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Added by Yellow Daisy on March 5, 2013 at 12:11pm — 6 Comments
Been awhile since I blogged, mainly as I have not really had any issues with Alopecia which I guess is a good thing. I can't actually believe in fact time has gone so fast. That is was Oct that I put on the blog about testing vitamins which I am not sure made any difference at all... But I did give up on them after one batch. I think taking a pill every day is just not my thing. I do still have a packet mind, which I pop one every so often when I think to myself it won't do me any harm for a…
ContinueAdded by KFlame on March 2, 2013 at 4:30am — No Comments
Is feeling relieved/frightened to be actually accepting of losing my hair; an odd mixture - like everything I've preached about health, wellness and loving Self decided to take a test ride with a very much thinning crown. So thankful to have found this site.
Added by Rebecca on March 1, 2013 at 1:30am — No Comments
You always hear : dont judge a person til you walked a mile in their shoes. This has become so apparent this past week, with my friends and family. You really cant blame or judge another for the choices they have made in life. We each have our own issues, adversities and ghosts in the closets. We each have made the best decisions with the resources we had at the time with the knowledge in which we had it. How can you sit in your glass house and judge them for those choices. I personally grew…
ContinueAdded by Bald and Fabulous AKA Terri on February 27, 2013 at 6:00pm — No Comments
Hi im Casey and Im 13 years old with Alopecia;) Dont worry...we can fight it together!!!
Added by tobincasey2 on February 27, 2013 at 6:00pm — No Comments
I wake up every day to light kisses on my cheeks, my sleepy eyes, my lips, the tip of my nose, my forehead, and lastly, my bald head. Lately I have been waking to heaven. The sight of my Superman smiling at me when I open my eyes is simply amazing. This seems to have been my husband’s morning routine lately. And I’m not the one to complain about it. I took it all with open arms. Like I said, it was heaven. This routine actually made me feel loved and accepted (first thing every…
ContinueAdded by IcedBit on February 26, 2013 at 12:00pm — 5 Comments
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…
ContinueAdded by amanda~ on February 25, 2013 at 4:21pm — 7 Comments
I thought I was alone with experiencing the itchy and sensitive skin. I can not wear the synthetic wigs or lace fronts.I can not use any fragrance type scents. If I wear perfumes, which are a little pricey. I believe that the alcoholis high in content and gives me some type of reaction. Does anyone have any suggestions?
I'm also looking to find the full lace fronts that are made with virgin hair and has not been treated
Added by Johnyette Sproles on February 23, 2013 at 9:30am — 2 Comments
Hey guys! I hope all is well with you guys. As you may have noticed my life got a bit crazy and busy. I haven't been on here in over a year so here is a little bit about what's been going on in my life. My divorce is almost final so that makes me happy and sad all at the same time. Marrying some one to me ment spending the rest of my life with them but when the person I was with couldn't handle my disease and abused me because he wanted me to feel like a piece of trash, took me a long time…
ContinueAdded by Izzy on February 23, 2013 at 2:30am — 2 Comments
Anybody here have success with hair up by schmuel gonen?
Added by MychildhasAT on February 22, 2013 at 5:30pm — 7 Comments
One of the joys of having Alopecia Areata and opting for the bald path is the need to shave every few days. I decided I will not learn to shave my own head, and have my husband do it to me instead. This way he’d have some participation in the delights of my Alopecia, because I’m nice like that. I have also decided to refer to him as “Superman” on this blog, because he is my superman (and this is my lame attempt at flattering him). So, every couple of days I would be niggling Superman into…
ContinueAdded by IcedBit on February 22, 2013 at 11:30am — 4 Comments
Still looking for a perfect hat for my wedding. Any ideas where to go to? I have tried google, etsy, everything.
Added by HeatherRae on February 21, 2013 at 5:00pm — 9 Comments
Anyone else experience this with their children. It's shedding everywhere and dr said its normal. I am freaking out cause my husband and I both have hair loss. Does anyone else seem to think it is stange that we all have hair issues. I am starting to think its our apartment or water. I don't know what to think anymore.
Added by Michelle on February 20, 2013 at 6:26pm — 3 Comments
Some people should really be reminded of their manners, from curious looks to downright stare fest, seriously. I have been getting this a lot lately. Yes, I am bald. Yes, I’m a woman. No, it wasn’t by choice that I’m bald. No, I’m not on Chemotherapy. Yes, those are extra-bald patches you see scattered all over the backside of my head. Yes, it’s a disease; and before you give me that look, no, it’s not infectious. It’s Alopecia Areata. Google it. Get over it.
I would say I found out…
ContinueAdded by IcedBit on February 20, 2013 at 5:00am — 6 Comments
Well my hair is growing back at a very rapid pace no bald spots just lots of hair don't like the colour grey and white though Hey but it's hair
Added by Annette on February 19, 2013 at 4:38pm — 15 Comments
Hey everyone, just dropping in to let everyone know that my hair did come back. Not perfectly, but beggars cant be choosers hey! Took 2 years though and still haven't got my facial back
Added by Shane Beard on February 18, 2013 at 7:12pm — 1 Comment
Hi - it's been a while since my last post about my nails that were lifting away from the nailbed. I've found something that seems to work - - although I have to say, it's pretty extreme. On two of my most affected nails where the nail had almost completely lifted away from the nail bed, I've received a cortisone injection at the cuticle line. Painful, but it seems to work. Next time, I'll apply some numbing agent the dr. prescribed before my next appointment.
Added by JMEL on February 17, 2013 at 1:00am — 3 Comments
Hi Everyone!
I am so so so so excited to be able to write on here to tell you all that the film that I have been talking to so many of you about over the years is finally on sale. My documentary - BABY LET YOUR HAIR HANG DOWN - about my journey with Alopecia Areata is available for you to watch. You can buy a DVD or download it from Amazon VOD.
The link to the film is here:…
Added by Georgia Van C on February 16, 2013 at 9:45pm — No Comments
Hi Everyone. It has been one year this month since I first lost all my hair and posted on Alopecia World.
I am happy to say it is growing back in. I still have a few small bald spots and the new hair growth is baby fine.But I will take what I can get.
I do want to say thank you to everyone on this sight for the support, it has really helped me cope.I did not feel so alone!!!!.…
ContinueAdded by Klo on February 16, 2013 at 4:58pm — 4 Comments
Added by Ryan on February 15, 2013 at 11:54pm — 2 Comments
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