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Brittany Bullard
- Female
- Winder, GA
- United States
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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 0 Favorites
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BaldGirlsDoLunch.org replied to Brittany Bullard's discussion Help on shaving my son's head-we are having problems"Just remember there's no timeline you have to follow. And as with all things related to our kids, alopecia or not, you get unlimited do-overs. Say the wrong thing? no worries..you always get plenty more chances to say the same thing again with…"
Brittany Bullard replied to Brittany Bullard's discussion Help on shaving my son's head-we are having problems"I don't. I will get on and check it out. I have pamplets and other material from the NAAF but his teacher didn't want to give it out!! She didn't even want to give out the letter I wrote to the parents. She said she wanted to wait…"
BaldGirlsDoLunch.org replied to Brittany Bullard's discussion Help on shaving my son's head-we are having problems"HI Brittany-
To help your son and his friends in school, do you have the materials from the Childrens Alopecia Project? In my experience, parents prefer them to the very tired, unattractive materials from another organization.
That org has a video…"
Brittany Bullard replied to Baldboi's discussion How many think ....screw it and bic off all the rest?"We have used both the Gillette Fusion and the headblade. My son Lane who is 6 shaved his head all by himself with the Headblade. I like them both."
Brittany Bullard replied to Brittany Bullard's discussion Help on shaving my son's head-we are having problems"Thank you for mentioning this Andis clipper and blade. I don't know when we will ever get to shaving him again. He has no interest at all. He had a Valentine's dance and he let my husband clean him up a bit. He has none up top and some on…"
Brittany Bullard replied to Brittany Bullard's discussion Help on shaving my son's head-we are having problems"Thank you so much for this, I needed it. Friday at school they are having wacky hair day and he has begged not to go. I tried telling him differnet things we could do but it doesn't want to go. He said I don't hair so what can I do. He has…"
Profile Information
- 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
Brittany Bullard's Photos
Comment Wall (17 comments)
- 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 8:31pm on January 19, 2009, BaldGirlsDoLunch.org said…
- Well one thing's for sure...kids have lurches and retreats.....very independent and then needing the cocoon no matter which decade....so you still have a little boy a long time with growth jumps along the way.
- At 5:00pm on January 16, 2009,
Cherylnz said…
- Hi Brittany
Welcome to Alopecia World
- At 1:23pm on January 12, 2009,
Cindy and Samantha 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 and Samantha 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
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