Guest guest Posted November 20, 2010 Report Share Posted November 20, 2010 Morning-I am one of those seldom heard from lurkers. I would appreciate talking with someone who is/has been on Tysabri. Also would love to connect with someone from Missouri who is taking Rebif or Copaxone. Appreciate your time tyvm. Sherri Quote Link to comment Share on other sites More sharing options...
Guest guest Posted November 20, 2010 Report Share Posted November 20, 2010 Hey Sherri! It's good to hear from you. Kate was on Tysabri so you will probably hear from her. Which drug are you on now? How are you doing? hugs SharonThis email is a natural hand made product. The slight variations in spelling and grammar enhance its individual character and beauty and in no way are to be considered flaws or defects. To: MSersLife Sent: Sat, November 20, 2010 7:53:44 AMSubject: Tysabri Morning-I am one of those seldom heard from lurkers. I would appreciate talking with someone who is/has been on Tysabri. Also would love to connect with someone from Missouri who is taking Rebif or Copaxone. Appreciate your time tyvm.Sherri------------------------------------ Quote Link to comment Share on other sites More sharing options...
Guest guest Posted November 21, 2010 Report Share Posted November 21, 2010 Sherri, I'm not from Missouri, but I do take Copaxone.. If I can be of assistance in this area, feel free to ask away on any questions you might have.. HUGS |)onna Morning-I am one of those seldom heard from lurkers. I would appreciate talking with someone who is/has been on Tysabri. Also would love to connect with someone from Missouri who is taking Rebif or Copaxone. Appreciate your time tyvm. Sherri Quote Link to comment Share on other sites More sharing options...
Guest guest Posted November 24, 2010 Report Share Posted November 24, 2010 Hi Sherri,I had been on Copaxone first, then on Tysabri from June of '07 til about Feb. of 2010. They only took me off because you are not supposed to be on it for more than 3 years or so.I found it helpful. I had been using a cane prior to the TY, and then no longer needed it about a few months into my infusions. I found the monthly infusions a lot less bothersome than every day shots, which I'm back on.If you have other questions, ask away or email me privately if you wish.Best of luck,glad to see you posting,KateTo: MSersLife Sent: Sat, November 20, 2010 9:53:44 AMSubject: Tysabri Morning-I am one of those seldom heard from lurkers. I would appreciate talking with someone who is/has been on Tysabri. Also would love to connect with someone from Missouri who is taking Rebif or Copaxone. Appreciate your time tyvm. Sherri Quote Link to comment Share on other sites More sharing options...
Guest guest Posted November 25, 2010 Report Share Posted November 25, 2010 what typems do tyou hae drs pout tis to me as a option for traing my spms have yoiu heard any suucces wth secosay and tysabri deb copeland > > Hi Sherri, > I had been on Copaxone first, then on Tysabri from June of '07 til about Feb. of > 2010. They only took me off because you are not supposed to be on it for more > than 3 years or so. > I found it helpful. I had been using a cane prior to the TY, and then no longer > needed it about a few months into my infusions. I found the monthly infusions a > lot less bothersome than every day shots, which I'm back on. > If you have other questions, ask away or email me privately if you wish. > Best of luck, > glad to see you posting, > Kate > > > > > ________________________________ > > To: MSersLife > Sent: Sat, November 20, 2010 9:53:44 AM > Subject: Tysabri > > > Morning-I am one of those seldom heard from lurkers. I would appreciate talking > with someone who is/has been on Tysabri. Also would love to connect with > someone from Missouri who is taking Rebif or Copaxone. Appreciate your time > tyvm. > > Sherri > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted November 27, 2010 Report Share Posted November 27, 2010 Hi Deb,I have 2 opinions. One is that I have RRMS, and the 2nd neuro I saw feels I have SPMS. I tend to go with the RRMS, but only G*d really knows the truth. I have no idea really. I've heard that a good many with secondary are good candidates for Tysabri.Let me know what you decide.hugs, KateTo: MSersLife Sent: Thu, November 25, 2010 11:53:38 AMSubject: Re: Tysabri what typems do tyou hae drs pout tis to me as a option for traing my spms have yoiu heard any suucces wth secosay and tysabri deb copeland > > Hi Sherri, > I had been on Copaxone first, then on Tysabri from June of '07 til about Feb. of > 2010. They only took me off because you are not supposed to be on it for more > than 3 years or so. > I found it helpful. I had been using a cane prior to the TY, and then no longer > needed it about a few months into my infusions. I found the monthly infusions a > lot less bothersome than every day shots, which I'm back on. > If you have other questions, ask away or email me privately if you wish. > Best of luck, > glad to see you posting, > Kate > > > > > ________________________________ > > To: MSersLife > Sent: Sat, November 20, 2010 9:53:44 AM > Subject: Tysabri > > > Morning-I am one of those seldom heard from lurkers. I would appreciate talking > with someone who is/has been on Tysabri. Also would love to connect with > someone from Missouri who is taking Rebif or Copaxone. Appreciate your time > tyvm. > > Sherri > Quote Link to comment Share on other sites More sharing options...
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