I would be questioning the Neuro about HIS interpretation of the brain MRI and what paperwork the hospital sent to you. I would say to the Neuro, either the brain is clear or it isn't. Apparently it is NOT!
If you have a herniated disk and the disk material is pressing on any area of the spnal space,..yes you can have problems. The disk material can bulge out and push on the spinal cord or cause stenosis of the spinal space. (narrowing) I have this porblem with four disks in my spine, but I also have an MS lesion in my upper spine. I DO have MS and was diagnosed over a decade ago.
You need to get back in touch with this Neuro and tell him that you want to discuss your brain MRI report. Find out why he says normal and the report says otherwise. If this guy isn't going to give you straight answers, then you will have someone who will.
There is obviously something wrong...you know that and apparently the report says that. Now you need to find a doctor that can figure that out too.
I am sorry that you are going through all of this....This happens to so many people, I want to pull my hair out and scream. You DESERVE answers and deserve them now.
Heather
Yeah, it's pretty depressing not knowing what the hell is going on with me. Especially as it's gradually getting worse. I was kinda hoping I had MS. At least I would not be wondering what is wrong with me anymore. I am only 24 years old and I can't help but wonder if I'm dying and don't even know it. I just e-mailed the neurologist about why I just recieved this letter in the mail. Thanks a lot for your response Heather. I appreciate it.
Hi there. It's really normal to almost hope you have MS. It would be much better if it all turned out to be some kind of little blip that could be fixed in 5 minutes, but since that isn't in the cards, we at least want SOME diagnosis. Limbo is wearisome at best, maddening at worst.
Just concentrate on seeing the best doctor possible. If that's not the one you have now, then read on this forum about how to find a better one.
Good luck.
ess
I know how depressing all of this wait and see game is affecting you. It must be awful to feel like "you are dying and don't even know it." I know that feeling. I hazard to guess that you are NOT dying, but just feeling overhwelmed at the prospects of possibly having MS and what it means for your future. This is a totally normal reaction. You are so young...this is so unfair.
Sweetheart, we will stand by you and with you, through every step of the process, no matter what that process is. You will never be alone. Most of all, we encourage you to express your feelings and emotions, as you wouldn't believe how many of us feel the same way.
You are not alone honey and will NEVER be alone, as long as this forum exists. Keep posting and today would be a good day to call that doctor with your report in hand. Find out what is going on. If you can't find the answers for him, it's time to find a doctor that CAN answer your questions. This "limboland," is hard on anyone.
We are with you dear heart,
Heather
Thanks a lot Heather. It helps to know I'm not alone.
The neurologist just e-mailed me back and said that they found a tiny spot of hyperintensity at the posterior horn of the lateral ventricle. Whatever that means... and to e-mail him if I have any new symptoms