Long Island-based wigstress Yael Hirsh, hosts a custom-made line of human hair wigs & pieces. In addition to custom wigs, ready made pieces & wigs are available to try on.
Expert cut, color, styling & repair services are all offered in her Long Island home, where luxury & quality meet in a private setting. Loyal patrons swear by Yael's know-how and flock from all over the world to sit in her chair.
Expertise
Raised in the world of human hair wigs Yael is a seasoned expert and veteran in her industry, backing the quality of all her products.
You tell Mia that I miss her too! It's been so strange seeing ordinary kids when I'm out now - ;-). I'm all alone in being bald again! LOL! Love you guys!
my sons in new york on business and he's been telling me to shave off my spars fluffy regrowth for years.
I recently received a freedom wig..suction wig..vacume wig.
My daughter is growing her sons hair in order to donate it for some child with Alopecia.
They can swim in it too.
Although I have gone without hair due to allergies to synthetic wigs..besides, they are way too big for my head.After all, they are really made for people with hair.
Suction wigs are the closest thing to having your own hair...so I'm happy.
I don't shave every day..yet do so when I wish to simply play fancy dress for myself...cause deep down..we still want to see how we look with hair.
hi Maria,
are you guys going to the alopeciapolooza in philadelphia in aug? we're going and Paige is so excited. let me know if you guys are going. say hi to Mia.
Hey Maria, How was your trip to Florida? We got back Wed and then Thurs was Sam's birthday and party. Needless to say I am wiped out for the week. I am trying to plan a trip to Ny in April to see my friends. I will keep you posted if I do. would love to meet up if we can.Let's chat online soon..Cindy
Hi Maria, of course we remember you! We will definitely be attending the Alopeciapalooza this August. I've already booked our room and I'm really looking forward to it. Will you be attending?
I love the pictures of Mia, there are so adorable. She makes a fantastic Snow White!
Have a wonderful Valentine's Day and I hope to see you in August!
Hi Maria! Nice to meet you. My daughter, Kendall, is also 4 (will be 5 next month). Kendall's alopecia happened very rapidly..we've been dealing w/ this since 10/08. It took a couple of months to overcome the shock before I realized I needed to seek a support group. Have met lots of nice people on AA. How's Mia handling what's happening? I'm surprised how well Kendall has adjusted to being bald, including losing her eyebrows/eyelashes/nose hairs (her hair was past the middle of her back). We have hope that it will all return, but preparing for if it doesn't.
Mia is such a cutie..
hi Maria,
how was your Christmas? ours was great. i'm happy to relax a little now. ok, so here's my latest thing. i started the kids on a gluten free diet. it's pretty hard but they seem to be adapting ok. i've read so much about it and bought some books today to better understand how to live without all those foods. i've seen some stories on line of people linking celiac disease with hairloss. who knows? how is mia doing? email me the pictures soon if you can. talk to you soon.
hi Maria,
how is Mia doing? Paige is completely bald at this point. her eyebrows had fallen out too. now strange things are happening. her eyebrows are growing back but they are brown. in the past she was extremely blonde with really light eyebrows. then last night while she was sleeping, i was staring at her head with a flash light. weird, i know, but it's the best way to see if there is any growth. her entire head is covered in a layer of fuzz. this is the way it happened last time when it completely grew back. i have no idea if this is growing back for sure, but i have such a feeling of hope right now.
how are things at school for mia? Paige has her school picture friday so that's on my mind. hope all is well.
Maria, Samantha is not minding the cod liver oil at all..All the reading I have done said it is good for hair and nails as well as lot of other things and it serves as an anti-inflammatory to fight the white blood cells. If you decide to try it get the Carlson's lemon flavor. Sam takes it in a medicine cup. I ordered the lozenges in 5000 mg too..
HI Maria, you have on tough kid. Have you sat done and talked to her about this treatment being the best thing to try to make her hair grow. We have told Samantha that when her head gets red and itchy her body is telling the bad guys to go away so her hair can grow. Sam is pretty good about treatments, but telling her that seemed to make her happy and distracts her from the irritation. During the hours you put the med on maybe you can do a special activity with Mia to distract her. For Sam when we put the stuff on we usually bake or read a book. It keeps her from touching her head to the let treatment dry. Make the hour a special time with Mia. I wish I had some magical powers. Have you thought about getting her a my-twin doll that has Mia's hair loss. If she likes dolls it may help...Sam has a doll from them, but she is not big into dolls. Have a good day.
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Maria, Mia's Mom's Comments
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How are you and Mia?
Tracy
Give Mia a big hug from me!
I recently received a freedom wig..suction wig..vacume wig.
My daughter is growing her sons hair in order to donate it for some child with Alopecia.
They can swim in it too.
Although I have gone without hair due to allergies to synthetic wigs..besides, they are way too big for my head.After all, they are really made for people with hair.
Suction wigs are the closest thing to having your own hair...so I'm happy.
I don't shave every day..yet do so when I wish to simply play fancy dress for myself...cause deep down..we still want to see how we look with hair.
are you guys going to the alopeciapolooza in philadelphia in aug? we're going and Paige is so excited. let me know if you guys are going. say hi to Mia.
I love the pictures of Mia, there are so adorable. She makes a fantastic Snow White!
Have a wonderful Valentine's Day and I hope to see you in August!
Mia is such a cutie..
how was your Christmas? ours was great. i'm happy to relax a little now. ok, so here's my latest thing. i started the kids on a gluten free diet. it's pretty hard but they seem to be adapting ok. i've read so much about it and bought some books today to better understand how to live without all those foods. i've seen some stories on line of people linking celiac disease with hairloss. who knows? how is mia doing? email me the pictures soon if you can. talk to you soon.
Cindy
how is Mia doing? Paige is completely bald at this point. her eyebrows had fallen out too. now strange things are happening. her eyebrows are growing back but they are brown. in the past she was extremely blonde with really light eyebrows. then last night while she was sleeping, i was staring at her head with a flash light. weird, i know, but it's the best way to see if there is any growth. her entire head is covered in a layer of fuzz. this is the way it happened last time when it completely grew back. i have no idea if this is growing back for sure, but i have such a feeling of hope right now.
how are things at school for mia? Paige has her school picture friday so that's on my mind. hope all is well.
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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.