Stacey, Olivias mom's Comments

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At 10:03pm on August 29, 2022, Kate amo said…

Hi Stacey my daughter zoe is 10 and was recently diagnosed with alopecia she's lost almost all her hair in under 3mths and is looking for friends with similar stories. I see ur in Truro NS. I just came back from pictou last week. Lol maybe ur daughter would like to chat with zoe. 

At 9:00pm on December 30, 2010, M said…
Ok so your name is Stacey and I see you from Truro.
At 8:09pm on December 30, 2010, M said…
Dear Stacey,

Thank you so much for your reply. I think you must be right about beautiful people having alopecia because I looked at your daughter's photos and she is such a little beauty. I love, love, love her pink wig. It's my favourite colour, how fun!!

Just realized that's your daughter's name lol. I'm from New Glasgow. Which part are you from , if you don't mind.

Sincerely
Marie
At 10:09pm on September 1, 2010, Liz said…
Your daughter is beautiful....I too love the picture of your daughter with the sand on the back of her head....cool pics...
At 7:04pm on February 11, 2009, emilie said…
Hi Stacey!
I think its amazing how you care so much about your daughter and support her!
I am sure she will keep her confidence especially knowing she has so much love and support around her.
I saw her pictures and she is really beautiful. So cute!! :)
Best of luck!

-emilie
At 8:08pm on February 9, 2009, Amber Lounder said…
Hi Stacey your girl is truely beautiful She's angelic
At 4:59pm on February 8, 2009, carly said…
thank you <3
tell her happy birthday!
At 11:04pm on February 6, 2009, carly said…
haha i love the picture of your daughter with the sand on the back of her head! its so cute!
At 2:39pm on February 6, 2009, Tracy said…
Well my email is tfisherthegreat@hotmail.com You can send me an email there and I will give you my address and I can take yours down and the girls can start writing letters to one another!
At 1:44pm on February 6, 2009, Tracy said…
Hey ! my daughter (8 years old) also has Alopecia, she has lost most hair on her head and just started losing it on her eyebrows. I find it hard, I think she is dealing just fine. I feel almost selfish for thinking her hair was the most beautiful ever, then she lost it! What do we moms do! lol. Your daughter is just beautiful!!!!
At 8:33am on January 17, 2009, Salmezan said…
Thanks Stacey. Olivia is a very beautiful girl and she does remind me of my younger years. I can see she is a very confident girl and she will get through her teenage years as easy as I did! How old she is now if you don't me asking?
At 10:28am on October 10, 2008, Cindy said…
We have to be blessed our kids are handling this so well. We can't say that about every child!! Do you find that your daughters eyes are exceptionally itchy with the hair coming in and are the lashes white? We are doing a treatment. Samantha has a layer of hair on about 60-70% of her head and getting thicker. I am seeing her brows starting to pop out, but no lashes yet. They were were the last to go in Feb...Cindy
At 7:35am on October 10, 2008, Cindy said…
Hi Stacey. I was reading your post about your daughter on the childrens board and it made me smile. You daughter shares a very similar attitude to mine. Sam would like her hair back very much, but she has the acceptance to live her life without hair if it is deemed that way. I hope not...Sam developed AA at age 5. She has been wearing a wig since Dec and lost her brows and lashes this year. That was harder I think..Are you doing anything to help her hair regrow or is it coming back on its own? Cindy
At 10:04pm on July 3, 2008, Christel Hertz said…
Hi Stacey,
Thanks for your comment. Yes they do sound a lot alike. Jennifer loves wearing her wig, she doesn't go out without it only on our back yard when she plays with her little brother. We have a new problem now ,he attends kinder at the same primary school and he has been telling his friends that Jennifer wears a wig and we prefer to keep it quiet to avoid teasing. So I have to try and convince a four year old to keep quiet. For him it is normal that Jennifer wears a wig, but he doesn't realize that other people may not understand. I love your quote I have to tell that one to Jennifer she will get a laugh out of that. All the best to you and your beautiful daughter.
At 11:58am on June 11, 2008, LeslieAnn Butler said…
Hi Stacey,
Sometimes it's harder for the parent than the child, isn't it!
Just wanted to say hello.
I've had aa for 30 years.
LeslieAnn
At 10:33am on June 11, 2008, tony said…
Hi Stacey nice to meet you, ya it gets fustrating and sad at times, but we have to stay strong and posetive for her sakes.Funny shes seems not to be botherd by it as much as I am and hopefully if hair doesn't return I do my part to make her be strong and confident to deal with it. I see some older girls on here who look vibrit and full of life. I've learned so much through this site and other websites that not to expect much but anything can happen, we made an appointment to see a specialists at sick kids here in Toronto who has done studies on alopecia just to hear more and maybe if find out anything we haven't already heard.My daughter's only 6 so any kind of steroid or heavy meds is out of the question but will be interesting to hear what she has to say. Well thanks for connecting ,oh shes hasn't had any eye problems yet but like your husband I've got all the things that can happen covered ,spent many nights on here researching all there is to know about alopecia. Again thanks for sharing and will let you know what the alopecia specialists says, chat again I hope take care stacey,
At 11:28pm on June 10, 2008, Cheryl, Co-founder said…
Hi Stacey, My mom was born in Truro, her maiden name is Paris. 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 4:31pm on June 10, 2008, Roger said…
Welcome.

Roger.
At 2:18pm on June 10, 2008, Carol said…
Hi Stacey
I grew up with alopecia since I was only one year old. This site is a wonderful resource and is full of support, I hope you enjoy it as much as I do. Welcome! :)
At 10:46am on June 10, 2008, Billie said…
Hi Stacey! Welcome. I am sure you will find alot of encouragement for you as well as your daughter as she grows up with this disease. It is great source of support for those who experience the same things daily.

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