MS diagnosis and symptoms Posted: 09-06-08 08:38am
Hello all, this is my first post.
Yesterday my brother was told that he
probably has MS. A little background...
About 1 month ago he got numbness on the
left side of his face and the right side
of his body. Went to doctor had cat scan,
nothing, numbness went away. About a week
later he developed tunnel vision, then
double vision, and lately blurred vision.
He went back to the doctor who sent him
for a MRI. After results came back they
referred him to a brain doctor. He had
his appt yesterday. The specialist didn't
have the scans (delivery service wasn't
working so he didn't get them) but he did
have the written report. He said that it
says my borther has 4 "spots" on his scan
that are consisent with MS. He also said
that his reflexs are "jagged" which is
also a sign. They of course are waiting
until Monday to view the scans but want to
sent him up for a spinal and for someone
to come out to the home 3 days in a row
for iv treatment. So onto my questions.
Could it possibly be something other than
MS with his symptons? Almost forgot, his
eyes dart like crazy when he looks to the
side. Is it already progressed if he has
4 spots? I saw other posts that mention 2
spots. Also what can we expect in the
next few weeks/months? Since it already
seems to be moving so quickly, should we
expect it to hit him hard? Thanks for any
advice/answers/comments you may have. We
are all at a loss right now.
Sorry for the long post which I am sure is
full of many errors:(
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zigemyster
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Posted: 09-10-08 19:04pm
There are other diseases out there that
mimic MS however with the lesions
(plaques) found on the MRI along with his
symptoms are highly suggestive of MS. His
doctor would want to rule out other
diseases before zeroing in on MS.
Spinal? Are you talking spinal tap? If
so, it is not needed for a dx nor to rule
out. I've had two and the last one I
wanted to curl up in a corner and
disappear.
As far as to what to expect...it's
unpredictable and your brother will need
to be monitored by his neurologist and
overtime it will be determined what form
of MS he has...it could be RRMS and then
10 years from now it goes to SPMS...it
just depends on how MonSter treats him.
There is no cure for MS however if he gets
on a treatment which slows down the
progression is the key to staying as
healthy and active that he can be under
the circumstances.
(below came from a previous post that I
had posted to another MS question)
MS is a tricky creature. It comes in
different forms...best way for me to tell
someone when they ask what it is? (some
think it is the same as Muscular
Dystrophy...so I educate them)...it is an
unpredictable disease of the central
nervous system...key word being
'unpredictable'.
nmss.org or mssociety.org are both great
websites to learn about MS. It is so
managable...I fall between benign and RRMS
(descriptions listed below)...I listen to
my body over the last 8 years than I ever
did...if I get a little too hot, I know to
find a cool spot as sometimes heat steals
the use of my legs...however if that
happens, I cool down and I'm good to
go...like going for a long walk...years
ago, I ended using a cane because my legs
did not want to function correctly, lasted
a few weeks, hasn't been back. If people
ask what happened...'it's an old injury
and just needs to heal once more'
To be honest, I hope you do not have MS
and that it is stress and / or B12 related
or something simple...but if you must join
our club, you'll have great support &
resources at your fingertips.
There are four types of MS, each with its
own characteristics, but each as
unpredictable as the other. It might not
be clear which type of MS you have when
you are first diagnosed. However, by
noting changes over time, your neurologist
should be able to clarify the type you
have.
Relapsing Remitting MS
Most people are diagnosed with relapsing
remitting MS. This is when you have
relapses (a flare-up of symptoms),
followed by remissions (periods of
recovery). Relapses are unpredictable.
They can last for days, weeks or months
and vary from mild to severe. During a
relapse you will either experience new
symptoms, or a reccurrence or worsening of
previous symptoms. During remission,
symptoms can disappear completely, though
sometimes people make only a partial
recovery.
Symptoms might not always be due to a new
relapse. For example, exercise or hot
weather can sometimes raise body
temperature and make symptoms temporarily
worse. Any changed or new symptoms must
last for at least 24 hours to be described
as a relapse.
