Hillary Howard
  • Female
  • Otis, MA
  • United States
Share on Facebook MySpace
  • Blog Posts
  • Discussions
  • Events
  • Groups (2)
  • Photos (2)
  • Photo Albums
  • Videos

Hillary Howard's Friends

  • Angie
  • Jasmine Quintero
  • Mya & Christine
  • Pradha
  • Lara (Becca's Mom)
  • Sherilyn and Tatum
  • Diane Dyer
  • Wendy Willeroy
  • Tracy and Amanda
  • kristin
  • LeslieAnn Butler
  • Cindy

Gifts Received

Gift

Hillary Howard has not received any gifts yet

Give a Gift

 

Hillary Howard's Page

Profile Information

Relationship Status:
Married
About Me:
My 6 year old daughter was just diagnosed with Alopecia Areata and we are searching for support, understanding, and information to help her through this difficult journey.
Do you have alopecia?
Parent or guardian of child with alopecia
Are you age 18 or older?
Yes - I am 18 or older

Hillary Howard's Photos

  • Add Photos
  • View All

Comment Wall (11 comments)

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

Join Alopecia World

At 10:57am on August 12, 2014, wclawvs said…

Hi Hillary,

I'm curious how your daughter is doing today. Our almost five year old was just diagnosed in early July. I'm interested in having her tested for allergies and trying to change her diet. I hope you are all doing well.

Thanks. Vikki

At 7:40pm on October 11, 2009, Cindy said…
Hi Hillary, did you make a apt at Children's with our doctor? How is everything going?
At 8:45am on September 28, 2009, Cindy said…
Hi Hillary, it was nice talking to you the other day. Did you call our doctor?
At 6:21pm on September 22, 2009, Hillary Howard said…
It's been a crazy few weeks- the two older kids are finally back in school and I get some peace and quite- sort of...Sophie is happy in school and we have had no problems with other kids questioning her hair. We had a few good weeks and her hair was growing back in all the bald spots. Now suddenly she is loosing a tiny clump or two a day. Luckily it is on the back of her head and isn't noticeable but we will see how it goes. We have an appointment next month with a doctor that specializes in autoimmune diseases. *fingers crossed*
At 8:55pm on September 2, 2009, Tracy and Amanda said…
Hi Hillary,
My daughter has had alopecia for 3 yrs now ever since she was 4. She is 7 now and just started back up at school today. She wasn't teased but alot of her classmates kept asking what was wrong with her hair. Most of the top of her hair is bald. She just has the back and the sides of her head with hair on it. She is going through a stage where she doesnt want to talk about it. She is keeping it inside which I dont think is good for her. But I wont push her at the moment, How is your daughter affected by it? I hope she is okay.

Tracy
At 1:46am on September 2, 2009, Cheryl, Co-founder said…
Hi Hillary, 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.

Cheryl
co-founder
At 1:36pm on August 31, 2009, Cindy said…
Hi Hillary, my name is Cindy and I am mom to a 7 yr old girl with this condition. Welcome to AW. It is a great place for support. I wanted to let you know that I am started a support group here in MA that meets bi-monthly in Hopkinton. The kids that attend thus far have been 4-9 yrs old. The group is supported by the Children's Alopecia Project. www.childrensalopeciaproject.org. You can find my contact info on their website or feel free to email me if your interested in learning more about our group. We are having a Big and Littles Event in Boston on Sept 26th. Details are on the website, but if your interested in more info feel free to email me..How is your daughter doing?
At 11:40am on August 31, 2009, LeslieAnn Butler said…
You might want to look into materials to take to school. There's a free children's video just for that purpose, and written info too, available from the National Alopecia Areata Foundation, at www.naaf.org. Go to the bottom right of the home page and you'll find a place to click to get more info!
At 11:33am on August 31, 2009, Courtney said…
Hi Hillary,
Nice to meet another local. I don't know of too many of us around! If I can be any help or support to you, please let me know. There are not a lot of resources in the area for alopecia. Best of luck to you!
At 11:23pm on August 30, 2009, LeslieAnn Butler said…
Hello and welcome, Hillary!
Just thought I'd stop by and see how you and your daughter are doing today.
LeslieAnn
 
 
 

Disclaimer

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