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« on: September 16, 2008, 09:24:19 pm » |
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It will cost $140 for Marie to do her part, design and create the bus bench back. Monthly funds will be needed to keep it up. We'll talk about that later
But for now, I want to know which design do you prefer?
Top or bottom?
I also would like for her to create our banner (remember the one I tried to make using purple tape?)
Matching business cards as well as postcards is on my list 
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« Last Edit: September 17, 2008, 12:17:48 am by Adminஐﻬ »
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 I look normal, as I have an "Invisible Illness". You can not catch it, you can not see it. It's called Lupus.My body is attacking itself on the inside.  www.LupusMCTD.com Represents: 1) We are patients helping researchers build a future for the lives of others... 2) Where HOPE is a WORK In Progress 3) Pay It Forward~Giving Back To The Future Lupus/MCTD Patients |
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Adminஐﻬ
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« Reply #1 on: September 17, 2008, 05:12:43 pm » |
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Don't forget to vote!!"
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I look normal, as I have an "Invisible Illness". You can not catch it, you can not see it. It's called Lupus.My body is attacking itself on the inside. www.LupusMCTD.com Represents: 1) We are patients helping researchers build a future for the lives of others... 2) Where HOPE is a WORK In Progress 3) Pay It Forward~Giving Back To The Future Lupus/MCTD Patients |
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Crabbyla279
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« Reply #2 on: September 17, 2008, 06:02:28 pm » |
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Momma~
I voted for the one on Top (I think... can't remember now lol) I just think that it looks better.
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Adminஐﻬ
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« Reply #3 on: September 17, 2008, 06:26:21 pm » |
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Momma~
I voted for the one on Top (I think... can't remember now lol) I just think that it looks better.
Thank you Honey for voting 
My poor charge card this year.... keychains, bracelets,tatoos, tank tops, trademark fees, now bus benches!!!
Will it ever stop on spreading lupus awareness? lol
My next plan is get a bus bench in say Kansas or Colorado (which ever is cheaper) then one more bus bench on the east coast.
That should finish up this years lupus and MCTD awareness
I did write to my newspaper which can be read online asking them to do write up on this site. I have not heard back from them yet.
Thank you for voting, I hope everyone does!!!
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I look normal, as I have an "Invisible Illness". You can not catch it, you can not see it. It's called Lupus.My body is attacking itself on the inside. www.LupusMCTD.com Represents: 1) We are patients helping researchers build a future for the lives of others... 2) Where HOPE is a WORK In Progress 3) Pay It Forward~Giving Back To The Future Lupus/MCTD Patients |
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Adminஐﻬ
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« Reply #4 on: September 18, 2008, 08:58:02 pm » |
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 BUMPING UP, AS I NEED AS MANY VOTES AS POSSIBLE ASAP
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I look normal, as I have an "Invisible Illness". You can not catch it, you can not see it. It's called Lupus.My body is attacking itself on the inside. www.LupusMCTD.com Represents: 1) We are patients helping researchers build a future for the lives of others... 2) Where HOPE is a WORK In Progress 3) Pay It Forward~Giving Back To The Future Lupus/MCTD Patients |
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chiara38
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« Reply #5 on: September 18, 2008, 11:14:05 pm » |
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Hi kathy..voted the top one..I like the edge around it better..black is soooooooo deathly looking..laugh out loud...great job gang..love you all..peace joy. love...we walk by Faith not by sight.....Hope for tomorrow...All this shall pass...rest well...hugs..Clare....
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Adminஐﻬ
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« Reply #6 on: September 18, 2008, 11:34:52 pm » |
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Hi kathy..voted the top one..I like the edge around it better..black is soooooooo deathly looking..laugh out loud...great job gang..love you all..peace joy. love...we walk by Faith not by sight.....Hope for tomorrow...All this shall pass...rest well...hugs..Clare....
Thank you for voting Clare, I need MORE members to vote so I can decide what to do
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I look normal, as I have an "Invisible Illness". You can not catch it, you can not see it. It's called Lupus.My body is attacking itself on the inside. www.LupusMCTD.com Represents: 1) We are patients helping researchers build a future for the lives of others... 2) Where HOPE is a WORK In Progress 3) Pay It Forward~Giving Back To The Future Lupus/MCTD Patients |
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chiara38
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« Reply #7 on: September 19, 2008, 12:17:54 am » |
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u r welcome...Do we vote only once? Clare |
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Adminஐﻬ
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« Reply #8 on: September 19, 2008, 12:31:29 pm » |
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u r welcome...Do we vote only once? Clare yes one vote only |
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I look normal, as I have an "Invisible Illness". You can not catch it, you can not see it. It's called Lupus.My body is attacking itself on the inside. www.LupusMCTD.com Represents: 1) We are patients helping researchers build a future for the lives of others... 2) Where HOPE is a WORK In Progress 3) Pay It Forward~Giving Back To The Future Lupus/MCTD Patients |
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Lupus/MCTD Awareness