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Replies to "Hi supernat10, You have been through so much, and we are all hoping for some spot-on..."
Autoimmune Diseases | Last Active: Oct 29 7:56pm | Replies (48)
Comment receiving replies
Replies to "Hi supernat10, You have been through so much, and we are all hoping for some spot-on..."
Thank you, it means a lot. I feel like I've been struggling to find a proper diagnosis for so long now, it's debilitating. I am seeing a neuro eye doctor actually. He did several balance tests, and I failed those, so have to go back in for more balance testing next month. He didn't really have a reason nailed down for the double vision yet. I have also suspected MS. My laundry list is so long I didn't include it in the original post, but I've had or have: double vision, brain fog, fatigue, chronic cough, trouble with breathing deep, random pains above my waist all over, pins and needles in both hands, muscle spasms/twitches random places, vertigo (only when I lay back), pulsatile tinitus, and weak muscles when I stand up after sitting a while (feel like I'll fall over sometimes although I never have). I also forget a lot and can't think of words often. I went to Harbor Freight with my son yesterday, and we were inside the store not more than a few minutes, and I had to ask him where we were, because I couldn't remember the name. These don't all come at once, but have been present over the years when I go through these flare ups. I had a brain MRI a couple years back due to these, which was normal, but have never had a spine MRI. My neurologist didn't think it was MS, because I still have good control over my muscles. I'm also aware that many people suffer from MS limbo, and I wouldn't be surprised to find that's what I've been in. I'm hoping it's not that, but finding out it was would be a relief.