← Return to Occular Myasthenia gravis (MG)

Discussion

Occular Myasthenia gravis (MG)

Autoimmune Diseases | Last Active: Oct 25, 2021 | Replies (47)
Comment receiving replies
@johnbishop

Hi @chorba -- welcome to Mayo Connect. We are glad you found us. Connect is a great place to ask questions and learn what others with similar health problems are doing for treatments. Did you have a chance to read through the MG discussion here?

@kanaazpereira posted a link in a post above yours on some very detailed care options for MG from Mayo Clinic which you may find helpful:
-- https://www.mayoclinic.org/diseases-conditions/myasthenia-gravis/care-at-mayo-clinic/mac-20352044

Do you have any questions you would like to ask of other members with MG?

John

Jump to this post

Replies to "Hi @chorba -- welcome to Mayo Connect. We are glad you found us. Connect is a..."
chorba | @chorba | Jan 25, 2018

Hi have had MG since 2013 this year my MG has started to get worse, harder to control lack of muscle control in jaws and mouth area, effecting speech, i.e. Speech becoming slurred, difficulty speaking , anyone have any knowledge on this or has it happened to anyone else, I would very much appreciate some feed back, cheers.

VIEW AND REPLY