Comment

Comment by John R on November 9, 2010 at 10:01pm

VG- I agree, it would be great to set up a meeting. Maybe early December or after New Years. Holidays coming up fast. I assume most of us are in NoVA? We can brainstorm location, I'm thinking happy hour...dinner...movie...not sure... I think just to meet some of you would be cathartic for me. I deal with this thing by ignoring it, fighting it, hiding it - so meeting you folks will be an interesting emotional event for me.

Comment by For VG on October 13, 2010 at 9:16am

Well folks, looks like in the past few weeks at least 4 us from NoVa have expressed interest to meet-Kristen, VG, John and Sarah. We can probably set up a date and location to have a group talk. Thoughts???

Comment by Kristen Ridenhour on October 6, 2010 at 7:54pm

Hey everyone. I grew up in nova and have lived down in Orlando, FL for the past 4 years. I just moved back up here this week for a job. It'd be nice to meet some of you up here.

Comment by For VG on October 3, 2010 at 11:13pm

Great to see a group for NoVa. Has there been any meeting so far?
Any future meetings? Tks.

Comment by John R on September 26, 2010 at 6:27pm

Hi all - I've been looking for a group in the NoVA area. Since diagnosis over 7 years ago I have never spoken to anyone with AA. It would be nice to have a group to talk to.

Comment by Sarah y. Clingman on August 17, 2010 at 9:15pm

Looking forward to see this come together. I'm just learning how to work this site so hopefully I will stay in touch. I'm about 1hr from Richmond so works for me:)

Comment by Laura on April 13, 2010 at 4:51pm

Here is the link at NAAF for info on community awareness activities.
http://www.naaf.org/site/PageServer?pagename=programs_events_fund

Comment by Laura on April 13, 2010 at 4:48pm

Hi all

First, I should be upfront here that I do not have alopecia, but my sister Sarah who lives in Texas has has alopecia universalis for 2.5 years. My ister goes by Sarah S on this site - not be confused with Sarah Seward though :) . I am a member of the group non-alopecians in alopecia world to help me find ways to more effectively support my sister.

Anyways, I would be happy to help out with any awareness event in the RIchmond area since I live here. I think that the national alopecia areata foundation (naaf) has some information on how to coordinate a run/walk event.

Comment by Sarah Seward on March 10, 2010 at 11:14pm

No problem! Yes I think we all should. Hopefully more people will join the group. I just think awarness needs to be brought to attention. Maybe in the long run I would like to hold a run/walk event to raise money for the organization. We should defintely all make some time to get together!

Comment by Shera on March 10, 2010 at 8:58pm

Hi Sarah .. thanks for putting this together. Sam and I were talking about getting together in Richmond once we can find a day & time that works.

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