Hello, Alocepia Support Group would like to invite you to our next event. It’s a New Year and New Beginnings! Join us for our meet and greet “ Cafe’ Conversations “ Saturday- March 23, 20192-4pm (PST)Renton,…"
"Hello all, Hope doing well, I miss and wanted to share an up coming retreat an hour & half of the U.S. border with http://www.alopeciasupport.org/:
Deeann will be one of the speakers and is a non-profit group:
Fri, Aug 31, 2018, 5:00 PM…"
"Hello all, Hope doing well. Here are 3 up coming events with http://www.alopeciasupport.org/:
Sat, August 11, 2018
1:00 PM – 3:00 PM PDT
Panel Discussion about Alopecia - Hair Loss. Hear the real life journey and personal stories of those…"
My heart goes out to you guys, I don't know as child or children but have a lot empathy for. I wonder if maybe she'd feel more comfortable wearing a cute winter hat or beanie? Maybe try set up your own children's support group,…"
"Hey Sarah! Thanks for posting and opening up! I hear you with fears and hang ups, but bravo for trying to face them and have a good game plan! I used wunderbrow and it stayed on a lot longer than other eyebrow makeup - had scrub off. I than recently…"
"Thanks for sharing Brian. I can't speak for you but when I took meds that were hard on my liver and had grandma die of liver cancer I had to stop. I feel like it would be really hard if I better results with drugs too, but am sensitive and have…"
Hi Lea, that you for your reply. It is my 7 year old granddaughter who has been recently diagnosed My daughter has several questions and wanted to attend a event while she is here. You see they live in Dubai, she comes once a year to stay with me for a few weeks.They will be here next month for only 16 days. I want to give them all the help and support that I can, but thats hard when they live so far away. So I have been doing my own research , reading post and learning so much from kind people like you and others in this group. She has ask me if I can find a Allergist in our area, Tacoma/Seattle. She has taken my granddaughter to two Derm doctors already there, but wants her to get checked out here in the states. Do you know of any? Also thank you for telling me about the up-coming meet up, but they dont arrive till August 9th . Thank you for your help.
There are a number of groups in Portland. On Alopecia World, there are two you can join: Active Alopecians in Portland, and Pacific Northwest Alopecians. NAAF lists this support group here in Portland: Denise Clopton/Brooke Ferguson 503.804.5315. I can't find the contact information on the group I have met with in the past! Sorry, I will try to find it for you.
And thanks for wanting to read my book! Let me know how you like it.
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