My husband was diagnosed with ILD (UIP) in 2010 with positive Anti Jo, Sjogrens and rheumatoid arthritis. Was diagnosed with dermatomyositis in the late 1990s. We live on Long Island.
Kelly, Portland, Oregon. Sudden onset severe ILD and subsequent diagnosis of OJ subtype of AS summer 2009. Loss of muscle strength in hands, forearms, rising CKs summer 2013 and then DM diagnosis via muscle biopsy. I refer to the entire situation as my DM AS.
Hi everyone I'm Lisa 50 something and I was diagnosed with an acute onset ASS with Jo1, ILD, DM and severe Osteoporosis in June 2011. Spent 9 months in hospital for 2 of those attempting to survive. Was on oxygen24/7 but lungs have now 66% capacity and for most normal life things I'm ok without it. Otherwise I use it at 2ltmp for gardening, major household chores. However, my muscles and joints do not work as they used to so life is definitely restricted.
Sorry from Brisbane Australia
Hi BarbieRose 66 I would be interested in finding out about the data you have on the numbers of f patient with ASS. I stated a Facebook group called Those of us with ASS.