In 2014 I was diagnosed with something called Lupus. I was unable to walk, was signed off work for 6 months , suffered major fatigue and couldn't use my right arm for a short space of time. I was told I had an autoimmune called Lupus SLE   this is where the body's healthy parts get attacked and unfortunately my brain was the organ that Lupus chose for me. I also got something called Chorea which is a neurological condition (I was told only three people had this me and two in India ) which lead to my use of my right arm being non existent for a short spell, it also meant my arm would involuntary move or jerk. After several lumbar punctures, MRI scans , blood tests to same a few, it as clear I needed chemotherapy to help the brain activity and control the Lupus. I also suffered a mini Stroke during the time that I was given my diagnosis. 

September 16th 2014 I had my first dose of chemotherapy and after 6 sessions and steroids my lupus was behaving as best as it could and my right arm was back to normal. 

I always promised my rheumatologist who saved my life with acting quicky with the diagnosis and chemo that when I could walk again I would take part in the Baker Hughes 10K in Aberdeen and I did and this year I'm taking part in the Kiltwalk. I also decided to set up a support group in Aberdeen for patients and family / friends of Lupus sufferers as we haven't got anything here in Aberdeen and a year on and we are a successful group and getting bigger. I have went on to have two beautiful children ( after being told I might not be able to after my chemo ) who will be encouraging me on the walk 

My Lupus went in remission in 2023 but it can come out of remission at any time and attack any of my organs. 

More awareness needs to be made for Lupus so I do my best to share my story and others. Lupus doesn't define me , I don't let it rule my life. 

Thanks Laura x