My story is similar to a lot of people with SREA. I was finally diagnosed in 2016 with this life changing disease after making 5 appearances at A&E and subsequent hospital stays. I lost my job because of all the absence. I missed my family and friends. My partner was neglected. My life had changed but I was in denial until I finally hit rock bottom. I was terrified of everything - going out, people etc just in case it prompted an exacerbation. My asthma is non-allergenic so I will never now what triggered this late-onset disease. This is a brief history of how it was...... You will all know the trauma, heartache, grief, despair that I felt. However it is now late 2018 and life is so much different. I have been on Mepolizumab for twelve months now with very little of my old symptoms. No steroids, no hospital admissions and now I am looking forward to the future. I recently applied and accepted an offer for a new job. It is not the same as before. It will not be as hectic and I will not be paid as much but I will be happy and feel valued again. I cannot wait to start my next new chapter. BRING IT ON......
My love, thoughts and support go to everyone with this devastating disease but there is light at the end of the tunnel and hope survives x