Thursday, 3 April 2014

You have parvovirus B19 & 99% you do not have Lupus! Famous last words.

The journey to diagnosis just got so much worse. In fact it was horrendous and so confronting. 
I'm finding writing all this stuff down from 10 years ago quite emotional. 

Looking at myself now I hardly recognise this person. 

I'm well, in remission and am very functional. Yes I'm like the tin man in the mornings. I have joint and fibromyalgia pain issues. I feel tired easily but I can run my own business. I can write. I don't do housework. I finally gave in a few months ago and I have a cleaner and it was one of the best things I have done. Why did I keep on trying to run myself into the ground? What was I trying to prove and to whom???!

Sometimes us Lupies are our own worst enemies. 

Giving in is OK. Some things are not worth the battle. I choose how I use my energy each day. There's a great theory called the Spoon theory. I love it and it helps explain our disease to others. I'm sure a lot of you have heard of it too. It's genius :-)


Not long after I started work as a Child & Family Health Nurse in Melbourne I contracted a virus. It was a particularly nasty virus called Parvo Virus B19 aka Slapped cheek syndrome. It hit me like a ton of bricks. 


I was ill for 6 months and at times felt I hadn't the strength to do anything. Getting out of bed was a big ask never mind work. But I was only on a permanent residents visa so no work...no money. I had joint pain, temperatures of 38-38.5C. I had a red face especially my cheeks. I felt like I had flu permanently. 

The rheumatologist I was referred to did a full blood screen. It was viral. It was Parvovirus B19 and I'd most probably contracted it from a child in my job as a Child & Family Health Nurse. He also said that I'd had Epstein Barr (glandular fever) in my past. That was something I hadn't known. He told me that 99% I didn't have Lupus. Famous last words. 

No comments:

Post a Comment