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hi there this is DragoNate's Mom I would
like to start by saying a big big thank
you to my son make them without him here
to support me and love me through this
journey I don't know where I would be
thank you so much hun and i love you so
much
also I'd like to thank my sister and her
boys they have been a huge support to me
and Nathan in throughout this journey so
my multiple sclerosis journey started in
april of 2013
it started with I had numbness in my
left foot which led to numbness in my
left thigh numbness in my right foot and
then numbers in my left cap so I went to
my car Proctor during this time thinking
that you know maybe it was something
that he could help put and he suggested
orthotics because nothing else was
working and my doctor also suggested
that I might need orthotics so we
decided to order them and i got them and
I started to use them the numbness did
go away but I was very off balance in
may of 2013 we went to a wedding and
back the day after the wedding we went
for a walk and i felt i was trying to go
up a little hill i went to grab a stump
to help me up the hill and I started to
Paul and I knew that if I felt the way I
was following that I would end up
rolling down the hill and I didn't want
that happen so I turn around and I
landed on my back my son and a friend
had to have help me up
I hurt my foot in the
process we got back home and I went back
to work but my legs start to feel like
jelly and they just didn't want to hold
me up um I thought I hurt my tailbone
really bad especially when things didn't
get better
during this time a friend from work
abroad in a walker which of course I
really didn't want to start using a
walker I was too young for a walker but
she didn't want to see me call so she
brought in the walk for me to use and I
used it
my legs just didn't seem to get better
so I want to see my doctor my doctor set
up appointments for me to check and and
see what was going on and he had me do
some tests and stuff
um during this time this was in june of
2013
I was working maybe one to two days a
week I was not hungry
I couldn't eat and it wasn't because
food made me feel sick
it's just that I wasn't hungry but
Nathan made me start to eat he would put
a piece of toast in front of me and say
you need to eat all this mom and so I
started to but i did lose a lot of
weight during this time while I was off
i can't go to into are covered colon and
my boss was very very understanding
he wanted to find out what was going on
with everything with me too because he
wanted to make the hawk and I wanted to
be back
so Nathan and I did some research
search join this time and all of my
symptoms led towards ms so when I went
in to see the doctor again he said to me
he um he SAT there and he's like my my
feelings are leaning towards and I
looked at him and I said ms and he said
which I kind of knew that that's maybe
what it was
so he go had an appointment set up with
the neurologist and I went to see her
and she can't understand why i was using
a walker why we thought it was ms my
legs were super super strong and all /
tests but I told her that my legs felt
like jelly
so she set up an MRI and she just wanted
to do an MRI of my back neck because she
still wasn't convinced that i could be
ms in july i started working again but
my eyes went wonky and it was during
this time that I went for my MRI my i
went back to see my doctor to let him
know that my eyes were you know really
really one care constitute be straight
and he wanted to try something with me
something new and that was to put me on
a massive dose of steroids to see if it
would help my eyes and my legs to get
better i had to take half days off work
to do this because i had to take them in
the afternoon i wasn't able to drive and
I needed to take them with food and milk
and the steroids did help my eyes but it
did not help my legs i'm still using my
Walker during this time I have to speak
a few more days off work because it only
happened three times but I had
tightening somebody's stomach just below
hurt
yeah just below my breasts line it was
super painful that it kept me awake i
couldn't fit i can't stand i couldn't
lay
nothing would help it just kept hurting
and the pain was unbearable
the second time it happened my son maybe
does have some water and the pains would
start to go away but not completely
it can't be home from work as I didn't
go to sleep that whole night and the
pain would go away in the morning when I
needed to get up and so I can't come
into work I need to sleep so my box was
very understanding at that time to in
early July I went for my first MRI just
have my back and my neck and the
neurologist i guess um talk to my doctor
and they had decided that I needed to go
for an MRI of my brain that found a
lesion in my lower knack and they needed
to you know make sure about lesions in
the brain and so when / number i have my
brain in which they found for lesions
three small ones which were dormant and
one larger one which was active which
with what was causing on my issues
my official diagnosis up ms was the end
of july and had an appointment set up to
CMS doctor for some time in the
beginning of august i'm going to in my
first vlog here this is a journey of
when I MS symptoms started to when I was
actually diagnosed in closing I'd like
to ask you to please check out
www.myspace.com / dragon eight dash
caring dashed he dr m.s this is a
charity charity teacher that nathan has
set up and seventy-five percent proceeds
goes to the MS Society for research for
ms also please check out dragonets
channel on youtube i will be putting the
links for both of these in the
description below if you help any
questions or anything regarding my
journey that may be able to help you
with your journey with what ever you're
going through
please don't hesitate to leave it in the
comments below if you like this video
please of like also if you'd like to see
more please subscribe and we will see
you in the next one
blessings to you one thing i would like
to say that I forgot is that I asked my
doctor is ms hereditary
and he said no it's not hereditary so
anybody who has any MS symptoms or is
going through from multiple sclerosis it
is not hereditary the biggest thing that
they said is for Nathan to start taking
vitamin D and he only has a 5 protect
percent chance of ever getting ms so no
it is not hereditary and you only have
to tell people who you want to tell due
to the fact that it's not hereditary
thank you
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