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Is anyone suffering with Anti MAG neuropathy?

Autoimmune Diseases | Last Active: Oct 17 10:03am | Replies (8)

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Hello John,

Thanks for the kind welcome to the group. It's much appreciated. It's nice to have an outlet, since this is not a topic that I share much with other people. Most people in my life don't know I have it. Yes, I am aware of the Foundation for Peripheral Neuropathy, thanks to my Kaiser neurologist. Very good site: I would also recommend the following: Shining through CIDP, the GBS/CIDP Foundation, the National Institute of Health (NIH) as well as other sites with data on PN, CIDP, and anti-MAG. Speaking of podcasts, my neurologist turned me on to this podcast/video by Dr. Richard Lewis. I guess I'm not allowed to post the link on here as a new member. Anyway, there are many others, most of which I haven't had the time to view yet. A little more about myself, I am a musician (drummer/percussionist), gardener/landscaper, athlete, and live a vegan/plant-based lifestyle. Have a good weekend everyone. -- Steve

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Replies to "Hello John, Thanks for the kind welcome to the group. It's much appreciated. It's nice to..."

Hi Steve @laporta, I thought I would share the podcast /video link for you since new members are prevented from sharing links for a short period of time to prevent advertisers and spammers from using our Connect community. Actually I think I have shared this one before but it is good - FPN Webinar: Anti MAG Peripheral Neuropathy: An Overview with Dr Richard Lewis, MD:


Hoping you have a great weekend also!
John