Category Archives: Internet

Writing and Lupus ~ Make Your Mark in Research

Here is an interesting opportunity for any of you who are living with lupus and use writing as a way of coping.  If you’re uncomfortable with getting involved in research using experimenta......

Meet Matt, MLWT Guest Blogger

I have been searching for a guy who is willing to share his experiences living with lupus.    There are many diseases out there that are often ‘labeled’ as a “man’s” or “woman’s” disease.  When ......

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......

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 ......

It’s that time of year again!

I’m sneaking in a greeting to all of you this Spring celebration of faith and renewal~  I want to share this precious card I received from my friend, Linda. of her sweet companion, Dagny.......

Celebrate Those Who Care

    A quick note, thanks to a reminder from Rheumatoid Arthritis Guy , about a very important day today.  Today is Kiss a Caregiver Day hosted by Caregiving.com .  Take a minute and stop by thi......

Seeing is Being

With this week being National Invisible Chronic Illness Awareness Week, there have been so many places to go and learn so much.  Not just about living with a chronic illness, but about living&#......

Hallo!

It took a little more than a few clicks of my heels, but I’ve made it back from vacation in one piece.  It may be a little early to tell about how I held up and I have plenty to write abou......

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: 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&......

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