Guest guest Posted September 28, 2005 Report Share Posted September 28, 2005 Thank you for sharing this Darlene! Didn't make me sleepy at all! LOL Hugs, Challis Sharon, I'm finally responding to your email. I was on the Antegren/Tysabri for the Phase II study in 2000. One of 213 patients. Scientist called me after the study and said I have the real stuff. This was a year study...the first few months they did MRI's, blood work, you name it. Tysabri is a monthly INFUSION not a shot. This is no exageration on how GOOD the Tysabri did for me. Before the study I was on the Avonex and had to stop the Avonex for a month before testing me to see if I qualify for the study. The first 3 months the scientists did MRI's blood work, NO infusion yet. I wasn't feeling very well and I tell ya, I went from walking/cane to BAM a wheelchair. Looking back I feel that it was a foggy dream/nightmare and not reality. I had no feeling from the waist down and my hubby had to carry be up/down stairs in our house. I was basically Wheelchair bound. OK so here I am having a major exacerbation taking my walking away so I asked the Doc's to give me steroids since that had always helped me in the past with optic neurtis and legally I knew they couldn't refuse me to receive steroids. The first monthly Antegren/Tysabri infusion I had, I started to feel a little better, next month -second infusion...better....third month infusion the best. I went from WC to COMPLETELY NORMAL. I continued to be completely normal during the 6 months of infusions. We had a barbeque at out house for the 4th of July. I was walking/talking completly normal. No cane, no balance problems, no numbness..... A neighbor came up to us and asked, if I was the young lady that she saw in the WC. She couldn't beleive her eyes how I was. I had a little pump (High Heel) on. Music was playing and I was on cloud nine. OK, I had my LAST infusion....the next 3 months would be going in for MRI's/bloodwork. The very NEXT month of my LAST infusion I started to loose my balance a little. It was amazing how I started to loose my balance. It has been 5 years since I had the Tysabri, and I am very fortunate that I did not go back in to a WC. I know this is a long email but all I have to say is that Tysabri worked wonders for me. Yes, I was a guinny pig and I chose to do that. I have NO regrets at all and once the Tysabri is approved I'm going back on it. The good news about Tysabri is that it is in a different catagory than the ABC/Rebif drugs. It has to do with the blood brain barier. My mom, hubby, daughter, neighbors all just shook their head in disbeleif to see how I went from WC to normal. I can tell and give everyone hope in regards to this........I was in the WC and had NO feeling from waist down and somehow my mylan repaired itself. Over 60% of patients on the study had good results. Yes, it was very unfortunate about the latest tradegy with the Avonex/Tysabri patient that died. That was the chance that I took too, when I signed on the dotted line to be in the study. Sharon, I'm glad to here that your Doctor is for the Tysabri. As we all know it is a very touchy subject. Reviewing the results of the study though says that something is there..................I didn't have any side affects that I remember. I was just so excited from WC to walking that I didn't pay much attention if I did. The good news is that it is MONTHLY and it is an INFUSION. Just like all of you receiveing the steroids through infusion. This is how I look at it. I'm currently on the Rebif shots and I don't know if it is helping me, of course since it is for future problems to slow it down. But since I saw it with my own eyes what the Tysabri did, I have to say that there is no better treatment for ME. I hope I didn't make you fall asleep with this long email. LOL Hugs Darlene Kickin Cane Covers http://www.canecovers.org/ Quote Link to comment Share on other sites More sharing options...
