Hello Strangers
Hi I'm back! It's been 200+ days since my last post; this is what happened. I was only getting comments from web crawlers and people who want me to enlarge my penis size so I got discouraged and quit. That's why I always ask for comments. I always quit things far too quickly that are good for me; I truly am my worst enemy. I started believing that the only people who visit my blog are web crawlers and spammers. But the other day I went on my website for the 1st time since my last post and saw how many of you visited. I couldn't believe my eyes! You are still here and growing. You didn't quit on me even though I quit on myself! I love you and thank you from the bottom of my heart for staying loyal. You made me believe again that I can make a difference.
So I am going to start posting again but turn off comments to avoid spam. If you want to contact me, you can on my Facebook page Lupus Celebrity. If you haven't liked me on Facebook yet, PLEASE do. See, now I am going to be begging for Facebook fans instead of comments :-). I am sorry if it gets old but I know me and if I don't think you are out there listening, I won't keep posting. I will also post on my Facebook page almost every day so you'll hear much more from me there than on the blog as long as you "like" my page. Again, THANK YOU, it is great to be back and doing what I believe I was born to do.
Once you have "liked" my page on Facebook, please consider liking the Alliance for Lupus Research. They are a voluntary organization founded by Johnson & Johnson owners. 100% of donations goes to lupus research which is kind of unheard of today and makes me respect the organization so much. So more important than liking my page, please help me and yourself by supporting the ALR by liking their page. See the end of this post for even more information on ALR.
xoxo
Lupus Celebrity
ALR: The Alliance for Lupus Research (ALR) is a national voluntary health organization based in New York City that was founded in 1999 and is chaired by Robert Wood Johnson IV, a member of the founding family of Johnson & Johnson. In just 10 years, the Alliance for Lupus Research (ALR) has become the world’s largest private funder of lupus research. To date, the ALR has committed $65 million to the most progressive and innovative research projects around the globe. 100% of your contributions to the ALR go directly to support lupus research programs because the ALR's board of directors funds all administrative and fundraising costs.
It's mission is to find better treatments and ultimately prevent and cure systemic lupus erythematosus (SLE, or lupus), a debilitating autoimmune disease through medical research.
Get in on it and help us find a cure. Give $10 by texting “Lupus” to 85994. Message and data rate apply. $10 will be added to your phone bill.
REMEMBER THE FULL $10 IS DONATED 100% TO THE ALR!!!
So I am going to start posting again but turn off comments to avoid spam. If you want to contact me, you can on my Facebook page Lupus Celebrity. If you haven't liked me on Facebook yet, PLEASE do. See, now I am going to be begging for Facebook fans instead of comments :-). I am sorry if it gets old but I know me and if I don't think you are out there listening, I won't keep posting. I will also post on my Facebook page almost every day so you'll hear much more from me there than on the blog as long as you "like" my page. Again, THANK YOU, it is great to be back and doing what I believe I was born to do.
Once you have "liked" my page on Facebook, please consider liking the Alliance for Lupus Research. They are a voluntary organization founded by Johnson & Johnson owners. 100% of donations goes to lupus research which is kind of unheard of today and makes me respect the organization so much. So more important than liking my page, please help me and yourself by supporting the ALR by liking their page. See the end of this post for even more information on ALR.
xoxo
Lupus Celebrity
ALR: The Alliance for Lupus Research (ALR) is a national voluntary health organization based in New York City that was founded in 1999 and is chaired by Robert Wood Johnson IV, a member of the founding family of Johnson & Johnson. In just 10 years, the Alliance for Lupus Research (ALR) has become the world’s largest private funder of lupus research. To date, the ALR has committed $65 million to the most progressive and innovative research projects around the globe. 100% of your contributions to the ALR go directly to support lupus research programs because the ALR's board of directors funds all administrative and fundraising costs.
It's mission is to find better treatments and ultimately prevent and cure systemic lupus erythematosus (SLE, or lupus), a debilitating autoimmune disease through medical research.
Get in on it and help us find a cure. Give $10 by texting “Lupus” to 85994. Message and data rate apply. $10 will be added to your phone bill.
REMEMBER THE FULL $10 IS DONATED 100% TO THE ALR!!!
Posted by lupuscelebrity at 9/17/2011 3:51 AM 
Categories: lupus activism, Lupus, Johnson and Johnson Company, lupus SLE, .pain, osteoperosis, summer, Alliance for Lupus Research, active SLE, malar rash
Tags: Lupus Sle systemic lupus erythematosus Alliance for Lupus Research ALR Lupus SLE Flare malar rash Sjogrens raynauds phenomenon fibromyalgia fibro
Categories: lupus activism, Lupus, Johnson and Johnson Company, lupus SLE, .pain, osteoperosis, summer, Alliance for Lupus Research, active SLE, malar rash
Tags: Lupus Sle systemic lupus erythematosus Alliance for Lupus Research ALR Lupus SLE Flare malar rash Sjogrens raynauds phenomenon fibromyalgia fibro
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