Alopecia World
www.alopeciaworld.com
Parents of Children with Hairloss
Information
Here you can talk amongst other parents about treatments, highs, and lows.
Members: 634
Latest Activity: May 17, 2020
My little lady...
Discussion Forum
Looking for the kids with alopecia at Jenkins Middle School in Colorado Springs
Started by Sara and William. Last reply by Austen May 17, 2020. 2 Replies 1 Like
My son and I are moving to Colorado springs this school year to join his dad, who has been there for a year and a half now. My son has alopecia, and naturally I was concerned. Both times he's gone…Continue
my daughter doesn't want to wear her hats to school anymore
Started by Saida Z. (Ariana's mom). Last reply by andirnaat Dec 11, 2019. 13 Replies 0 Likes
This is my first time starting a discussion and i'm fairly new to alopecia world im sorry if im off topic but i am worried about my daughter she is 6 yrs old in first grade and has been wearing hats…Continue
Food Allergies
Started by Hillary Howard. Last reply by HarrisonPorshe May 2, 2019. 29 Replies 0 Likes
We have taken our daughter to a Naturopath and she was tested for food allergies. Sure enough she tested positive for quite a few (wheat, soy, dairy, white beans, eggs, cabbage, shellfish...to name a…Continue
Newly diagnosed child
Started by Alexandra. Last reply by Ebs Family Oct 18, 2018. 1 Reply 1 Like
Hello i noticed a week ago my daughter lost a clump of hair I thot she needed a hair treatment (my daughter is mixed) we got a treatment trimmed her hair and then 4 days later I found the bald spot I…Continue
Friends?
Started by Dusti. Last reply by VelmaJDennis Sep 22, 2018. 6 Replies 0 Likes
Hello, I am a mother of an 8 yr old beautiful little girl. She was diagnosed with Alopecia when she was 3 yrs old. It started with just bald spots and they would grow back, but last year she…Continue
Comment Wall
Comment
-
Comment by Susan - Jon's Mum on February 21, 2010 at 6:00am
-
Thanks Thea for the Info
Appreciate all you do
-
Comment by Monique (Mom) on February 20, 2010 at 8:23pm
-
Thank you for sharing this news. I will check out your blog at BaldGirls. Appreciate all the info. we can get.
-
Comment by margaret and nicole on February 19, 2010 at 8:51pm
-
I hesitate to put our story out there because I'm not sure how unique our situation is, and because I know we can lose ground anytime, but Nikki's hair is almost all back. The very last hold out spot is showing signs that it will fill in. Most of her spots have thin fine coverage at this point. We had lost about 1/3 of her hair by September. She is a former micro preemie and through my research I came up with a theory that one of her meds was causing nutritional deficiencies. Long story short, we started giving her tiny amounts of aqueous zinc and we got our first signs of regrowth within 4 days. I'm praying she can get off her meds soon but until then at least we are addressing one of her issues. She has also started to grow better, gain weight better, and is sick much less frequently. Again, not sure if this story helps but at least food for thought about different causes for alopecia.
-
-
oh, this is such wonderful news to hear. Thank you Angie for telling us that. I could use some good news about Alopecia. I feel as though we are a lost cause many times and no one is working for it. I guess because we don't hear anything about it in the public...at all. Thank you for saying this. I am curious to see where it will go. The NH study? You've done this? What is involved exactly. I have been debating it. How is little Gracie doing by the way?
-
Comment by Fizza on February 18, 2010 at 10:26pm
-
Angie - I really hope that comes to fruition. I thinkt he teen years will be the worse for our kids. I hope they find a cure and that it has no side effects!
-
Comment by Ellie on February 15, 2010 at 7:01pm
-
I am not planning on going to the NAAF conference. I think that it is really expensive and I can't afford it for me not to mention my daughter as well.
-
Comment by Mya & Christine on February 12, 2010 at 8:45pm
-
Does anyone plan to go to the NAAF conference in June? We are new with alopecia and we are definitely going to Alopeciapalooza, but I am wondering if I should go to this one, too.
-
Comment by Sandra Christianson on February 11, 2010 at 11:03pm
-
I had no idea how many people have AA. when i came up with my product i thought of kids and teens who suffer mostly from cancer. It open my eyes
-
-
The most ironic thing is that I saved her stem cord cells when she was born. I keep thinking that I could be sitting on a cure. lol
-
Comment by rebecca finlaw on January 9, 2010 at 8:27am
-
I can relate to you Monique, I feel the same.
© 2024 Created by Alopecia World.
Powered by
You need to be a member of Parents of Children with Hairloss to add comments!