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Multiple Sclerosis Tysabri #5 update vlog part 1

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Uploaded by on Oct 19, 2009

I am on my fifth Tysabri infusion and all is going well! I also have a new love in my life and pose the question asked to me 'Do you think of MS all the time?'
I talk so much, that there is a part 2!

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Uploader Comments (teslagirlM)

  • When do I need to call my doc, I am still able to function, I keep telling myself that this is all psychosomatic and that's why i am constantly thinking about this...Glad to know there are people out there that get it. Any tips?

  • I would say it is time to call your dr now. I do this too. I wait and wait, because even after five and a half years, I STILL don't always link my problems together! It could be a relapse, or a flare up, but the doctor should determine it. Also note that in the first year, many people get a higher amount of relapses. That was my cae, so don't put off calling the dr because you dont want to hear him/her say you are in a relapse! You can take steroids and speed recovery! Especially if u R in pain.

  • I think of my MS when I'm alone. Why I try to surround myself with people.

  • Thanks for your honesty, as always. I think many people will feel the same way.

    Good luck with Tysabri. I wish you much good health on it!

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  • I really liked your comment which relates to the question is it MS or is it PMS... I can relate, i have probably had Ms for 10 years but only known about it since april last year

  • I just had my first Tysabri infusion yesyerday. It went really well. I dont think iI had any side effects.

  • i think about my MS daily. when i was first diagnosed 4 months ago, i thought about nothing else. the thought was constant and overbearing, because the symptoms were constant and overbearing. now that i'm out of that relapse and learning my "normal", it's not a constant in my mind, but still a daily thought. a tingly hand, a jello leg, blurry vision... there's something every day.

  • Thanks for posting this. I was diagnosed in April and just yesterday was driving and thought to myself, "crap, am I going to have to think about this everyday?" Granted my right arm is numb, heavy, and cold. I have been getting pain in my eyeball and face, and so tired (is this a relapse). I am a novice at this and don't know any better.

  • I believe you wouldn't be with this new boyfriend if you truly wanted to be alone. You deserve love and you are right about not being able to turn it down. I wish you guys all the best and he is a lucky man :).

  • Dear Margot,

    It's hard to live without thinking about MS but going home back to Italy allowed me to let go of the disease and I was able to LIVE in the real sense of the word.

    Being back home, to a place where I didn't have MS allowed me to go back to the time when I was still healthy and every single time I go back to Italy, I get to feel so good that I realize that my type of cure is not just a medicine. It is also in my mind.

    I stopped thinking about MS and I started living again.

    Hugs

  • I try not to think, its hard, reminder follow every step I take so I just sitting and surfing internet ocean. Listen music, reading jokes. I want lost myself.

    Why I see big question marks in your eyes, Can I, Should I

    Life too short.

    No one knows what happens tomorrow.

    Waiting vlog part 2.

  • to find (no to gind ?! :()

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