Sabrina-

Sorry that you have been dx w MS. Thinking back it may explain a few odd things- certainly did for me.

If you are going to start on an RX, a think Copax is a good choice. I realized how depressing the interferons were the week I went off of them. The depression (which i didn't fully realize) was worse than the "interferon flu."

My best to you!
ANN in 6th year of Copaxone

Welcome to our little club...sorry that you qualify

Copaxone seems to be the mildest drug in terms of side effects. I've been on it for 4 years now, ever since being dxd. I have to say that when I got the diagnosis I was relieved to finally have an answer...but when the Copaxone arrived I cried-made it so real.
I look forward to next year when the drug company will come out with a formulation that only requires a few injections per week instead of daily.

Don't forget to keep a symptom journal! It's important to bring to each exam and gives the neuro an idea of how things are going.
Eat good food, try to stay active, get a bit of exercise, and balance this with rest. We are all veterans here-ask anything and one of us will probably have some idea of what you need to know.
You're not alone!! Be a pro-active patient...your doc and nurse are a part of your team. And sites like this one help keep you sane.

i was also dx'd by my MRI.
i'm sorry you were dx'd with MS. but, now that you know what you're dealing with you can make plans and take action.

i'd research copaxone. look it up and become knowledgeable. around here we say that knowledge is power. and power gives you control. you are your own best advocate.

i've been on copaxone for almost 10 yrs. i picked it because i didn't want the side effects of the interferons. i'm one of those people that believe in an MS med. some don't. some have started meds and gone off. each of us have our story with MS which is different for each.

my neuro thought i'd be in a WC in 5 yrs but i'm still walking with a cane and still driving. i'm independent. because of the copaxone???? or just my MS course. i guess i won't know but i'm sticking with it.

you get used to the daily routine. you may have some local site reactions but they decrease with time. i've found shared solutions to be very helpful in helping you. they also will send an RN to your house to get you started. and they will come back if needed.

keep us posted.

Hi Bri,

You are at a good place as you go through the MS process. Come share as you go and find a lot of good information here.