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Erin posted a discussion

A Fundraiser for the Children's Alopecia Project

If you are in or around the St. Louis area please consider joining us for "A Night at the Ballpark" with the River City Rascals on June 13th at 5:00. The Rascals will be taking on the Washington Wildthings, tickets will be sold for $9.00 each and all proceeds will go to support CAP programming. Contact Erin Burke at erinjane1@att.net for more information or to purchase tickets.
Apr 7, 2010
0 Comments
Erin replied to Lisa's discussion Meeting Friends
"We're just outside of St. Louis. Our son, 4 y.o., has AA. We're always looking for new friends...."
Jan 24, 2010
Erin replied to Lisa's discussion Depressed
"We live just outside of St. Louis, our son has AA. We are always looking to meet people that are experiencing similar things. Send us a message if you would be interested in meeting."
Jan 24, 2010
Erin and Children's Alopecia Project are now friends
Sep 23, 2009
Erin posted an event

CAP MO/IL Support Group at MO/IL

September 12, 2009 from 3pm to 5pm
Come join the MO/IL support group for our September get together on Sat., Sept. 12th at 3:00. Email Erin at capkids@charter.net for more information.
Sep 1, 2009
0 Comments
Erin joined rj, Co-founder's group
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Non-alopecians in Alopecia World

If you're a member of Alopecia World and you do NOT have alopecia, you should join this group. Share your unique concerns as a non-alopecian who's truly supportive of alopecians. Let us learn from our shared experiences.
Apr 11, 2009
30 Comments
Erin joined Children's Alopecia Project's group
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Children's Alopecia Project

CAP is the only non-profit devoted specifically to children living with alopecia. Please continue to visit all the other great groups and sites but visit here with questions about CAP and how you can become involved.
Apr 11, 2009
6 Comments
Erin updated their profile
Mar 31, 2009

Profile Information

Relationship Status:
Married
About Me:
I am the mother of a wonderful 3 year old little boy with alopecia.
Do you have alopecia?
Parent or guardian of child with alopecia
Are you age 18 or older?
Yes - I am 18 or older

Comment Wall (6 comments)

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At 5:00pm on January 16, 2009, Cherylnz said…
Hi Erin
Welcome to Alopecia World
At 10:48pm on January 8, 2009, Eileen Simpson said…
Hi and welcome,
I hope you find your time spent here well spent. If I can help in any way please let me know.

Eileen
At 4:54pm on January 4, 2009, LeslieAnn Butler said…
Hello and welcome, Erin!
How are you and your boys today?
LeslieAnn
At 6:42am on January 4, 2009, 3wwasha said…
Hello,

Welcome to alopeci World.

Aysha
At 1:14am on January 4, 2009, Cheryl, Co-founder said…
Hi Erin, I wanted to take this opportunity to welcome you to Alopecia World. I have been living with Alopecia Areata since 1991 and know full well the struggle it can be. I look forward to getting to know you. Cheryl, Co-founder
At 10:30pm on January 3, 2009, rj, Co-founder said…
Hi, Erin. Welcome to Alopecia World! This is a great place for great people, so be sure to make your positive presence known. :-) - rj, Co-founder
 
 
 
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