advertisement
Reply
 
Thread Tools Display Modes
Old 05-08-2012, 06:26 AM #1
Lynn's Avatar
Lynn Lynn is offline
Member
 
Join Date: Sep 2006
Location: Australia
Posts: 660
15 yr Member
Lynn Lynn is offline
Member
Lynn's Avatar
 
Join Date: Sep 2006
Location: Australia
Posts: 660
15 yr Member
Default Tysabri and JC+

Hi everyone

I got the result of my JC test back today, and I am JC positive. I am up to about infusion 40 on Tysabri, and I am wondering what others are doing in this situation.

The question now, is do I continue with something that works brilliantly for me - and take the risk (which is about 1 in 400 of getting PML as opposed to 1 in 10,000 for JC negative). I am thinking I willl stay on Ty, but remain vigilant. Any other knowledge, ideas or opinions are more than welcome.

Thanks

Lyn
__________________
Lyn
.



Multiple Sclerosis Dx 2001 Craniotomy to clip brain aneurysm 2004. ITP 1993.
Lynn is offline   Reply With QuoteReply With Quote
"Thanks for this!" says:
Kitty (05-09-2012)

advertisement
Old 05-08-2012, 12:13 PM #2
SallyC's Avatar
SallyC SallyC is offline
In Remembrance
 
Join Date: Sep 2006
Location: SW Ohio
Posts: 17,844
15 yr Member
SallyC SallyC is offline
In Remembrance
SallyC's Avatar
 
Join Date: Sep 2006
Location: SW Ohio
Posts: 17,844
15 yr Member
Default

I'd run like a bunny as far away as I could get. But that's me and you are you. I'll pray for you and wish healing thoughts for you whatever your decision..
__________________
~Love, Sally
.





"The best way out is always through". Robert Frost



~If The World Didn't Suck, We Would All Fall Off~
SallyC is offline   Reply With QuoteReply With Quote
"Thanks for this!" says:
Dejibo (05-09-2012), dmplaura (05-09-2012), Kitty (05-09-2012), Lynn (05-09-2012)
Old 05-08-2012, 12:20 PM #3
Kitty's Avatar
Kitty Kitty is offline
Wisest Elder Ever
 
Join Date: Jan 2008
Location: Deep South
Posts: 21,576
15 yr Member
Kitty Kitty is offline
Wisest Elder Ever
Kitty's Avatar
 
Join Date: Jan 2008
Location: Deep South
Posts: 21,576
15 yr Member
Default

I'm like Sally. It scares me! But everyone is different and I can imagine how hard it would be to stop if it's helping like it is. Why does it all have to be so difficult?
__________________
These forums are for mutual support and information sharing only. The forums are 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.
Kitty is offline   Reply With QuoteReply With Quote
"Thanks for this!" says:
ANNagain (05-08-2012), Dejibo (05-09-2012), dmplaura (05-09-2012), Lynn (05-09-2012), SallyC (05-08-2012)
Old 05-08-2012, 05:23 PM #4
ANNagain ANNagain is offline
Senior Member
 
Join Date: Nov 2011
Location: Boston
Posts: 1,105
10 yr Member
ANNagain ANNagain is offline
Senior Member
 
Join Date: Nov 2011
Location: Boston
Posts: 1,105
10 yr Member
Default

Lynn,

I am with the others, i think I'd stop it but I'm not in your shoes. I have a close friend who is somewhere in her 40+ doses and she is JC positive and she stayed on it. She had good reason- it's the only thing that got her MS under control. I was scared for her before and more now but it is her life.

It is a very tough decision.
ANN
ANNagain is offline   Reply With QuoteReply With Quote
"Thanks for this!" says:
Dejibo (05-09-2012), dmplaura (05-09-2012), Kitty (05-09-2012), Lynn (05-09-2012), SallyC (05-08-2012)
Old 05-09-2012, 06:50 AM #5
Dejibo's Avatar
Dejibo Dejibo is offline
Elder
 
Join Date: Jan 2008
Location: New Hampshire
Posts: 7,332
15 yr Member
Dejibo Dejibo is offline
Elder
Dejibo's Avatar
 
Join Date: Jan 2008
Location: New Hampshire
Posts: 7,332
15 yr Member
Default

Do your research. I know you have looked up the odds, but have you looked up what happens to that 1 in 400? have you seen the heart crushing videos of those that woke one morning feeling great, and then the next unable to feed themselves? Have you contacted anyone who has gotten PML? They usually welcome contact. Have you spoken to those that have been on it long term and have had not a single thing go wrong, other than it helped?

As long as you are making an informed choice, and not one with your fingers crossed and your eyes closed I will cheer lead you all day. Please dont make such a sizeable choice based on a wish. There are too many unknowns in this silly disease. Arm yourself and then decide.

if it were me on #40 and was found to be + I would stop. Ima chikin and scared to death of that stuff, but thats just me. i wish you the best of luck, no matter what you chose.
__________________
RRMS 3/26/07
.

Betaseron 5/18/07
.

Elevated LFTs Beta DC 7/07
Copaxone 8/7/07
.



.
Dejibo is offline   Reply With QuoteReply With Quote
"Thanks for this!" says:
ANNagain (05-09-2012), dmplaura (05-09-2012), Kitty (05-09-2012), Lynn (05-09-2012), SallyC (05-09-2012)
Old 05-09-2012, 08:50 AM #6
Lynn's Avatar
Lynn Lynn is offline
Member
 
Join Date: Sep 2006
Location: Australia
Posts: 660
15 yr Member
Lynn Lynn is offline
Member
Lynn's Avatar
 
Join Date: Sep 2006
Location: Australia
Posts: 660
15 yr Member
Default

Thank you all so much.

I really appreciate everyone's opinion - Dejibo, you have really made me stop and think - what a great post.

I have a lot of thinking to do.

Hugs
__________________
Lyn
.



Multiple Sclerosis Dx 2001 Craniotomy to clip brain aneurysm 2004. ITP 1993.
Lynn is offline   Reply With QuoteReply With Quote
"Thanks for this!" says:
Dejibo (05-09-2012), dmplaura (05-09-2012), Kitty (05-09-2012), SallyC (05-09-2012)
Reply


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
Anyone else on tysabri? barb02 Multiple Sclerosis 19 08-28-2008 09:06 PM
Tysabri? coletaterbug Multiple Sclerosis 4 08-19-2008 11:21 PM
Tysabri Snoopy Multiple Sclerosis 71 08-05-2008 08:39 PM
to take tysabri or not? debbie0395 New Member Introductions 6 04-16-2008 11:18 PM
To Tysabri or Not To Tysabri--That is the question! Keely Multiple Sclerosis 3 03-10-2008 11:46 AM


All times are GMT -5. The time now is 03:29 AM.

Powered by vBulletin • Copyright ©2000 - 2024, Jelsoft Enterprises Ltd.

vBulletin Optimisation provided by vB Optimise v2.7.1 (Lite) - vBulletin Mods & Addons Copyright © 2024 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.