Hi, I'm Ron, and I'm an ME/CFS survivor (so far anyway), 24 years and counting. I am, at the time of writing, pretty much housebound. This restricts me to mostly sedentary pastimes - reading, blogging, occasionally sloping off to the pub, and cooking when I can, which isn't as often as I'd like. I do, though, make my own bread by hand, at least once a week - good food and physio in one...
29 year old mom and wife who have been diagnosed with lupus since 2002.
at the course of having lupus, i got operated in the lungs due to pleurisy, suffered pulmonary embolism and cyst in the ovary.
but now i am in remission.
I am a 28 year old who has recently received a lung transplant after an agonising wait. I have pulmonary fibrosis and it is thought to have developed as a result of aggressive cancer treatment received for a childhood cancer called Wilms' tumour. Sadly, I had a number of post transplant complications but I am determined now to get my life back on track. I am making slow...
My name is Rachael Wakefield. I'm 20yrs old from north west England. I suffer from a rare lung disease for which there is no cure. I host a couple of support websites to help support other patients and families affected by rare lung disease.
I am a 23 year old with Cystic Fibrosis. However in january of this year I underwent a bi-lateral lung transplant, and now my lung function is 99%, and I feel completely normal. I also suffer from CF related diabetes, which is a walk in the park compared to not being able to breathe.
