I've only come across this thread today after melissa's post...but it's very interesting and I am wondering what people think about it in relation to IVIg as a treatment for CRPS? More and more, CRPS seems to be linked to auto-immune system failings, and having coeliac disease myself and arthritis, it's easy to think that perhaps my immune system is just cruddy. I also had glandular fever as a young woman, and was very poorly for nearly 2 years.

Any thoughts?

Bram.

Melissa,

Sorry that it has taken me this long to respond. Apparently I''m easily confused these days and sent a PM to someone else, thinking it was you .
They have responded and now it is all sorted out.

I too have been diagnosed with Parvo; and have been dealing with the joint symptoms for the past 4 months. The docs are looking into using IVIG as a therapy to help the body get over the virus.
Have you had any therapy suggestions?

I posted a thread on the MS forum (was diagnosed over 30 years ago and have SPMS).
http://neurotalk.psychcentral.com/thread200717.html

With love, Erika