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Looking for info and people with Neuromyelitis Optica (NMO)

Brain & Nervous System | Last Active: Nov 22, 2022 | Replies (49)
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@ann123

I was diagnosed with NMO six months ago, and am having trouble understanding what is going on with my body and how exactly to help myself. When I have a flare up, how should I respond to it? Any ideas?

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Replies to "I was diagnosed with NMO six months ago, and am having trouble understanding what is going..."
John, Volunteer Mentor | @johnbishop | May 21, 2018

Hello @ann123, welcome to Connect. I don't have NMO but do have several other autoimmune diseases. I'm tagging other members in this discussion in hopes that they can offer some suggestions or ideas to help you. @oregongirl and @aathins can you offer any suggestions or infomation/tips for @ann123?

Ann the following is a link to a post earlier in the discussion that may also offer some helpful information:
-- https://connect.mayoclinic.org/comment/91765/bookmark/?ajax_hook=action&_wpnonce=76ef07e468

John

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ann123 | @ann123 | May 23, 2018

Hello,
Thanks for responding to my message and tagging others with the disease. I tried to use the link that you posted, but I got a ‘page not found’ message. Could you try posting it again? Thanks!
Ann

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John, Volunteer Mentor | @johnbishop | May 24, 2018

Hi Ann @ann123 - I just clicked on the link and it takes my up to the earlier post? I will post it again to see if this works for you:

-- https://connect.mayoclinic.org/comment/91765/bookmark/?ajax_hook=action&_wpnonce=264dce940b

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