Elaine
  • Female
  • Memphis, TN
  • United States
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  • Jeremy PIerce
  • lauren
  • Kelsey O'Ree
  • Michael
  • Jessica
  • Olivia Rusk
  • Rose Marie'
  • Jason Wright
  • JeffreySF
  • Cheryl, Co-founder

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Elaine's Page

Latest Activity

Michael and Elaine are now friends
Jan 4
Elaine replied to Jen's discussion I need someone who knows what I'm going through/been through
"I know what you're going through! I had alopecia universalis when I was 8yrs old and it grew back five years later. This year I lost it all again. Coming to this site help me to realize I wasn't the only one. There were others who…"
Nov 8, 2011
Elaine's blog post was featured

A little bit of info I found

I just found out today that the National Alopecia Areta Foundation set up an Ascot Fund that provides financial assistance toward the purchase of a hairpiece to individuals who have alopecia areata and are struggling financially. I was also on this other website that seemed to have a lot of wigs and hairpieces that were very natural looking...there were some on there even for kids that I really wished was around when I was a kid.…See More
Oct 23, 2011
Elaine commented on Chellie Bell's blog post New wig :) !
"Amen to that! If you like it that's all that matters! Wigs and weaves are much easier than natural hair. And if your co-worker can't handle it, it's his lost!! Good luck"
Oct 21, 2011
Elaine posted a blog post

A little bit of info I found

I just found out today that the National Alopecia Areta Foundation set up an Ascot Fund that provides financial assistance toward the purchase of a hairpiece to individuals who have alopecia areata and are struggling financially. I was also on this other website that seemed to have a lot of wigs and hairpieces that were very natural looking...there were some on there even for kids that I really wished was around when I was a kid.…See More
Oct 20, 2011
Elaine commented on Chellie Bell's blog post Excited
"I just did my own lil research on lace front wigs and I think I should give it a try...they look very realistic!"
Oct 20, 2011
Elaine's 2 blog posts were featured
Oct 20, 2011
Elaine posted a song

 play Fistful of Tears - Maxwell

Blacksummer'snight
03:37
Oct 19, 2011
Elaine and Jessica are now friends
Oct 19, 2011
Elaine commented on Elaine's blog post What a day!
"LOL!! Yea, I tried to get my mind off of it and ate plenty of chocolate cake last nite. It doesn't help any our kids go to the same school so I have to see him every afternoon. I've done my nails, put some nice eyelashes on, and I'm…"
Oct 19, 2011
Elaine joined Megan's group
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Christians With Alopecia

Come chat about how your alopecia has affected your faith,how your faith has affected your alopecia,or just for plain old chatter.Open to questions,debates etc.But please always respect others beliefs.
Oct 19, 2011
Elaine commented on Elaine's blog post What a day!
"Thanks Karen!! I guess when it rains it pours"
Oct 18, 2011
Karen Smith commented on Elaine's blog post What a day!
"We are here to listen and help if we can.Sorry about your break up."
Oct 18, 2011
Elaine commented on Dominique Cleopatra's group Women Who Never Want to be Bald in Public
"I'm so glad I'm not the only one who just can't get up enough nerve or courage to walk around all natural. For me I can't even say the word "bald". I guess it comes from bad childhood experiences. But I have a hard time…"
Oct 18, 2011
Elaine posted blog posts
Oct 18, 2011
Elaine joined Alopecia World's group
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Alopecia Totalis

Join today to meet, support and share information and resources with others who are also living with the complete loss of scalp hair.
Oct 18, 2011

Profile Information

Relationship Status:
Single
About Me:
Single mom of 3. Very involved in my kids life. Grew up with alopecia universalis, and it just came back again about 2 months ago. Avid weave wearer (just don't feel comfortable going natural yet). I love music, hate going to work and I am a foodie!!
Do you have alopecia?
Alopecia universalis
Are you age 18 or older?
Yes - I am 18 or older

Elaine's Photos

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Elaine's Blog

A little bit of info I found

Posted on October 20, 2011 at 9:30pm 0 Comments

I just found out today that the National Alopecia Areta Foundation set up an Ascot Fund that provides financial assistance toward the purchase of a hairpiece to individuals who have alopecia areata and are struggling financially. I was also on this other website that seemed to have a lot of wigs and hairpieces that were very natural looking...there were some on there even for kids that I really wished was around when I was a kid.… Continue

Curious about discoloration

Posted on October 18, 2011 at 10:19pm 0 Comments

On my scalp there are discolored areas that are much lighter than my natural skin tone. What is that about?

What a day!

Posted on October 18, 2011 at 9:00pm 4 Comments

Around the age of 8, I was diagnosed with alopecia universalis. About 5 years later, it came back in and ever since I've been with hair...until about 2 months ago. I'm now 31 and the hair is completely gone. I will admit I had to get re-adjusted to not having hair again, but at least I knew what to expect. My mother is my confidant through this and I don't feel comfortable with telling anyone else. But I come on here and spill my guts? Yes! I feel this is the only place where people understand… Continue

Injections: Cure or Needless Pain?

Posted on April 12, 2009 at 11:12pm 4 Comments

I remember back when I was about 8 or 9 my dermatologist telling my mother about receiving injections in my scalp. Even though my mother waited a while and discussed it over with me before agreeing with the treatment, nothing could've prepared me for these injections. Everyone is different and everyone don't have the same experiences that I may have had, but it was not a pleasant experience. I can't remember what the exact name of the medications were, but the results were not enough for me to… Continue

Just Me!!

Posted on March 13, 2009 at 10:55pm 4 Comments

The thing that I like most about this site is that it provides a lot of support and answers to those who don't know. I used to have so many unanswered questions when I was in school. I used to wonder why me? Out of all these kids at school--why ME!! I remember things like how hot it was to wear a wig in the summer. The constant thought of "I hope nobody snatches my wig off." It really stopped me from participating in things like field trips because i didnt know what the kids would do once i got… Continue

Comment Wall (6 comments)

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At 12:40am on March 26, 2009, lauren said…
thanks for the comment. it was very nice. im glad you think i should keep writing!
At 5:42pm on March 24, 2009, Kelsey O'Ree said…
hi my name is kelsey.i have aa
At 11:32am on March 14, 2009, JeffreySF said…
Hi Elaine,

Welcome to Alopecia World.

Jeffrey
At 11:03pm on March 13, 2009, Rose Marie' said…
Hi Elaine

Welcome to Alopecia World, it's a great place to spend a little time.

Rosy
At 11:33pm on March 10, 2009, LeslieAnn Butler said…
Hello and welcome, Elaine!
How are you today?
LeslieAnn
At 10:48pm on March 10, 2009, Linda said…
Hi Elaine, welcome to alopeciaworld!
 
 
 
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