Category Archives: Challenge and Opportunity
So Much to Learn — So Little Time
“What advice would you give, or what would you want non-chronically ill people to know about your illness and your life?”
This question brought up something I hadn’t thought about in years. Alt......
A Picture Worth a Thousand Flares
I’ve been around the block a bit when it comes to knowing what I should and should not do because of my lupus. (Note: the lower case “l”) For over a decade, I have managed my living with illnes......
A Cautionary Tale
For this next edition of Patients For a Moment (July 28th), hosted by Queen of Optimism on her blog, she presents the question:
“What is the nicest thing (or things) anyone has done for yo......
Knowing Where Illness Stops and Love Begins
I’m working down my catch up list of posts and have reached this trailer for a new movie that addresses living with illness (lupus) and learning to love right along with it.
Check out Love......
My Version of Physical Comedy
I will apparently go to great lengths to avoid exercising on purpose. This Wednesday, July 7th, was to be a Target Practice gathering at Cooper Mountain. It has to be postponed, but I still en......
Scleroderma Foundation OR Chapter on AM Northwest This Thursday
I received a note from the Oregon Chapter of the Scleroderma Foundation that they will once again be on our own KATU Channel 2 AM Northwest morning show! This Thursday,July 1st, AM Northwest ......
People First!
Today, BloggersUnite is hosting an online event entitled People First: Empowering People With Disabilities .
I’ve been having unusually prominent symptoms from my lupus. I always anticipate a ......
Thank you Veterans~
Monday was a day set aside to reflect on personal sacrifice, dedication to values, making commitments to those we share our lives with and things to believe in. It was a day when we said “Than......
Playing the matching game
My good friend, and fellow blogging buddy, Leslie, who authors Getting Closer To Myself recently posted about a topic that is at the core of my work here in our Pacific Northwest lupus and chr......
A Day of Empowerment
After about three weeks of the most painful headaches I’ve ever had, I’ve been a little overwhelmed with trying to make up all that time off. I don’t know what brought them on......










