Brittany Bullard
  • Female
  • Winder, GA
  • United States
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  • Paula Bowman
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Brittany Bullard's Discussions

Help on shaving my son's head-we are having problems

Started this discussion. Last reply by BaldGirlsDoLunch.org Mar 3, 2009. 22 Replies

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Relationship Status:
Married
About Me:
I am married to Michael and we have 3 wonderful children-Parker 9, Lane 6 and Madilyn 4. My husband sells/manages real estate and is a firemen. I work for our local city taking care of the fleet in town. Our middle son Lane who is 6 has AA. He has had AA since he was 3. I was so excited to see this. I try to get more informed everyday about what I can do and how to help Lane.
Do you have alopecia?
Parent or guardian of child with alopecia
Are you age 18 or older?
Yes - I am 18 or older

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Comment Wall (15 comments)

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At 1:25pm on February 8, 2009, Paula Bowman said…
You have a wonderful looking family and Lane is a cutie, I see he likes to play football too. It's nice to meet you. There is a camp for children with alopeica and it starts in Aug. 7,8 and 9th in Pa. Im going to try to take Ray. I think this will be good for him, we don't no one around here who has AA. It would be something to think about. You can look it up at Childrens Alopecia Project (CAP) bestywoytovich@yahoo.com. Besty and her husband is over.
At 1:27am on February 7, 2009, Paula Bowman said…
Hello Bullard family, My son Ray is 9 and his had AA since he was 3. I was so glad to find this site also. You have a great looking family.
At 4:42am on January 28, 2009, Zoe said…
Hey Brittany,

has Lane lost all his hair or just some hair? How does he cope with it? HAve other members in your family AA?
At 5:00pm on January 16, 2009, Cherylnz said…
Hi Brittany
Welcome to Alopecia World
At 1:23pm on January 12, 2009, Cindy said…
We went to a Boston Meet and greet last April and had a nice time. We missed the Boston one this year..We are not going to NAAF, we have never been to one of their events. check out the www.childrensalopeicaproject.org. They are holding their first kids conference in PA this summer. There event is geared towards the kids. It is their first one. Also, if you contact Betsy she will put you on their contact list and can even tell you if there are other kids in your area Lane's age with AA that are registered with them. They have profile on this board too..Cindy
At 2:50pm on January 5, 2009, Cindy said…
Lane sounds like a great kid and well adjusted!! I wish the best for him..Are you going to go the Alopeicapalozza in Aug that CAP is putting together?
At 5:06pm on January 4, 2009, LeslieAnn Butler said…
Hi Brittany,
Hello and welcome. How are you and Lane doing today?
LeslieAnn
At 4:33pm on January 4, 2009, Buffy, Alicia's Mom said…
Welcome, Brittany! I, too, was very excited to find this site! I have gotten lots of great ideas from many caring people. You have a beautiful family!
At 4:38pm on January 3, 2009, rj, Co-founder said…
Hi, Brittany. 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 9:34pm on January 2, 2009, Cindy said…
Hi Brittany, Samantha has been doing squaric acid for the last year. We tried topical steriods with no avail. I took her to 3 doctors before finding a doctor willing to be more aggressive. Of course I would never subject Sam to anything she did not want to do or that we thought would not be safe to try. She does well tolerating the irritation and rash she gets from the treatments. They are part of the response she should have to the treatment. We apply it twice a week now. It took several months before seeing any results. Now, she has patches of hair coming in. Around March she lost her lashes and rest of her brows. Still no signs of them coming in yet. Alopeica really snuck up on us. We have no family history of it and all her blood work is normal, nor does she have any symptoms that are commonly associated with AA. She started wearing a wig a year ago and really likes it. I was hoping by her b-day next month she will be wig less, but I don't think so. It is hard to watch a young pretty girl lose her hair and have to go through this. I am fortunate she has a good spirit and sees the positive in everything. She is an old sole as many say to me. Is your son doing any treatments?
 
 
 

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