Category Archives: MLWT

My longest post EVER?

Windows seem to frequently represent possibility or potential. At least, they do for me. I had a window open up for me a few days ago and the view was unsettling. During a recent conversation w......

January and February are Discovery Months!

As I try to finish up those holiday gifts that I still haven’t  finished, I’m seeing my weekly schedules begin to fill up with work.  Before I get too swamped and overbooked, though,I want......

Welcome 2013!

    I want to share my mantra for 2013 with you.   We spend a great deal of time defining ourselves with our brains – using terms or phrases that everyone ‘out there’ will underst......

Working hard to meet those shipping deadlines

I was a little swamped today and don’t have much of a post to put up. I can’t believe it is already the 13th! Yikes! The clock is ticking and I’m not even close to mailing anything yet~ I’m head......

Calling all elves~

I’ve been busy trying to stay on track for the gifting season.  I’ve also finished up with my last Wellness Doula client for the year.  That’s what I’ll cover today and catch up in a post tomorr......

Meet Guest Writer, Jennifer, and the new direction in her life with pain

I have known my wonderful friend, Jennifer, for a few years now and have been privileged to watch her create a life for herself that leaves me in awe.  When we first met, she was young and strug......

The Cycle of Support

This month, I had the pleasure of stopping in and spending some Discovery time with the Tacoma Lupus Group.  I was heading up to Seattle for SeaFair and it was a nice break from driving. It’s a......

So, a little updating is in order

Now that summer is here and the garden in finally gaining some momentum, I like to dive in to domestic practices like concoctions in jars, experimenting with new recipes and living off the land......

What the Lupus Research Institute’s $1 million initiative in the 2013 Senate Committee Bill Means

Good news for lupus sufferers and lupus researchers dedicated to finding effective treatments for the rare and difficult to detect disease.  A US Senate Appropriations Committee committed $1 mil......

June 2012 Patients For A Moment is here June 15th!

I recently facilitated a group Discovery Dialogue during a “Retreat for the Soul” event hosted by the Portland Fibromyalgia- ME.CFS Group .  The theme for the day was “self-care” and the partici......