Aaron Taylor

Your Replies

  • August 14, 2020 at 10:14 am

    Thanks, pdarwin, for your post on this. I know it’s been a while since you posted, so I am late to the party on this. But, it helped me when dealing with a recent “relapse” of my CIDP. Been tough sledding to this point, and it’s been helpful to read what someone else deals with.

    August 27, 2018 at 5:05 pm

    I have been getting weekly IVIG for 5 years. I thought it was a bit much. Then, I started a new job and had to cut back the frequency of my infusions. The decrease in the IVIG as well as the increased time on my feet have equaled what I believe to be a relapse in symptoms.

    Got to tell you, I really like this job and it will devastate me if I have to give it up. Not sure what I am going to do. I have to support my family. I have been okay for a few years dealing with this god-awful disease, but I may just lose it if it takes away yet something ELSE from me.

    I’m sorry, I’m ranting. But, I just don’t know what to do at this point. Thanks for reading.