← Return to Worsening diplopia with no explanation

Discussion

Worsening diplopia with no explanation

Autoimmune Diseases | Last Active: Dec 27, 2020 | Replies (47)
Comment receiving replies
@ethanmcconkey

Hi @beka those symptoms must be so frustrating.

I wanted to introduce you to fellow Connect member @sarcomasurvivor who has experience with diplopia and also to Connect member @user_chdb5e8ac who has experience with ocular myasthenia gravis as they may be able to provide support for you.

I also think you may find this thread on myasthenia gravis interesting https://connect.mayoclinic.org/discussion/hi-everyone-let-me-begin-by-telling-you-some-of-my-story/

Back to you @beka, have your doctors prescribed any treatment at this time or are they looking for the cause first?

Jump to this post

Replies to "Hi @beka those symptoms must be so frustrating. I wanted to introduce you to fellow Connect..."
beka | @beka | Mar 11, 2019

Thank you @ethanmcconkey I greatly appreciate it. And I will definitely check out that thread.
None of my doctors have prescribed any treatment for this since they can't find why it's happening. I had one that at least assured me it was real and not in my head, which is awesome because women are often told it's all in their head. But I'm getting what I call "the big shrug".

VIEW AND REPLY