lea
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Latest Activity

lea commented on Tanya's group Vancouver Alopecia Areata Support Group
"PS the retreat people can do just a day or so, not just full weekend too.."
Aug 10, 2018
lea commented on Tanya's group Vancouver Alopecia Areata Support Group
"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…"
Aug 10, 2018
lea commented on JeffreySF's blog post 11 Years of Alopecia
"Sweet, thanks Jeffrey !! Am excited and thanks again"
Aug 6, 2018
lea commented on JeffreySF's blog post 11 Years of Alopecia
"Ah sweet, thanks Jeffrey!! Looking forward to seeing there :-D"
Jul 28, 2018
lea commented on JeffreySF's blog post 11 Years of Alopecia
"Hi Jeffrey,  Thanks, awesome! I had heard a rumor least it be on the west coast :o) hugz~"
Jul 27, 2018
lea commented on JeffreySF's blog post 11 Years of Alopecia
"Awesome Jeffrey, thanks for sharing and just being YOU Too! =) Hope to meet some day and go to the conference! Thank you again - much love ~"
Jul 26, 2018
lea liked JeffreySF's blog post 11 Years of Alopecia
Jul 26, 2018
lea commented on Lauren Simpson's group Seattle Area Alopecians
"Hello all, Hope doing well. Here are 3 up coming events with http://www.alopeciasupport.org/: 1) 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…"
Jul 26, 2018
lea replied to Sandy K.'s discussion Tears, Fears and uncertainty
"Hello! 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,…"
Nov 8, 2017
lea commented on BrianH1972's blog post Off the Xelganz
"PS I did microblading and really happy with the results. Have a friend who uses water proof liner on her husband when he like to have brows (he has alocpeia too) and says no one notices."
Sep 13, 2017
lea replied to Sarah's discussion eyebrows & sex
"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…"
Sep 13, 2017
lea commented on BrianH1972's blog post Off the Xelganz
"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…"
Sep 13, 2017
lea replied to Seanyy210's discussion Hair system too dense, wrong colour?
"hows it going? hope well! cheers"
Sep 13, 2017
lea commented on Sara's group Pacific Northwest Alopecians
"Hello all, this is a good group in Seattle and upcoming event... 21314832_2067243813301051_5093081426557200209_n.jpg https://www.eventbrite.com/e/asg-panel-discussion-tickets-375602747... Sep 30 ASG - Panel Discussion by Alopecia Support…"
Sep 13, 2017
lea commented on Lauren Simpson's group Seattle Area Alopecians
"21314832_2067243813301051_5093081426557200209_n.jpg https://www.eventbrite.com/e/asg-panel-discussion-tickets-37560274793?aff=erelexpmlt Sep 30 ASG - Panel Discussion by Alopecia Support Group Date and Time Sat, September 30, 2017 3:30 PM…"
Sep 13, 2017
babyk23 and lea are now friends
Aug 24, 2017

Profile Information

About Me:
Here to check out
Do you have alopecia?
Other type of alopecia
Are you age 18 or older?
Yes - I am 18 or older

Comment Wall (6 comments)

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At 9:01pm on August 10, 2017, Madbrown said…
I mean I am fine with going to the Seattle one to start.
At 8:27pm on August 10, 2017, Madbrown said…
I am fine with trying to setup something down here if there are people in the area that would want to. I can definitely do Seattle area also to start. Where would the Seattle one be at?
At 3:20pm on July 25, 2017, ayshia2000 said…

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.

At 2:13am on June 11, 2014, LeslieAnn Butler said…

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.

 

At 1:02pm on June 5, 2014, LeslieAnn Butler said…

Hey thanks, let me know how you like the book. And yes, there is a meetup group in Portland. Do you go to one in Seatte?

At 5:31pm on December 12, 2012, LeslieAnn Butler said…

Hello and welcome, Lea!
How are you today?
Leslie Ann

 
 
 

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