MRI Set up

[LadyQ0]

Got my MRIs set up and my follow up with an EMG. I'm going to have all kinds of tests done with in the week. As sucky as it will be let there be something new (changed) on the MRI to get me out of this CIS limbo boat.

[jimeka]

LadyQ0 hoping and praying that you get the results you are hoping for, keep us posted, blessings Jimeka 🦋 🌈 🙏

[Qt314grl]

I completely understand wanting to get out of limbo. I’m new here so I don’t know your story but I hope you get the resolution you seek.

[LadyQ0 in reply to Qt314grl]

I'm new too, but I've been having symptoms progressing from 2012 I was with a RA and switched in 2015 b/c he kept writing me off as things progressed and the new RA sent me to Neuro which is were I'm working through things back and forth since late 2015 and most of 2016 with a break after lose of Insurance and here we are today. I'll have to add a longer back story somewhere later.

[mrsmike]

Good luck. Hope everything turns out ok.

[WAshingtongirl]

It sounds as though your doctor is aggressively pursuing an answer, LadyQ0 . I know how being in limbo can make you long for a diagnosis...any diagnosis! I hope it isn't MS, but if it is, you're among a great group of friends here...ready to answer questions, listen, and encourage. I don't believe I'm met you before, so welcome! If I have met you, I apologize. I blame it on MS brain. 😉 Please keep us updated! 💕

[LadyQ0 in reply to WAshingtongirl]

Nope first time, signed up awhile ago, but been in a non motivated state since like January. Finally getting some get up and go so here I am posting

[WAshingtongirl in reply to LadyQ0]

Welcome! Happy to hear you've been feeling 'better' lately. 💕

[LadyQ0]

Well part 1 of 2 is done. I had my MRIs today. They went well, no sudden movements so no repeated parts. Not a fan of the contrast solution but whatever LOL. 3 more days and I have my F/u to discuss the MRIs and get/discuss my EMG.