Category Archives: Advocacy

Arthritis Road Show Free Education Presentations

This traveling community presentation offering will be available beginning this Saturday and provide speakers, e-advocacy opportunities and more information about theOregon’s Arthritis Foundatio......

Summertime, Summertime, uh, oh, Summertime ♫

Today we are hosting Patients For A Moment (PFAM) and the theme was to divulge the wishes, dreams, goals and plans for the summer months ahead.  I’m noticing a slow-down in PFAM participation an......

Today is National Fibromyalgia Awareness Day

I am pleased to introduce author and pain archeologist, Sue Ingebretson, as our guest for today.  You may already know her from her website Rebuilding Wellness and/or from her book, FibroWHYalg......

It is World Lupus Day – got your armor on?

  If you are living with lupus, or know someone who is, you will undoubtedly come across references to it live or via internet.  Over the last three years of MLWT, I have watched the presence of......

May 7th~ World Ankylosing Spondylitis Awareness Day

I have had the pleasure of meeting and collaborating with some amazing people, including the crew at the Spondylitis Association of America. Although there isn’t an official chapter of the Spon......

May and Lupus back in the spotlight

Here we are again~ National Lupus Awareness Month.  International Lupus Awareness Day is May 10th.  In Oregon, SB348 (Senate Bill 348 designates May of each year as Lupus Awareness Month and ma......

Sound the trumpets, but heed the call

This was a big week for me and I intend to write about all that is going on in the next few days.  I want to begin with one of those “big” items, though, that has caused some mixed feelings and ......

New MLWT Partnership: Meet the APSFA

I would like to welcome Tina Pohlman, as our newest MLWT Guest contributor.  She is the President, Co-Founder, Executive Director of the APS Foundation of America, Inc. .  She is also an APS an......

No matter where I go, there you are~

I have been followed around by lupus for over a decade now, but there are still times when I actually expect to be able to fly solo.  In comparison to many people living with this disease, I am ......

Putting it out there

Today begins National Invisible Chronic Illness Awareness Week 2010.  For the entire week, I will be posting mini-posts including photos that bring a little more visibility to how I view living ......

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