Ok this is a day late, but
yesterday was the 14th January, marking my MS birthday – basically
it was two years ago on the 14th January 2014 that I got my
diagnosis of MS. Did I celebrate? No of
course not, not something to be celebrated. Did I reflect on how the last two
years have been? Yes I did. And I think I have been a huge improvement from how
I was in January 2014, and even how I was January 2015.
Last year on the one year
anniversary I wrote that I felt I had reached complete acceptance of my
illness, well thinking back I think that was not 100% true. However, I can now
say that yes two years on I have now reached complete acceptance of my illness,
have a peace about it and am content in my situation. Ok, that doesn’t mean
that every day is rosy, no there are hard days, easy days, bad days and good
days – is that not the same for everyone?
There are days I wish I was cured,
days I wished I could wake up not feeling tired, days I wish I had no pain,
days I wish that I did not have to take so much medication and days that I wish
MS didn’t stand for Multiple Sclerosis
but instead stood for Mystery Solved meaning no more MS. However most days I just get up and plod on
with life.
What other differences from last
year? Well last year I was working part time but now I am working full time,
well nearly full time, I work 30 hours a week which is 10 hours up from January
2014’s working hours.
In August 2015 I left my part
time job and moved to a full time job. I worked five days a week from August 24th
to November 30th, but my body was not able to cope with this and
either was my concentration etc. so I asked to go down to 30 hours a week and
now have Wednesday’s off. So work two days, off one day, work two days and off
two days for weekend. It is helping me. I am able to give my all at work and
not come home completely sore and exhausted.
In 2015 I decided that I would
get on with life, though I wasn’t really sitting on my bum for the previous
year. But I wanted to do fun things, and
I did. So what did I do that was fun? Well the three highlights are:
1) I
did a zip line over the Lagan River in Belfast. It was so exhilarating. The hardest thing was
stepping off the platform into thin air. My brain was telling me to stop being
stupid as there was nothing there, but I did it. I stepped off the platform and
went zipping across the river. So why did I do it? To raise money for MS and I raised
nearly £700. Which was great, and am so thankful to all those who supported me
3) I
went to Spain in August 2015. And despite it being stupidly hot, I had a great
time and enjoyed seeing Spain (it was my first time), practising my Spanish and
enjoying the culture as well.
2015 was a better year than 2014
but it has had its downs but am so grateful to God for always having me in his sight,
never letting me go and containing to see me though the journey of MS as well
as the full journey of life. He has opened my eyes and put some amazing people
in my life so help me through. He is the one constant and I know he always will
be. Despite what happens, God is always going to be there for me.
Now am looking forward to seeing
what 2016 has to offer and the third year of MS. Maybe this will be the year of
a cure!!
you sound more active the most people these days
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