New boy in town ..,
looking for friends and a new life ... LOL Thanks for beeing strong and beutiful .., I like youre oictures very much ... The Author
Hey Kimberly. You have arrived! Nice. I won't be at the meeting because I have class tomorrow night. You should go for sure. They meet for pizza at Georgios Pizza at Clement and 3rd at 6pm before the meeting which starts at 7:30pm. If you give me your email I will send you the flyer!
I'll be at the meeting tomorrow night at 730
It's at Geary and Divisadero streets. I dont have the exact address but it's on the 5th floor in the Jade Room.
Fred is our Support Group Leader you can call him for more info. 650-759-4760. Look forward to seeing you there.
yep, im a concert junkie, the last show i went to was mudvayne and static-x, before that was 311, and yes i do play an instrument, i have been a drummer for 13 years, and i'm closer to LA then SF but i do frequent santa cruz when i can.
Hey Kimberly! I'm glad to hear you are moving back to San Fran. We have a pretty good group of alopecian friends out here. We get together for lunches and meetings all the time. I look forward to meeting you and including you in our little get togethers!
Hi everyone, thanks for sayin hello to me. i haven't met anyone else yet with my condition, im nervous if i do waterworks may not be held back.im welling up now just knowing you guys have been struggling with me but seem to be handling it better(sound so positive).i cant bring myself to wear a wig or just shave it.and i hate it when i get brushed off by friends or family by saying"kim, i can't even tell you are losing hair" like its no big deal if they cant see it...they have no idea what i do everyday to hide it best with different hair parts, hairspray,brown colored talcom powder, hair pieces i clip in, hats hats and more hats etc.........it wears me down, not to mention the constant anticipation of what changes my hair will go through next month more growth or more fallen out.argh emotionally and physically draining. to think this could be the rest of my life.depressing.all the adjustments like what jobs can i do with least amount of embarrassment, where can i live, do i hide in the country(im doing now), or shave and be cool shnead o'connor in the city(but my head is too small and weird shaped for shaving,just not my style). I am 4 years into this dilema.sometimes 50% hair gone(the part under the top layer of hair luckily so i can hide it), some year it was a good portion of the top(it was a hat and colored powder year), just keeps duin its thing moving all around then growing back. well this is long. feels like a jounal.i check my emails every 2 weeks or so, but if anyone reads this that knows of actual meetings with others in my area, please let me know. that means you jeffrey that lives in San Francisco, let me know puh-lease(wed nites?) thanks y-all kimberly
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Kimberly Foote's Comments
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No worries. I didnt realize you are living up at The Russian River.
Have a great weekend. I'll be working.
Jeffrey
Let me know. I booked a table for 10 so far.
Jeffrey
What you doing 12/12/09? I am putting together an alopecia holiday bash.
Jeffrey
I was going to tell you about pizza but looks like Matt allready did.
See you tonight!
Jeffrey
-Matt
I'll be at the meeting tomorrow night at 730
It's at Geary and Divisadero streets. I dont have the exact address but it's on the 5th floor in the Jade Room.
Fred is our Support Group Leader you can call him for more info. 650-759-4760. Look forward to seeing you there.
Jeffrey
Would be great to see you there.
Jeffrey
Whats going on?
We have a NAAF Meeting coming up in November if you want to attend.
It's the 3rd wed at 7pm.
Hope all is going well with you.
Jeffrey
Joel
Good news you're in Napa Valley (hope you are enjoying the wine)
Bad news hair shit sucks but it does get better (just like the wine)
Cheers,
Jeff
What kind of aa do you have? I have had au for 20 years -- started with aa 30 years ago.
How are you today?
LeslieAnn
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Any mention of products and services on Alopecia World is for informational purposes only; it does not imply a recommendation or endorsement by Alopecia World. Nor should any statement or representation on this site be construed as professional, medical or expert advice, or as pre-screened or endorsed by Alopecia World. Alopecia World is not responsible or liable for any of the views, opinions or conduct, online or offline, of any user or member of Alopecia World.