Don’t try this at home!

I have been sitting here for an hour trying to start writing about MS.  I don’t have writer’s block, I have too many topics that I can’t focus on just one.  I’ve reviewed my pre-written list of Ramblings, and instead of selecting one, I’ve added 20 more.  While this is good for the future, it’s not what I want to do right now, so I have sat and stared at the screen literally for an hour.  Thankfully? I have places I have to be today and can’t continue to sit here for another hour.

The first place I have to go this morning is to the Eye doctor, SILLY DOCTOR gave me BIFOCALS last time, which in hindsight is utterly ridiculous for a person with MS. (I watch the ground when I walk, because I can’t feel my feet).  It’s not justified, but I am a bit upset with said doctor for not thinking of that considering they watched me walk in and out of their office several times.  Why didn’t they warn me?

I did admit that my upset is unjustified (doesn’t change the fact that it is there though).  It was MY mistake.  While I did notice my issues when leaving the doctor that first day, I thought I could manage and learn to deal with it.

Yeah Grace add another thing to your list of “deal with it”?!?!?

 I think I mentioned before that I make a lot of mistakes, and I believe that is ok as long as you learn from them.  In my case, it took me not one, not two, but 3 WIPEOUTS before I came to the conclusion that I REALLY, REALLY need new glasses.

Did I mention a person with walking and balance issues should NOT wear bifocals?!?!?

A PERSON WITH WALKING AND BALANCE ISSUES SHOULD NEVER WEAR BIFOCALS!!!!!

A PERSON WITH WALKING AND BALANCE ISSUES SHOULD NEVER WEAR BIFOCALS!!!!!

A PERSON WITH WALKING AND BALANCE ISSUES SHOULD NEVER WEAR BIFOCALS!!!!!

Well as they say, 3rd time is a charm?  Please learn from my experience and DON’T TRY THIS AT HOME!!

I do hope to post about MS later today…wish me luck?

MS Multiple Sclerosis Diagnosis

Many people that have been diagnosed with MS can look back in their lives and identify times that they had MS symptoms long before they were diagnosed with the disease.  When I tell my story though, I am only speaking about the events directly leading up to my diagnosis.  In hindsight, I can tell you that I am grateful for the way things played out, but I certainly wasn’t when it was happening to me.

I was at work and a coworker friend of mine was kicking the back of my knee with her foot as we were walking down the hall.  I don’t remember how many times she did it, or how many times I avoided tripping, but I do remember the one I went down on.  Not only had I torn my nylons, but two fingers in my left hand went numb within the hour.  It seemed strange, since I don’t remember landing on my fingers, but I shrugged it off.  There were more important things to think about like how was I going to get even with Michelle for bruising my pride.  I went to sleep that night, figuring the numbness would go away in the morning and didn’t give it a second thought. When I woke up the next morning my entire left hand was numb, and by noon from my fingertips to the middle of my forearm was numb.   Over the next few days the numbness continued to spread up the rest of my arm and down the left side of my body to my left knee.

Call to the doctor

The order of events that happened next are kind of a blur to me.  Maybe because they happened so quickly, maybe because I was terrified and tried to block them out, maybe because they happened almost 20 years ago.  Within a week my doctor ordered Evoked Response tests, 3 MRI’s, a spinal tap, and enough bloodwork to save a nation.  Then the call came.  “We need you to come into our office to discuss your test results, TODAY.

As I type this, the hairs on my arm are beginning to stand up, and I can feel my breath catching in my throat.  I don’t remember the words she used to tell me I had Multiple Sclerosis.  I remember the silence that followed and the hopeless and pitiful looks she and her nurse were giving me.  Somehow the numbness that I had been feeling during the past week seemed to take over my brain and my emotions.  (pun intended).  The doctor ordered a course of steroids for me and gradually I started to regain feeling in the reverse order that I had lost it.  First my trunk, then my chest and shoulder, and eventually my arm except for my left hand which is still numb.

As I mentioned earlier that was almost 20 years ago, but that is where it started for me.  In the last 2 decades I have learned and experienced so many things due to this disease that I think may be helpful to share with others.  Living with MS is not new to me, but blogging is.  If you’re willing join me on this new adventure of mine, please follow the blog, or Look me up on Facebook. Grace Fullnot (same picture I use here) If you do add me on facebook, please send me a short message saying “Hi”, I saw your blog, or something to that effect, so that I know you aren’t a robot.

If you are reading this because you have MS or think you might, please know that yes it can be scary, it’s ok to be mad, but it really is NOT the end of the world! There are many resources out there to help you with this!!!!!!