Jake's Comments

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At 3:38pm on April 14, 2013, Rachel Taylor said…

Hey Jake! I just re-connected to Alopecia world and saw you on my friends. I clicked on your profile and noticed that you live in NC! So do I! How are things going with your alopecia?

At 6:46pm on May 22, 2012, Ashley said…

Hey I dont know if you still use this or not but I have alopecia as well and im turning 16 this summer. if u need to talk to someone who has alopecia as well I'm here (: I dont know what its like to deal with it as a guy but I know with me being a girl without hair it can be hard

At 7:37pm on February 19, 2010, Gale Moorman said…
Hi Jake and his mom, the only thing i know is that you have to find a support group in NC where others have alopecia and possible children will have the strength and determination to come with their mom. I am in NYC and my last support group there was a 12 yr. old. So it is possible for Jake to meet others his age with alopecia.
At 10:58pm on December 11, 2009, Angie(Austin and Lily's Mom) said…
Hi there, we havent signed on for a while and just noticed you have accepted our friend request. Thank you!...Its really awsome to see another boy close to the same age with alopecia! Austin really liked your pictures and he knows its not only him. so thank you for accepting our friendship!.
At 5:24pm on November 23, 2009, Jesus Chick and Mom-Abre said…
Hi Jake and Mom.
My name is Kayden. I am 13 years old and in the eighth grade. I have had AA since Feb.,but I wasn't diagnosed untill March 27. Like Jake, I am the only kid at my school who has Alopecia. My mom also made a profile for me too. Have a great Thanksgiving! Dress warm!
At 7:26pm on November 4, 2009, Leah Turlo said…
Hi Jake (and mom). I am also the only one in my school of about 200 kids that has alopecia. There is a girl in fith or sixth grade that has alopecia universalis (is that it? I don't know the terminology yet) my uncle also has alopecia unirversalis.
At 8:29pm on October 4, 2009, Metoaka Perez said…
Hi, my mom told me about you. My name is Wakiza. I am 13. I have AA. I am the only person in my school that has alopecia too. I'd like to talk to other people my age that also have alopecia. I was diagnosed a year and a half ago after donating my hair to Locks of love because my mother also has alopecia. about 3 months after that I lost my first patch of hair. My mom thought I had shaved a part of my hair off. LOL After she realized I hadn't and that I had become scared of the fact of having lost my hair, she believed me and had me diagnosed. That hair has grown back, but I later had three more spots show up on the top of my head at the same time.
My mom thought it would be a good idea if I were to find other people my age to talk to that were going through the same thing. That way I would understand it better and maybe to help others that may be having a hard time with it. I am ok with having AA. Besides me and my mom have a deal. If I loose more of my hair than she does then I get to shave her head. It goes the same if it happens the other way too. We are ok with it.
I'd like to talk more with you sometime. Feel free to type anytime. My mom is going to set me up my own site here later. I'll let you know what it is later.

Wakiza
At 9:25pm on September 28, 2009, Sharon Beckham Hinson said…
Yes it is!!! Thanks so much for sharing. I sent the email out last night sharing the website and then sent that invitation to several this afternoon. This is really cool!!
At 8:35am on September 28, 2009, Cindy said…
What kind of help are you looking for?
At 12:41pm on September 27, 2009, Sherilyn and Tatum said…
From Tatum: I am 7 and I started losing my hair when I was 2, also. I have Alopeica Areata. I hoppe you will be my friend!
At 7:24am on August 27, 2009, Cindy said…
Hi Jake and Nicole, welcome to AW!!! I hope Jake meets alot of great kids on here to chat with there. There are so many! How are you? Cindy
At 12:43pm on August 25, 2009, pamela s mcnurlen said…
Welcome Jake, you are adorable, you will have a lot of friends here to talk to. : )
At 6:14pm on August 24, 2009, Roger said…
Welcome.

Roger.
At 2:40pm on August 24, 2009, Cheryl, Co-founder said…
Hi Jake, 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 12:19am on August 24, 2009, Brandy Snap said…
Welcome to this site. Everyone here is great.
At 11:11pm on August 23, 2009, Tracy and Amanda said…
Hi Nicole,
How are you? I have a 7 yr old with AA. This is a great site for support.
Tracy and Amanda
At 9:16pm on August 23, 2009, John M. said…
No worries Nicole...saw your instant message. Ask and ye shall receive! :-)

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