Secondary Progressive MS
Most people who have relapsing remitting
MS later develop a form known as secondary
progressive MS. This type of MS is
identified when your condition becomes
steadily worse, and your disability
progresses, for a period of six months or
more, whether you continue to have
relapses or not.
Benign MS
If you have a small number of relapses
followed by a complete recovery, you may
be described as having benign MS. It is
only possible to make a diagnosis of
benign MS once you have experienced little
or no disability for a period of 10 to 15
years. However, a diagnosis of benign MS
does not guarantee that you will be free
of problems; a relapse may occasionally
occur after many years in which your MS
has been inactive.
Primary Progressive MS
With primary progressive MS, symptoms
steadily worsen, resulting in a continued
progression in disability. You will not
have distinct relapses and remissions.
~Zig
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NikkiS78
New User, Becoming EHEALTHy
Joined: 06 Sep 2008 Posts: 2
Posted: 09-11-08 07:14am
Thanks! Yes I was referring to a spinal
tap. His doctor was really pushing for it
so he has one scheduled for tomorrow:(
I have been doing alot of reading over the
past few days and to be honest the more I
read the more scared I am for him. He
works in a foundry where heat is a major
downfall. It is beyond tolerable in that
place. I wonder how this will come to
effect him after reading your post.
Gotta run to get my kiddos on the bus.
Again thanks so much for replying to me.
Edited to ask...why was your last spinal
tap so bad?
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zigemyster
Moderator
Joined: 16 Aug 2008 Posts: 353 Location: ,
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Posted: 09-11-08 20:29pm
2nd spinal: I was in alot of pain in my
lower back and legs, could not stand up
straight or walk even a short distance
without crying for about 2 weeks. The
person who did the spinal said he was very
careful however per the neuro and other
specialist...apparently they hit a nerve
... like the siatic... Spinals are not
error proof...injuries can happen and if
it is a risk that one is willing to take.
First spinal I ended up with a what they
call a 'spinal headache' and I had to go
back and have a bloodpatch and also took
Zomig due to the back to back migraines it
created.
MS treats all of its victims
differently...your brother may be able to
handle heat...lately I am able to handle
it, unsure why but I don't push my
luck...if I start to get weak, cool place
I search for.
They make cooling vests and other things
that help people with MS cope with these
strange symptoms. There are two mags that
I subscribe to, MSFocus (free) and MS
Motivator (free as well). There are great
support groups & siminars / events
which are put on by some of the companies
that make the drugs to slow down MS and it
is also a great place to meet others who
are in your same shoes...whether you are
the MSer or caregiver, family member or a
person who just wants to be educated on
this disease.
I do hope your brothers spinal tap will go
well. Before the epidual is done they
will inject him with a numbing agent...it
feels like a bee sting...(I took a couple
of my husband's hydrocodones before I had
mine...I know, I know, I should not have
taken somebodys elses meds however I
needed something more than an
aspirin)...if he needs something
beforehand, they may be able to give him
something to relax him.
If it turns out that he can not continue
with his current job function, could he be
transferred to maybe an inside job
(office) or another location or go back to
school and learn new skills?
Several years ago spinals were routinely
done for MS purposes however recent
research has id'd that bands or no bands
in the spinal fluid does not indicate or
rule out MS as research shows that some
people with MS will not have bands and
some who have MS and are having an active
attack will have bands...so in truth it is
a guessing game.
Let's see my 1st & 2nd were
inconclusive and I had MS lesions and
clinical findings of MS however my neuro
did the wait and see (how many attacks,
symptoms, etc) and then I got the dx...but
because of his not wanting to label me as
MS I missed several years of injectibles
that slows down the progression of MS. At
the time he was for certain that bands
were needed in the spinal fluid to be
absolutely sure of MS and now that
procedure has been dismissed...he no
longer requests spinals for MS dx.