Hi all, I am brand new here, and glad I found this place :)
In late March, I was very stressed out with work piling up and very
little rest. 10 days later, I was going blind in my right eye, went
to urgent care 2x, and finally got to an ophthalmologist who diagnosed
me with Optic Neuritis, and told me it could be a symptom of MS.
Before he diagnosed me, he had asked if I'd had any numbness or
anything, and I remembered that yes, there had been some instances of
numbness in my left leg last fall. I thought maybe I was getting a
little too chunky (!), and soon after lost about 25 pounds. Haven't
had the numbness since then. Then we started the MRI process. The
whole thing took 3 (annoying!) weeks -- from ophthalmologist to MRI to
meeting with a neuro to discuss the results.
It didn't show any definitive lesions! There was one bright spot that
the radiologist pointed out on his report (a "high signal focus"), but
it said it didn't look conclusively like anything in particular.
There were a few other bright spots not mentioned on the report, but
which the neurologist pointed out just to show that there could be
"unidentified bright objects" that usually don't mean anything, and
that he woul dfind these in a large percentage of the general population.
He didn't take a very detailed history at all -- I was all prepared
with details of other things that I thought may or may not be related.
(The leg numbness from last fall, very painful sciatic nerve a few
months ago, shingles on my left leg about 8 years ago.) When I asked
specifically about the leg numbness, he pretty much blew it off and
told me historical symptoms like numbness are of very little help for
diagnosis -- unless it had been severe, like 3-week paralysis, he
couldn't use it. He said that if I had any more symptoms, I should
come back, have them documented, and possibly repeat the MRI at that
time. He also said I had the option to do a spinal tap, but that it
also would not be conclusive.
Since then, I've had the same kind of numbness in my left foot, mostly
in the mornings, that comes and goes some days. It's numb right now.
I guess what I want to know is, should I get a 2nd opinion? Should I
get the spinal tap? I feel like I should. I didn't feel like the
doctor really listened to me... My symptoms are not as severe as
many, until the blindness, of course. THAT was kind of a problem :)
The leg numbness was strange, and slightly troubling as it recurred
and recurred -- until they went away.
Hello. My dear husband just had an MRI last week to rule out MS. He is 51. We have two sons, 3 and 7. I am 39. We live in southeast TN. We have been...
I started with blurry vision, fatigue, trigeminal neuralgia, cramps in back, and chronic depression. I was lucky enough to start my treatment with a wonderful...
I took my first shot today! i used the autoject and put the shot in my leg. It didnt hurt at all, until after ... it stung just a little and I have a big red...
And...I'm glad they caught it so quick. There are some wonderful treatments out there that slow down the progression of MS. I've been on the Beta Seron for 5...
Hi, I've been on copaxone for several years now. It's a daily injection just under the skin so a small needle. There are no flu-like symptoms with Copaxone....
Hooray for you. The Copaxone is usually well tolerated. The injections become very routine. I have been using Copaxone for several months now and had one...
Hey Everyone I have a question that I would like to ask. I have been on Copaxone for 2 yrs now. I am thinking about changing over to Avonex. If you are on...
Hi all, I am thankful I found this site. I am currently being tested for MS, and really confused. All my troubles started with an electric type shock...
I don't recommend switching to Avonex -- it's been found to be the least effective MS treatment -- plus the interferon side effects were tough on me, I had...
Hello everyone, Sherry here. I've been on vacation in TN, great time. Just read some of the last posts. I've been on Avonex and Copaxone. Currently on the...
Good evening everyone! I had just typed a long message when I hit the wrong key - oops! I'll try to remember most of it, but I was rambling :-) Thank you for...
Hi everyone - I went to my family reunion this past weekend. It was entertaining, to say the least. I had been trying to figure out how to tell them about my...
Hi! I was diagnosed with MS a year ago ~ my neurologist told me all the options for meds and I chose Copaxone. When I 1st started my shots - I had some...
My husband, who is 52, was just diagnosed with progressive MS. We're not sure about the primary/secondary part. He has balance isssues. We have been going to...
Hi all, I am brand new here, and glad I found this place :) In late March, I was very stressed out with work piling up and very little rest. 10 days later, I...
Hi! I'm new to all this but was so impressed with the message about the family reunion etc. The positive attitude will take you far and not let this disease...
Hi, I'm new with questions too & I'm hoping to get to know you all and interact. So sorry for what you've gone thru. I was told about 20 years ago I might...