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!! :)
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
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
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.
You are so cute! Stay positive and don't let the other children get you down. They don't understand how to accept others who are different. You are the first local person that I have met on this site.
Mom & Dad, You are right. Education is so important to foster acceptance. Good luck in your efforts!
Hi Jose, 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
Hey Jose and family...welcome to alopecia world, hope you find the support you need here, its a great place with a great bunch of people. You're looking pretty cool with bald head dude, keep your chin up.
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JOSE CHARQUENO's Comments
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Thank you for your invitation to be a friend.
Sincerely
Marie
Hope you're having a great day
Jeffrey
christina
You are so cute! Stay positive and don't let the other children get you down. They don't understand how to accept others who are different. You are the first local person that I have met on this site.
Mom & Dad, You are right. Education is so important to foster acceptance. Good luck in your efforts!
I´m happy to meet you
-Drew
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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.