Comment

Comment by Caged_liberty on September 22, 2017 at 3:49pm

Hi. I am a henna artist and one of the founders of the non profit metamorphosis project. We provide free henna body art, makeover and photoshoot to selected candidates who need a little reminder of their true beauty. As it is alopecia awareness month, I am looking to connect with people with alopecia. If you are interested in getting a free henna crown and creating awareness through body art, please email me at contact@ineedhenna.com. Thanks

Comment by Jody Gorski on March 6, 2017 at 1:51pm

There is a support group meeting for Michigan 

Tuesday March 7th, 2017

6:30pm-8:30pm

Clinton Macomb Public Library (Conference Room B)

40900 Romeo Plank Rd.

Clinton Twp, MI 48038

Please RSVP and let me knowsbooza814@hotmail.com

Comment by Katscratchfvr on June 10, 2016 at 4:50pm

Kalamazoo here. Looking for support for my 8-year-old son.

Comment by Liisa on April 26, 2015 at 12:04pm

Anyone from Upper Michigan?

Comment by Dedi on July 2, 2014 at 5:14pm

Hey...I'm an alopecia in K-Zoo

Comment by Gooberoobu on June 22, 2014 at 3:00pm

Any Alopecians near Kalamazoo??

Comment by Jody Gorski on September 6, 2013 at 10:32am

Hello Michiganders
I cannot make the Naaf baseball game...are there any other events for alopecia awareness month that you know of?
thanks
jody

Comment by alamogirl/ aka Judy on December 27, 2012 at 8:32pm

Is there anyone with alopecia living in the Grand Rapids area? I would LOVE to connect with some face time. The boards are great but not totally satisfactory.

Comment by Caitlin Riley on December 8, 2012 at 8:52am

First Support Group Meeting in Ann Arbor!!!
Saturday, JANUARY 12, 2013
1PM – 3PM
Ypsilanti Public Library
229 West Michigan Avenue
Ypsilanti, MI 48197

RSVP caitm.riley@gmail.com

Comment by Caitlin Riley on November 4, 2012 at 6:48am

Hello alopecia world community! I am starting an alopecia support group in Ann Arbor, MI. The group will have its first session in January. For more information, contact me by email caitm.riley@gmail.com or message me for my number.

Caitlin Riley
Support Group Leader
National Alopecia Areata Foundation

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