Showing posts with label life with lupus. Show all posts
Showing posts with label life with lupus. Show all posts

Thursday, September 6, 2012

My First Pearl


My experiences through the past 25 years have been priceless. The many faces of lupus are imprinted on my heart and  there are sixty inches of  precious pearls on my strand, so I had better get started.

I was nine when my journey started.

There were many theories on what ailed me as young child.  One was Rheumatic Fever, another was mono.

My first pearl on my strand would be my mother, Rose.  When I first came down with symptoms she was the driving force behind my wellness.  My mom had four children and worked full time.  As I look back and reflect on our many hospital stays and doctor visits, I am now aware how cumbersome the task of caring for me was.  Since lupus was very mysterious, I was not correctly diagnosed with lupus until I was 27.

Doing her very best to take care of me, she and dad would pull me out of school each winter (we live in Ohio) so that we could be in Florida. After all isn’t the sun healthy for everyone? Obviously not true for lupus patients.  So, each winter I had rashes and sunburns.  They did not know that the sun was my enemy.  

**Do you know that the sun is the enemy for lupians? This is true.  Long exposures to the sun can bring a dormant lupus to surface.  We are very sun sensitive and many of us suffer from photosensitivity.  Sun tan booths are an absolute no for us.  Sunbathing too!  We need to limit the amount of time we are exposed to the sun.  If you must go in the sun at its peak, be sure to use the highest level of sun block you can find.  Remember to read the instructions completely.  There is a company that sells sun protective clothing for those that must be in the sun.  Also I have seen UV umbrellas. Try to limit your exposure and do not go out in peak times. Remember too that because we lack the sun we will most likely need vitamin D to take its place. ( Ask your doctor about it).

The other challenge was at the same time, I took penicillin every day of my life until I was 18.  Really?  How crazy was that? You need to know that the biggest challenge a lupian can face is infections.  We have a very difficult time fighting off infections and often infections are the cause of our demise. 

Since I was taking large doses of antibiotics, I was at risk for my body becoming complacent to the drug.  I was constantly fighting off colds, strep throat, etc.

So, at the end of the day, my family thought they were helping me but were actually contributing to my illness.  How sad is that? They did not know. They thought they were doing what was best for me.  Still… my mom was the one who brought me to the Lupus Foundation of America when I was 27.  She was a member first.  She was determined to make up for the past and get me on the road to wellness.  I remember fighting her tooth and nail, not wanting to attend that first meeting.  I followed her and bless her heart; she knew it was exactly what I needed.

To be in the presence of others that have walked in my shoes was such a relief. Finally, there where others out there in the world that had similar challenges.  Through the years, I have learned so much from the LFA and most importantly, I have fostered relationships with my fellow lupians that have lasted my lifetime.  Together we have met challenges, and together, we have championed them.  One of my favorite sayings is “There Is no I in lupus, but there is an US!”

I will be eternally grateful for my mom dragging me to that first lupus meeting.  Today I lead a support group.  Wow!  It is better for me than most of my meds I take! 

Get involved with the Lupus Foundation of America; I promise you, it will change your life.  There is no reason today that a lupus journey should be a lonely and misunderstood one.   Mom knows best, and I am grateful she took charge and did not give up on finding what was wrong with me.  It was through her tenacity that I got diagnosed.

Why the Pearls?


I have this tremendous fascination with all that glitters. I was a jeweler for ten years when a stroke changed the direction in my life. I am especially drawn towards pearls. As my journey continued with lupus and I let go of my old life, I learned a way to welcome my new life with lupus. As I left the jewelry industry and the world of glitter, gemstones, gold and pearls, I embraced all those with lupus. They became my new gems. Some were rubies, emeralds, or diamonds, but most of the time I thought of them as pearls.

Each person with lupus that I met was different.  They were one of God’s creations. The shells for the most part the same, but the insides were pearls. In them, I saw a lustrous beauty that was a work of art that had layers of a type of nacre. Unique and complicated: yet still beautiful.

The definition of a pearl can differ but here are my thoughts. A pearl is a living gem, and each pearl is a miracle of nature. A pearl is the accumulation of a slightly translucent material, called "nacre" (better known as "mother of pearl"), similar to the lining found on the inside of nacreous chells. This is what gives a pearls its unique lustre and iridescence. It takes thousands of very thin layers of this nacre to make a single pearl. It is the composition, structure, thinness and evenness of these microscopically thin pearly layers that distinguishes a high quality pearl worth thousands of dollars from another worth a great deal less. It is a remarkable feat of nature that a living oyster produces such an exquisite work of art.

Thus here is my story of my strand of pearls. For the sake of this blog it will be called Suzy’s precious pearls.
In my blog I will introduce the many pearls I wear around my neck. There will be many. This year I celebrated my 60th birthday. For a gift I received a 60 inch strand of lustrous pearls. I wear them proud. It is a privilege to wear them. Each pearl is named after someone that has impacted my life with lupus. I am excited to share each pearls story one at a time with all of you.
I pray that someday I will have a strand of pearls that is endless. I pray that I will be able to continue my lupus journey and share even more pearls with you.
Each pearl has shared a special place in my life. Often times a lesson came with each.  Some other times empowerment.
To all my fellow lupians.... stay tuned you are most likely on my strand of pearls that I wear around my neck.