Hi everyone. I'm 34years. I was diagnosed with civd in 2004 after being sick my entire life. I started monthly iv treatment mid 2004 till 2009. Afterwards I lost my medical insurance and relied on exercise, supplements and immediate antibiotics whenever I got sick. My next iv was mid 2012. In 2014 I started getting iv once every 6 months till today. I take supplements, exercise and wear a respiratory musk at work whenever a colleague has flu/cold. I am a warrior of life.
Ok - I'll start a new thread.Anyone have issues with duodenal/peptic ulcers ?That's my latest, at first docs thought it was kidney stones but turns out it ulcers. I actually think I've been dealing with this for some time, it just got quite worse (painful !). Waiting for a scope in the next day or so. Ugh.
Hello everyone!! I have such a broad array of feelings at this to have finally found a group of people who also suffer from CVID. I was diagnosed with PID 4 years ago and specifically CVID a year ago. I had a successful run with sub q Ig, then changed insurance companies and have been denied tratments for almost 3 months. I am really beginning to feel alone in a way I never have before. I'm...