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.
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.
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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.
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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.
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
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