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Madisonsmom's Friends

  • Abby TerHaar
  • Kimberly
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  • Maria, Mia's Mom
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Relationship Status:
About Me:
I'm a mother of 3 boys & 1 beautiful little girl. Madison is 7 and has alopecia universalis since age 4.
Are you age 18 or older?

Comment Wall (15 comments)

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At 1:21am on August 20, 2009, Tracy and Amanda said…
Hi Madison,
How are you?
At 4:31pm on May 27, 2008, LeslieAnn Butler said…
Hi Sharon,
I have had au for 20 years. Just wanted you to know that if you need support, I will help...
At 6:37pm on April 16, 2008, Mommy said…

Does this mean you she will soon be sporting a wig? What does she think of about it? Lynn
At 9:07pm on April 15, 2008, Mommy said…

Madison is very cute, especially in her dress up clothes. Since you said you are participating in the M.D. Anderson study I was wondering if you live in Houston?. We live locally and would love to meet if you do! My daughter is about to be 4 next month. She has had it since her 3rd birthday. She wears hats when we go out and nothing when inside. Occasionally she takes off her hat with close friends & family. As we approach the 1 year mark, I have kind of been thinking about maybe getting a hair hat in case she wants to wear it sometimes? What do you think of those? When did you start discussing/ accepting that her hair might not come back with Madison? Lynn
At 11:06am on April 14, 2008, Cindy said…
Happy Alopecia Day Madison!!!

your friend, Samantha
At 10:04am on March 25, 2008, Janine-Connor's mom said…
What a beautiful girl! This is a very supportive group of moms/dads
At 2:00pm on March 24, 2008, Janna said…
Hello! Welcome to the website. This place seems unlike any other, with so many supportive people. I, too, have a daughter with alopecia. She's adorable, sweet natured and confident. (Can't say the same for myself some days) lol. She's going to be 3 in July, and has had it since the age of 8 months. Madison looks like a little princess!

I look forward to getting to know you both!
At 12:30pm on March 22, 2008, Jessica said…
She's so BEAUTIFUL!!! Thanks for the comment, I'm so happy I have found this site it makes everything a little bit easier to know are not the only ones going through this.
At 11:07pm on March 19, 2008, Cindy said…
Hi Sharon..

Nice to meet you...Your daughter sounds comfortable with who she is..I am glad to hear she is having a good experience in school. I have to say that I admire your daughter and all the other kids out there who have the courage to go to school hairless..Samantha does not leave the house without her wig on. She loves it so I am lucky..I never allowed her to be seen with patches and once we could not cover them any longer we got her a wig..We did not have to push her to wear a wig..She thinks it is cool and I think Hannah Montana helped. I am private about her AA and only our close friends and family know..It is my choice, but of course I can't stop Samantha from sharing if she chooses to do so. Samantha has had AA for almost a year now and once summer was over she aggressively lost her hair..It has been hard and now she has almost no lashes or brows..It will be nice to get know some of the other parents on this board who are facing the same issues...I hope to see you around..Cindy
At 10:02pm on March 19, 2008, kastababy said…
I've had alopecia since I was 4 years old; during that time I have lived mostly with alopecia totalis, but more recently I have dealt mainly with severe alopecia areata. I have a special affinity for children with alopecia, seeing as how I was a child with alopecia myself.


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