T
  • 43, Female
  • nowhere
  • United States
Share on Facebook MySpace
  • Blog Posts
  • Discussions
  • Events
  • Groups
  • Photos (25)
  • Photo Albums
  • Videos

T's Friends

  • JenNy
  • Nini
  • Kimberly
  • François
  • Zoey
  • Mandy
  • Amanda
  • Jennifer
  • Lolin
  • as
  • Jennifer White
  • Sharalynne Robertson
  • LeslieAnn Butler
  • andrea
  • John Smith

Gifts Received

Gift

T has not received any gifts yet

Give a Gift

 

T's Page

Profile Information

Relationship Status:
Married
About Me:
I hate filling out online forms that give too many losers from my past the resource they need to find me *lol*
Hello..I'm Taylor, I have had Alopecia Universalis for 20 years. I'm skeptical when joining 'new' alopecia "groups" because I usually find that while I was searching for other individuals to share something in common with, I find that not having hair doesn't mean a damn thing. I'm extremely against self pity, I can't stand for someone to tell me they are sorry I don't have hair! (I mean really, HAIR! I'm not, have never been and will never be handicapped!) I am just as normal and awesome as the hairiest person out there ;)
In all seriousness, I join this group hoping to connect with people going through a similar situation. Those I can relate to. Some I could possibly support. Ya know, it would be wonderful if the whole world was supportive and polite and tactful when dealing with others differences...but the truth remains that human nature is curious and not every human feels comfortable enough with themselves to respond to our differences in a positive manner. Please don't miss your hair. Hair is just...hair! YOU are not your hair!
I think I found this site accidentally, while hoping to find a site of Peggy's stylist...she ain't got one dammit!
I'm open to alllllll kinds of chit chat....
What's on your mind?
Are you age 18 or older?
Yes

ME, MY BEAUTIFUL SON, EZRA AND MY WONDERFUL HUSBAND, JASON.



T's Photos

  • Add Photos
  • View All

Comment Wall (29 comments)

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

Join Alopecia World

At 12:31pm on July 4, 2010, Kimberly said…
T, you crack me up. Love what you said on your page. I love, love the wig in the pic with you holding the coffee cup. That looks just like my "old" hair. What is the brand, if you don't mind? The baby is toooooo cute BTW.
At 10:23am on December 30, 2008, Nini said…
Hi T

I love what you wrote on ur page, that is soooooooooo true. I love ur pictures and ur eyelashes, I am trying to find out where to get them and how to wear them. Please help.

Thanks,
Nini
At 4:36pm on October 23, 2008, jo chesson said…
hi T,

I seem to have the same approach to my alopecia as you! I wear a wig or scarf when I go out but am generally bald around the house, I have a 9 month old nephew and I often wonder if he thinks he has 3 aunty jo's!!
At 1:42am on August 5, 2008, Jessica said…
ps you are the second gal on here with a husband named Jason. Mine too so that makes 3.
At 1:40am on August 5, 2008, Jessica said…
Hey t,

Love the hair who is it by can you give me some info.

Jessica
At 3:40pm on July 25, 2008, Jessica said…
Hey T,

Love all the pics and your baby is sooo cute. I have a little baby also his name is Aiden he is 11 months. When i can I will add pic's of him soon. I also have 2 girls Grace 7 and Ava 3
At 3:19am on July 10, 2008, Roger said…
Congrat with the baby!

Roger.
At 10:38pm on July 9, 2008, T said…
Gosh! I'm such a nerd...Sorry new friends that I did not accept for WEEKS!! I just now figured out how to accept new requests *lol* I'm so awesome...love it!

Have a nice Thursday tomorrow ;)
At 5:30pm on June 14, 2008, as said…
Hallo.
I don't know whether that will prove well tell.Your words are very wise.They may much people here assist in better manage its baldness.Say why. 28 ys backward I fell ill serious neurological illness movement.Mine doctor me said, that the longest behind 10 ys I'll on disabled armchair.It was shock and I mentally was on that very badly.
One elderly gentleman same illness me but learn heaven this infliction of like illness,but as a something due back to me.
Thanks that I have got though big severity,but always go.Therefore I think, that the most incurable illness or infliction of puts manage.Only man
mustn't it treat as ill and be sorry for oneself.So won't help.Get, that the female be bald,is very heavy,unpleasant and stressful.Alone I don't know how would it managed be woman.Right its baldness is for me always quite heavy namely am man.
My alopecia scar began within days on May 2007.Was it for me very heavy,but came to be it slowly manage.Came but January 2008 and to us unexpectedly obiit son.Mentally am again was on that very badly.Doesn't know am what shell I do and began be looking for on Internet cafe,different help.Found am Alopecia world.For the first time am here found out,that also women and little children are bald.Was I shocked and was me of all very sorrow.
Began be read various sections and examine photo and slowly find out how strong and primely personalities are.I said to myself,that when this female heavy thing know how to manage further prove assist in and second.So it I have to manage so did I.I wanted also somehow assist in.It but I don't know.Place Alopecia world and largely instance you brave and wise women on the contrary me much assisting manage its baldness and even mitigate pain above death child.Also me turns view of eye - appeal women.Not to be angry if it say badly,but for me bald woman has only other kind hairstyle and be like each other beautiful like if has hair.
Therefore again I say ,yes your words are very wise !Also ; access to baldness,as well as of several of other members and founders hereof seats is for us other instance.
Thank you and other.My English is very bad so I hope, that the me do you understand.Unless,please about erasure mine benefit.
Keep lovely day.as
At 5:46pm on June 9, 2008, Roger said…
Wow! Nice comment to yourself =)

Roger.
 
 
 

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.

© 2024   Created by Alopecia World.   Powered by

Badges  |  Report an Issue  |  Terms of Service