tysabri september 2010

( I am not thrilled w Tysabri at this point. Was doing really well on it, from Jan 2010 until the summer when I lost my voice for 3 months. Tysabri was D/C then per Neuro. In case that was a side effect. I went back on Tysabri in Dec. My voice is still an issue. Neuro doesn't know still if side effect, and is leaving it up to me if I want to stay on. She would like me to stay on it, as there is no other alternative for me at the moment.

I've been on Tysabri since 2012 and tested + before I started. Some months I feel better, some I don't.

I have read on here by several members, that they have not considered Tysabri or Gilenya because their MS is not that aggressive. What does that mean? I was dx Jan 2010, MRI showed approximately 10 lesions, I had a real hard time accepting my dx....I really wasn't sure I had MS, so I refused a DMD. Then in Oct 2010, I had a new MRI that showed an additional 5 lesions. My Neuro said that we needed to get aggressive and he suggested Tysabri and/or Gilenya.

I am trying to do a current post for all the September 2010 due dates, since by now almost everyone should have found out (if they wanted to) what gender their baby/babies is/are going to be. Just thought it would be fun to view everyone whos due around the same time =0) So if you would like to join just go ahead and send me a message with your due date and baby/babies gender. I will post this in a few days, so get back to me ASAP.

i did get my meds and they take up an entire shelf of my refrigerator. so i know what you mean hey the thread moved to the cycle buddies september 2010> there are i think 6 of us on there and we would love to have you. i start my lupron injections on this friday morning then i begin my fsh and lh on the 4th with lupron still projected er is the 17 of september with a 5 day transfer planned for the 21st or 22nd.... so how far have you gotten do you have your calendar?

Due to 3 new lesions since the start of my Copaxone in September 09 and a failed 6 month attempt at Rebif my neurologist wants me to consider Tysabri. Yes PML is a concern but a very small one....my concerns with Tysabri are the other side effects like joint pain, increased depression, and weakened immune system. I work in healthcare in an outpatient lab and draw blood from ill people daily. Last year a co worker contracted H1N1 quite possibly from another patient.

Hi, Yes I have MS, I was diagnosed in Dec. 2010, I have being with a lot of symtoms, especialy that invisible symtoms, like ms hung, electricity and more. I was in Copaxone for about one year, then my neuro decided to move me to tysabri, I started tysabri two months a go. But I don't feel good.

t - I have been on copaxone and am now on Tysabri. Perhaps someone else here has experience with Aubagio and will speak up.From you name I am going to assume you are on Rebif?

Hi, I am Barb. I was diagnosed with MS in late February/March this year. My first symptoms started in May 2010 but I really got "sick" in the fall of 2010. That is when I really felt the stress on my body. That stress really took a toll on me. I felt sick for about a year and half. I still do feel sick (fatigue, neurological symptoms and overall weakness) but there has been some improvement between flares it seems. For the last year and half, though, I was sick.

Could you give us a little background on what meds you've tried and for how long? I'm sure you've mentioned it before but I have a hard time keeping track of so much.

) Think I am sticking with Tysabri for now, seeing neuro as well tomorrow and I know I will get a good report. Having a great summer with my boys... Just a quick update. I haven't been on the boards for some time, not too much extra time right now. I imagine September I will be back more often. (It is strange, i rarely think of MS anymore. I would love for that to stay.0 The only thing that has been increasing is Migraines.

I just went to the neurologist yesterday and he didn't tell me anything good. I was diagnosed in August of this year and I have been on Copaxone for two months. I just recently started having tingling in my back and some numbness in my bottom lip. I thought I might be having another attack. The neurologist said he does think it's another attack and that it is probably effecting my brain stem because of my symptoms.

I have been on Rebif for 8 years but my most recent MRI shoes several new lesions since 2010 and dr wants me to change therapies. I have ruled out going to another type of injection and don't think I should do Tysabri yet. Does any one have experience with switching over to Tecfidera, Aubagio , or Gilenya ? The new lesions are in the cerebellum and have caused walking and balance issues. Thank you in advance for any advice or info.

My neurologist says that the symptom flareups I've had since 2010 are only pseudo-exacerbations because the MRI I had in 2010 showed no enhancing lesions so the MS isn't active. Thoughts?

Last September 8, 2010, I donated blood. The blood was screened negative for HIV 1 and 2, Syphilis and Hepatitis B and C. I had a high risk activity last August 19, 2010. It involves an unprotected anal sex with a male stranger. I was the "top." My question: Is the blood screening last September 8, 2010 a reliable one to secure that I'm free from HIV at this point? I had been anxious for weeks already.

Hi, After using the glasses a long time almost around 18 Years while having a high nearsightedness (L: -11.0,-2.5 R: -12.0,-2.5) I had gone for Lasik in the year 2004. After Lasik I was very happy as there was a great improvement in vision in both of my eyes. Since than I was not using any glasses till September 2010. What went wrong in September 2010 I don't know but one day I notice that I have scattering from the edge of the bright objects in my right eye.

i had sex on the 4th of september 2010 and i was supposed to see my period on the 29th of september 2010 but it didnt come. i did a pregnancy test and it said i was pregnant.i took gynaecosid on the 6th of october but i still have not started bleeding.

he has been on betaseron for 2 years, ivig for 2 years and tysabri for 2 years. he has not ben on any meds since aug 2010. he is now on steroids and has to decide what med to go on. he had to stop the tysabri because he was building up antibodies against the medicine. he former doctor suggested he go off it and consider the oral medince. since then his doctors prtice closed and now we are seeing a new doctor. we are very confused. does any one have any advice?

Tysabri september 2010

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