747 days ago I was sitting in the same hospital with my parents, not sure if I had a choice to cry, laugh, or just sit there in disbelief. As the words came out of his mouth, my suspicions were confirmed, "You, without a shadow of a doubt have Multiple Sclerosis."
Looking at him with his funny glasses, after all these silly tests and questions he had asked me for what felt like the dozen-th time I felt a sense of peace. A sense of clarity washed over me. No more weird unexplained symptoms. I had the answer. I had multiple sclerosis.
Without a doubt.
I don't remember every moment of that day, but I remember most of the time after I walked into the hospital. I remember trying to figure out where the MS clinic was and navigating a strange hospital. I remember sitting in the waiting room watching the many different people walk in and out of the hallway, some with their canes because MS had affected their eyes to the point where they couldn't see. Or their loved ones wheeled them down the hallway because MS had affected their ability to walk.
At that point I still felt like I didn't have a hope to live a what I would call a "normal life".
But then the doctor came back into the room and to tell me there was hope. His face lit up as he said, "This drug is going to knock the socks off MS."
As he handed me a stack of papers, he tole me and my parents we should read through them, and if I said yes to being a part of his clinical trial, he would put me to the top of his list and I would start by the end of the month.
I remember leaving that room and the nurse asked, "So, what did he say?" I replied naively, "He said he would put me to the top of the wait list and I would start the trial by the end of the month."
She looked at me in shock and said, "Okay."
At that point I didn't know that the wait list was at least a year and even then, it was unlikely to get to be apart of the study.
What else I didn't know was how my life would change in two years...
I didn't know how much MS would affect my life.
I didn't know how hard it would be to live with MS.
I didn't know how much love and support I would receive from my friends and family.
I didn't know how much I would learn and grow.
I didn't know that in two years I would say, "You know, I wouldn't give back what I've learned, how much I've grown, or the challenges I've faced for the 'normal life' that I thought I'd lost"
Today it's back to the UbC hospital for my first "knock the socks" off MS drug infusion. It's still going to be a while before I feel the effects of the drug and will potentially start to feel "normal" ...or at least what I remember to be 'normal'.
I am excited. But also prepared that there is a slim chance it won't do anything for me at all. I'm ok with that too, and ready to take on this next stage of life.
So thanks guys for keeping me in your prayers, thoughts and lives.
I will continue to keep you updated.
(Stay tuned for Pt. 2 in two weeks when I come back down for my second half of my first dose!)
--Kate
My name is Kate. I was diagnosed with Multiple Sclerosis when I was 20 going into my second year of Nursing. It has been a long year, but I have come out on top of all of it and I plan on continuing to do so. Please feel free to share my blog, and come along on this journey with me.
Monday, 22 September 2014
Saturday, 6 September 2014
TWO Years and Counting...
It's official. I have had MS for the past 2 years, as of September 5, 2012.
It has been a long two years and so much has changed. I have changed so much. Learned more about myself that I ever may have wanted to and or thought I could.
Looking back it's been good, summers have been great and a sweet way to break up the year. The people I have met, especially this summer, and old friends I have gotten to know better has been really sweet and encouraging. They are relationships I would like to continue on with for sure!
Well... what is new with me?
Yesterday I had my last first day of classes ever! That is definitely exciting.
I am doing my placement this semester in Fort St. James in Northern BC. I am really excited to get out of PG for a bit and experience a new hospital.
Things I have learned in the past TWO years:
2. I have learned independence by moving out officially on my own! (with friends.)
3. I have experienced much more of the world, travelling to London twice as well as Northern Ireland.
5. I have felt valued while working as the photographer/videographer for Echo Lake Bible Camp.
6. I have battled MS on a daily basis and so far have come out on top.
7. I have practiced counting it all joy when faced with trails of many kinds.
8. I have done my best to remind my self that I have to live life one day at a time and live it to the full. For me this means doing things like learning to Fox Trot, throwing around a baseball with friends until I cannot see the ball anymore, exploring train tracks, playing on bridges in the fog, sharing hidden secrets of Prince George with friends, and going for runs at 9:30 at night with my roommate.
9. I have learned to not take life so seriously and to laugh always.
10. I have learned that crying and feeling sorry for myself is a waste of energy that is better spent being productive, sleeping, exercising etc.
And what is coming down the pipe for me?
However, as excited as I am about this new drug I also am not putting ALL of my hope in it, as there is a chance it might not help. All I can do is wait and see, right?
As I have said to some people before, looking back I am so happy to see how far I have come. I am not saying its been easy, but I will say I've had good days and bad days. I do my best to make the good days out-weigh the bad ones, but sometimes I need to take a break and reflect on the good/great things in my life.
I am so thankful for the things God has taught me over the past while, depending on Him, living life the way He wants me to, and counting it all joy. I am unbelievably thankful for those around me who have supported me in my journey with MS. Having people trust in me helps me remember that I can do succeed in life and that I don't have to be run by MS.
So thank you, for continuing to read my blog, pray for me, think of me, support me as I continue to navigate these foreign waters.
Love, Kate
HIGHLIGHTS OF 2012-2014
Leaving for London the first time!
I love these two! Always up for the bant |
....when you have moments like this. Steroids...not always my favourite.
If I could live in mud I would. |
This is what made some early mornings this past year worth it
Sista Time! Waiting on the parents... |
Spent a weekend this summer at the base of Mt. Robson. |
I LOVE adventures... this one was a highlight of the summer. |
I know its good when I get this reaction from Tim. |
3 inches away from highway traffic flying above our heads |
Mt. Robson- Kinney Lake |
Glaciers are always a neat thing to explore. |
Northern Ireland Adventures |
Heel clicks--always a classic. |
I was constantly blown away by the scenery in NI. This place was one of my favourites. |
Queens University, Belfast, Northern Ireland. |
Worked on star trails this summer. |
Double Barrel 20G shotgun. I actually hit my target... in thet air! |
Friends, lakes, rivers, creeks, forests, inukshuks, hanging out on the beach...
I wouldn't give back these moments for anything!
Sometimes I just like being 10. With a bear towel! |
The last night of camp this summer: took advantage of a clear, cold (-2), frosty-sleeping-bag kind of night. The view in the morning was incredible, as you can see. |
Highlights of 2012-2014
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