Hey Red,
I do not know any new information as of right now. I was hoping to get a call from either my PCP or my neuro, but alas, I am still waiting. :S
I will post new information as soon as I get it, I promise! :)
Have a good night all!!
Victoria
OK we are waiting Victoria!! If you have info. now or not we want to hear from you:-)
Red
hey victoria,
totally understand wanting the results to come back as positive in some regard.
i think i read in one of quix's posts that she was just so happy to know the name of her enemy. this makes complete sense to me.
i do hope you get some answers, and then some relief soon!!!
xo michelle
Thank you. I will look those evoked potentials up on the internet and ask about them at my appointment next week.
I am also waiting on my Lyme Disease test to come back. All the other blood work, vitamins, CBC, and all that came back normal.
I hope this weekend goes by quickly (they always do even when I want it to go by slowly), but I hate playing the waiting game. Especially since I've been playing it for way too long. I'm sure everyone here can relate.
Thanks for the suggestions Red! I really appreciate it, because I wasn't even thinking about evoked potential, I don't even know what they are yet. Google...here I come!!
:) <3 Victoria <3 :)
It doesn't sound wierd at all to sort of want something to show up on the MRI. When you suffer for a long time without a diagnosis it becomes more frustrating not knowing than to know what it is.
I hope that you do get answers soon. Treatment now can make a huge difference in your life and get you get back to your life and hopefully halt the progression.
It's a very bid deal that your doc is already thinking about a possible LP in case the MRI is inconclusive. Also, maybe he will order the evoked potentials too, that could make the LP unecessary.
There are a number of things that may be done to exclude every other possibility.
Hang in there and we will be here for you!
Red
I had my MRI last night. My neurologist said it would take around an hour to two hours. It only took 45 minutes. I hope they didn't skimp on anything. I don't know if it is a T1, T2 or T3. I have no idea.
He said I should have my results at my doctors by mid next week.
I know this sounds weird, but I just hope it shows something. It sounds weird saying it, but I am so sick of being in limbo. I just want to know what and why and how. And I really want to start some kind of treatment so I can run around and play with my kids without having to take a 4 hour nap in the afternoon, rest every few minutes and be able to take them to the park even if it is 80 degrees outside.
I'll let you all know what the results are next week. My neuro said that if they don't know anything that he would like to do a LP on me. Which I would do, if the MRI doesn't show anything.
Have a wonderful day everyone!!!
Victoria