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Good Days…Bad Days With Maureen Pratt
Good Days...Bad Days With Maureen Pratt Archives

Premission to sleep! Chronic illness, whether lupus, fibromyalgia, MS, or another culprit, can bring on fatigue. Not just the “normal” kind brought on by a busy night or day, or strenuous exercise. No, our fatigue is usually called “unrestorative,” that […]

The human spirit can endure a sick body, but who can bear it if the spirit is crushed?                  Proverbs 18:14, New Living Translation These few words from Proverbs say it all about the importance of a strong spirit when […]

Last week, some friends of mine participated in a lupus event, and they invited me to come with them. I cannot tell you how wonderful it was to see their caring in action. Truly, the benefit of being enveloped by […]

When I was diagnosed with lupus, I found it extremely helpful to immediately organize all the information, appointments, and other things pertaining to life with the diagnosis. That, then, was my “Coping Skill # 1.” Next, I set about finding […]

Before this Lupus Awareness Month gets too far underway, I wanted to highlight a few activities that will be taking place to educate, encourage, and raise funds for research. I realize that budgets can get stretched and energy sapped easily […]

When you are diagnosed with lupus, you have to absorb a lot of information in a brief period of time. Lupus is a very complex disease; even if your case is mild and you do not have to take any […]

The first significant symptom that I had that indicated something was seriously wrong was that my hair began coming out of my scalp in thick, cylindrical clumps, leaving behind smooth, round bald patches from which no further hair would grow. […]

One of the most confounding things for many people when they first hear the term lupus is, “Why is it called ‘lupus?’” The name doesn’t resonate with people today; it doesn’t seem to describe any kind of body part or […]

May is Lupus Awareness Month, and during this time, I’ll be blogging frequently about aspects of the disease, living with it, and coping with it. I realize my personal experience is unique; each person with lupus has his or her […]

Never say “give up!” That’s one of my mottos for life with lupus. The flare that was stirred up after I had to go off one of my lupus meds has also made me extremely sun- and fluorescent light sensitive, […]