EMILIE's Comments

Comment Wall (24 comments)

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

Join Alopecia World

At 3:48pm on March 20, 2010, Tallgirl said…
I am in Lincoln. Ever come down Hwy. 65? We could meet in town or at Starbuck's!
At 3:36pm on March 16, 2010, Mary said…
Welcome to the National Bald Out Group, Emilie.

I was where you are not too long ago. I thought my life would be over if I lost my hair. Then I thought it would be over if I lost my eyebrows. Two years later, and my life is great and I'm comfortable going everywhere bald. It's who I am now. Take care,
Mary
At 3:36am on January 16, 2009, Jamie said…
Hello Emilie,
I know how you feel believe me, I am also tired of covering up the spots. And also in the spot of I don't know what to do. I've been going through that alot lately in trying to make a decision. I was so happy to find this site, anytime you want to chat, I'm here.
At 8:28pm on January 2, 2009, Eileen Simpson said…
Hi Emilie, I've been meaning to say hi,
So hi, how are you doing? My name is Eileen and I will be oving to Sacramento in June to live with my son and grandson. So maybe we could chat sometime. I think that your a very brave young lady with a beautiful baby. I hope that you have a great New Year.

Eileen
At 2:12am on December 14, 2008, Eileen Simpson said…
I just joined tonight didn't even know there was such a sight out here. So this is very late in posting to you. I have had AA for less then a year and already about 30 of my hair is gone. its just such a weird disease, I can't understand it, my moods are up and down. I have felt like shaving it all off many times, but until I can find a good wig I wait.
Anyway looks like there are some good people out here,
Hugs to you, and keep your chin up you are not your hair, you are unique and special with or without it.
At 6:48pm on September 22, 2008, Gina said…
Hi Emilie,

I know exactly what you're going through and how you feel about it. My hair started to fall out right after my second baby was born but didn't get that bad till a year ago. I too tried to cover until I couldn't anymore; got a wig but didn't shave what I had left of my hair, it fell out short after that anyways. I still hate this, and some days really are a challenge but it gets better, you get to the point where you realize you can't let alopecia prevent you from enjoying your life, especially when you're a mom; I know my kids are happier when I'm happy :-) It's great that you have your husband's support and I'm glad you found this site, it helps to know we are not alone. So hang in there...
At 4:29pm on September 4, 2008, Zoey said…
I think families would be welcome, but I am not really sure. This will be the first meeting I will be attending. So, I am not really sure about anything. Sorry I am no help!

I was born and raised in Los Angeles area. Valencia California. Do you know where that is? Its right by Magic Mountain.

I wouldnt worry about what your little cutie will think when he gets older. I can tell you from my experience, my son being 9 years old in 5th grade. He hasn't been teased at all. Infact, all the kids come up to me and talk they want to hang out..lol Its cute!
I am the only parent they all run to on the block and ask questions.. Makes me feel pretty good that none of them run and scream from me. I am not sure if anyone asks my son what's wrong cause they have never asked me.
I have had one of his teachers ask if I was okay. I think they thought I had cancer. (I wear my scarf all the time)
Anyways, its so far away. I am sure everything will be okay!

Zoey
At 2:28pm on September 2, 2008, Rachel said…
Your son is so stinkin' cute!!
At 2:17pm on September 2, 2008, Dawn said…
Hi and welcome Emilie
At 1:40pm on September 2, 2008, Dotty said…
Hi Emilie,
Welcome to Alopecia World. Just wanted to stop by and let you know that we are just like family here so if you need anything, be sure to let me know. I love your pics. Your son is adorable and it sounds like you have a very supportive hubby. That makes a huge difference.
Love and Hugs,
Dotty
At 1:27pm on September 2, 2008, Billie said…
Hi Emilie! I am so glad to welcome you here to our place in the cyber world. I can understand what you are going thru. This place is a great source of support for all of us who have this dreadful diease.
You have a beautiful little boy and I am so glad to hear a loving & supportive husband.
Feel free to ask what you may have questions on. I will answer honestly.
Again, welcome!!!!
At 9:59am on September 2, 2008, Cheryl, Co-founder said…
Hi Emilie, 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. Cheryl, co-founder
At 8:25pm on September 1, 2008, Zoey said…
Where did you move from? Your son is sooo cute!
Treasure each moment.. I already miss my son being a little guy. He is almost ten.. He thinks he is an adult now...
At 2:08am on September 1, 2008, JeffreySF said…
Welcome to Alopecia World Emile.

Jeff
At 2:01am on September 1, 2008, EMILIE said…
I just want to say THANK YOU!! to everyone that has already welcomed me!! I apprecite it so much and am so happy to know there is SO much support out there in the world!!! I look forward to getting to know all of you!
Again.. thank you.... :)
At 11:11pm on August 31, 2008, Dawn said…
Hi and welcome Emily. We are here for you.
At 8:20pm on August 31, 2008, carly said…
hi emilie
welcome
how are you doing?
At 7:48pm on August 31, 2008, rj, Co-founder said…
Hi, Emilie. Welcome to Alopecia World! This is a great place for great people, so be sure to make your positive presence known. :-) - rj, Co-founder
At 4:33pm on August 31, 2008, LeslieAnn Butler said…
I am here for you!
Big hugs!
At 4:22pm on August 31, 2008, Roger said…
Welcome.

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