Category Archives: Diagnosis

OR Scleroderma Foundation’s Cheri Woo Education Seminar This Saturday!

Just a reminder about the Educational Seminar going on this Saturday, offered through the Oregon Chapter of the Scleroderma Foundation.  Even if you don’t have this particular disease, the......

Meet Becca Seitz, our new MLWT Guest Blogger

Hi All!  I’m Becca Seitz, licensed acupuncturist and owner of Thrive Acupuncture in NE Portland.  You can read about what got me into acupuncture and Chinese medicine at the link Maria ga......

Lupus and men: Dr. Oz is making an office call soon~

I received an email from Kathy Casey, Executive Director of the Lupus Foundation of America -Pacific NW Chapter letting me know about an event that I want to pass along to all of you: “Hello, We......

Making Connections (Part One)

“My life has a great set of characters; I just haven’t figured out the plot.”                                                                                                     ~Ashleigh Brilli......

National Invisible Chronic Illness Awareness Week 2009

Here we go! Monday, September 14th is the beginning of National Invisible Chronic Illness Awareness Week 2009  and there will a lot of great people out there offering a great deal of informatio......

A new lupus book that speaks from the heart

            When facing my lupus diagnosis, I sought out many books covering medical terms, confusing symptoms, current and potential treatment options – all to quench my thirst for conque......

Every Day is Father’s Day!

I had some trouble with my computer beginning Thursday and throughout this weekend, so I just wasn’t able to post a Happy Father’s Day in time~ I do hope all you guys out there, who ......

Our Voices For Lupus Awareness: Sara finds her way and shares her story Despite Lupus

I am so excited to present my blogging friend Sara as our final Guest Blogger for MLWT’s ” Our Voices For Lupus Awareness ” event this May.  I have been reading her blog for mo......

Our Voices for Lupus Awareness: Jess will roam if she wants to

My life with lupus.  Hmmm, I’m not even sure what that means to me just yet.  Last year I began the journey to a lupus diagnosis. I’m not quite finished with the diagnosis, but we......

Our Voices for Lupus Awareness: Maureen’s 25 Random Things About A Day With Lupus

Living Every Day with Autoimmune Diseases            It’s been about 15 years now that I’ve woken up feeling hungover.  Sound crazy, or maybe like I have a “problem”?  I&......