Quote:
Originally Posted by MAT52
Thanks Loulou this is really helpful. However I'm fairly sure that a London doctor wouldn't be able to sort out IViG for me up here in Scotland. I am about to post about the immune mediated thing but very interesting to know what your neuro thinks about NLD SFN and the immune aspects of it. Mat x
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Hi Mat,
There was a lady on here a while back who lived in Scotland, she had PN for 8 years, her local neuro referred her to Hammersmith Hospital in London, it was advised that she try IVIG by the professor there. I believe she has this every 3 weeks in Scotland and it helps.