tahnie elizabeth grant
  • Female
  • nsw
  • Australia
Share on Facebook MySpace

Tahnie elizabeth grant's Friends

  • Heather
  • Tatum
  • lee willsmer
  • Josephine Bihl
  • ashley mcmullen
  • Laurie Blundell
  • Clara S.
  • Vince Tooley
  • Susan - Jon's Mum
  • Tracy and Amanda
  • lynne
  • LeslieAnn Butler
  • Cheryl, Co-founder

tahnie elizabeth grant's Groups

 

hope everyone is having a gr8 day

Profile Information

Relationship Status:
Single
About Me:
i lost my hair when i was 7 and i am a couple of days from being 18 so i gess i have had alopecia universalis for 11 yrs now
Do you have alopecia?
Alopecia universalis
Are you age 18 or older?
Yes - I am 18 or older

tahnie elizabeth grant's Photos

  • Add Photos
  • View All

Tahnie elizabeth grant's Blog

just wanting a opinion

Posted on April 10, 2010 at 1:38pm 0 Comments

how do u get respect well i do it by macking a compleat fool of ur self for people that probly dont even like me n there are the ones that do respect me for just being there for them n being a friend.Like i dno i feel like people only respect me when they benifet from me its been like that my whole life so far n i just get to the point were u just dont care so what i do when that happens is just block it all out n i eventualy forget what happend n yeah like my pash is like a puzzel with peaces… Continue

Be strong

Posted on April 8, 2010 at 9:00am 3 Comments

what ever u go through it will make u stronger and 4 that a better person 'but' it can also make u just as bad as the people that tease u take it from me be the better person because you will hate the person that u become.It is not worth the pain of being 'well in my words a bad person'. u have to stay true to your self no matter what others do.

to realy understant what i am saying ill tell u my story.

I got alopecia when i was 7 and every thing changed i was in the popular group and… Continue

Enjoy yourself and have fun

Posted on April 6, 2010 at 8:00am 1 Comment

what i have learnt is that what ever anyone says or dose to me,u and or anyone is that we all can choose to let it effect us or we all can choose to not let it effect us.we all can just have fun be normal in ower owen ways not what anyone elce thinks is normal its ower appinion that counts not theres.

so yeah that is now my way of dealing with what other people think of me :)

so just remember what ever is wrong just have fun and enjoy your self :)

Love yourself

Posted on April 5, 2010 at 12:59am 1 Comment

it is allwayes hard to move on but the best thing to do is love the new you.
if u have doughts just look in the mirror and see how beautiful you are no mattere how much hair you have :)

Comment Wall (7 comments)

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

Join Alopecia World

At 9:15pm on April 09, 2010, Susan - Jon's Mum gave tahnie elizabeth grant a gift
At 9:15pm on April 9, 2010, Susan - Jon's Mum said…
Hi Tahnie
Glad that you have joined us here on Alopecia World.
I live in Northern NSW. My son Jon, 13, has had Alopecia since he was 6. He just developed AU in July last year.
Read your last blog. Be proud girl!!
At 5:51am on April 8, 2010, Clara S. said…
I'm doing pretty good. :) I want to buy some new shoes but have spent so much over the last 2 weekends just going out..so am going to hold back a bit. haha
At 11:24pm on April 6, 2010, Clara S. said…
Welcome to AW Tahnie! How are you?
At 7:39pm on April 6, 2010, LeslieAnn Butler said…
Hello and welcome, Tahnie!
Sounds like you have a very healthy attitude.
I have universalis, too.
LeslieAnn
At 11:39am on April 6, 2010, Josephine Bihl said…
HI!
well, we´re "free" from school, cause of Jesus (I don´t know the word, påsk ? :) It´s the swedish word in any case ;)
But, yes, it´s good, I think ;)

How are you?
At 11:03am on April 6, 2010, Cheryl, Co-founder said…
Hi Tahnie, I wanted to welcome you to Alopecia World. I can honestly say that we are a great community here and I hope you enjoy the time you spend with us.

Cheryl
co-founder
 
 
 

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