Sarah bradley's Comments

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At 7:28pm on March 4, 2016, Mary said…

Hi, Sarah! How are you?

I love your hair in the first picture, colud you tell me what wig were you wearing, please?

At 5:10pm on April 6, 2015, Nammer said…

Sarah sarah how are you?!

At 1:00am on March 18, 2015, Josh McDowell said…

It's been awhile since you've been on the site. Hopefully everything is going okay?

At 10:15pm on January 13, 2012, Sarah said…

Hello other Sarah :-) My personal advice would be to not take oral steroids (like ****nisone). I took them for a month to help with the burning on my scalp, but it did nothing, and the side effects are nothing to laugh at. There are different types of steroids, this kind can thin your bones with long-term use, decrease muscle mass and even contribute to hair loss!! Anyway, they're not worth it, and can risk dependance meaning you'd have to be on it for a LONG time, months even. Work on eating healthy, exercising, accepting yourself for who you are. I've been on antibiotics, steroids, hormones, etc all trying to remedy this condition (mine may be different from yours) but nothing seems to work. I think you're a lovely lady, enjoy being young! Go and do fun stuff, people will accept you... and who cares what everyone thinks anyway? It only matters what you think, and the confidence that you hold inside. Sarah K.

At 4:37am on November 19, 2011, Josef said…

thank you for the friendship :)

At 8:52pm on November 6, 2011, Megan said…
Hi Sarah,
I was looking at you profile some and I think it's amazing that you have had alopecia areata sinse you were 13! I'm 13, and it has probably been around 3 months since I found out. I also was wondering if you have ever got the injections?
At 2:08pm on October 11, 2011, Nathan Paul Prince said…
I haven`t ever taken steroids, nor any other type of pill or chemical... none of the "remedies" ever really work, and though there is still a lot of research going on (particularily in the pharmaceutical industry) nothing concrete has ever arisen yet. I think you are beautiful just the way you are. Cheers from Montreal!
At 12:59pm on October 11, 2011, Julija gave sarah bradley a gift
Gift
Have just saw your pictures must say you look lovely :)
At 5:51pm on August 26, 2009, alyssa said…
hey sarah, i am 17 and a senior in HS. i am totallly bald and brought my frst wig about 3 months ago when i was still going to AA. i see you have alot of blog about help... i would love to help you out with anything you need
At 2:15am on August 7, 2009, Susan - Jon's Mum said…
Hi Sarah, Welcome to Alopecia World. Hope you get the support you need. My son Jon is 12 in Year 7 and having a hard time of it. He has had AA for 6 years. He hates it and hates being different from everybody else.
Since being a member of this site I have noticed that alot of people have come to terms with AA and are out there living their lives and not worrying about what anyone thinks. There are alot of people without Alopecia that can't do that so I think they are very special and I am sure that you will get alot of support from them.
At 8:07pm on August 5, 2009, Cheryl, Co-founder said…
Hi Sarah, 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
At 11:02pm on August 4, 2009, Cherylnz said…
Hi Sarah,
Welcome to Alopecia World
Cheryl
At 4:48pm on August 4, 2009, LeslieAnn Butler said…
Hello and welcome, Sarah!
I know how hard alopecia can be; I have had it for about 30 years. Let me know if you need help or support. One thing that you might be interested in is my book, written for women, called "If Your Hair Falls Out, Keep Dancing!" (It just won two national awards!) It has a lot of good info in it, it can answer many questions, and it's a fun read, too. You can find out more on my page. It's available on Amazon.com, and on this site under "Bookshelf."
Let me know if there's anything else I can do! I am here to help.
LeslieAnn
At 9:18am on August 4, 2009, kastababy said…
Welcome to Alopecia World!

I hope your time here is educational, inspirational, and overall sensational! We're more than alopecians here; we're family -- if you need anything all, just ask -- we're all here to support and love one another!

Hope to get to know you better!

Your new friend, YoKasta

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