Kelli Tysabri.wmv

A quick video of me getting first Tysabri infusion.

Category:

People & Blogs

Tags:

• kwazykelli
• kelli
• ms
• m.s.
• multiple sclerosis
• tysabri
• infusion
• therapy

[vbeachy]

I hope you see VAST improvements Kelli. I have for sure. :)

[joanie383]

I have been on Tysarbi since 2008 just over 45 infusions! I didnt notice any benefits expect no relapses for first year. Now its been over 4yrs and I recently had 1 relapse where I was admitted to hospital, I think I had more but they werent bad enough for me to go to doc and say i need steriods.

[jesusroxheaven]

my mom was going to go on tysabri

[shammy0007]

Kelli, I don't see any mention of CCSVI and the liberation treatment in any of your videos that I've watched. Do you have any opinions on them? Thanks for your videos.

[angelusa73]

Good luck with Tysabri, Kelli!

I hope it will work for you and for everyone that has to take this medicine!

I have had 14 infusion and, in just a few days, I will have to take it again!

Take care and thanks for the update!

Angela

[AutumnOh12]

aw, i'm glad it has worked out for you so far. my mom tried tysabri a couple of years ago and it didnt wok out for her. hope it does for you. (:

[OneScruffyOne]

Hello Kelli

I started Ty in Feb 2010 so I've had two infusions. Absolutely no side effects so I'm really happy about that. Haven't seen any improvement yet but no flares so I'm happy about that. Was on Beta for two years but too many flare ups. I wish you and everyone else with this Monster the best of luck as we try and carry on with life.

Bill

[Brodyb0087]

Good Luck kelli! hope all goes wll

[Brodyb0087]

Is this treatment only if you have severe ms because iv only had one attack and im taking an injection every day called copaxone. so far it doesn't bug me but im sure after time it probably will have it's side effects i started about 3 days ago and the only side effect that i'v had is a fast heat flash and soreness but after a few hours it feels like nothing happend no soreness around the injection site.. have any of you tried this method of treatment?

[qualisarx]

After the infusions and for the next couple of days I work out as hard as possible till I can take no more. Tysabri takes a while to act but anything is better than pricking yourself with a needle 3X a week! Patients and then it will get better in time..

[WORRO01]

IM still doing my betaseron, as i said in another video post to you, i havent taken a shot in 2 months due to injection site pain. i gotta get back on them though!! at least with tysabri it's a once a month deal, and that in itself should make it worth while??? Take care Kelli, and best of luck to you!!