Guest guest Posted September 28, 2005 Report Share Posted September 28, 2005 Gee, I will keep you in my prayers!!!! Here I complain about taking 3 shots a week with the Rebif. Is your body marked up with red welts. I only take my Rebif shots on the left/right hip/buns area. It is always sore and you can visable see my marks. Monday night when I took my Rebif shots, I had a BAD night. My whole body felt like sand paper and I felt like I was freezing. My feet always feel like frozen blocks as I call it. Darlene Kickin Cane Covers www.canecovers.org --------- Tysabri & Darlene Sharon, I'm finally responding to your email. I was on the Antegren/Tysabri for the Phase II study in 2000. One of 213 patients. Scientist called me after the study and said I have the real stuff. This was a year study...the first few months they did MRI's, blood work, you name it. Tysabri is a monthly INFUSION not a shot. This is no exageration on how GOOD the Tysabri did for me. Before the study I was on the Avonex and had to stop the Avonex for a month before testing me to see if I qualify for the study. The first 3 months the scientists did MRI's blood work, NO infusion yet. I wasn't feeling very well and I tell ya, I went from walking/cane to BAM a wheelchair. Looking back I feel that it was a foggy dream/nightmare and not reality. I had no feeling from the waist down and my hubby had to carry be up/down stairs in our house. I was basically Wheelchair bound. OK so here I am having a major exacerbation taking my walking away so I asked the Doc's to give me steroids since that had always helped me in the past with optic neurtis and legally I knew they couldn't refuse me to receive steroids. The first monthly Antegren/Tysabri infusion I had, I started to feel a little better, next month -second infusion...better....third month infusion the best. I went from WC to COMPLETELY NORMAL. I continued to be completely normal during the 6 months of infusions. We had a barbeque at out house for the 4th of July. I was walking/talking completly normal. No cane, no balance problems, no numbness..... A neighbor came up to us and asked, if I was the young lady that she saw in the WC. She couldn't beleive her eyes how I was. I had a little pump (High Heel) on. Music was playing and I was on cloud nine. OK, I had my LAST infusion....the next 3 months would be going in for MRI's/bloodwork. The very NEXT month of my LAST infusion I started to loose my balance a little. It was amazing how I started to loose my balance. It has been 5 years since I had the Tysabri, and I am very fortunate that I did not go back in to a WC. I know this is a long email but all I have to say is that Tysabri worked wonders for me. Yes, I was a guinny pig and I chose to do that. I have NO regrets at all and once the Tysabri is approved I'm going back on it. The good news about Tysabri is that it is in a different catagory than the ABC/Rebif drugs. It has to do with the blood brain barier. My mom, hubby, daughter, neighbors all just shook their head in disbeleif to see how I went from WC to normal. I can tell and give everyone hope in regards to this........I was in the WC and had NO feeling from waist down and somehow my mylan repaired itself. Over 60% of patients on the study had good results. Yes, it was very unfortunate about the latest tradegy with the Avonex/Tysabri patient that died. That was the chance that I took too, when I signed on the dotted line to be in the study. Sharon, I'm glad to here that your Doctor is for the Tysabri. As we all know it is a very touchy subject. Reviewing the results of the study though says that something is there..................I didn't have any side affects that I remember. I was just so excited from WC to walking that I didn't pay much attention if I did. The good news is that it is MONTHLY and it is an INFUSION. Just like all of you receiveing the steroids through infusion. This is how I look at it. I'm currently on the Rebif shots and I don't know if it is helping me, of course since it is for future problems to slow it down. But since I saw it with my own eyes what the Tysabri did, I have to say that there is no better treatment for ME. I hope I didn't make you fall asleep with this long email. LOL Hugs Darlene Kickin Cane Covers www.canecovers.org -------------- Original message -------------- Okay, Darlene... tell me how you felt on Tysabri. How long were you on it? Tell me all about it, please. My neuro gave me a "talk" about Tysabri and said he wanted me to "really seriously consider" going on it when it comes back on the market. I AM seriously considering it. I really trust my neuro and I know he believes in this drug. I am so seriously considering it that I think I'll go see my other good former neuro, Dr. K., and see what he says. Dr. K. is the neuro who dxed me and I quit seeing him only because the insurance stopped covering him. But now I have Medicare and I know he takes that. Sharon Sharon (MSersLife creator/owner) “One minute it's a giant cabbage and the next, ka-boom! You've got cole slaw all over you." V.R. , Palmer, Alaska, where Cabbages grow huge Yahoo! for GoodClick here to donate to the Hurricane Katrina relief effort. Quote Link to comment Share on other sites More sharing options...
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