lea
  • Female
Share

Lea's Friends

  • Bon
  • babyk23
  • Madbrown
  • KReed
  • sam
  • gldean1988
  • Carman
  • Nakia
  • sadele
  • Livkerp
  • Shari
  • SweetlyFree
  • Andy
  • Modern Monarch
  • ANVan

Gifts Received

Gift

lea has not received any gifts yet

Give a Gift

 

lea's Page

Latest Activity

lea left a comment for Bon
"PS private messages."
16 hours ago
lea left a comment for Bon
"Hi Bon, I message you my number, is at bottom of my messages and going to again (right after this). I get a lot goin on and with doctors and hope the injections work for you. I seemed to have dermatologists chase my spots and areasmissibg hair. In…"
16 hours ago
Bon left a comment for lea
"Hi Lea, I'm sorry I've been so dangned busy.....yesterday my naturopath gave me my first LAI injection....the LDN seems to have slowed the shedding of what I have left of hair, but left upper eyelash, outer edge of right eyebrow and nails…"
Tuesday
JeffreySF replied to lea's discussion Meeting end of 3/2020 or in 4/2020 in the group Seattle Area Alopecians
"I could Skype in if the times work out."
Monday
JeffreySF liked lea's discussion Meeting end of 3/2020 or in 4/2020
Monday
lea added a discussion to the group Seattle Area Alopecians
Thumbnail

Meeting end of 3/2020 or in 4/2020

Hello all, Wondering who would be up for meeting end of March - April? Also if possibly online through Skype or Zoom, as an online option with people living all over too. ThanksSee More
Monday
lea commented on Lauren Simpson's group Seattle Area Alopecians
"Dear Bon,  I am sorry for typo with my first message to you and how may have missed some of mine/delay. I have messaged you my number and been seeing if there are any scheduled upcoming WA meets without luck yet. Please call or text me. As I am…"
Saturday
lea left a comment for Bon
"Hi Bon Thanks and sorry delay and you didn’t see my msgs on Seattle group page. I am sending you a private message with  my number, on this site you can once people accept friend request. Or least that’s my experience and…"
Saturday
Bon left a comment for lea
"Good Morning Lea, this is Bon still not sure how this site works.  I have been so busy learning about my 'condition' that I haven't been able to spend enough time perusing it.  I REALLY want to connect with the Seattle group…"
Feb 20
Bon and lea are now friends
Feb 20
Bon replied to lea's discussion Get together in the group Seattle Area Alopecians
"Yes, I would attend.  Just been diagnosed with Lichen Planopaliris.  Tough to hear.  I live in Everett and don't care for driving long distances but I will. I've tried to get responses on this site to no avail.  Perhaps…"
Feb 17
lea commented on Lauren Simpson's group Seattle Area Alopecians
"PSS Bon and all who are interested : NAAF has meets and local leaders for support and lists of people in WA. NAAF.org June S. rjsecreto@comcast.net also checkout AlopeciaSupportGroup.org for upcoming meets /events. If I hear of any will share too."
Feb 12
lea commented on Lauren Simpson's group Seattle Area Alopecians
"PS please excuse typos talking to my phone, no excuse after long on the way home. Thanks "
Feb 12
lea commented on Lauren Simpson's group Seattle Area Alopecians
"Hi Bob, Thank you ! I’m sorry about diagnosis I don’t know that one and shall research. I haven’t had an official term for what I have, since I got disillusioned with the dermatologist - it was super expensive and they didn’t…"
Feb 12
lea posted a video

Exclusive: Rep. Ayanna Pressley Reveals Beautiful Bald Head and Talks Alopecia for the First Time

Ayanna Pressley loves playing with her hair. Before she became a Massachusetts Congresswoman (and a high-profile member of “The Squad”), Pressley would exper...
Jan 18
lea liked Cheryl, Co-founder's video
Jan 8

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

lea's Videos

  • Add Videos
  • View All

Comment Wall (8 comments)

You need to be a member of Alopecia World to add comments!

Join Alopecia World

At 6:14pm on February 25, 2020, Bon said…

Hi Lea, I'm sorry I've been so dangned busy.....yesterday my naturopath gave me my first LAI injection....the LDN seems to have slowed the shedding of what I have left of hair, but left upper eyelash, outer edge of right eyebrow and nails are being affected that latter 3 in last 2 weeks! Anyway, where do I find your number to get in touch through texts or calls?  I have 3 new sites I'm learning to navigate and just created a FB account, which I wanted to avoid, but they all use it. Please advise and THANK YOU for being there, you've no idea how much it means. I am not freaking out over this but I do want to do everything I can to arrest the 'issue'.  Be well, Bon

At 9:25am on February 20, 2020, Bon said…

Good Morning Lea, this is Bon still not sure how this site works.  I have been so busy learning about my 'condition' that I haven't been able to spend enough time perusing it.  I REALLY want to connect with the Seattle group but am not getting a response from the contact.  Not sure why. Eventually I would like to start a group North of Seattle from say....Millcreek to  Standwood or Arlington. I am in the process of learning about alternative treatments (naturopath) is trying LDN and LDA very interesting possibilities! Faux hair of course, nothing new to me as I was a hairdresser and have loved faux hair since then. I have 9 wigs of various colors and styles, fun. Problem is as I lose hair my scalp is so tender! Am looking to have them retrofitted with silicon around hair line.  They are Jon Renau....around $300 with tax?  If you have any suggestions re: Thank you for friending me,  Bon 

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

 
 
 

Disclaimer

Any mention of products and services on Alopecia World is for informational purposes only; it does not imply a recommendation or endorsement by Alopecia World. Nor should any statement or representation on this site be construed as professional, medical or expert advice, or as pre-screened or endorsed by Alopecia World. Alopecia World is not responsible or liable for any of the views, opinions or conduct, online or offline, of any user or member of Alopecia World.

AlopeciaWorld.com: It's hair loss support at its best!

© 2020   Created by Alopecia World.   Powered by

Badges  |  Report an Issue  |  Terms of Service