Alopecians in Wisconsin.

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Alopecians in Wisconsin.

A group for Wisconsinites to meet and greet. We also welcome Wisconsinite friends and folks who have been here and love our state as we do. Remember if you don't have anything kind to say about our Midwest accent, best not to say anything at all:).

Members: 53
Latest Activity: Oct 15, 2017

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Comment by Josh and Kiah on February 9, 2015 at 3:11am

Greetings All!

Quick update informing everyone of the upcoming support group meeting on Thursday, Feb 26 at 7pm. Whether you need support, or can offer some to someone else who may be going through a difficult time, we really hope you all can attend. Details can be found on the flyer above.
We recently launched a facebook group to help local families communicate with one another and discuss issues that are important to them or ask questions. This is a CLOSED GROUP, which means it is not open to the public to view. This is so everyone feels comfortable sharing thoughts or feelings in a safe place. You can find the group at 
Join the group and help us continue to build our community! Parents of children/teens with alopecia...please share this page so they can join as well! 
Comment by Susan Innes on December 18, 2014 at 7:37pm
Hope love, compassion and kindness is bestowed upon all of you over the holidays, and thanks Josh and Kiah for all of your wonderful events and support! Susan
Comment by Damani on December 4, 2014 at 5:37pm

Josh. Wishing you a great meeting tonight. Unfortunately with schedule changes, I won't be able to join, tonight. Appreciate you and your leadership!

Comment by Josh and Kiah on December 4, 2014 at 2:55pm

Hey all here are the details of tonights support group meeting. Hoping some of you can make it. 

Comment by Josh and Kiah on September 11, 2014 at 4:12pm
Hey Josh. Not positive when next support group meeting will be. We just finished held or big fundraising event, Rock for Locks and Morgans Ride for Alopecia last weekend and are still wrapping that up. We do however, have another event tomorrow. Alopecia Awareness night at Miller Park. I still have free tickets available for anuome who wants to join! Let me know asap!
Comment by JoshMcCann on September 10, 2014 at 10:41pm
When, if any. Is the next support meeting/gathering? Id love to make it!
Comment by Josh and Kiah on March 26, 2014 at 3:16pm

ATTENTION WISCONSIN WOMEN WITH ALOPECIA!!! 

2011 Miss America Finalist Kayla Martell has teamed up with a local hair clinic in Milwaukee to offer a women's HAIR MAKEOVER GIVEAWAY!!! Currently, they are trying to gauge interest in this. If you or someone you know would be interested please email Kayla at kaylaruthmartell@gmail.com with "Milwaukee Makeover" in the subject line! Please contact Kayla ASAP so we can show that there is indeed interest. Participants should be between the ages of 13-45. Thank you and let me know if you have questions!!

Comment by Josh and Kiah on March 26, 2014 at 3:15pm

Comment by Josh and Kiah on March 26, 2014 at 3:14pm

Well if weather permits we would love to have you! I can ask around to our group about the dolls. I have some newsletters too... but could certainly make yours available to hose who might want them at a meeting. Keep me posted!

Comment by Susan Innes on March 24, 2014 at 10:46am
Josh and Kiah..thank you for the update. It doesn't look like the weather is going to present dry road conditions for a trip there; however, I'm determined to attend one of the upcoming sessions. Also, I've male and female Komfy Kid dolls, 1 each, that need to find homes, as well as about 50 editions of past NAAF newsletters in case people would like to read the very inspiring articles. I'd love to bring these when I come (or if someone would like something shipped to them, please let me know.) Hope all survived the winter well. "Hugs" Susan
 

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