Category Archives: Advocacy
Lupus makes the TV lineup tomorrow
Have any of you noticed the increase in lupus talk happening in the media? Lady Gaga, Snoop Dogg’s daughter, and John Stewart comparing lupus to the FOX News Network? You don’t only have to s......
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......
A Penny For Your Thoughts
On Tuesday night, July 6th, I watched the PBS NewsHour (on OPB Channel 10 ) segment (reported by correspondent Betty Ann Bowser and funded by Robert Wood Johnson Foundation ) about the new he......
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 ......
Local Arthritis Events to Join in on!
I want to mention a couple of great things going on through the PNW Chapter of the Arthritis Foundation and our own local branch here in Oregon~
There will be a free Public Education Seminar off......
LFA’s Advocacy Day on Tuesday, March 16th
We’ve been asked by the National Lupus Foundation and our own Pacific Northwest LFA Chapter to post reminders about this annual awareness event. Both offer important and convenient way......
Why The Pecking Order?
We live next to a water way and have more varieties of fowl than you would expect to be here in the suburbs. With the mild temps this winter and heading into spring, the size of our backyard f......
Interview opportunity discussing insurance lifetime caps
An announcement from our local Scleroderma Chapter:
Have You Experienced a Lifetime Cap on Your Health Insurance?
The Scleroderma Foundation is interested in speaking with scleroderma patients w......
Wishing Everyone An Adventurous 2010!
I’ve been off the radar for too long here and plan on getting back into writing in January. It’s tough to keep putting up posts when there are so many amazing people to be connecting with perso......










