More disease progression blah,blah,blah
 

Went to the neuro today, he is a really sweet guy, very smart and understanding, got my MRI results. Why is it that I never hear Hey Great! No new lesions! No Progression! Nope every time it's well....there's been a little more disease progression from your last MRI same thing today, I am always positive but it is kind of discouraging! he asked how everything was I told him having some visual issues, the heat is killing me, tremors are awful some days, spasms are awful some nights yada, yada. Just bummed cause for once I would love to hear GOOD news!!

Awwwww, so sorry Nae, that's stinky..:(

I'm glad you like your Neuro, though. He probably hates giving you bad news too.

Join the summer blah's club...you're not alone and I hope you feel better soon..

(((Renee))) Progression is supposed to be a positive word but for us MSers it's not. Sorry about your appointment.:hug:

Positive Progression - I think you are amazing! You are strong and have endured so much and yet you continue with your happy personality, wit, and getting done what needs to be done despite everything. That is positive progression.

Hang in there!:hug:

THANKS GUYS!!!! Tkrik I meant to tell you I was looking at all of your artwork the other day and there are couple in there that I absolutely love, they are all good, I am in the process of doing a waterfall. The ones of yours I liked were the radial colors, misty, and flowing!

renee,

i'm sorry you got bad news.
i forget, are you on any DMD's?
i hope this ratty disease leaves you alone for a while.

Sorry you didn't get the good news you were hoping for. (((hugs)))

Another member here of the summer blah club (wish there were t-shirts for that!) and sorry about the news from the doctor.

Feel better!

Niko:cool:

Sorry to hear that Renee. You are strong that's for sure with all you've been through. I remember when Jim would get the same news each time he went to the neuro. It sucks for sure. :hug:

Renee sorry to hear of your bad news. I got my bad news the end
of May.

For the first time in 24yrs. dx with ms I agreed to take Rebif.

Hoping all gets better for you.

As Sally has said the Summer Blaaaahs. We will blame that for
waking up this horrible monster in us.



Jappy :hug:

Judy, I was on Rebif but had to quit due to side effects, then I was on Tysabri....had to quit due to side effects (horrible kidney pain) Now I am on Copaxone and all is well.