JOSE CHARQUENO
  • Male
  • DALLAS, TEXAS
  • United States
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JOSE CHARQUENO's Friends

  • erica herrera (elijahs mom)
  • M
  • Lesa M - Jess's mummy
  • Diana Carter
  • Kim Karacz Caudill
  • Samantha (:
  • Liz
  • Makayla M
  • rlc
  • emine hasoglu
  • Lilly
  • Cindy (Duncan's Mom)
  • Camille Paddock
  • Karine , Xavier
  • Paula Bowman

JOSE CHARQUENO's Groups

JOSE CHARQUENO's Discussions

USEFUL INFO ON ALOPECIA IN POWERPOINT

Started this discussion. Last reply by JOSE CHARQUENO Nov 5, 2008. 3 Replies

ANYTHING OR PEOPLE IN DALLAS AREA

Started this discussion. Last reply by Shanea Matthews Mobile 4 Beauty Nov 19, 2008. 4 Replies

 

HI MY NAME IS JOSE BUT THEY CALL ME PELON!!!

Profile Information

Relationship Status:
Single
About Me:
MY NAME IS JOSE AND I AM 8 YEARS OLD. I HAVE ALOPECIA UNIVERSALIS. JOSE IS A VERY CARING KID AND HE LOVES TO PLAY SOCCER. MY SON DEALS WITH ALOPECIA VERY WELL ALTHOUGH I HAVE FIGURED OUT THAT HE DOESNT LIKE TO GO ANYWHERE BECAUSE HE DOESNT LIKE THE ATTENTION. WE ARE DOING ALOT OF AWARENESS IN DALLAS TO MAKE SURE THAT PEOPLE KNOW ABOUT THIS ILLNESS. ITS BETTER THAT PEOPLE KNOW SO THAT THEY ARE NOT AFRAID.
Do you have alopecia?
Alopecia universalis
Are you age 18 or older?
No - I am not 18 or older
Your Website (Leave blank if you don't have one):
http://josecharqueno

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Comment Wall (16 comments)

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At 10:14pm on June 02, 2011, Diana Carter gave JOSE CHARQUENO a gift…
Gift
Red Ribbon
Red Ribbon
From the Gift Store
At 6:49pm on January 4, 2011, M said…
Hi Jose,
Thank you for your invitation to be a friend.
Sincerely
Marie
At 11:46pm on July 5, 2010, Liz said…
Thanks for the add...
At 11:32am on September 8, 2009, Robert said…
HAPPY BIRTHDAY JOSE!

Hope you're having a great day
At 1:21am on September 7, 2009, JeffreySF said…
Happy Birthday Jose.

Jeffrey
At 11:01pm on March 12, 2009, Christina Bostwick said…
thank you for responding to my question. i actually had some ggos new today i wen to the doctor and she told me the chance of a mother or father giving this to their child is less than 11%. so needless to say slim to none. so that makes me happy. thank you again for taking the time to share for knowlegde with me it mean alot!! your lil guy and you families is in my prayers i hope one day soon they find a cure so noone has to suffer with this disorder forever..but until then know that my heart goes out to you and your son and i wish you guys all the best in dealing with this crazy disorder. oh and please tell your son i think he is a very handsome li guy with a great smile!! :)
At 9:55am on March 11, 2009, Christina Bostwick said…
Reading your sons story is heart breaking! I know as anadult this is painful to go thru but as a child i can only imagine. I had alopecia wreta when i was in high scholl and it was horrible ..long story short i was treated and for 1o years nothing no patchs no hair loss nothing and now i have patchs all over agian. As i have been doing research i have found out that they are considering this to be hereditary....so my ? is (if this is not to personal) do you have any other children with this diorder or do you and your husband have it? I am so worried that i will have given this to my children i feel sooo guilty. If the do seem to get it for whatever reason i hope god gives me the will he has given you guys to face all the challenges that go along with this disorder. you child looks so handsome he looks like a really great kid you guys should be proud! :) well if you could find the time to answer my ?'s i would truly be grateful. thank you again for your time and god bless you and your family.
christina
At 12:05pm on March 1, 2009, Cindy said…
Hi Jose, I have a 7 year old daughter with Alopeica,Samantha. You are a handsome young man and like you Sam is strong and handles her Alopecia well. It is always nice to hear stories about children who don't let a lack of hair stop them from being who they are or want to be...Don't ever stop being who you are and keep smiling! Cindy
At 6:53pm on January 15, 2009, Shannon M said…
that would be great and i would love to meet jose, but we are going to need to sceldule something that will work for the both of us
At 10:35am on December 19, 2008, sandyk said…
Thanks for the reply. Let me know if you meet others who are local. I would love to get together with you and others and form a social group. It would also be great to find a group of kids who have alopecia so they can make friends. It would be good for Jose to have a friend or two like him or even friends who don't care about his condition.

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