Amanda~'s Blog (8)

How do you tell your children?

It has been a really long time since I was last on this site but I am in need of some suggestions, ideas or input please...

I have a new baby (girl) and I am wondering how others with children have chosen to tell their kids about their alopecia? I know that I have time (though it goes fast) before she will be able to ask questions, but I am still uncertain about how I'll respond.

I have never hidden my alopecia from my baby, nor have I hidden my wigs. However, when she's old…

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Added by amanda~ on February 25, 2013 at 4:21pm — 7 Comments

People have no boundaries

I am back in NY for the summer to complete my masters degree and be done with school officially. Just like last summer I have been wearing a scarf around my head and have not been wearing my wig as it's too much bother and gets too warm. I have now, just this week, had two different people come up to me and ask me if I am "receiving treatment".



I think this is so horribly and unbelievably rude. 1) no i do not have cancer 2) when and where did people learn that this was socially… Continue

Added by amanda~ on June 20, 2009 at 9:00pm — 6 Comments

Finally...

Sorry it's taken me so long, but I finally put up a new (updated) picture of my new wig. Here it is!

I'm getting married soon (Sept) and this is just after my makeup trial. Hope you like it. I know that I love it. It's so thick and lucious in comparison to my old wig and I love the rich dark color too.
Hope everyone is doing well.
amanda~

Added by amanda~ on April 18, 2009 at 8:08pm — No Comments

Change change change

So it's been awhile since I was last online here and awhile since I last posted anything in my blog.I wanted to talk about my very new wig...I just picked it up 2 days ago. Backtracking a bit here, over the summer I was in NY and got myself a full lace wig and had nothing but problems with it. I learned that I am allergic to the adhesive. I also learned that since it was "off the shelf" instead of custom made it didn't really fit as well as it should/could have.



After much… Continue

Added by amanda~ on November 9, 2008 at 8:39pm — 3 Comments

The wig saga continues...

To continue on my storyline about my search/experience for a new wig. Last time I wrote about how I had learned that I am allergic to the adhesives used in my (thought to be) perfect new lace front wig. Then I wrote about how I had learned that I am hooped and instead of sharing my alopecia with the world of people I work with, I opted for some bright red extensions. I did this to divert attention from the fact that one day I had longer brown hair and then the next I came back with my old hair… Continue

Added by amanda~ on August 15, 2008 at 11:09am — 3 Comments

Positive temporary outcome...

First and foremost thank you to everyone who read and commented on my horrible horrible wig experience the other day. I am both pleased and proud to say that



1) with the help of a truly wonderful friend and some great sales people in other stores I was able to figure out how to "fix" my lace wig and remove almost all of the darn glue & tape that was stuck on it. I also have found a wig place in town that I think might be able to help me with different adhesive options or some… Continue

Added by amanda~ on August 7, 2008 at 12:45am — 2 Comments

I know it's a long one, but please read. I need advise

So last month while I was in NY I decided to purchase a "lace wig" according to the website, this wig is different from a lace front wig although don't ask me how because I really don't know. Anyways, when they attached it (approximately 10 days ago) they told me that they were using the "sensitive skin" glue & tape and that with this combination the wig can stay on my head for up to 5 weeks. Of course I realize there are no guarentees in life, but I have quite a story for… Continue

Added by amanda~ on August 5, 2008 at 1:22am — 8 Comments

Am I ready for this ???

I have had aleopecia universalis since I was 15 yrs old. I remember the day my hair truly fell out. It's been 15 yrs and it sometimes still feels like just yesterday. I cannot belive that it took me so long to find this website and others living with, dealing with and surviving life with aleopecia. I guess it's possible I just wasn't ready to.



I have been wearing wigs since I was 15. I started out with the experience of going into a store where an older woman basically sat me in… Continue

Added by amanda~ on July 20, 2008 at 9:00pm — 13 Comments

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