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Lupus Adventurer

Phoenix, Arizona
I am a lupus patient, wife, mother, grandmother, musician, legal professional, certified public manager, local government employee and Christian. Living with lupus is an adventure, and that adventure is often found between the lines.
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Prognosis and Hope: Lupus Fact #29 – Pregnancy successes with lupus

Prognosis and Hope: Advancing technology and better understanding of the disease have improved pregnancy outcomes. Today, 80 percent of women...

Prognosis and Hope: Lupus Fact #28 – Normal life span expected with current treatment standards

Prognosis and Hope: With current methods of therapy, 80 to 90 percent of people with non-organ threatening lupus can look forward to a normal...

Prognosis and Hope: Fact #27 – Lupus is not contagious but is often invisible or misunderstood

Prognosis and Hope: Lupus is not contagious and cannot be “given” to another person. Lupus is unlike and unrelated to HIV/AIDS or any other...

Living with Lupus: Fact #26 – Neonatal lupus in the littlest autoimmune patients

Living with Lupus: Neonatal lupus is a rare condition that affects infants of women who have lupus. With proper testing, physicians can...

Living with Lupus: Fact #25 – Cutaneous lupus may someday be more than skin deep

Living with Lupus: About 40 percent of people who were originally diagnosed with cutaneous lupus, which affects only the skin, will go on to...

Latest Activity

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Lupus Adventurer updated their profile. Oct 05 2011
Lupus Adventurer updated their profile. Aug 19 2011
Charlene Y. Atchison and Lupus Adventurer are now friends. Apr 28 2011
Lupus Adventurer and ATHOMAS are now friends. Apr 19 2011
Lupus Adventurer's Whiteboard
Feb 28 2011 by TiffanyAndLupus
:) Stay strong lovie! Keep fighting! Also feel free to add my blog to your blog webroll! Just wrote a new post yesterday. Hope you like it!
 
Feb 20 2011 by Lupus Adventurer

SR:  I agree with Tiffany, there just aren't enough of us lupus patients sharing our experiences.  Thanks!  LA

 
Feb 07 2011 by TiffanyAndLupus
Thank you! There aren't enough of us sharing our experiences fully. I try to be as open as possible within our lupus community. ^_^
 

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