Thanks Kiwi33,

Over the past 18 months I’ve tried to read everything about Anti-MAG PN that I can get access to! Your article from the GBS/CIDP Foundation was one of the first that I ever read.

There are different views on effective treatments. Most people agree that more research needs to be done but, as with most rare disorders, it is difficult to get the necessary funding.

I’m thankful that in Australia we do have access to government funded treatments and can try different options without suffering financially. And, so far, COVID-19 has not prevented me from continuing treatment in hospital.