Thread Tools Display Modes
Prev Previous Post   Next Post Next
Old 12-03-2010, 09:47 PM #11
clarkstar's Avatar
clarkstar clarkstar is offline
Member
 
Join Date: Aug 2010
Posts: 316
10 yr Member
clarkstar clarkstar is offline
Member
clarkstar's Avatar
 
Join Date: Aug 2010
Posts: 316
10 yr Member
Default

Quote:
Originally Posted by Riverwild View Post
Clark, first of all, welcome to the Tysabri thread.
I had my 46th infusion today, piece of cake when I compare it to giving myself a shot, whether it's daily, every other day, or once a week!

Infusion is the same as starting an IV because it IS an IV. It's called an infusion because that's what you are doing with the drug, infusing it. They start you with saline solution, then start the drug, then you go back to the saline for the observation period. If you've ever had steroids, it's the same procedure except for the wait time for observation afterward.

Most infusion centers will have lidocaine on hand to numb the area, They use a tiny needle and they inject a tiny amount of lidocaine under your skin where they are doing the stick for the IV and wait a minute or two for it to numb up and then go for the IV stick. Tell them you have pain and needlephobia and ask for the lidocaine if they don't offer it.

It took me 2.5 hours today from start to finish.

It sounds like your doctor is already a part of the JC study and that you won't have any trouble with testing for PML. A lot of us have been on Tysabri since before the test came out for the trial and some folks are having a hard time being tested.

Good luck with whatever you decide. Let us know how it goes!
Thanks! my only problem is that they never even spoke to me about the program, jsut said they wanted to start me on it. i was disappointed i am still waiting on any treatment besides gabapentin. i'm worried i wont get any better (i currently use a walker but can walk without it through the house- sometimes). i got an "infusion blanket" in the mail the other day but other than that havent heard anything. someone from the clinic called me on thursday, but only asked me to call, then didnt answer or return my call...................... frustrating!
__________________
Multiple Sclerosis Diagnosed August 2010
clarkstar is offline  
"Thanks for this!" says:
Grammie 2 3 (12-04-2010), Natalie8 (12-07-2010), Riverwild (12-07-2010), shayna (12-09-2010)
 


Posting Rules
You may not post new threads
You may not post replies
You may not post attachments
You may not edit your posts

BB code is On
Smilies are On
[IMG] code is On
HTML code is Off


Similar Threads
Thread Thread Starter Forum Replies Last Post
LDN Information & Check-in 2 SallyC Multiple Sclerosis 827 07-07-2017 09:46 PM
Tysabri Information & Check In Curious Multiple Sclerosis 988 04-16-2009 05:09 PM
LDN Information & Check In SallyC Multiple Sclerosis 844 01-15-2009 11:40 AM
Part 2...Medicare Part D/Prescription Coverage Stitcher Parkinson's Disease 1 12-17-2006 12:50 AM


All times are GMT -5. The time now is 08:41 AM.


Powered by vBulletin • Copyright ©2000 - 2025, Jelsoft Enterprises Ltd.

vBulletin Optimisation provided by vB Optimise (Lite) - vBulletin Mods & Addons Copyright © 2025 DragonByte Technologies Ltd.
 

NeuroTalk Forums

Helping support those with neurological and related conditions.

 

The material on this site is for informational purposes only,
and is not a substitute for medical advice, diagnosis or treatment
provided by a qualified health care provider.


Always consult your doctor before trying anything you read here.