Hi All
My son, 23yrs, started getting chest pains 4yrs ago and they diagnosed him with pericarditis - inflammation - sac around the heart - he had to have fluid which was building up, drained. At the time we did not link it to SLE, but having had the chest pains every year for the past 3 years he was diagnosed this year to have SLE. The is year he had a really bad flare up - inflammation of bowels, excessive weight loss, vommitting, diaorrhoea - this continued for wks, which resulted in - me contactting the GP to admitt him to hospital. He lost so much weight, going from 11st to 8st. The docs have prescribed him on predisilone and azathiaprine. His lupus is not visible, his is internal so I don't know if that is good in a sense it is not visable.. I know either way visable or not, it is not a nice thing to go through for anybody who has to go through with it. My son is doing well now, he is monitored regularly by the docs and has his bloods screened every 2 weeks, he is taking his meds and he is back in uni and working. I just hope we don't have to go through any more flare ups... the amount of heartache and tears we shed when he is not well.. is just so hard to bear... :sad:
My son, 23yrs, started getting chest pains 4yrs ago and they diagnosed him with pericarditis - inflammation - sac around the heart - he had to have fluid which was building up, drained. At the time we did not link it to SLE, but having had the chest pains every year for the past 3 years he was diagnosed this year to have SLE. The is year he had a really bad flare up - inflammation of bowels, excessive weight loss, vommitting, diaorrhoea - this continued for wks, which resulted in - me contactting the GP to admitt him to hospital. He lost so much weight, going from 11st to 8st. The docs have prescribed him on predisilone and azathiaprine. His lupus is not visible, his is internal so I don't know if that is good in a sense it is not visable.. I know either way visable or not, it is not a nice thing to go through for anybody who has to go through with it. My son is doing well now, he is monitored regularly by the docs and has his bloods screened every 2 weeks, he is taking his meds and he is back in uni and working. I just hope we don't have to go through any more flare ups... the amount of heartache and tears we shed when he is not well.. is just so hard to bear... :sad: