#140Conf Panelist, Amanda Greene – @LALupusLady On… Sharing Passions and Hugs at the #140conf

#140Conf Panelist, Amanda Greene – @LALupusLady On… Sharing Passions and Hugs at the #140conf

Press Announcements FDA approves Benlysta to treat lupus

Here is the official news release.... Press Announcements FDA approves Benlysta to treat lupus

the long wait is over the FDA has approved a new drug for Lupus. Welcome Benlysta!

Alliance for Lupus Research Mobile Giving!

There are a lot of great activities and Lupus awareness projects coming from the Alliance for Lupus Research.  Tomorrow is the first day when the mobile giving campaign will be up and running for the ALR, I can't wait to tell you about the great news - especially if you live in the Boca Raton or Chicago areas.


Sunday March 6, 2011 I am excited to share that the Alliance for Lupus Research mobile giving campaign will take place during the Boca Raton Walk.  Text the word "WALK" to 85944 to make a $10 donation.  Forward this information to all your friends so that they can help too.


Can’t make it to the Walk? Any text donation made between Sunday, March 6, 2011 and Sunday March 13, 2011, will be credited towards the 2011 Boca Raton Walk. It’s quick, it’s easy, and it’s fun. Help the Alliance for Lupus Research lead the way to find a cure for lupus!


This Sunday (March 6, 2011) is the Alliance for Lupus Research Chicago Wolves’ Lupus Awareness Hockey Day against the Manitoba Moose at the Allstate Arena in Rosemont. The game starts at 3:00 p.m. with doors opening at 2:00 p.m. Before the game, be sure to stop by the ALR table in the concourse and enter our raffle to win an Anthony Stewart game worn jersey.


For every ticket purchased, $3.00 will be donated to the Alliance for Lupus Research.
In the Chicago area but you can't make it to the game, be sure to watch it on WPWR Channel 50. 11 year old Chicago Walk family volunteer, Gus Kalivas, will be dropping the puck at the beginning of the game!


The Alliance for Lupus Research will also be holding their mobile giving campaign during the game on March 6, 2011  Text the word "Lupus" to 85944 to make a $10 donation or text "ALR" to 85944 to make a $5 donation. Any donations that are texted on March 6, 2011 to the ALR will be credited towards the 2011 Chicago Walk.  It’s quick, it’s easy, it's fun. Help the Alliance for Lupus Research lead the way to find a cure for lupus!  


A one-time donation of $10 will be billed to your mobile phone bill.  Messaging & data rates may apply.  Donations are collected for the Alliance for Lupus Research by mobilecause.com.  Reply STOP to 85944 to stop. Reply HELP to 85944 for help.  For terms, see www.igfn.org/t. All donations made through this program go to the specific Walk and not towards a specific team.  Alliance for Lupus Research
If you have any questions please feel free to email haldama@lupusresearch.org.

Wonder is where you find it...

Barbara Biziou, is an inspiring life coach and author whose books and workshops have tremendously enhanced my enjoyment of life.  Her website offers insights and lessons on how to celebrate today.  Earlier today I received the March Newsletter from Barbara Biziou and www.joyofritual.com I feel compelled to share this with you:

The man whispered, God, speak to me, and a meadowlark sang. But, the man did not hear.

The man looked around, hearing nothing so the man yelled, "God, speak to me! And the thunder rolled across the sky.

But, the man did not listen.

The man looked around and said, God let me see you"

And a star shined brightly. But the man did not notice.

And the man shouted,

"God show me a miracle!" and a life was born.

But the man did not know. So, the man cried out in despair, Touch me, God and let me know you are here!"

Whereupon, God reached down and touched the man, but the man brushed the butterfly away and walked on."

Don't miss out on a blessing because it isn't packaged the way that you expect.

I know that dreams come true and visions work.  Listen to your world and be aware of everything because you never know where you will find your spirit.  I believe that every thing in my life has come together to help me become the woman I am today.  Still figuring out how to be comfortable in my skin, while living and thriving with Lupus.  I am so much more than the disease.  I am learning how to be who I am a spirited woman who finds healing in many ways.

Tonight I am going to find healing at the El Rey Theater as Veronica Varlow performs with Emilie Autumn and the Asylum.  May you find healing wherever you are.  Happy Wellness!

Lupus Advocacy is important!

I know what it is like to go to Washington, DC to advocate for Lupus Research.  I remember the exhaustion... I remember the sore feet... and I remember why I did it.  I went to our nation's capitol because over 1.5 million Americans have Lupus.  Lupus is one of the lesser-known major diseases in the United States, Lupus is an autoimmune disease that effects each individual patient differently.  If I was on Capitol Hill today I would be joining the team of Lupus Advocates that are meeting with members of Congress, (or more likely, a Health Legislative Aide) today to discuss the importance of funding Lupus medical research by telling my story of what living with Lupus has been like for me the past 28 years.  I would tell you that it may not have been easy but it was "much better than the alternative".

If you have Lupus or someone you know has Lupus.  Please raise your voice and let your Senators and House members know that you are a constituent who is an advocate for Lupus and you vote.  Let your voice be heard...

The Lupus Foundation of America is going to Capitol Hill today to ask for:

 

Increase funding for Lupus Medical Research at the National Institutes of Health (NIH).

 

Fund the establishment of a Lupus Medical Research Program, established under the Congressionally Directed Medial Research Program (CDMRP), Defense Health Program (DHP), Department of Defense (DoD).

Continue funding for:

The National Lupus Awareness Campaign at the U.S. Department of Health and Human Services' Office on Women's Health (OWH) which increases public awareness of Lupus in order to increase early diagnosis of Lupus.

The Health Provider Education Campaign at the U.S. Department of Health and Human Services' Office of Minority Health (OMH) which increases health professional providers' awareness of Lupus to improve Lupus diagnosis and treatment.

Lupus has a tremendous financial cost to the nation, estimated at $31.4B annually, but the cost of inaction will only make those numbers grow.  We cannot afford to wait.  

http://capwiz.com/lfa/home/

I am a writer for ButYouDontLookSick.com ~ Put Your Best Face Forward!

I am so excited and proud to announce that I am one of the new Staff Writers on the website ButYouDontLookSick.com

Product Review Nicole Paxson “Mimosa” Liquid Foundation: Put Your Best Face Forward!

My Review of Junk Food New York Jets Vintage Distressed Triblend T-Shirt

Originally submitted at NFL

Like players need their uniforms, you need your game day gear! The Junk Food® vintage distressed triblend tee looks great whether you're hitting up a tailgate or hosting at home. Your team's script name, logo and "Football" are each screenprinted onto the chest in a distresse...

Junk Food New York Jets Vintage Distressed Triblend T-Shirt

J-E-T-S T-shirt!

By LA Lupus Lady from Los Angeles, CA on 1/18/2011

 

4out of 5

Sizing: Feels too small

Pros: Stylish, Shows Off Team Pride

Best Uses: Around Town, At The Game, Watching The Game on TV, Anytime

Describe Yourself: Sports Enthusiast

Super t-shirt! Bought using the Wildcard Network to help support the Jets for Wild Card Weekend ~ my new lucky shirt, it works!

(legalese)