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Comment by Children's Alopecia Project on January 12, 2012 at 11:05am

Our Children's Alopecia Project Group leader in the Cleveland area can be emailed at stacy.friedman@trelleborg.com, I am not sure of any other meetings from other groups. Take care!

Comment by Mr. Skinart on November 17, 2011 at 5:07pm

Hey guys, i'm new here. I dont have alopecia, my daughter does and I'm just trying to show her that she isn't alone. I know it is a very hard in todays society where the media demands we conform to the various boundries set by them. So please invite our friend request us. I am doin this all on my phone... My laptop its down for the count, so please show a patience in our response times. I'll be updating soon. Thanks.. Chris and Alaydren ite

Comment by Margie Jelar on November 7, 2011 at 8:33am

Alopecia Awareness Contest at My FB page: Margie Jelar (Mueller)





November 6, 2011 at 6pm to December 15, 2011 at 7pm

Alopecia Awareness Contest..getting the WORD OUT with Media attention!One click voting to spread the word..Details on FB-Friend me for details..(it won't let me add the direct link to the contest page-tried for 2 days now-i surrender!)See More.

Event posted by Margie Jelar

Comment by Margie Jelar on October 30, 2011 at 2:51pm

FELLOW OHIOIANS:here is my submission to ABC NEWS--What would you do, submitted today Sunday October 30th, 2011...(lets bring this show to OHIO!)
I am asking all my twitter and FB gal pals to send them a message as well..CoMON lets do this thing!!!!!

http://abcnews.go.com/WhatWouldYouDo/

TO ABC NEWS:
Alopecia Areata and the "Bald" woman! The reaction to this autoimmune disease in different settings/scenerios.!
Alopecia Areata is a VERY Emotional and Devasting disease!
In today's society, men are still acceptable to be "BALD", but women on the other hand get the looks,stares,the finger pointing OR the mistaken identity for having CANCER.
Our hair does not grow back, IF it does it usually ends up falling back out again.
We ARE victims of our H A I R...and NEED public AWARENESS to this disease and a CURE!!
STILL not sure-ask your wife, girlfriend. sister,mom,grandma, or any female you know, how she(they) would feel with having this condition!!
For more information on this subject please visit my website where you will read HONEST opinions on my ALOPECIA AREATA...www.omgmyhair.com

Comment by Margie Jelar on October 27, 2011 at 2:02pm

Cindy-yes I did receive that flyer...I am forming a group for the Northeast Ohio area,reaching CLeveland/Medina and all the way out past Orrville Ohio..it will b a 20 minute drive from any location!
Unless someone wants to drive further for some fun group times!
I still would like you to reconsider about the 2 groups getting together and cranking out some awesome fundraisers tho...
United we stand!

Comment by Margie Jelar on October 27, 2011 at 1:57pm

MAN, got to love this Ohio weather-today rainy,cold and no sun here today in the Wads area--BRR..when I get more time I will upload some awesome photos for everyone to see!
I'll put it on my:100 things to do list-LOL..my humor-ME BAD!

Comment by Cindy Molnar on October 26, 2011 at 4:55pm

Hi Margie - Did you get a flyer in the mail about our support group meeting on Mon Nov 14th in Akron? Hope you can come, haven't seen you in awhile.
I don't know of other support groups in Ohio. I run the Canton/Akron Support Group. There used to one in Cincy and Columbus, but they stopped having them.

Comment by Margie Jelar on October 26, 2011 at 1:27pm

I am in the Wadsworth Ohio area.
I have had AA for 1 year and 4 months now.
It will be great to talk with other Ohio people about Alopecia.
Thanks,omgmyhaircom

Comment by Colleen on October 25, 2011 at 2:58pm

Hi everyone, I am new to the site. I was diagnosed with AA almost a year ago, I am in the Columbus area and would love to meet other people from around here! Or if anyone knows of anythign going on in the Columbus area let me know =) !

Comment by Children's Alopecia Project on July 25, 2011 at 7:30pm

CHECK OUT ALOPECIAPALOOZA!!

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