tysabri webcast

http://www.clinicaloptions.com/Hepatitis/Live%20Events/Webcast/All-Oral%20HCV%20Therapy/Tabs/Agenda.aspx I have registered to watch this free webcast on Sunday, Nov. 9th. Agenda Welcome and Introduction Program Director: Nezam H. Afdhal, MD, FRCPI Showing Interferon the Door: HCV Therapy That’s Safe, Easy, and Effective Jordan J. Feld, MD, MPH The Patient Perspective on All-Oral Therapy All-Oral Therapy for Previously “Hard-to-Treat” Patients Paul Y.

Hi, We are pleased to announce that our partner the Cleveland Clinic is hosting a free live webcast about Lung Surgery. This webcast will be hosted by a thoracic surgeon from the Cleveland Clinic who will answer questions regarding lung surgery, new advancements, research and options for patients suffering with lung diseases. The free webcast is on 1/15 at 12:00 EST. To sign up, please go to http://www.clevelandclinic.org/health/ChatReg?

You can listen to the webcast from the presentation ARC gave yesterday by the first link given. They responded on ARC-520 as well as some others they are testing. Also, if you click on the 2nd link below it gives a presentation that I believe was presented at the IBC's 17th Annual TIDES Conference in San Diego a few days ago. Webcast link: http://ir.arrowheadresearch.com/events.cfm Slideshow link: http://files.shareholder.

the American Academy of Neurology and the NMSS have a live webcast on April 14, noon ET on this CCSVI topic. I understand that Dr. Zamboni will be part of the panel. http://register.mediasite.com/?nd=login&setsite=15 You have to register in advance and there is a place to write a question, if you wish. If you can't attend this webcast live, it will be available for replay later. I'm not sure if you still need to register to have access to the recorded version.

Well; yes and no. : ) I should have could have mentioned that 3x posted the wrong link. The one posted is for the annual shareholders meeting; good in 1 week Feb 11. Just go to Vertex home, click on presentations (it's on the left) and then choose the Feb 5 webcast. I would bet that the Feb 11 webcast will be a promising one. They won't post so much data but there may be some hints about the future. I got the vibe that the Prove 3 results were good.

The recorded webcast is now up at http://hosted.mediasite.com/mediasite/Viewer/?peid=5625f9f8badd40eab1b1a3ebb41a8ba6 I haven't watched all of it yet between lack of time and the fact that it's been a little glitchy for me and keeps hanging. If you don't want to watch the whole thing, here are a couple summaries: http://www.wheelchairkamikaze.com/2010/04/comments-on-april-14-ccsvi-live-web.html http://www.facebook.com/pages/CCSVI-in-Multiple-Sclerosis/110796282297#!/note.php?

//www.patientpower.info/listenhealthtopicdetails.asp?showid=NMH102808&Topic=Thyroid%20Cancer Evaluation and Treatment of Papillary Thyroid Cancer ____________ Papillary thyroid cancer is the most common form of thyroid cancer in the United States. The symptoms of thyroid cancer can include a lump in the front of the neck, hoarseness or voice changes, trouble swallowing or swollen lymph nodes in the neck. In this webcast, Dr.

I like to recommend this webcast by Professor Anna Lok, presented by invitation at the recent CROI: webcast: https://www.croiwebcasts.org/console/player/51538?

VRUS) today announced that it will webcast an investor event from the European Association for the Study of the Liver (EASL) on Saturday, April 2, 2011 starting at 8:00pm CET. During this webcast, management will review Pharmasset's progress on the programs that are the subject of presentations at EASL.

I was exhausted on Tuesday to go LIVE on the webcast offered with Dr. Oz with the series Oprah is promoting for better health. I did however get up today and watch the whole broadcast with many topics I'd like to share with you. Most of it WAS Thyroid related. Today - Tuesday, January 15 her show will go into an indepth look at the endocrine system- hormone imbalances (THYRIOD) and others glands too.

They found out the reason people contracted PML was because they were taking Avonex/and the other MS medications with Tysabri. I think the Tysabri has given me a second chance at helping slow my disease progress, but with out it I would be on no MS medications to slow the disease. I did alot of research before I decided to start the medication and the one resource that helped me make my decision was reading the Tysabri diaries on line. www.msrc.co.uk/index.cfm?

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.

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.

I would like some information/details from anyone who has had (or seen) the rash you can get from Tysabril and/or PML?? I have been on Tysabri 10 years so far without any major issues. I was outside after my treatment for 10 minutes or so. After taking my shirt off, my husband gasped and asked what was wrong with my back.

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.

My new neuro suggested Tysabri based on increased lesions on Interferon (Rebif). Any persons out there on Tysabri that could share their experience?

He feels that Tysabri is the way to go. I know that there are others here on it or used to be. I would love some insight on what to expect, how long it takes, etc... Thanks!

I will start tecfidera in 3 months I hope I dont have the rebound effect I have heard about after stopping tysabri. Tysabri has really changed the way I feel was using a walker now nothing and I do Zumba too. I hope I stay like this but having doubts. anyone using tecfidera? How was your experience.?

So now he wants to take me off of the Copaxone, I have been on for a month and a half, and put me on Tysabri. I started the application process and now waiting for them to call me and get the ball rolling on that. Now he mentioned that this is the top of the line MS medication so that does give me some relief. P.S. I did test negetive for the JC Virus. Any thoughts, experiences etc on this Tysabri??!!

The research side of my MS Practice has identified a CSF biomarker for disease activity. The research is featured on the cover of this month's Multiple Sclerosis Journal. http://tischms.org/news/tisch-ms-breakthrough-biomarker-research-featured-cover-article-october-2013-issue-multiple I'm a beneficiary of this discovery. I had been on Tysabri for 20 months. At 18 Months I converted to JCV +, and we discussed switching from Tysabri to Tecfidera.

The campaign will culminate with a real-time webcast from Massachusetts General Hospital on Sept. 24, featuring members of the coalition, survivors of ovarian cancer and their family members, and physicians discussing the disease's diagnosis, treatment, and heredity To view the live webcast: URL: http://styleforfree.com/OCA.html To view the recorded, on-demand webcast: URL: http://styleforfree.com/OCA.

side effects for each other medicine and now this with tysabri. Has anyone else been on tysabri and developed c. Diff from it? If so, what did they do to help it? Stop tysabri? Any information would be greatly appreciated.

There is an alogirthm for the chances of contracting PML while on tysabri. I believe it is on the tysabri website among other places. I will see if I can find it for you and report back.

Tysabri webcast

Common Questions and Answers about Tysabri webcast

tysabri