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Michelle Female Alameda, CA United States: Like

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Alopecia Universalis

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Michelle's Discussions

Salmon patch on nape of neck

Started this discussion. Last reply by Lori Van Decker Oct 21, 2014. 9 Replies 0 Likes

Need support

Started this discussion. Last reply by Rose Marie' Oct 15, 2014. 1 Reply 0 Likes

Reaching out to parents who have AA

Started this discussion. Last reply by Vanessa Nov 14, 2013. 4 Replies 0 Likes

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Profile Information

Relationship Status:: Married

About Me:: I have had AU since 1994

Do you have alopecia?: Alopecia universalis

Are you age 18 or older?: Yes - I am 18 or older

Comment Wall (9 comments)

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At 11:08pm on September 13, 2014, JeffreySF said…: NAAF will be in your backyard next June!!!

At 9:20pm on August 11, 2013, Rob said…: I joined this site to tell everybody how I cured my AA. I am not here as a psychological support group person. I cured it. It took a lot of research and thinking outside the box. Look at the bottom of my home page by clicking on my avatar picture and look below my profile. Iodine(best in the form of kelp at 100% or slightly more but not too much and biotin and I went from nearly bald for a year to hair everywhere in just a few weeks. I have helped two other people with patchy bald spots to recover.

At 8:36am on February 8, 2009, Eileen Simpson said…: Hi Michelle, welcome to AW, just want to let you know that there is a group in Northern California. I am flying down to Sacramento with my son on the 15 of FEB, next weekend, and we are going to have lunch in Citrus Heights with other fellow Alopceians at the Olive Garden at 12:30 they have a gluten free menu also. If you could make it that would be nice.

Eileen

At 9:29pm on January 29, 2009, Michelle said…: Thanks to everyone for welcoming me to Alopecia world, I will try to get more involved with the site in the next few weeks.

At 7:34pm on January 29, 2009, LeslieAnn Butler said…: Hello and welcome, Michelle! How are you today?
LeslieAnn

At 2:23pm on January 27, 2009, Cherylnz said…: Hi Michelle
Welcome to Alopecia World

At 9:10am on January 27, 2009, JeffreySF said…: Hi Michelle,

Welcome to Alopecia World.

Jeff

At 12:11am on January 27, 2009, Cheryl, Co-founder said…: Hi Michelle, I wanted to take this opportunity to welcome you to Alopecia World. I have been living with Alopecia Areata since 1991 and know full well the struggle it can be. I look forward to getting to know you. Cheryl, Co-founder

At 11:04pm on January 26, 2009, Linda said…: Hi Michelle, welcome to alopeciaworld!

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