Saturday, May 2, 2026

Lupus Awareness Month

Hi Everyone!
May is
 
First for those of you who don't know.
Lupus is a chronic autoimmune disease where the immune system is over stimulated. This makes the immune system mistakenly attack healthy tissues, causing widespread inflammation and damage to organs, joints, muscles and skin. It's characterized by periods of flare ups and remissions. Symptoms vary widely, including but not limited to extreme fatigue, joint and muscle pain, and a marlar rash that takes on the shape of a butterfly across the cheeks and nose. Giving the Butterfly one of the mascots. The other is the Wolf. Lupus is the Latin for Wolf. I will get into some history in later posts. 
Some more but not all of the symptoms We can have one or a host of these at one time.
Now that you have an idea of what lupus is and how it affects the body, here are some facts.
 
  
 
Here are some myths and facts.
 
If you suspect you have lupus contact your health care provider and ask for lupus blood work, that's where you start. There are a set of criteria questions as well.
For me living with lupus really does suck.
When I wake in the morning I have to gauge what my body wants to do.
Everyday is different. 
Nicole
 

13 comments:

jabblog said...

My neighbour has lupus and has to avoid sunlight.

Anvilcloud said...

All the best in continuing to engage and deal with this horrid disease.

Margaret D said...

It's certainly not a nice disease to have, Nicole.

Tom said...

...it surely causes some awful health concerns.

Fundy Blue said...

Thank you for sharing accurate information, Nicole! What a miserable disease. I admire how you handle it greatly. ❤️🌺❤️

Debra She Who Seeks said...

I wonder why women are so much more susceptible to lupus?

Lowcarb team member said...

Thank you for posting these details.

All the best Jan

Carola Bartz said...

I have learned so much over the years about Lupus thanks to you, Nicole. It is an awful disease I don't wish on anyone. I don't think we can ever fully understand what it means to live with it. Best wishes to you.

peppylady (Dora) said...

Interesting

Anonymous said...

Thanks for raising awareness-Christine cmlk79.blogspot.com

Iris Flavia said...

Dear Nicole. What can I say. I go with Debra and am sorry "we" spend money to go to the moon instead of research for health...

David M. Gascoigne, said...

I was aware of Lupus before reading your blog, Nicole, but you have made sure that I learn a whole lot more about this dreadful affliction.

Ananka said...

I didn't know of it until I started following you. Thanks for the information Nicole :-D