More awareness is never a bad thing.

Today is World Lupus Awareness Day. I sometimes wonder if the proliferation of awareness days, weeks and months desensitize us, making us immune (no pun intended) to the message we are intended to receive.

While visiting last weekend, my mother saw tv sports commentators wearing green ribbons. She asked why they were wearing green ribbons? I replied for the Humboldt Bronchos hockey team. She knew that had been done, but was surprised they were still wearing those weeks after the accident. Having celiac disease, she commented that green ribbons are also worn for celiac awareness. I added my two cents: green is also for organ transplant awareness too. We are running out of colors, sadly not out of diseases or causes.

Since starting my blog, I’ve had the same thought while composing every post about Sjogren’s’s Syndrome – everyone who reads my blog knows about this already. But thanks to the world wide web, new readers continue to find me here and inevitably after each post a new reader e-mails me, or leaves a comment after a post saying they never heard of Sjogren’s before. Sometimes people thank me, because they have Sjogren’s themselves, or know someone who has it, or suspect that someone they know and love is suffering the symptoms but has yet been diagnosed. I am willing to gamble on reader fatigue if it means one more person in the world will become aware.

Beyond awareness, I hope my writing will also generate understanding. Awareness that a certain disease or cause exists is absolutely the first step. It is great to know today all over the world people will wear purple ribbons acknowledging it is World Lupus Day. I hope people ask the person wearing a ribbon why they are doing so; that they get a response creating an understanding of Lupus and its impact on the person wearing it, whether they are afflicted or wearing the ribbon for someone they know.

Several years ago my Rheumatologist believed I had Lupus, but as my symptoms evolved and blood tests were repeated over and over through the years, I was diagnosed with Sjogren’s Syndrome, Raynaud’s Syndrome, Autoimmune Hepatitis, and Undifferentiated Connective Tissue Disease (UCTD) “with multiple symptoms of Lupus and Dermatomyositis” instead.

LUPUS overlap diseases

Although I meet the criteria for Lupus based on the characteristics used for diagnosis, because it has not affected my brain, lungs, heart or kidneys, and I have not tested positive for the definitive antibodies anti-DNA, rather only the more general ANA, my current Rheumatologist does not want to say I have Lupus. Instead I was diagnosed with UCTD, which is basically a catch-all disease category (hence the word undifferentiated) for people with symptoms of several connective tissue autoimmune diseases including Lupus.

To do my part on World Lupus Awareness Day here are the diagnostic criteria for Lupus as per the Canadian and American Rheumatology and Lupus Associations. A person must have at least four of the eleven criteria on the list. If you currently have four or more of these, or have had in the past, there is a strong chance you have Lupus.

1. Malar rash – a rash over the cheeks and nose, often in the shape of a butterfly
2. Discoid rash – a rash that appears as red, raised, disk-shaped patches
3. Photosensitivity – a reaction to sun or light that causes a skin rash to appear or get worse
4. Oral ulcers – sores appearing in the mouth
5. Arthritis – joint pain and swelling of two or more joints in which the bones around the joints do not become destroyed
6. Serositis – inflammation of the lining around the lungs (pleuritis) or inflammation of the lining around the heart that causes chest pain which is worse with deep breathing (pericarditis)
7. Kidney disorder – persistent protein or cellular casts in the urine
8. Neurological disorder – seizures or psychosis
9. Blood disorder – anemia (low red blood cell count), leukopenia (low white blood cell count), lymphopenia (low level of specific white blood cells), or thrombocytopenia (low platelet count)
10. Immunologic disorder –anti-DNA or anti-Sm or positive antiphospholipid antibodies
11. Abnormal antinuclear antibody (ANA)

(In case you are curious, # 1, 3, 4, 6, 9, and 11 have applied to me. Because I am currently taking a chemotherapy immune-suppressant drug for the AI Hepatitis, most of those symptoms have been lessened by the same drug, which is a very good thing.)

Remember if you see someone wearing a purple ribbon today, maybe take a moment to acknowledge it. Be aware and even better, try to understand the complexity of Lupus.
It is not an easy disease to diagnose; it is just as difficult to live with. Be patient, be kind.

10 thoughts on “More awareness is never a bad thing.

  1. Thank you for reminding me, I slept until after 3:00 pm EST today-Allergies and a heat wave to boot here. My immune system is going nuts. My best friend Barry passed away of Lupus complications at age 34- I was not aware of Lupus or Sjogrens -I was only 28 then. I know am all to aware.. I am living with Sjogren’s, UCTD, Peripheral neuralgia, Fibromyalgia, and a they cannot rule Lupus, and who knows what else. I should be wearing alot of different ribbons-but I think I will find some colorful pajamas-lol. I hope you are doing well with your treatment. Stay strong like the Warrior’s we are!

    Liked by 1 person

    • Hi Lisa – Yes, colorful pyjamas are a good plan! 😀 We gotta do the best we can with what we have to work with. Sorry to hear you too have multiple diagnoses. Stay strong my friend. (((hug)))

      P.S. Sorry to hear about the loss of your friend at such a young age. So sad that these illnesses can have dire consequences for so many, especially when heart, lungs, kidneys become involved. People don’t realize that there is no cure and treatments are hit and miss in too many cases. 😦


  2. GREAT !!! Well Done !!!!….and NOT just because I am your Mom…..Clear and understandable definition….Hopefully most can understand 🙂 Interesting note…..Yesterday was Celiac Awareness Day….My Day….today is yours…………………………..Love you 🙂

    Liked by 1 person

  3. What a horrible disease with so many symptoms and such pain. Thank you for making others aware so that they may be informed and share with others. Know that I love you my friend and wish you good days ahead.

    Liked by 1 person

  4. I know sometimes it’s hard to write about this, especially because you are in the middle of it, but it serves to encourage us to share your information and be aware of what goes on around us. Keep writing, my friend. I may be late in getting back to you, but I always come back.

    Liked by 1 person

    • Hello dear Claudia,
      Better late than never (lol Just like my reply!)

      Thank you for always coming back, I appreciate you reading and being supportive and encouraging of my writing. Hope you are having a good summer. ((((hugs)))


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