
My Tysabri Diary...
Brief update from me...I would encourage all Tysabri users to send a brief (or long) progress report to: mspatientsforchoice.org/contact.htm. This will help many MS patients looking for information about how other MS patients are doing on Tysabri therapy :)
and copy and paste the following questions (with your answers) in the comment section.
Questions for his Tysabri Poll:
Your Name:
Your email  address: 
Your  Location: 
How long ago  Diagnosed with MS? 
Are you diagnosed  with RRMS (Relapse Remitting)?            
If  not, please provide your current diagnosis: 
Have you noticed a  progression of your disability since being  diagnosed?
If so, to what  extent? 
Prior to Tysabri,  which MS (FDA approved) medications had you  used? 
In what order, in  what order and for how long and with what  results? 
Why did  you  decide to switch to Tysabri? 
When (in 2006/2007)  did you begin taking Tysabri?
How many infusions  have you now had since Tysabri re-commenced in June  2006 ?
Had you previously  been on Tysabri? If so, when and for how long? 
How long did it take  for you to get started on Tysabri once you  decided you wanted to  start?
Has the infusion  process gotten easier for you?
What favorable  remarks do you have since beginning Tysabri  Infusions?
(ie: infusion  process, fatigue  factors , strength, pain, walking ability,  etc.)
Do you  have any negative comments to inform  to others?
(if yes, please  explain)  (ie: infusion process, side effects,  etc.)  
What are your  expectations of Tysabri ? 
What if anything  have you heard from others, who are using  Tysabri?
Do you have any other comments:
______end of survey* Can I have your first born? <---laughing - I'm just kidding (wink) ... Stu will probably kill me for listing a joke question in his poll - but I did add a (*) !
*not in original survey (some parents were probably muttering to themselves, "darn it!") - lol - take care all :)
(((hugs)))
Lauren
A very proud member of www.MSpatientsforchoice.org




3 Comments:
At 3:11 PM, Cyndee said…
 Cyndee said…
Lauren, I tried to fill out the form and email it to your friend, but the link didn't work. Help.
At 10:10 AM, Anonymous said…
 Anonymous said…
Lauren,
I also tried to send you an email but it didn't work. I was diagnosed with ms three yrs ago and I have taken Copaxone and Avonex. Now they want to put me on Tysabri and I am terrfied! Please email me and give me some words of wisdom. I'm 31 yrs old and my last MRI says that it is going to my neck now :( I'm just scared of the the warning signs. My doctors want to put me on a 5 day steriod injection this week in order to slow down the fare up I'm having, but the warning label on the Tysabri state NO STERIODS. HELP
Thank you
Teresa
At 1:45 PM, Lauren said…
 Lauren said…
Michelle/Teresa,
Check your e-mails dearheart.
Lauren :)
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