Tysabri on utube

Common Questions and Answers about Tysabri on utube

tysabri

535822 tn?1443976780 Check out something interesting happening its a video on utube called 'We the People Declaration to Revoke and abolish M.MV' its very long but worth the time ...
535822 tn?1443976780 a video on utube called 'We the Peoples Declaration to Revoke and Abolish M.MV' read and listen its very interesting ..
Avatar f tn I WAS WONDERING DO ANY1 ON HERE DO VIDEO LOGS ABOUT PREGNANCY OR TTC ON YOUTUBE???
572651 tn?1530999357 Thanks for the update! Good to know the only side effect was a one nighter. Looking forward to hearing more as your journey continues.
8398640 tn?1398042546 m hoping this sort of discovery gets us closer to finding an actual cause, and not just developing a pharmaceutical band-aid, for MS. I glad to be on Tysabri.
233622 tn?1279334905 I am not doing well on any DMD. After 2.5 years trying my neuro has decided to try Tysabri. I have to have a blood test first. I am looking forward to trying it after reading the results others have had. I personally know someone on it and she is doing so well now. I am tired of being sick!
Avatar n tn Look up Magellons Disease on Utube. Tons of people have it but there is much info on Utube about it. Also, it could be muscles and the nerve bundles within them or lower back problems. If you slowly stretch very slowly sitting trying to reach for toes and after wards you get that feeling then it is the nerves within the muscles that have not been stretched out enough. Be gentle.
645390 tn?1338555377 I never got nauseous on Tysabri. After 8 months on it, I started getting skin lesions, and my skin was REALLY dry. Much drier than usual. I still love the stuff, though. I will probably go back on it by the end of the summer.
Avatar f tn Hello, I just finished #12 of tysabri. they did a 5 day infusion of Solmedrol,after that I noticed my scalp was itchy and I had little bumps ALL over my head. anybody else??? it is driving me CRAZY. IAM TO START a pill soon.
Avatar f tn I recently had my 9th infusion. I've noticed a fiery joint pain in my knees 3-5 days after my infusion for the past few months. It eases after a week or so but doesn't go away completely. My doc doesn't think it is Tysabri because only my knees were effected. As time goes on I feel like more joints are involved. After my last infusion (5 days) I'm experiencing the same "fiery" feeling in my toes and stiffness in my hands.
738075 tn?1330575844 Dang! I started taking Baclofen a week and a half ago, and within 2 days, I became extremely weak. I had a gig coming up, and I couldn't even complete one song in rehearsal, let alone 2 hrs worth of stuff. So, last Saturday, I weaned myself off the Baclofen to see if my strength would bounce back - and it didn't! It got worse! By Tuesday (yesterday) I was so dragged out I went into my Neuro's office while he was finishing his lunch.
572651 tn?1530999357 from Tysabri could affect its sales growth, and that prospect weighed on shares of Biogen and Elan on Friday. Shares of Cambridge, Mass.-based Biogen recently fell 5.8% to $44.49, while the American depository receipts of Dublin-based Elan plunged 20% to $5.17. Biogen spokeswoman Naomi Aoki said the incidents of PML remain rare, reiterating the company's contention that the rate remains within the 1-in-1,000 patient level implied by its label. As of Sept.
Avatar f tn t know what you ultimate decision will be on going with Tysabri but hope that you will get the relapses under control. I have been on copaxone for 6 months now and my doctor thinks it is not working as well as he'd hoped, but I'll stick with it awhile to be sure. Take good care and thanks for bringing up a very good and relevant question.
1088527 tn?1425313375 Hi Kat - I will get my 11th infusion in about 10 days. I have had no issues of any kind in conjunction with Tysabri. From the follow up MRI's I've had Tysabri seems to be doing the trick. No new lesions or relapses since I started. You will be tested for the JC virus prior to starting.
2015036 tn?1332997788 Some of you probably received the same email I did. Biogen sent me an email saying they could now help people get financing, even if you're on a Medicare plan. So far, only Biogen is working with Medicare patients. There's a lot of paperwork involved, but it look like I'm finally going to start a DMD again. All of Biogen's MS meds are available for the program: Avonex Plegridy Tysabri Tecfidera It's worth calling about.
382218 tn?1341181487 Have MS but only on sx control - currently Gabapentin - but live in UK so nothing unusual.
Avatar m tn My initial diagnosis was SPMS. My doc started me on Tysabri immediately. He wanted to be as aggressive as possible. I've been on it for 17 months now, and so far, so good!
Avatar f tn Are any of you on Tysabri? My doctor has suggested that I consider starting Tysabri treatment. His neurology practice runs a TOUCH infusion center. I've been on Copaxone for four years and have just had my first flareup. My recent MRI shows progression of MS with T2 hyperintense white matter lesions in the pons of the brainstem and the frontal lobe. Several of the older lesions have increased in size. Five years ago I was on Avonex. I had multiple flare-ups the whole year on this med.
Avatar f tn I have had MD for 18 years. Been on Avonex, Betaseron, Tysabri, and now Tecfidera. Unfortunately, I'm also on lots of other medications, mostly due to terrible central pain. My neurologist made me stop the Tysabri after 24 infusions because of safety concerns. I felt my overall best while on Tysabri and have asked him if and when I might be able to go back on the monthly infusions. He does not have an answer for me at this point.
1948771 tn?1324402334 there are quizzes on the net you can search for, and if you check out utube there are lots of videos of moms to be doing fun tests or talking about the different ones they have done... there is the ring test, the pencil test, the cabbage test...all on utube... check it out theres some other too...
572651 tn?1530999357 I've been tested twice in the last year, and they were both negative. Since you can acquire JCV at any time, I opt to have my status tested once a year since I'm on Tysabri. There is also a Tysabri antibody titre available, now. I plan on doing that once a year, too, although development of Tysabri antibodies is relatively rare.
1827617 tn?1317703371 My new neuro suggested Tysabri based on increased lesions on Interferon (Rebif). Any persons out there on Tysabri that could share their experience?
620923 tn?1452915648 I like the idea of chiari awareness, I watched this thing on the news about how a girl posted a video on MS to raise awareness and it ended up going global. It would be great if there was something like that that we could put together. I find in Canada that there really needs to be more information, there are not many people or NS that are familiar in this field.
Avatar f tn Do you mean you have something on your eyelid? if on eyelash the eyelash is usually just pulled out. If on the eyelid I have no way of telling how big of a deal this is. You really need to ask your surgeon.