Kristen Viveros
  • 43, Female
  • Canton, OH
  • United States
Share on Facebook MySpace

Kristen Viveros's Friends

  • amy
  • hannah sophia holland
  • Enriquillo Manuel Melendez
  • Nicole
  • Lalo Guerrero
  • Irene
  • erick
  • Thomas
  • tarik
  • NiCKoLe
  • despina
  • Kymm
  • Misty Boggs
  • Bonnie Ajan
  • Ana

Gifts Received


Kristen Viveros has not received any gifts yet

Give a Gift


My regrowth turned into a full head of hair!


Kristen Viveros's Photos

  • Add Photos
  • View All

Profile Information

Relationship Status:
About Me:
I am Native American Cherokee Indian and the love of my life is Mexican. We have 5 beautiful children between the two of us. I have two from a previous marriage and he does also and then we have one together. I was diagnosed with Alopecia Areata on May 12, 2009. I was also diagnosed with Fibromyalgia Disease on the same day. Although I have just recently been diagnosed with Fibro, I have been dealing with the pain and other symptoms for 4 years. I am very familiar with Alopecia Universalis because my best friend Clara has been dealing with this since she was 12. I was the girl who watched her back in junior high school and beat up all the kids who liked to snatch her wig off and laugh. Now we get to look out for each other. I am very comfortable being bald. I chose not to wear wigs, I think that people need to get used to seeing me bald. I love my bandannas and that's just the way it is. A friend once told me "Hair is so over-rated!" lol (thanx C@). No matter what happens in my life, I have been able to hold my head high and swim to the other side. I'm not sure where I get so much confidence, but it's a great feeling to be able to be myself and not care what other people think. People may say what they want, it doesn't effect my life. As my husband says "I don't eat from your pocket so why should I listen to what you say." In other words, I take care of myself and you are not going to tell me how to live my life. I am here on Alopecia World to share my experiences and learn something new from someone else. Feel free to comment on whatever you feel like commenting on. I always enjoy reading someone else's experiences in life with Alopecia and/or Fibromyalgia.
Do you have alopecia?
Alopecia areata
Are you age 18 or older?
Yes - I am 18 or older
Your Website (Leave blank if you don't have one):

Kristen Viveros's Blog

My Daughter's Emergency Surgery!

Posted on July 17, 2009 at 9:30am 1 Comment

On Saturday June 11th in the evening, my 13 year old daughter Monica started to complain that she wasn't feeling well and her belly was hurting on the lower left side. She took a tylenol and didn't say anything else about the pain for the rest of the evening.

On Sunday morning she was again complaining of the same pain on the lower left side of her belly again. She went to next door to my grandmother's house for lunch (this happens every Sunday) but she came back within 30 minutes, telling… Continue

No where to go for national bald out.

Posted on July 14, 2009 at 9:30am 0 Comments

Hey guys... I was just sitting here thinking... sunday is national bald out day (Now International Alopecia Day) and I have no where to go. Maybe I'll go visit a friend or a family member or maybe I will venture to the store bald and see what kind of reactions I get. lol. I'm not really sure what exactly we are supposed to do for national bald out day. Any suggestions?


Posted on July 7, 2009 at 10:33am 2 Comments

Days turn into weeks, weeks turn into months. I just can't understand why I am still here. I haven't seen my husband for 6 long months and I am almost at my breaking point now. Every morning I wake up alone and a realize once again that I must spend yet another day with out him. Every night I cry myself to sleep. No one understands. My family sees my cry, although I try to stay away when I cry. But, lately I have been crying nearly everyday. My own mother never offers any reason or comfort for… Continue

Mexico is getting closer!

Posted on June 29, 2009 at 7:12pm 0 Comments

For those of you who have been reading my blogs and such about moving to Mexico... I now have all of my loose ends tied up. I of course have my passports. I now have my birth certificates and my S.S. cards I have been waiting for. The baby is totally up to date on his shots and my meds are all squared away for the duration of my trip. The only thing that is missing now is the money to purchase the ticket. I have some friends rallying around me to try to help me raise the money by doing various… Continue

I'm Still Ok.

Posted on June 28, 2009 at 9:41am 0 Comments

Hello everyone, I thought I would post a new blog since I got a couple of emails asking me if everything was ok with me since I haven't posted or commented lately.

I am happy to say that everything is perfectly ok with me. I still have a bald head and I am still having fun with it! The thing that has kept me from posting is my Fibromyalgia. With this disease I get what is referred to as "Fibro Fog"... this means that it's hard for me to concentrate and finish a project, even as small as… Continue

Comment Wall (25 comments)

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

Join Alopecia World

At 8:55pm on October 25, 2009, beatriz castillo said…
Hola Kristen,, me llamo Beatriz tengo universal desde los 3 meses de bebe,, ahora tengo 31 me ha causado una gran alegria ver a mi querido Xalapa ver,, precisamente de alli soy , espero saber de ti pronto,, hasta la proxima.
At 11:27am on July 27, 2009, Julia said…
Canton, are in my used to be neck of the woods. I'm from Mansfield..."not exciting" lol

Also, on FaceBook find and join the group "Alopecia (Hair Loss) Awareness" we want to be 1 Million strong by September due to Alopecia Awareness Month. AWARENESS is Key! make sure you share the group with all of your FaceBook Friends too. By the way my new book that showcases 22 women and stories about living with's called "Metamorphosis~Inspirational Stories of Women Living with Alopecia" by Julia Crittendon. You can go to your local Borders or order online at Barnes and Noble or Amazon!
At 3:00pm on June 29, 2009, ROCKSTAR: ROCKY MANUEL MARTINEZ said…
i am Puerto Rican & Cuban ma'i form the island of Puerto Rico yo.
At 7:14pm on June 14, 2009, Ana said…
Awww, thanks Kristen for the compliment. Thank you. The only reason why I said it's hard to believe is because noone believes me when I tell them LOL. So you're moving soon you said, I hope everything goes well for you in the move to Mexico. We'll surely keep in touch.
At 6:44pm on June 14, 2009, Ana said…
Hi Kristen, thanks for the love and support. Yes, I am Latina, born in the Dominican Republic...I know, I know...Dominican hard to believe. LOL. Sure all the support is welcomed. For the first time ever since I have been diagnosed I am actually seeking support from others that share the same emotional stresses I do.

Keep in touch!
At 2:12pm on June 13, 2009, JeffreySF said…
Oh Good!!! I'm glad you got the passports.
When is the move?

At 12:11pm on June 13, 2009, JeffreySF said…
Hi Kristen,

Thanks for your coments.
How is you day going?

At 8:01pm on June 12, 2009, Jesus Chick and Mom-Abre said…
kirsten, same thing here! i haven't gotten back to you in a while. sorry. i have been doing fine. how about you? hope everythings fine.
At 11:06pm on June 6, 2009, Jesus Chick and Mom-Abre said…
hey kirsten! how's it going? i just looked at "my friends". i saw you were online. i hope everything is goin' good for you. have you checked out my mom's page. her name is Stephanie Kuykendall. talk to you soon.
At 6:11pm on June 2, 2009, lynne said…
hello, how r u doin, i have been readin ur blogs and really feel for u, i hope ur doin ok tho, i also think im losin more hair around my body as it seems like its gettin thinner, my eyebrows and down below, im also very scared of this happenin, i hope we can help each other thro this, i dont think i can talk to my friends n family about it, speak sn x


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