Tag Archives: MRI


Good morning, all. I kept the promise to myself on Friday that my post for Celebrate the Small Things would be all positive. I did that. Now, it’s time for me to post the not so great news. It would be an understatement if I said I wasn’t freaking out just a little bit but I’m doing my best.

When I saw my neurologist Dr. G on Friday, he went over my MRIs with me. The brain MRI was as expected. No new aneurysms or anything like that. Yay, for that. I wasn’t so lucky with the cervical spine MRI.


Photo from the Mayo Foundation

It seems that I’m one of the few that suffers from syringomyelia. It’s a disorder where cysts (syrinx) forms within the spinal cord. There are two types:

  1. In most cases, it’s related to an abnormality in the brain called Chiari I malformation. This causes the lower part of the cerebellum to protrude from its normal position in the back of the head into the cervical or neck portion of the spinal canal.
  2. The second form occurs as a complication of trauma (like my car accident in 2011), meningitis, hemorrhage, tumor, or arachnoiditis. In these cases, the cysts (syrinx) develops in a segment of the spinal cord damaged by one of these conditions.

According to the National Institute of Neurological Disorders and Stroke (NINDS), approximately 40,000 people in the US are affected. Couldn’t I have just won the lottery instead? Just sayin’…

Many of the symptoms are similar to the ones I currently have from the bleed, but it could explain why I’ve had a couple of falls lately. Dr. G wants another MRI done in six months to see if it’s grown or expanded. The usual treatment is surgery if the cysts increase or expand, but I’m trying to remain optimistic that I won’t have to go that far. I’ll be monitored by Dr. G and have a follow-up cervical spine MRI in six months to check.

Oh, and I’m back to having to use my cane indefinitely. Blah. Thank goodness he’s got me going to physical therapy soon.

If you’d like more information on this disorder, you can go to the NINDS site.

Like I said, I’m going to try remaining optimistic that the syrinx won’t grow or expand and routine follow-ups will be all that’s required. I love you guys and would appreciate any positive thoughts and prayers you can send my way.

Have a great week. Xoxoxo



Good morning, everyone. Hope you all had a wonderful weekend.

There’s been a lot of stressing here for the last week, give or take a few days. As I mentioned in a previous post, I had my three MRIs done about a week and a half ago. My neurologist appointment was supposed to be on Friday, but I received a call that morning that he wouldn’t be in the office. The earliest ‘late’ appointment I could get was the beginning of March.


Photo courtesy of FreeDigitalPhotos.net

Normally that wouldn’t bother me but with the whole medication thing up in the air, it leaves me frustrated. In an attempt to stay more alert, I’ve started taking my 30mg Duloxetine every other day instead of daily. I won’t chance any other changes until I see and speak to Dr. G.

It’s helped with the sleepiness, but minimally. The thought of lowering the number of meds I’d have to take daily fueled my excitement. Now I have to wait another month. I haven’t received any phone calls from him regarding the MRIs. I don’t know if it’s because he hasn’t seen them, or if it’s because no news is good news.

Not sure if I mentioned this before, but the purpose of two of the MRIs was to rule out spinal stenosis (like I need any other issues).

I suffered through two days with a monster headache a few days ago. In my bed was where I spent most of my time.

Other than that, I’ve been taking things day by day. Staying positive has been a task but between my friends, family, and Sophie, I’ll make it through. I might call during the week to see if he has any cancellations prior to March.

Thank you guys for always allowing me to vent, and for being there when things get tough. I appreciate you.

Have a great week. Hugs.