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I hope this is ok to post.. February 06, 2008 4:29 AM

 

Announcing the inaugural Las Vegas Walk for Lupus Now!

The Lupus Foundation of America (LFA) is responding to requests from our Las Vegas constituency for more direct patient services in your community.  To meet these needs, the LFA will be hosting our first fundraising Walk to provide the funds necessary to deliver these imperative services.  The money raised in your community will stay in your community!

Your help is needed to ensure a successful event!  If you would be interested in learning more about the event and how you can be involved, please plan to attend our organizational meeting!

Las Vegas Walk for Lupus Now!

                  Organization Meeting                 

Feb 19 10:00 AM

At 2797 S Maryland Parkway sweet 12 Anthem near the blue sheild cross in Las Vegas NV


Please RSVP to Terry Sanders at Sanders@lupus.org
or 877-910-9779.   
If you are comming please contact Terry Sanders at
Sanders@lupus.org or 877-910-9779.

Providing research dollars for the future

and help for persons living with lupus today!

~Passionate, Purposeful, Mission Driven~

The Lupus Foundation of America

 

Terry Sanders
National Walk Director
Lupus Foundation of America
2000 L Street NW
Suite 710
Washington, DC  20036
VM/Fax: 877-910-9779
Cell: 219-718-4565
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anonymous  February 06, 2008 4:48 AM

this is ok to post.  i cant get on there site i wanted to check it out.  [report anonymous abuse]  [ accepted]
 
anonymous  February 06, 2008 5:37 AM

me too.. i cant get to it. my next door neighbor has lupus.  i know quite a bit about it. watching her suffer over the years.   [report anonymous abuse]  [ accepted]
 
 February 06, 2008 6:54 AM

Try this: http://www.lupus.org/newsite/index.html

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anonymous  February 06, 2008 6:55 AM

thank you jim, got it.  [report anonymous abuse]  [ accepted]
 
anonymous  February 06, 2008 10:39 AM

Thank you for this update. I have a dear friend that has Lupus and she has been put on a respirator now for the rest of her life. It is a very heartbreaking disease.  [report anonymous abuse]  [ accepted]
 
Filling you in on the walk.. February 10, 2008 1:46 PM

We got the date for the Lupus walk so thought I would fill you in.
Our Lupus Walk in Las Vegas Nevada is in April

At: Mission Hills Park
551 E. Mission Drive
Henderson, NV
Saturday, April 26, 2008 9am-12pm

You do not have to live in NV to help.

I would like to share with you about what The Lupus Foundation Of America is
trying to Do. The Lupus Foundation Of America is trying get an office here in Las Vegas we have doctors who will volunteer their time to help Lupus patients that have no insurance.

I invite you to join my team to help get donations so Las Vegas can
have an office for Lupus patients you can join my team or just donate
on to my page, if you choose to join the team and are able to have your family
and friends donate it would help us get to our goal a lot faster.
here is the link.
This link explains even more so on our cause.

https://www.kintera.org/faf/donorReg/donorPledge.asp?ievent=265274&lis=0&kntae265274=B40DA008085A48989001B7A860C3D142&supId=204526128



I do not think people out of USA can donate because of the exchange rate has to be converted. But those in USA can..

Please if you can pass this on to those who are in USA and who would like to help us.

Thank you Hugs Angela

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Sorry about your friend who has Lupus February 10, 2008 1:49 PM

So sorry to hear about your friend who has Lupus.

Lupus can do a lot to a person we just never know. My prayers are with her and family.

Sorry I took so long to get back to post.

Hugs Angela

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anonymous  February 10, 2008 3:14 PM

Angela, Thank you for your concern. She has also had triple by pass in the last 2 years. Her name is Linda and she has been through alot. She has a great husband that gives her support also. Blessings, Jaylena  [report anonymous abuse]  [ accepted]
 
 February 10, 2008 5:29 PM

It is good she has a husband who is supportive.

Sending prayers for Linda. Hugs Angela

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