Ryan
  • Male
  • Christchurch, New Zealand
  • New Zealand
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  • Amaka
  • Jory
  • courtney
  • loryn!
  • Nachiketa Sanyal
  • Emory
  • R0BB
  • x3Awesome'TTx3
  • Megan Willmott
  • PaulJ
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Profile Information

Relationship Status
Single
About Me
Found out I had alopecia 16/9/2011
Do you have alopecia? (Choose appropriately)
Alopecia areata
Are you age 18 or older?
Yes - I am 18 or older

Comment Wall (9 comments)

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At 6:45pm on November 3, 2011, Megan Willmott said…
Hi! sorry for late reply.. haven't been on this site in a while. Yeah well I suppose it is hard but you have to learn to live with these things. Everyone has something wrong with them or an illness they have to live with... we just have alopecia, nothing too heavy haha. x
At 5:58am on October 29, 2011, Nachiketa Sanyal said…
Hi Ryan.. i also discovered i had AA in Sept 2011.. and I'm also undergoing steroid shots like you.. thought we could connect and share our progress..
At 2:55pm on October 21, 2011, Megan Willmott said…
hey, how're you? i'm actually so jealous you live in New Zealand, England is not soooo nice.

How are you taking the news of finding out you have alopecia?

I've had it all my life, so i'm 100% used to it, but finding out you have it midway through life after having hair all those years is going to be tough, but you'll be fine :) x
At 6:07pm on October 18, 2011, x3Awesome'TTx3 said…
Hii Ryan :)
At 4:41pm on October 17, 2011, PaulJ said…
Welcome to Alopecia world mate,

I'm in Chch too, been AU since I was 4, there a few of us here. I grew up with alopecia so if ya have any questions or just want a rant send me a PM.

Cheers
At 3:05pm on October 17, 2011, JeffreySF said…
Hi Ryan,
Welcome to Alopecia World.
Jeffrey
At 6:06am on October 17, 2011, Eliza alisa abgail said…
there are having an alopecian meeting in new zealand in Nov Do you want to meet up with them? In your area. If you are interested add a paul jackson on here. Though he is 30 plus.
At 5:23am on October 17, 2011, Tallgirl said…
I often ask the students who start to whisper behind my back (but enough for me to know I am about to be outted on my alopecia) to either discuss or write a paper on what they would feel and do if they suddenly lost a body part due to an incurable disease (and had rude comments made about it from so-called "friends"). Sometimes, midway through the paper, one savvy student will get an "Aha!" look on the face, and figure out that MY lost body part is my hair. You might soften the blow for your FB friends by asking this on your status (without telling what is happening to you yet), and deleting any friends who have moronic answers. Do this before your alopecia gets worse. Those people will NOT be good for you. Keeps the sensitive ones out of the 600.
At 1:35am on October 17, 2011, Cheryl, Co-founder said…
Hi Ryan, 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 and we look forward to your input. Be sure to check out "10 tips for getting the most out of Alopecia World” which include a few tips to get you started! Cheryl, co-founder
 
 
 

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